Category: Health

  • MIL-OSI Global: Parents with disabilities have faced discrimination for years in the US, but new rules will help ensure that child welfare systems treat them more fairly

    Source: The Conversation – USA – By Elizabeth Lightfoot, Distinguished Professor of Social Policy, School of Social Work, Arizona State University

    Parents with disabilities have new legal protections. Westend61/Getty Images

    Parents with any kind of disability are much more likely to have some type of interaction with the child welfare system than other parents. This means they are more likely than other parents to be reported for child abuse and neglect and more likely to have abuse or neglect substantiated by child welfare workers. They are also more likely to have their children placed in foster care and more likely to permanently lose their parental rights.

    More than one-third of mothers with intellectual and developmental disabilities have an interaction with the child welfare system within four years of their child’s birth, and about one-fifth of all children in foster care have a parent with some type of disability.

    However, there is little evidence that parents with disabilities abuse or neglect their children at higher rates than anyone else. Instead, there’s evidence that many young adults raised by a parent with a disability have very positive childhood experiences.

    New rules that went into effect in July 2024 provide the first federal protections specifically for parents with disabilities. These new rules ban discrimination against parents and caregivers with disabilities throughout the child welfare system.

    Government is changing these rules

    I’m a social work policy researcher who has studied policies affecting parents with disabilities since 2007.

    In 2010, I found that three-quarters of states had laws which said that a parent’s disability could be used as the grounds for terminating their parental rights. Most of these state laws focused on parents with intellectual and developmental disabilities or mental health disabilities, though some listed physical disabilities and other types as well.

    Many of these laws were vague and used outdated language such as “mental deficiency.”

    Parental disability is the only grounds for termination of parental rights that focuses on a condition of the parent. The rest focus on behaviors. For example, parental poverty is not listed as grounds for termination of parental rights in any state, but neglect – a behavior – is.

    State laws were only one of the issues parents with disabilities encountered related to child protection. For years, there had been confusion as to how the Americans with Disabilities Act, the federal law banning disability discrimination, applied to parents in the child welfare system. Until 2015, most state courts denied ADA claims by parents with disabilities who believed they were discriminated against.

    In addition, most child welfare workers do not receive formal training on working with parents with disabilities. They are not trained in how to assess parenting skills or how to make accommodations to services that they typically provide, such as providing in-home parent training or conveying information in plain language. They might not know about the overwhelming evidence that parents with intellectual disabilities can learn parenting skills.

    This has historically led many child welfare workers to make decisions based on stereotypes or speculation.

    One of the main biases that parents with disabilities face is the “presumption of unfitness bias.” This is a widespread bias that parents are unable to parent solely because of their disability.

    This bias can lead child welfare workers to not consider that parents with disabilities can rely on “parental supports” to assist them in parenting, ranging from adaptive cribs and baby monitors to in-home helpers. It also can result in parents with disabilities being held to a higher standard than others.

    State laws specifically naming parental disability as a for termination of parental rights, the lack of federal protection, and widespread biases left parents with disabilities vulnerable in encounters with the child welfare system.

    Gaining national attention

    Two federal actions in the early 2010s brought national attention to parents with disabilities.

    First, the National Council on Disability, the independent federal agency that advises the federal government on disability issues, released a report in 2012 called Rocking the Cradle. That report focused on the widespread discrimination faced by parents with disabilities; highlighted and called for changing the state child protection laws; and called for the application of ADA protections in child welfare cases involving parents with disabilities.

    This report received a lot of media attention and led to more awareness of the plight of these parents.

    Then, in 2015, Justice Department and the Department of Health and Human Services released guidance directing child welfare agencies to protect parents with disabilities from discrimination. This was the first federal action indicating that the ADA and Section 504 of the Rehabilitation Act applied to child protection services.

    This guidance followed the departments’ investigation of the Massachusetts Department of Children and Families’ removal of a newborn baby from Sara Gordon, a new mother with a developmental disability, in 2012. The Department of Justice and the Department of Health and Human Services found that the state agency had made assumptions that Gordon was unable to take care of her child and unable to learn parenting skills. The state agency had also failed to take into account that Gordon had support systems in place. She lived with her parents, and her mother had quit her job to assist with parenting.

    Making progress for parents with disabilities

    The momentum for protecting parental rights has led to some positive changes.

    A few states changed their own child protection laws to address some of these problems before the federal government took action by providing new protections for parents with disabilities. In addition, the Department of Justice and Department of Health and Human Services have reached agreements with state agencies in Oregon, Georgia and Massachusetts related to discrimination against parents with disabilities.

    Despite this progress, parents with disabilities are still discriminated against by the child welfare system in many parts of the country.

    At the same time, I have no doubt that the federal government’s revision of the rules of Section 504 of the Rehabilitation Act is a major step forward for parents with disabilities.

    In particular, it is promising that Section  84.60 of the rule clarifies that disability discrimination is not allowed in any part of the child welfare process. Child welfare agencies throughout the United States now must ensure that they are not making decisions based on speculation, stereotypes or generalizations.

    Thanks to changes in the federal rule, when a child welfare agency evaluates how a child is being parented, the tools it uses must be backed by research. The evaluations must be conducted by a qualified professional and tailored to the needs of the individual parent. Agencies must ensure that parents with disabilities can participate in any services they provide. These services include parent-child visitation, parenting skills programs, family reunification services and child placements in foster care settings or in the care of another relative.

    Disability advocacy groups applauded this new rule when it went into effect in the summer of 2024.

    I believe these new rules will protect parents with disabilities when interacting with child protection authorities. They will also make it easier for child welfare agencies and state courts to recognize disability discrimination when it appears in their caseloads or on their dockets.

    Elizabeth Lightfoot receives funding from the National Institute on Disability, Independent Living, and Rehabilitation Research and the Arizona Developmental Disabilities Planning Council.

    ref. Parents with disabilities have faced discrimination for years in the US, but new rules will help ensure that child welfare systems treat them more fairly – https://theconversation.com/parents-with-disabilities-have-faced-discrimination-for-years-in-the-us-but-new-rules-will-help-ensure-that-child-welfare-systems-treat-them-more-fairly-238185

    MIL OSI – Global Reports

  • MIL-OSI Africa: World Health Organization (WHO) in Africa, International Federation of Red Cross and Red Crescent Societies (IFRC) bolster partnership for enhanced public health emergency response

    Source: Africa Press Organisation – English (2) – Report:

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    World Health Organization (WHO) in the African Region and the International Federation of Red Cross and Red Crescent Societies (IFRC) have endorsed a regional collaboration framework to strengthen public health emergency response, especially at the community level, and bolster health security.

    With the WHO in the African Region’s presence in 47 countries and the IFRC’s Africa Regional Office’s support of 49 National Red Cross and Red Crescent Societies in sub-Saharan Africa as well as over 1.4 million volunteers and 12 000 branches, the two organizations are leveraging their vast networks and presence on the continent to support governments in scaling up response at the community level.

    To address the ongoing mpox outbreak, WHO in the African Region and IFRC are reinforcing their long-standing collaboration to support Burundi and the Democratic Republic of the Congo to ramp up measures for an effective response to halt the outbreak. The collaboration can be expanded to include other countries facing active mpox cases, as well as other public health emergencies.

    “As the continent and the world face new and emerging threats, our enduring partnership remains crucial in safeguarding health, enhancing emergency preparedness, and building a healthier, more resilient Africa,” said Dr Matshidiso Moeti, WHO Regional Director for Africa.

    WHO and IFRC have collaborated for decades on the continent, driven by a deep-rooted commitment to save lives. The new collaboration framework will facilitate closer coordination and alignment in the response to health emergencies in Africa. It aims to enhance capacity-building in national health workforces, strengthen disaster preparedness and risk reduction, increase vaccine access and expand evidence-based action. The partnership will also streamline and integrate preparedness approaches within ministries of health and address the health impacts of climate change, among other priority areas for collaborative action across the continent.

    Approximately 500 000 IFRC volunteers are in the Democratic Republic of Congo, a country that accounts for 90% of all mpox cases in Africa. They have been trained in community-based surveillance, community engagement, risk communication and case management. 

    “Our volunteers are members of the community who have built social trust over many years. They generate large reservoirs of applied research and data on the health status of communities,” said Mohammed Omer Mukhier-Abuzein, IFRC Regional Director for Africa. 

    With an estimated ratio of one volunteer for every 200 people living in the Democratic Republic of Congo, the IFRC workforce will play a crucial role in passing real-time information about suspected outbreaks to WHO’s national mpox response team. This team includes polio experts who have demonstrated considerable effectiveness in previous disease eradication initiatives. 

    “By combining WHO’s technical expertise and national coordination with IFRC’s grassroots community mobilization, we can create a powerful and complementary response mechanism. This partnership ensures interventions are scientifically sound and locally relevant, setting a new standard for integrated and effective outbreak responses,” said Dr Abdou Salam Gueye, WHO’s Regional Emergency Director for Africa. 

    Epidemiological surveillance conducted in collaboration with IFRC will support the mpox vaccine rollout in the Democratic Republic of Congo, which is set to begin in the coming weeks. WHO will be able to use data to guide vaccines to where they are needed most. 

    WHO is supporting countries experiencing mpox outbreaks through multiple response strategies, including enhancing disease surveillance, vaccine introduction readiness, contact tracing, training and combating misinformation. 

    Distributed by APO Group on behalf of WHO Regional Office for Africa.

    MIL OSI Africa

  • MIL-OSI Asia-Pac: EDB launches “Love Our Home,Treasure Our Country 3.0” joint school national education activities to celebrate 75th anniversary of founding of People’s Republic of China (with photos)

    Source: Hong Kong Government special administrative region

    EDB launches “Love Our Home,Treasure Our Country 3.0” joint school national education activities to celebrate 75th anniversary of founding of People’s Republic of China (with photos)
    EDB launches “Love Our Home,Treasure Our Country 3.0” joint school national education activities to celebrate 75th anniversary of founding of People’s Republic of China (with photos)
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         The Education Bureau (EDB) today (September 24) held the “Love Our Home, Treasure Our Country” – Celebration of the 75th Anniversary of the Founding of the People’s Republic of China and Joint School National Education Activities Kick-off Ceremony. The Bureau announced that it will collaborate with Tung Wah Group of Hospitals, Po Leung Kuk, the Hong Kong Council of the Church of Christ in China, the Lok Sin Tong Benevolent Society, Kowloon, Hong Kong Subsidized Secondary Schools Council, Hong Kong Direct Subsidy Scheme Schools Council, Hong Kong Aided Primary School Heads Association and Subsidized Primary Schools Council to jointly organise the “Love Our Home, Treasure Our Country 3.0” series of joint school national education activities in the 2024/25 school year, with an aim of deepening students’ understanding of Chinese culture and strengthening their affection for and sense of belonging to the country.      The Deputy Chief Secretary for Administration, Mr Cheuk Wing-hing; the Secretary for Education, Dr Choi Yuk-lin; the Convenor of the Working Group on Patriotic Education, Ms Starry Lee; the Division Director of the Education, Science and Technology Department of the Liaison Office of the Central People’s Government in the Hong Kong Special Administrative Region, Dr He Jinhui, together with representatives from school sponsoring bodies, school councils and school head associations involved in the activities, jointly officiated at the kick-off ceremony. About 2 500 representatives from school sponsoring bodies and the EDB, principals, teachers, students and parents attended.      Addressing the event, Mr Cheuk said that the “Love Our Home, Treasure Our Country 3.0” joint school national education activities will further expand the scale of the event. Participating schools cover kindergartens, primary schools, secondary schools, special schools and sister schools on the Mainland. Joint school collaboration not only strengthens exchanges among schools but also combines strengths to develop resources, enabling a patriotic atmosphere and sentiments to extend continuously across school campuses in all districts of Hong Kong.      Mr Cheuk said, “Love for the country should be the value and sentiment of every Chinese national. Patriotic education and activities play an important role in nurturing the growth of patriotic sentiments.” He thanked practitioners from the education sector for remaining steadfast in their roles. Through learning inside and outside the classroom, students are given the opportunity to gain an in-depth understanding of the country’s history, culture and values from an early age, and experience the distinctiveness of traditional Chinese culture, thereby fostering their pride in being Chinese and enhancing their national pride and sense of responsibility and ownership.       The kick-off ceremony featured a variety of rich programmes, including the performance of the magnificent “Hymn to the Sun” by a joint school Chinese orchestra formed by nearly 90 students. In addition, over 100 students performed lion dances, martial arts and other dances. A choir composed of 75 principals from school sponsoring bodies, school councils and government schools marked the finale of the ceremony with a song to express their warm congratulations on the 75th anniversary of the founding of the People’s Republic of China.      Highlights of the kick-off ceremony will be broadcast on RTHK TV 31 at 1.30pm on September 28 (Saturday).

     
    Ends/Tuesday, September 24, 2024Issued at HKT 21:25

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    MIL OSI Asia Pacific News

  • MIL-OSI USA: Friends With Paws celebrates therapy dog at Calhoun County Middle High School

    Source: US State of West Virginia

    CategoriesEnglish, MIL OSI, US State Governments, US State of West Virginia

    MOUNT ZION, WV –  First Lady Cathy Justice announced today that one of the state’s newest therapy dogs through the Friends With Paws program is thriving and doing incredible work at Calhoun County Middle High School.

    Coco is a male Chocolate Labrador Retriever and was celebrated during a Pup Rally held at the school. Representatives from the First Lady’s Office, along with students, faculty, staff, and several other local leaders, were in attendance. 

    While Coco is the 29th dog placed through the program, a total of 38 Friends With Paws therapy dogs have been placed throughout the state.

    “We are thrilled to celebrate Coco at Calhoun County Middle High School,” First Lady Cathy Justice said. “Therapy dogs like Coco offer so much more than just a friendly face—they provide comfort, reduce stress, and create a calming environment for our students. These dogs are making a real difference, offering support when it’s needed most, helping children feel safe, and encouraging emotional well-being. Coco will be a cherished companion and an important part of this school’s journey toward a brighter, healthier future.”

    The Friends With Paws program places certified therapy dogs in several schools across the state, providing companionship and comfort for students in need of a boost. 

    Therapy dogs are specially trained to provide comfort and support to people in various tense environments. They can help people feel at ease, improve their mood, relieve anxiety, and remove social barriers. Therapy dogs are highly trained and certified to show their ability to work in stressful environments, ignore distractions, and provide therapy to people with diverse backgrounds and circumstances.

    “Coco fosters meaningful relationships and provides comfort to both students and staff, showing us that compassion and connection can profoundly enhance our school community,” Michael Fitzwater, Superintendent of Calhoun County Schools, said.

    Following today’s assembly, students and staff had the chance to spend extra time with Coco.
    “Calhoun Middle High School believes that every child deserves a safe and nurturing environment to thrive,” Michelle Paxton, Principal at Calhoun Middle High School said. “Therapy dogs, such as Coco, provide unique emotional support, and we are excited to see how this initiative can positively impact our students at Calhoun Middle High School.”

    The Friends With Paws program is a partnership between the Governor’s Office, West Virginia Communities In Schools (CIS) Nonprofit, and the West Virginia Department of Education. Therapy dogs are placed in schools within CIS counties where students are disproportionately affected by poverty, substance misuse, or other at-risk situations, and are in the greatest need of a support animal. The dogs serve as a healthy and friendly outlet for these students to address trauma and other social-emotional issues.

    “Coco has made an incredible impact at Calhoun Middle High School,” Assistant Superintendent of Calhoun County Schools Jeannie Bennett-Yoak said. “His presence brings joy, comfort, and a sense of calm to our students and staff alike. We are immensely grateful to First Lady Justice, her dedicated staff, Ultimate Canine, and Communities in Schools for providing such a valuable resource. The bond Coco has formed with our school community is truly uplifting and has significantly enhanced the emotional well-being of everyone here.”

    More information about Friends With Paws can be found in Communities In Schools: Friends With Paws, a documentary produced by West Virginia Public Broadcasting. Click HERE to view the documentary.
     
    A 2019 study published by the National Institute of Health found that a dog’s presence in the classroom promotes a positive mood and provides significant anti-stress effects on the body.

    In addition, research shows that the simple act of petting animals releases an automatic relaxation response. Therapy animals’ lower anxiety and help people relax, provide comfort, reduce loneliness, and increase mental stimulation. They are also shown to lower blood pressure and improve cardiovascular health, reduce the number of medications some people need, help control breathing in those with anxiety, and diminish overall physical pain, among other profound benefits.

    MIL OSI USA News

  • MIL-OSI USA: Governor Hochul Discusses Youth Mental Health at Summit

    Source: US State of New York

    Earlier today, Governor Kathy Hochul participated in a Concordia Summit Fireside Chat on Youth Mental Health in New York City.

    VIDEO: The event is available to stream on YouTube here and TV quality video is available here (h.264, mp4).

    AUDIO: The Governor’s remarks are available in audio form here.

    PHOTOS: The Governor’s Flickr page will post photos of the event here.

    A rush transcript of the Governor’s remarks is available below:

    Penny Abeywardena: Good afternoon. So, we’re going to talk about something that really should be on the top of minds for all of us, and that is the many aspects of phones and schools to explore today. And there is no one better to reflect on this than our mom-Governor, Governor Hochul.

    So there are two massive clusters of changing norms colliding over this past decade. Parents driven a lot by anxiety and concerns have been buying smartphones for their kids. How do I keep my kids safe in school? With mental health challenges and bullying, how can I make sure my kid is okay during the day?

    And then, can I ensure my kid is keeping up with the technology? And then let’s not forget that the smartphone and video game and social media industries have focused on maximizing and monetizing screen time. So now these trends are complex and interdependent, but there is leadership that is going to help address this. And so it is a pleasure to be in conversation with Governor Hochul on this.

    Now, I want to know what your aha moment is, and I do think this is a moment to reflect on personal experience. We were just talking backstage, I have an eight-year-old in the public school system here in New York City. This became a big issue over the last few weeks. And I was properly shocked because he’s eight. And so this is something that quite honestly all of us need to be thinking about. And so, Governor Hochul, through your personal experiences or insights, can you tell us what influenced you to really focus on this issue from a legislative perspective?

    Governor Hochul: Thank you, Penny, and for Concordia for elevating this issue. I was here last year talking about climate change, and I’m always happy to talk about that. I can give you the speech I gave a few hours ago. But this is something a year ago I would not have thought we’d be talking about here. But I am so happy that this has finally taken hold because as a mom, a parent, you are hardwired to protect your children. Full stop. You wake up in the morning, start thinking about them when they’re little, late at night when they’re out with their friends you don’t sleep until they’re back home. That’s how we are. And as the Governor of New York, my number one job also has to be to protect all New Yorkers.

    So, you asked what my aha moment was. About a year and a half ago, I started convening mental health roundtables because we knew we were starting to see the signs that young people in particular had not fully emerged from the pandemic. They are still stressed out. The statistics on suicide, especially for teenage girls contemplating suicide, the depression, the anxiety, it was off the charts. So, I started having meetings and gathering kids and talking all over the state, and there was one not that long ago where the young woman – we started talking about the impact of social media and how it really takes hold of them. They’re held captive to these algorithms that are designed to bombard them with information that they will like because it’s taking personal information about them and turning it around and pulling them in deeper and deeper.

    And I said to this young woman – she was telling me how “I’m getting bullied during the day and all these social media and everybody’s doing this and I’m missing out and I have FOMO,” I said, “What do you want us to do?” She goes, “You have to save us from ourselves.” And that was my aha moment, when I realized it’s hard for parents to say you’re going to be the only teenager in the school without a cell phone, it’s hard for the school district to take it on and say, “We’re going to be the heavies,” teachers have enough on their plates, they don’t have to be the enforcers. And I realized this calls for government intervention, and I’m not afraid to take on the fights, especially when we’re fighting for our kids’ mental health.

    That was when I said, “Let’s find out what we can do to control these social media companies,” and we can talk about our nation-leading legislation, but also I’m right now developing a policy that’s going to say, “Bell to bell, full school day, phones should not be in the hands of children because they’re being denied the chance to learn, the teachers are frustrated that they’re not paying attention anymore, but also it has taken them to negative places, and it’s horrible for their mental health.”

    Penny Abeywardena: It really is. And different levels at different ages and grades, the impact is even more optimized, right?” Now, it would be great if you could talk about the significance of the first-in-the-nation law you signed to combat addictive social media feeds. And I will say, I hope many of you realize this, Instagram changed their policy last week, and I’m assuming it’s because they’re seeing the serious movement that’s coming from around the country, led by –

    Governor Hochul: Well, that’s true. In the era of – waiting for industries to self-regulate in the best interest of consumers is probably never going to happen. So, I’m not holding my breath. We encourage the tech companies, social media companies to work with us. Obviously, you’re always threatened by lawsuits. And I said, first I have a lot of lawyers, I can hire any lawyer in the state I want so bring it on. But I’d rather not. I said, “Why don’t you get out of the courtroom and come into my conference room and help devise solutions, because you know what you’re doing. You know exactly what you’re doing. You design these algorithms that’ll capture all this personal data about any age, a 10-year-old, 12-year-old, 15-year-old,” and they’re using it to structure messaging around your interests.

    We worked with them, they resisted, they built a campaign against us, they spent a lot of money. And I was able to work with our Attorney General, Tish James, here in New York, and legislators, and work with a coalition of parents and Common Sense Media, and formed a coalition where we were able to fight back. And our legislation – which we encourage every other state to adopt, I hear California’s looking at this now – it basically says a couple of things: one, is you cannot collect private data about anyone under the age of 18. You can’t collect it, you can’t sell it. You cannot monetize our children’s mental health any longer, you’re barred from that. Secondly, you are forbidden, barred from being able to target young people with algorithms designed based on their tastes.

    Now, a young person is not prohibited from going to your sites. They can talk, they can go to all kinds of chat rooms, they can talk to their friends, they can do whatever they want. But you cannot target them. And that was a heavy lift for them, and it’s a heavy lift to get through in legislation, but we did it. I just signed it into law a few months ago, and I’m really proud of it.

    We’re working on the regulations, but I always think about the fact that they told us, “Well, we have no capacity to identify who’s under the age of 18. This is an impossibility.” It’s like, “You’re tech companies, you can do anything, figure it out.” And somehow, magically, Instagram announced last week, they figured it out.

    I have immense faith in their ability to solve problems even if it’s against their self-interest.

    Penny Abeywardena: And that’s really bringing everybody to the table. When we think about the efficacy of what you’ve been able to do, it really came down to really strategic collaborations. Can you talk about how you worked not only with parents and teachers, but unions? We talked about authorities and the police; I’d just be curious how everybody’s playing a part in all of this?

    Governor Hochul: That’s a great question because you can’t go into these battles alone, right? You have to have allies as you march into war. And here’s what we needed to have. First of all, many parents on their own have said they know how bad it is. They’ve seen their children, especially if they were able to get a cell phone at age 12, 13, 14, they turn into a different person. First of all, they lose the capacity over time to have real, genuine social interactions. They don’t make eye contact. They don’t talk to other students. In school, the cafeteria is silent. They’re silent when they’re in the schoolyard. They’re silent in the halls. And the school districts that – on their own – were courageous enough to ban them said they now hear children laughing, talking, even arguing, they’re communicating more.

    And it was stopped. It was a dead silence. It was so unnatural. So, I had to get teachers on board, that was the easiest one. 72 percent of teachers across this country say that they are tired of the distractions and their inability to communicate with students or make connections in a way that are positive relationships.

    This is, outside a parent, the most influential person in their lives is a teacher. And the teacher is trying to do the best they can, and they’re being thwarted. They’re not learning, but they’re also not making connections.

    They’re stunted in their growth. They’re not turning into young adults eventually, over time, and ultimately adults. And we needed teachers on board, principals on board, school districts on board, and I said in all my – I did roundtables all over the state with all these parties at the table. I said, “I’ll be the heavy, just blame me, say, ‘that mean Governor made us do this,’ I mean I’ll take that on.” Because as a mom, I know how important this is and it would have helped me enormously to tell my kids, “I would have let you have the cell phones in school, but hey, it’s the law, I can’t let you do that. I still love you and I’d let you do anything else.”

    It’s about relationships, the ability to say no, which I have no trouble saying to my kids, but some do. But I also need law enforcement, and this is interesting, because my kids were in middle school during Columbine, the very high-profile mass shooting, and you still say the word ‘Columbine,’ I get chills because I know what it did to my sense of security. And we have so many other cases since then, I just spoke about Uvalde at another forum.

    So I thought, I have to think about how this affects parents’ sense of security when they say goodbye to their most precious little child, whether it’s kindergarten or 12th grade. I talked to law enforcement, what they said was so striking. If there is a crisis on campus or in the schoolyard, in the school, a mass shooting, worst case scenario, the last thing you want children to be doing, the last thing, is looking at their cell phone, texting mom and dad, sending messages, maybe videoing because they want to be the one who captures this. First of all, you’re telegraphing where you are, okay? You’ll hear this. Also, the police said to me the place their attention has to be is not on their smartphone, it has to be on the front of the classroom where the teacher is going to lead them to safety.

    When I heard that, it was like the clouds parted. I said, that’s the argument for parents. They need to hear that. So we’re not through yet. I’ve proposed this and loosely I said I’m going to be developing a policy. I will be working with these same groups I just mentioned. Everybody to let them understand how important this is and it’s also when I think about employers in my state, I want to be able to let them know that when young people emerge from their educational process, they’ll be fully functioning adults who have social interaction skills, who’ll be able to have the creative collisions and talk to someone else, a colleague, and work in teams and strategize together and really be more productive instead of someone who’s, again, their existence for a number of years has just been with the virtual world.

    And I can’t control what happens after school. Like my nieces are on all night long. I said, who are they talking to all night long? Isn’t anybody sleeping? And so they’re not, because they’re talking to kids on the other side of the world, literally. So we also say no notifications, and parents have the ability to turn it off. Sorry, kids, you can’t have it on from midnight until 6 a.m. I think Instagram actually said 10 p.m. to 7 a.m., which I thought was extraordinary. So parents are being empowered. So now we have to educate the parents. This is what it looks like, this is how you handle it, and when your teenager gets, tries to get around it, this is how you undo what they did. We have to help the parents get through this as well, but ultimately, imagine a world where this never happened. We’re not dealing with these high rates of depression and anxiety in young people and the bullying that goes on in schools.

    One mom said her husband has to leave work every day to be there at the end of the day when the child comes home from school because he gets picked on so badly on his own cell phone, watching it all day long, people are saying that he’s about to commit suicide and they want to keep an eye on him.

    If that doesn’t hit you as a parent – what is happening? But a world where we say, no cell phones, we just go back to the way it was when we were younger.

    Penny Abeywardena: Yeah.

    Governor Hochul: And if you need to – forget your lunch or you need to figure out how you’re getting home at the end of the day, guess what? There’s phones in the office. It’s a radical idea. Go down the hall, talk to your counselor, talk to your principal, can I use the phone?

    Penny Abeywardena: Talk to someone.

    Governor Hochul: And maybe forget your lunch and you go hungry; you won’t do it the next day. That’s called learning about life, right? Consequences. So it’s, that’s how I was raised. I don’t know. Maybe I’m old school, but I want to save our kids. It’s this important. I have to work on this intensely to at least save our state’s kids and hopefully other states will follow. And a number have, there have been other states that have done it.

    Penny Abeywardena: I was curious what kind of advice you would give to other state lawmakers because we talk about these coalitions as groups, but they’re important constituents who vote. So they’re concerned about making parents angry and losing that support. And I’d be curious what strategies and ideas you would offer to other state lawmakers to take this on.

    Governor Hochul: Just looking at it globally, the easiest thing in the world is to do nothing. Just wait for someone else. “It’s too hard.” Believe me, there’s a lot of challenges in New York to be a lot easier to pass on to somebody else. And that has happened. And I’m the cleanup Governor. I have a lot of work to do to try and invest, we never invested in mental health in the state.

    For example, never, no one ever talked about mental health as if it was an issue at all. I invested a billion dollars in my first budgets and said, we have to deal with everything from the lack of training for more professionals to be in the field to school-based clinics, so we can treat the kids right in schools if they have challenges to the homeless on the subways, more beds in hospitals. We looked at it holistically and we’re making real progress. So my advice to them is just show some profiles and courage once in a while. Shock everybody. Do something that’s a little bit difficult on the front end, but we’re in the world to make a difference.

    And these positions are positions of great authority, but they also hold a lot of responsibility for us. If you’re not making a difference every single day when you’re in a position like I am, then just stay in bed. I mean just don’t even bother because your job is to make a difference. Find problems – the easy problems my brilliant staff will solve, the hardest ones are on my desk and that’s what a Governor is supposed to do. It’s just, and if you’re not going to fight for kids, who are you wanting to fight for? That’s a statement about your values.

    Penny Abeywardena: And building on that. So there’s a middle ground, right? There are these bags you can have in school, so the kids get their phones, they get to show up at school with their phones, but then put them in. We had an interesting conversation backstage, and I was wondering if you can share, you know, our kids are smart.

    Governor Hochul: Yeah, kids are very smart. There are a few school districts in New York, Schoharie School District, up near the Capitol. They went full board, they did it a couple years ago, they said it was hard, there was a lot of resistance, parents said no, teachers didn’t want to be enforcers, and now they’re so glad they didn’t. And people now, and they had signs in front lawns, protesting taking cell phones away from kids.

    Give me a break. So I know it’s coming. I know it’s coming. But, these, so they have these bags, and there’s all sorts of ways to do this, but there’s these bags that are magnetic. Teacher watches the children put them in the bag at the beginning of the school. Only the teacher can unlock it so at the end of the school day they’ll get their phone back.

    No one’s going to steal it. It’s safe. Some kids are showing up at school, the teachers told me, with two cell phones. They lock one up in front of the teacher. Okay, kids have burner phones now? Okay, or what parent is buying their kid two cell phones? Okay? And then they use the other one all day.

    The other thing I think is important for parents to know. One of the teachers, she said, “We have to deal with the integrity issues.” I said, “What’s that mean?” It’s a nice way of saying they’re cheating. The whole world, all the answers are sitting there on their lap, and they’re not learning because they don’t have to. Or they run off to the lavatory with their phone, even the schools that ban it but let you have it during lunchtime or during breaks. They’re looking up information that they’re never going to learn properly from. And people say they’re not going to learn how to use technology. What do you think they’re doing the second they get home?

    They have all night long they’re doing that. I can’t control that. That’s up to parents. The last thing I’ll say on this is – parents, watch what you’re doing too. Kids learn from you. If you won’t put down the cell phone at the dinner table, or when you’re talking to them after dinner, by the time they’re mid-teenagers, they don’t even want to see you, so work on them before that. I believe I speak from experience. But show the kids they matter. Go to one of your meetings and leave your cell phone on your desk. The world will not fall apart. Somehow, we got to this age of 2024, surprisingly, throughout most of history, without being able to be connected and scrolling while your boss is talking to you, or while your colleagues are trying to present something. Just show basic respect to each other. Let’s not forget those skills. Respect each other, put down the phone.

    Penny Abeywardena: Put down, and that they’re paying attention to you and what you’re doing. I want to, we’re about to run out of time, but you mentioned, can we just talk about the investment that you made in mental health and other educational initiatives. Can you just share some of the programs and initiatives you have coming up that essentially reinforce this legislative –

    Governor Hochul: Yes. Again, one of the most significant things we’re doing is the mental health services in schools. Yeah. And so we’ve had to ensure that we’re funding workforce training for a whole new generation of more people going into the mental health professions, because I can open up a clinic in every single school. I could never staff it. I have to work with the unions and the training programs and put money behind this and training in hospitals. And so part of ours is creating a whole new generation of more healthcare workers, especially focused in this area. So that’s one big area, but I would say this, we also just need services, wraparound services from the get-go. My job is to make sure that our children emerge with healthy minds and not needing a lifetime of mental health services because we didn’t do our jobs when we had them in school.

    Penny Abeywardena: That is a perfect conclusion. Thank you so much, Governor Hochul.

    MIL OSI USA News

  • MIL-OSI: China Medical System: New Drug Application for Vitiligo Indication of Ruxolitinib Phosphate Cream Accepted in China

    Source: GlobeNewswire (MIL-OSI)

    SHENZHEN, CHINA, Sept. 24, 2024 (GLOBE NEWSWIRE) — China Medical System Holdings Limited (the “Company”, together with its subsidiaries, the “Group” or “CMS”) is pleased to announce that on September 24, 2024, the New Drug Application (NDA) for vitiligo indication of ruxolitinib phosphate cream (the “ruxolitinib cream” or the “Product”) has been accepted by the National Medical Products Administration of China (NMPA). This is another substantial milestone for ruxolitinib cream in China, following the approval for Urgent Clinical Import by Hainan Medical Products Administration and approval for marketing in Macau for vitiligo, and it is also a key step in benefiting over ten million of patients with vitiligo in China.

    Ruxolitinib cream achieved positive results in Chinese Real-World Study. The primary efficacy endpoint was the proportion of patients in the treatment group who achieved F-VASI 75 response at week 24, which was 49.5%, significantly higher than the target value of 14.1% (p<0.0001). The study met its primary endpoint, demonstrating that ruxolitinib cream is effective in treating patients with nonsegmental vitiligo, reducing the area of the lesions, and repigmenting the skin. All secondary efficacy endpoints showed a trend of benefit consistent with the primary efficacy endpoint, and the treatment effect for vitiligo continued to improve with longer treatment duration. Adverse events mostly had severity levels of grade 1 or 2. No adverse event (AE) leading to discontinuation or withdrawal, and no serious adverse event (SAE) related to the study drug occurred.

    While advancing the process of NDA for the Product, the Group is conducting the transfer of ruxolitinib cream from overseas production to domestic production (localization technology transfer), which is being orderly promoted by the Contract Development Manufacturing Outsourcing Organization (CDMO), and the lab-scale and pilot trial studies have been completed and under scale-up production. The Group strives to complete the localization study as soon as possible, register in Mainland China and obtain marketing approval, so as to enable the Chinese patients with vitiligo to use the innovative product.

    Vitiligo is a chronic autoimmune disease characterized by depigmentation of the skin, which results from the loss of pigment-producing cells known as melanocytes. It is estimated that there are approximately 14 million vitiligo patients in China[1]. Non-segmental vitiligo patients account for approximately 85% of them. Topical corticosteroids (TCS) and calcineurin inhibitors (CI) are used off-label for non-segmental vitiligo, however, these therapies have clinical deficiencies with long-term adverse reactions of long-term treatment or limited efficacy[23]. If the Product being successfully approved for marketing in China, it will be the first prescription drug approved for repigmentaton in vitiligo in Mainland China, bringing novel treatment hopes for Chinese vitiligo patients.

    CMS has always adhered to its mission of providing competitive products and services to meet unmet medical needs. Guided by innovation strategy, the Group continuously strengthens its independent R&D as well as external collaboration, enriching its product pipelines. Looking ahead, CMS will continue to identify products with differentiated advantages globally and efficiently promote their clinical development and commercialization, bringing more novel and effective drugs to patients.

    About ruxolitinib cream
    Ruxolitinib cream, (Opzelura), a novel cream formulation of Incyte’s selective JAK1/JAK2 inhibitor ruxolitinib, is approved by the U.S. Food & Drug Administration for the topical treatment of nonsegmental vitiligo in patients 12 years of age and older, and is the first and only treatment for repigmentation approved for use in the United States[4]. Ruxolitinib cream (Opzelura) is also approved in the U.S. for the topical short-term and non-continuous chronic treatment of mild to moderate atopic dermatitis (AD) in non-immunocompromised patients 12 years of age and older whose disease is not adequately controlled with topical prescription therapies, or when those therapies are not advisable[5]. In Europe, ruxolitinib cream (Opzelura) is approved for the treatment of non-segmental vitiligo with facial involvement in adults and adolescents from 12 years of age[6].

    The Product is not approved by the NMPA for any indication in Mainland China. However, on 12 August 2023, the Product was approved by Hainan Medical Products Administration for Urgent Clinical Import, and officially became available to applicable patients in the Hainan Boao Lecheng International Medical Tourism Pilot Zone (the “Pilot Zone”) on August 18, for the topical treatment of non-segmental vitiligo in adults and adolescents aged 12 and above with facial involvement. Benefiting from the Early and Pilot Implementation Policy granted by the state to Hainan Free Trade Port and the Pilot Zone, patients with vitiligo in China can apply for the Product in Boao Super Hospital first and receive treatment from the expert team. In addition, ruxolitinib cream was approved by the Pharmaceutical Administration Bureau (ISAF) of Macau on 11 April 2024 for the topical treatment of non-segmental vitiligo with facial involvement in adult and adolescents form 12 years of age.

    On 2 December 2022, the Group through a subsidiary of the Company, a dermatology medical aesthetic company (“CMS Skinhealth”) entered into a Collaboration and License Agreement (the “License Agreement”) with Incyte for topical formulations of ruxolitinib for the treatment of autoimmune and inflammatory dermatology diseases. In accordance with the  License Agreement, the Group through CMS Skinhealth received an exclusive license to develop, register and commercialize the Product in Mainland China, Hong Kong Special Administrative Region, Macau Special Administrative Region, Taiwan Region and eleven Southeast Asian countries (Indonesia, Philippines, Vietnam, Thailand, Myanmar, Malaysia, Cambodia, Laos, Singapore, Timor-Leste and Brunei Darussalam) (the “Territory”) and a non-exclusive license to manufacture the Product in the Territory. The License Agreement commenced on its effective date and has a royalty term of ten years from the date of the commercial sale of the Product in the Territory (the “Royalty Term”). Upon the expiration of the Royalty Term, the License Agreement may be renewed for a period of ten years thereafter (the “Initial Extended Royalty Term”) as per certain conditions defined in the License Agreement. Upon the expiration of the Initial Extended Royalty Term, the License Agreement may be extended for a period otherwise agreed by both sides as per certain conditions defined in the License Agreement.

    Incyte has worldwide rights for the development and commercialization of the Product, marketed in the United States and Europe as Opzelura®. Opzelura and the Opzelura logo are registered trademarks of Incyte.

    About CMS
    CMS is a platform company linking pharmaceutical innovation and commercialization with strong product lifecycle management capability, dedicated to providing competitive products and services to meet unmet medical needs.

    CMS focuses on the global first-in-class (FIC) and best-in-class (BIC) innovative products, and efficiently promotes the clinical research, development and commercialization of innovative products, enabling the continuous transformation of scientific research into clinical practices to benefit patients.

    CMS deeply engages in several specialty therapeutic fields, and has developed proven commercialization capabilities, extensive networks and expert resources, resulting in leading academic and market positions for its major marketed products. CMS continues to promote the in-depth development of its advantageous specialty fields and expand business boundaries. While strengthening the competitiveness of the cardio-cerebrovascular/gastroenterology business, CMS independently operates its dermatology and medical aesthetics business, and ophthalmology business, aiming to gain leading positions in specialty therapeutic fields, whilst enhancing the scale and efficiency. At the same time, CMS has expanded its business territory to the Southeast Asian market, striving to become a “bridgehead” for global pharmaceutical companies to enter the Southeast Asian market, further escorting the sustainable and healthy development of the Group.

    Reference

    1. Ezzedine K, Eleftheriadou V, Whitton M, van Geel N. Vitiligo. Lancet. 2015;386(9988):74-84. doi:10.1016/S0140-6736(14)60763-7
    2. Consensus on the diagnosis and treatment of vitiligo (2021 version)
    3. Kubelis-López DE, Zapata-Salazar NA, Said-Fernández SL, Sánchez-Domínguez CN, Salinas-Santander MA, Martínez-Rodríguez HG, Vázquez-Martínez OT, Wollina U, Lotti T, Ocampo-Candiani J. Updates and new medical treatments for vitiligo (Review). Exp Ther Med. 2021 Aug;22(2):797. doi: 10.3892/etm.2021.10229. Epub 2021 May 25. PMID: 34093753; PMCID: PMC8170669.
    4. Drug approval information can be found on the FDA official website, as follows: $1
    5. Drug approval information can be found on the Incyte official website, as follows: https://investor.incyte.com/news-releases/news-release-details/incyte-announces-us-fda-approval-opzeluratm-ruxolitinib-cream
    6. Drug approval information can be found on the EMA official website, as follows: https://www.ema.europa.eu/en/medicines/human/EPAR/opzelura

    CMS Disclaimer and Forward-Looking Statements
    This press release is not intended to promote any products to you and is not for advertising purposes. This press release does not recommend any drugs, medical devices and/or indications. If you want to know more about the diagnosis and treatment of specific diseases, please follow the opinions or guidance of your doctor or other medical and health professionals. Any treatment-related decisions made by healthcare professionals should be based on the patient’s specific circumstances and in accordance with the drug package insert.

    This press release which has been prepared by CMS does not constitute any offer or invitation to purchase or subscribe for any securities, and shall not form the basis for or be relied on in connection with any contract or binding commitment whatsoever. This press release has been prepared by CMS based on information and data which it considers reliable, but CMS makes no representation or warranty, express or implied, whatsoever, and no reliance shall be placed on, the truth, accuracy, completeness, fairness and reasonableness of the contents of this press release. Certain matters discussed in this press release may contain statements regarding the Group’s market opportunity and business prospects that are individually and collectively forward-looking statements. Such forward-looking statements are not guarantees of future performance and are subject to known and unknown risks, uncertainties and assumptions that are difficult to predict. Any forward-looking statements and projections made by third parties included in this press release are not adopted by the Group and the Company is not responsible for such third-party statements and projections.

    Media Contact

    Brand: China Medical System Holdings Ltd.

    Contact: CMS Investor Relations

    Email: ir@cms.net.cn

    Website: https://web.cms.net.cn/en/home/

    Source: China Medical System Holdings Ltd.

    The MIL Network

  • MIL-OSI United Kingdom: Blind and partially sighted supporters to avail of new commentary service at Brandywell games

    Source: Northern Ireland – City of Derry

    Blind and partially sighted supporters to avail of new commentary service at Brandywell games

    24 September 2024

    Visually impaired or blind spectators attending Derry City games at the Ryan McBride Brandywell Stadium can now avail of a new service that will give them a live audio description of games.

    The new programme has been designed to allow the supporters to listen to descriptive commentary that will be transmitted to a radio receiver through a headset from anywhere within the stadium. The commentary will be provided by Drive 105. 

    The new service will be available for Derry City’s forthcoming games versus Sligo Rovers, Bohemians and Shelbourne and is available to home and away supporters.              

    The equipment has been installed by stadium owners Derry City and Strabane District Council following a report on accessibility improvements at the stadium being approved by Elected Members of Council’s Health and Community Committee in May.

    Mayor of Derry City and Strabane District Council, Councillor Lilian Seenoi Barr, said it will allow more supporters to enjoy the match day experience.

    “This is brilliant news for blind and visually impaired supporters who can now be more involved and enjoy an enhanced match day at the Ryan McBride Brandywell Stadium.

    “I have had the opportunity to attend a number of games in recent months when I experienced the noise and excitement for myself, and I am so delighted more people can now feel included and part of that.

    “I would like to thank Council Officers for bringing the project to fruition so quickly, the RNIB for their input in the project development, Derry City FC who will manage the service at games and Drive 105 for providing commentary from their Match Night Live service.”

    The service at the Ryan McBride Stadium is similar to the Soccer Sight programme that was successfully implemented at Windsor Park in Belfast.

    Campaigns Officer for RNIB Northern Ireland, Michéal Smith, attended Friday’s match at The Brandywell and said: “RNIB Northern Ireland is delighted to be involved in this initiative.

     “Blind and partially sighted fans should be able to enjoy watching a live football match in an accessible environment which welcomes both participants and those who visit sporting facilities to follow the action.

     “Too often, access to and within grounds and stadia, the facilities on offer, the accessible communication and the return travel, can be difficult to negotiate or completely absent. In many cases this deters sports fans with sight loss from getting involved.

    “Football is for everyone and we commend The Brandywell for introducing Audio Description technology to the stadium. Many thanks to stadium announcer Martin Bradley for all his assistance.

    “We thank local RNIB volunteer Rory McCartney and Richard Moore from Derry’s Drive 105 community radio station for their brilliant work together to make this happen. We also thank Derry and Strabane District Council – particularly Councillor Emma McGinley, Councillor Aisling Hutton and Leisure Area Manager Steve Setterfield, for helping bring this project to fruition. This is a great example of the Council’s ongoing partnership with RNIB to help Derry/Londonderry become a ‘Visually Aware City.’”

    Derry City’s Robert Martin added: “Derry City FC is delighted to note the success of the new ‘Brandywell Audio Assistant’ service that was trialled in our home game against Shamrock Rovers on Friday night.

    “Anything that enhances the match night experience at the ground is warmly welcomed and no doubt our visually impaired supporters will be happy to make use of the headsets going forward.

    “We congratulate all involved in the development of this project and encourage anyone who feels they may benefit from the service to speak with stadium stewards.

    “The sets will be stored in the Communications room and signed in and out by an appointed club delegate.”

    For further information on accessing the new service contact Rory McCartney (RNIB),  [email protected].

    MIL OSI United Kingdom

  • MIL-OSI United Kingdom: Preparing health and social care for winter

    Source: Scottish Government

    Record high NHS 24 workforce to meet increased demand.

    A record number of NHS 24 call handlers will support the public to access the most appropriate care this winter as services deal with increased demand.

    Through the Scottish Government and COSLA’s joint Winter Preparedness Plan, continued investment for NHS 24 will increase service capacity to provide clinical supervision for at least 150,000 additional calls per year and help prevent unnecessary A&E attendances.

    Key measures to support services in the face of increased demand, include; improving discharge planning for patients admitted to acute or community hospitals, maintaining established care at home packages and a Government led delayed discharge response team to directly support Boards in need of assistance. Planned care capacity will also be safeguarded with a continued focus on clearing long waits.

    The annual winter vaccination programme, which includes respiratory condition RSV for the first time, will support a reduction in severe disease, hospitalisation and mortality – while protecting health and social care service capacity. The joint plan also sets out action to support the mental health and well-being of service staff through increased flexible working options and dedicated mental health resources.

    This year’s plan has been published a month ahead of last year, and earlier than ever before, to allow more time for NHS Boards and care providers to prepare for winter surges in demand.

    Health Secretary Neil Gray said:

    “As winter approaches, the NHS will see surges in demand across all health, social care and social work services. Our joint-plan Winter Plan with COSLA is just one part of a wider programme of work to respond to heightened demand.

    “A record number of NHS 24 call handlers will be available this winter to direct people to the most appropriate care, helping reduce unnecessary A&E attendances. We will continue our work to reduce delayed discharge in hospitals with an increased focus on effective discharge planning and protecting care at home packages. We will also ensure planned care capacity is protected as much as possible in the face of winter pressure so patients are seen as quickly as possible.

    “We are prioritising frontline services with over £14.2 billion investment in our boards this year – an almost 3% real terms uplift – and also investing £2 billion in social care services.

    “I thank all health, social care and social work staff for their continued efforts and dedication to deliver high quality care. It is fundamental we safeguard their wellbeing, and improved options on flexible working and continued access to mental health resources will ensure staff are supported over this challenging period.”

    COSLA Health and Social Care Spokesperson, Councillor Paul Kelly said:

    “It is our shared responsibility to ensure that people and communities have timely access to quality care and support when they need it most. We know that Local Government and Health and Social Care Partnerships across Scotland are working hard to plan and deliver the essential health and social care services our communities rely on every day.

    “The context within which this takes place is increasingly challenging, which is why COSLA have worked jointly with the Scottish Government to produce this plan. Local Government plays a key role in supporting people to experience better wellbeing and better outcomes, so it was only right that this plan reflects the whole system of integrated health and social care, from acute and primary care to social work, our care homes, community settings, and our partners across the sector.

    “Winter is often a time of exceptional pressure on our services so I am pleased that this plan, produced with our partners across the sector, reflects the challenges and the opportunities we face.”

    Background

    Health & Social Care Winter Preparedness Plan for 2024-25

    MIL OSI United Kingdom

  • MIL-OSI USA: Congresswoman Sylvia Garcia Statement on First Known Post-Dobbs Death

    Source: United States House of Representatives – Congresswoman Sylvia Garcia (TX-29)

    WASHINGTON, D.C. – Congresswoman Sylvia R. Garcia (D-TX-29) issued the following statement based on ProPublica’s recent reporting on the tragic death of Amber Thurman, a 28-year-old mother who lost her life due to Georgia’s extreme abortion ban shortly after the Dobbs v. Jackson Women’s Health Organization decision:

    “American women woke to learn their worst fears have been realized—a 28-year-old mother in Georgia was left to die because of the Trump abortion bans. A son lost his mother, a family lost their loved one.

    “Two years after her death, she is the first confirmed casualty in the MAGA war on women. It begs the question, how many more women have died, their stories hidden away?

    “What we know for certain is this will happen again. It will happen in Texas, and across the country, until we end these cruel bans.

    “We must defeat these Trump abortion bans and ensure every woman has access to comprehensive reproductive health care without fear of losing her life.”

    MIL OSI USA News

  • MIL-OSI USA: U.S. House of Representatives Unanimously Passes Trahan’s Bipartisan Legislation to Advance Rare Disease Treatments for Kids

    Source: United States House of Representatives – Congresswoman Lori Trahan (D-MA-03)

    WASHINGTON, D.C. – Today, Congresswoman Lori Trahan (D-MA-03), a member of the House Energy and Commerce Committee’s Health Subcommittee, celebrated the unanimous passage of her bipartisan Creating Hope Reauthorization Act of 2024 in the U.S. House of Representatives. The legislation will reauthorize a key program that incentivizes the development of new drugs and treatments for children battling rare pediatric diseases. Trahan introduced the legislation earlier this year alongside Representatives Michael McCaul (R-TX-10)Anna Eshoo (D-CA-16)Gus Bilirakis (R-FL-12)Michael Burgess (R-TX-26), and Nanette Barragán (D-CA-44).

    “When a child is battling a rare disease like cancer, currently one of the leading causes of death for kids, they deserve access to the best treatments possible,” said Congresswoman Trahan. “The Creating Hope Reauthorization Act is a critical bipartisan effort to make sure those treatments are available while newer and more effective treatments are being advanced to save children’s lives. The unanimous support for this legislation in the House is a testament to the necessity and effectiveness of this initiative, and I look forward to working with our colleagues in the Senate to send it to the President’s desk to become law.”

    Approximately 30 million Americans are affected by rare diseases, two out of every three of whom are children. However, treatments intended for adults are often too harsh for children, limiting their treatment options or even leaving them with life-altering complications after their disease is cured. The Creating Hope Reauthorization Act seeks to solve this problem by reauthorizing the U.S. Food and Drug Administration’s (FDA) cost-neutral priority review voucher (PRV) program, which incentivizes the development of treatments for rare pediatric diseases. Since 2012, the PRV program has spurred the development of therapies for nearly 40 different diseases, 36 of which previously had no safe or effective FDA-approved treatments for children.

    The Creating Hope Reauthorization Act was included in the Give Kids a Chance Act, a bipartisan legislative package created to advance pediatric disease treatment. During a markup last week, members of the House Energy and Commerce Committee unanimously passed the Give Kids a Chance Act. In addition to Trahan’s legislation to advance pediatric rare disease treatments, the package also authorizes the FDA to direct companies to research combinations of therapies and cancer drugs in pediatric patients. The FDA is currently only authorized to direct pediatric cancer trials of single drugs, and the majority of these trials are conducted on children with relapsed cancer. However, kids with relapsed cancer are very rarely cured by one-drug treatments because their diagnoses are so advanced.

    Since her appointment to the House Energy and Commerce Committee in 2021, Trahan has spearheaded multiple bipartisan initiatives to expand and improve pediatric health care. Last week, she secured passage by the full House of Representatives of her bipartisan Accelerating Kids’ Access to Care Act, legislation that will break down barriers for children with complex medical conditions to make it easier for families to access out-of-state care. In July, she introduced the Bolstering Research and Innovation Now (BRAIN) Act, bipartisan legislation to strengthen research and treatment development for brain tumors, the leading cause of cancer-related death among children and young adults. In May, the House passed her bicameral and bipartisan Youth Poisoning Protection Actbipartisan and bicameral legislation that would ban the consumer sale of products containing high concentrations of sodium nitrite, a meat-curing chemical that has been popularized in online suicide forums because of its lethality when ingested.

    The legislative package containing Trahan’s Creating Hope Reauthorization Act now moves to the Senate where companion legislation has been introduced by Senators Bob Casey (D-PA) and Markwayne Mullin (R-OK).

    ###

    MIL OSI USA News

  • MIL-OSI: Investment Management Update

    Source: GlobeNewswire (MIL-OSI)

    THAMES VENTURES VCT 2 PLC
    LEI: 21380035MV1VRYEXPR95

    INVESTMENT MANAGEMENT UPDATE
    20 SEPTEMBER 2024

    Following the novation of the investment management agreement from Downing LLP (“Downing”) to Foresight Group LLP (“Foresight”) comprising management of the Company’s Venture, AIM and DP67 share classes in July 2022, the Board is pleased to confirm that Foresight has now also been appointed as Manager of the Company’s Healthcare share class following completion of a Put-Option Agreement between Downing and Foresight on 20 September 2024.

    For further information, please contact:

    Company Secretary
    Foresight Group LLP
    Contact: Stephen Thayer Tel: 0203 667 8100

    Investor Relations
    Foresight Group LLP
    Contact: Andrew James Tel: 0203 667 8181

    The MIL Network

  • MIL-OSI Canada: Statement from Minister McLean and Minister McPhee on supporting 2SLGBTQIA+ Yukoners

    Source: Government of Canada regional news

    Minister responsible for the Women and Gender Equity Directorate Jeanie McLean and Minister of Health and Social Services Tracy-Anne McPhee have issued the following statement:

    “Today, we saw many Yukoners join together and show their support for our youngest 2SLGBTQIA+ community members.

    “To Yukon’s transgender community, allies and advocates, we say ‘thank you”. Your dedication and unwavering care in protecting our communities’ rights to freedom of opinion and expression, as well as the right to security and safety, is respected and deeply valued.

    MIL OSI Canada News

  • MIL-OSI Canada: New Health and Wellness Centre opens in Old Crow

    Source: Government of Canada regional news

    The Government of Yukon and the Vuntut Gwitchin First Nation announce the opening of Old Crow’s new Health and Wellness Centre, named Natr’idizhii Srii Tr’agwandaii Hah Zheh, meaning “place for healing and wellness”. The new Health and Wellness Centre is based on a collaborative care model and provides a range of health care and social services for the residents of Old Crow.

    MIL OSI Canada News

  • MIL-OSI Canada: Government of Yukon urges Yukoners to protect themselves from rising pertussis cases through vaccination

    Source: Government of Canada regional news

    The Government of Yukon and the Chief Medical Officer of Health is encouraging all Yukoners to ensure they are up-to-date with their vaccinations to protect themselves and their families from pertussis (whooping cough) as the territory experiences a rise in cases. Over the past two months, seven cases have been reported so far in 2024. While most cases have been linked to travel, some have not been connected to a known source, indicating the possibility of community transmission. Nationally, rates of pertussis are also increasing and the Yukon is not immune to this trend.

    MIL OSI Canada News

  • MIL-OSI USA: Read More

    Source: United States House of Representatives – Representative Richard Hudson (NC-08)

    WASHINGTON, D.C. – In case you missed it, Representative Richard Hudson and Heritage Foundation Director of the Center for Health and Welfare Policy Nina Owcharenko Schaefer wrote an op-ed for the Washington Examinerslamming Vice President Kamala Harris, Governor Tim Walz, and the Democrats’ government-run healthcare policies that are leaving patients and families with fewer, lower quality choices and higher costs.

    In theop-ed, Rep. Richard Hudson and Nina Owcharenko Schaefer wrote, “While issues such as the border crisis, global conflicts, and persistent inflation continue to dominate headlines, healthcare remains a key concern for voters.

    That’s especially important because, last month, Vice President Kamala Harris picked Gov. Tim Walz (D-MN) as her running mate, solidifying the duo as the first ticket ever to feature two candidates who have fully embraced government-run, single-payer healthcare.

    It would cost tens of trillions of taxpayer dollars and reduce medical productivity, giving patients fewer healthcare choices, worse quality care, and longer wait times while hiking taxes for everyone.

    Harris and Walz have also embraced the Biden administration’s disastrous prescription drug price controls. In North Carolina, these liberal policies are actually making prescription drug costs more expensive while limiting future access to life-saving drugs for seniors.

    Democrats once promised people that the ACA would solve our healthcare woes. But a decade later, their efforts are more focused on masking its failures than fixing what is wrong. Premiums are still rising, families have fewer choices, and the choices that are available are more limited and lower quality.

    Instead of addressing these shortcomings, the Biden-Harris administration’s solution has been to simply slap a Band-Aid over them with more taxpayer-funded subsidies.

    A Harris-Walz administration would take away the coverage you have today and put the government in charge of your care, giving it the power to decide what kind of care you get, where you get it, when you get it, and if you can get it at all.

    While Harris and Walz are focused on expanding government control and eroding your freedom, conservatives in the House of Representatives are focused on making coverage more affordable, prices fully transparent, care more accessible, and overall costs more reasonable.

    It’s time to move away from the Democrats’ failed big-government policies and toward a healthcare agenda that is patient-centered, not government-centered.”

    

    Read the full op-ed in the Washington Examiner HERE.

    -###-

    MIL OSI USA News

  • MIL-OSI USA: Medical readiness: The right prescription for US, Africa partnership

    Source: United States Army

    Kenyan Army Lt. Col. Moses Mdzomba speaks with U.S. Navy Petty Officer 1st Class Wyche during the U.S. Army Southern European Task Force, Africa (SETAF-AF) medical readiness exercise (MEDREX) and global health engagements (GHE) concept development event (CDE) held in Vicenza, Italy, Sept.16-20, 2024. The MEDREX GHE CDE brought together military medical professionals, planners, and experts from SETAF-AF, U.S. Africa Command, U.S. Medical Command, and others, along with medical providers and representatives from 17 African partner nations. Participants worked collectively to refine the fiscal year 2025 MEDREX and Global Health Engagements execution strategy and discussed the framework for fiscal years 2026 through 2028. (U.S. Army photo by 1st Lt. Katherine Sibilla) (Photo Credit: 1st Lt. Katherine Sibilla) VIEW ORIGINAL

    Back to 

    U.S. Army Southern European Task Force, Africa

    VICENZA, Italy — Strengthening partnerships through medicine is exactly what U.S. and African military forces prescribe for a more stable future.

    Military medical professionals from the U.S. joint force and 17 African nations came together here from Sept. 16-20, 2024, to shape the future of medical engagements on the African continent.

    U.S. Army Southern European Task Force, Africa (SETAF-AF) hosted a concept development event (CDE) for global health engagements (GHE) and medical readiness exercises (MEDREX). Planners from U.S. Africa Command, U.S. Medical Command, and other military units discussed and refined the medical strategy for fiscal year 2025 alongside African partners. Together, they also laid the groundwork for future collaboration through 2028.

    Benin Army Lt. Col. Mahounakpon Hounkpevi listens during the U.S. Army Southern European Task Force, Africa (SETAF-AF) medical readiness exercise (MEDREX) and global health engagements (GHE) concept development event (CDE) held in Vicenza, Italy, Sept.16-20, 2024. The MEDREX GHE CDE brought together military medical professionals, planners and experts from SETAF-AF, U.S. Africa Command, U.S. Medical Command and others, along with medical providers and representatives from 17 African partner nations. Participants worked collectively to refine the fiscal year 2025 MEDREX and GHE execution strategy, and discussed the framework for fiscal years 2026 through 2028. (U.S. Army photo by 1st Lt. Katherine Sibilla) (Photo Credit: 1st Lt. Katherine Sibilla) VIEW ORIGINAL

    “We’re coordinating activities across Africa to meet the medical needs of our partners,” said U.S. Army Capt. Jeffery Sparda, SETAF-AF GHE officer. “This event is about planning for the next three years and finalizing our medical activities for fiscal year 2025.”

    Some participants in the CDE have partaken in previous MEDREXs, bringing firsthand experience to the event. U.S. Army Chief Warrant Officer 3 David Kloberndaz, a MEDREX planner from the 30th Medical Brigade, highlighted the hands-on training aspect of the program.

    “MEDREX gives us the opportunity to train in real-world environments, treating cases we don’t see at home,” said Kloberndaz. “It’s a critical part of our readiness and allows us to share best practices with our African partners.”

    As both a planner and participant, Kloberndaz emphasized the mutual benefits of the knowledge exchange between U.S. and African medical teams.

    1 / 3 Show Caption + Hide Caption – U.S. Army Col. Kelly Togiola, global health engagements chief, U.S. Army Southern European Task Force, Africa (SETAF-AF), speaks to participants at the SETAF-AF medical readiness exercise (MEDREX) and global health engagements (GHE) concept development event (CDE) held in Vicenza, Italy, Sept.16-20, 2024. The MEDREX GHE CDE brought together military medical professionals, planners, and experts from SETAF-AF, U.S. Africa Command, U.S. Medical Command, and others, along with medical providers and representatives from 17 African partner nations. Participants worked collectively to refine the fiscal year 2025 MEDREX and Global Health Engagements execution strategy and discussed the framework for fiscal years 2026 through 2028. (U.S. Army photo by 1st Lt. Katherine Sibilla) (Photo Credit: 1st Lt. Katherine Sibilla) VIEW ORIGINAL
    2 / 3 Show Caption + Hide Caption – U.S. Army Lt. Gen. Mary Izaguirre, U.S. Army Surgeon General, speaks during the U.S. Army Southern European Task Force, Africa (SETAF-AF) medical readiness exercise (MEDREX) and global health engagements (GHE) concept development event (CDE) held in Vicenza, Italy, Sept.16-20, 2024. The MEDREX GHE CDE brought together military medical professionals, planners, and experts from SETAF-AF, U.S. Africa Command, U.S. Medical Command, and others, along with medical providers and representatives from 17 African partner nations. Participants worked collectively to refine the fiscal year 2025 MEDREX and Global Health Engagements execution strategy and discussed the framework for fiscal years 2026 through 2028. (U.S. Army photo by 1st Lt. Katherine Sibilla) (Photo Credit: 1st Lt. Katherine Sibilla) VIEW ORIGINAL
    3 / 3 Show Caption + Hide Caption – U.S. Army Lt. Gen. Mary Izaguirre, U.S. Army Surgeon General, listens to a brief during the U.S. Army Southern European Task Force, Africa (SETAF-AF) medical readiness exercise (MEDREX) and global health engagements (GHE) concept development event (CDE) held in Vicenza, Italy, Sept.16-20, 2024. The MEDREX GHE CDE brought together military medical professionals, planners, and experts from SETAF-AF, U.S. Africa Command, U.S. Medical Command, and others, along with medical providers and representatives from 17 African partner nations. Participants worked collectively to refine the fiscal year 2025 MEDREX and Global Health Engagements execution strategy and discussed the framework for fiscal years 2026 through 2028. (U.S. Army photo by 1st Lt. Katherine Sibilla) (Photo Credit: 1st Lt. Katherine Sibilla) VIEW ORIGINAL

    With each medical exercise lasting about two weeks, SETAF-AF plans to conduct eight MEDREXs in Africa, spread throughout fiscal year 25. Host nations include Angola, Burundi, Cabo Verde, Chad, Ghana, Rwanda, South Africa and Zambia.

    With clear plans for the next three years, SETAF-AF and its African partners worked diligently to ensure that these engagements will not only enhance medical capabilities, but also strengthen the relationships critical for future cooperation across the continent.

    1 / 2 Show Caption + Hide Caption – U.S. Army Maj. Gen. Andrew C. Gainey, commanding general of U.S. Army Southern European Task Force, Africa (SETAF-AF), greets Italian Army Lt. Col. Dragotta during the SETAF-AF medical readiness exercise (MEDREX) and global health engagements (GHE) concept development event (CDE) held in Vicenza, Italy, Sept.16-20, 2024. The MEDREX GHE CDE brought together military medical professionals, planners, and experts from SETAF-AF, U.S. Africa Command, U.S. Medical Command, and others, along with medical providers and representatives from 17 African partner nations. Participants worked collectively to refine the fiscal year 2025 MEDREX and Global Health Engagements execution strategy and discussed the framework for fiscal years 2026 through 2028. (U.S. Army photo by 1st Lt. Katherine Sibilla) (Photo Credit: 1st Lt. Katherine Sibilla) VIEW ORIGINAL
    2 / 2 Show Caption + Hide Caption – Kenyan Army Lt. Col. Moses Mdzomba speaks with U.S. Navy Petty Officer 1st Class Wyche during the U.S. Army Southern European Task Force, Africa (SETAF-AF) medical readiness exercise (MEDREX) and global health engagements (GHE) concept development event (CDE) held in Vicenza, Italy, Sept.16-20, 2024. The MEDREX GHE CDE brought together military medical professionals, planners, and experts from SETAF-AF, U.S. Africa Command, U.S. Medical Command, and others, along with medical providers and representatives from 17 African partner nations. Participants worked collectively to refine the fiscal year 2025 MEDREX and Global Health Engagements execution strategy and discussed the framework for fiscal years 2026 through 2028. (U.S. Army photo by 1st Lt. Katherine Sibilla) (Photo Credit: 1st Lt. Katherine Sibilla) VIEW ORIGINAL

    About MEDREX

    MEDREX is a medical readiness exercise, planned and executed by SETAF-AF, enabling military health professionals from the U.S. and their African partners to exchange medical practices, procedures and techniques that enhance treatment capabilities and result in lasting relationships between the participants.

    About SETAF-AF

    SETAF-AF provides U.S. Africa Command and U.S. Army Europe and Africa a dedicated headquarters to synchronize Army activities in Africa and scalable crisis-response options in Africa and Europe.

    Follow SETAF-AF on: Facebook, Twitter, Instagram, YouTube, LinkedIn & DVIDS

    MIL OSI USA News

  • MIL-OSI USA: All Ages, All Stages NC — A Roadmap for Aging and Living Well Plan Kickoff Event

    Source: US State of North Carolina

    Headline: All Ages, All Stages NC — A Roadmap for Aging and Living Well Plan Kickoff Event

    All Ages, All Stages NC — A Roadmap for Aging and Living Well Plan Kickoff Event
    rmbeck

    Credentialed media are invited to attend the North Carolina Department of Health and Human Service’s kick off event to announce the unveiling of the All Ages, All Stages NC – A Roadmap for Aging and Living Well Plan. This multisector plan for aging is designed to help enhance the quality of life for all North Carolinians as we get older. The plan comes at a time when the number of older North Carolinians is growing rapidly. Today, nearly two million North Carolina residents are age 65 or older — that number is expected to rise to three million by 2050. 

    The plan is the result of a collaborative effort across sectors including consumers, providers, government entities, and aging and disability advocates in North Carolina. 

    Join NC Health and Human Services Secretary Kody H. Kinsley to learn more about this work to help North Carolina transform its infrastructure and coordinate services to better serve people across the state.

    What: All Ages, All Stages NC – North Carolina’s Multisector Plan for Aging Kickoff Event 

    Who: Kody Kinsley, Secretary, NCDHHS
                Constantinos Miskis, Regional Administrator, Administration for Community Living, U.S. Department of Health and Human Services
                Joyce Massey-Smith, Director, NCDHHS Division of Aging; Co-Chair All Ages, All Stages NC Steering Committee
                Jill Simmerman Lawrence, Deputy Director, NCDHHS Division of Aging
                Mary Bethel, Chair of the NC Coalition on Aging’s Board of Directors; Co-Chair All Ages, All Stages NC Steering Committee

    When: Friday, Sept. 27, 2024
                  10-11 a.m.

    Where: Adams Building, Dorthea Dix Park Campus
                    101 Blair Drive
                    Raleigh, NC 27603 

    Media: Please RSVP news@dhhs.nc.gov to confirm attendance.  

    Sep 24, 2024

    MIL OSI USA News

  • MIL-OSI USA: Lieutenant Governor Primavera Visits School-Based Health Center at George Washington High School

    Source: US State of Colorado

    DENVER – Today, Lt. Governor Primavera and Director of the Office of Saving People Money on Health Care visited a school-based health center at George Washington High School to learn more about the importance of these facilities to students and communities. The Lt. Governor was joined by a student, school staff, leadership from Denver Health and Denver Public Schools, the Youth Healthcare Alliance, and Senator Janice Marchman and Representative Emily Sirota. 

    “The Polis-Primavera administration has been working since day one to break down barriers to health care and these facilities are important avenues where students and staff can get important care in a convenient location. I appreciate the collaboration that goes into these centers and the opportunity it gives young people, helping them fulfill their potential,” said Lt. Governor Dianne Primavera. 

    Since taking office, the Polis-Primavera administration and the Office of Saving People Money on Health Care have made Colorado a national leader in reducing health care costs. The creation of Reinsurance and Colorado Option are connecting Coloradans with insurance coverage outside of an employer while saving them money. Through the Prescription Drug Affordability Board and capping the cost of insulin at $100 per month, the administration is helping Coloradans save money on prescription drugs. Colorado is also pursuing a waiver from the federal government to import lower-cost prescription drugs from Canada. These are just a few of the ways Colorado is increasing access to health care while lowering costs. 

    Earlier this year, Governor Polis signed SB24-034, which expands eligible uses for the grant program at the Colorado Department of Public Health and Environment (CDPHE) that supports school-based health centers to school-linked health services. These grants currently fund 59 operating SBHCs and four planning sites throughout Colorado. The SBHC Program also partners with other state agencies and grant programs to expand the services available in SBHCs.

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    MIL OSI USA News

  • MIL-OSI USA: House Passes Kaptur Bill to Increase Healthcare Access for Military Families

    Source: United States House of Representatives – Congresswoman Marcy Kaptur (OH-09)

    Washington, DC – Today, Congresswoman Marcy Kaptur (OH-09),Senior Member of the House Appropriations Subcommittee on Defense, celebrated the House of Representatives’ unanimous bipartisan passage of the Care for Military Kids Act. The legislation, which Congresswoman Kaptur introduced alongside Congresswoman Jen Kiggans (VA-02), ensures that military families can maintain essential healthcare coverage and medical services for their children, regardless of where their service takes them.

    The Care for Military Kids Act amends the Social Security Act to ensure that the dependents of active-duty servicemembers receiving long-term care through a state-administered Medicaid plan will remain eligible for these services even if their family is relocated to another state. The bill is endorsed by major advocacy organizations, including the National Disability Rights Network (NDRN) and The Arc of the United States.

    “I introduced this bipartisan legislation alongside Congresswoman Kiggans, and am thankful to those who helped ensure its swift passage,” said Congresswoman Marcy Kaptur (OH-09). “Our servicemembers commit their lives to the safety and security of all Americans. It is essential we ensure that dependents of active duty servicemembers do not lose their critical healthcare coverage through Medicaid and CHIP as their families transfer locations while in service to our nation. Through this bipartisan effort we will prevent military families from facing the burden of healthcare insecurity and uncertainty. I am grateful for the bipartisan support this bill and our military community have received and look forward to Senate passage so we can send this legislation to the President’s desk to be signed into law.” 

    “Our men and women in uniform sacrifice so much for our country, relocating frequently and spending months apart,” said Congresswoman Jen Kiggans (VA-02). “As a Navy spouse, mother of four, and a veteran who served for nearly 10 years myself, I firmly believe servicemembers should be able to maintain healthcare coverage for their children when they are relocated. I am thankful my colleagues agree and passed my bipartisan bill unanimously. I urge the Senate to act on this legislation quickly so we can ensure military children have access to the consistent healthcare coverage and medical care they need to lead healthy, happy lives. They should never have to forgo critical care because of their parents’ selfless decision to serve.”

    Medicaid is operated by states, meaning that portability of benefits related to home and community-based healthcare services is not guaranteed from one state to another. This puts individuals and their families at risk of a loss of services when they leave their state, which particularly impacts dependents of military servicemembers who frequently transfer locations as part of the family’s commitment to serving their country. A new report from the Children’s Hospital Association underscores Medicaid’s significance in enabling healthcare access for nearly three million children in military-connected families. The Care for Military Kids Act provides clarity and consistency by ensuring that military children with disabilities or long-term healthcare needs remain eligible for Medicaid services across state lines.

    # # #

    MIL OSI USA News

  • MIL-OSI USA: Grassley Leads Bicameral Colleagues in Calling Out Abuses in the Biden-Harris Unaccompanied Migrant Children Program

    US Senate News:

    Source: United States Senator for Iowa Chuck Grassley

    WASHINGTON – Sen. Chuck Grassley (R-Iowa), a senior member and former chairman of the Senate Judiciary Committee, today led 43 bicameral Republican colleagues in a letter urging President Joe Biden and Vice President Kamala Harris to work with Congress to root out abuses in their administration’s unaccompanied migrant children program and stop the Department of Health and Human Services (HHS)’s cover-up of the crisis. HHS has failed to comply with two out of three Department of Homeland Security (DHS) subpoenas and other information requests issued amid its investigation into more than 100 suspicious sponsors identified as a result of Grassley’s oversight.

    Program Abuse

    More than 500,000 unaccompanied migrant children have crossed the southwest border under the Biden-Harris administration, while cartel trafficking activity surged an estimated 2,500 percent. Amid this crisis, the lawmakers note that the Biden-Harris administration limited background checks for sponsors of unaccompanied children, cut back on familial DNA testing at the border and decreased information sharing with law enforcement.

    In addition to hampering DHS’s child exploitation investigation, the Biden-Harris HHS attempted to obstruct Grassley’s oversight of HHS contractors, including Southwest Key. HHS has also defied House Judiciary Committee subpoenas.

    Seeking Solutions

    The lawmakers are urging Biden and Harris to “make changes to [their] policies and procedures” in order to “end this public safety crisis.” They are specifically calling on the Biden-Harris administration to enhance information sharing with law enforcement and Congress, fully cooperate with DHS’s child exploitation investigation and thoroughly respond to all congressional oversight requests.

    “[The Biden-Harris HHS] must stop its cover-up and cooperate with law enforcement and Congress to end this crisis and protect unaccompanied children and the American people,” the lawmakers concluded.

    Read the full letter HERE.

    Joining Grassley on the letter are Sens. Bill Cassidy (R-La.), Ron Johnson (R-Wis.) and House Judiciary Chairman Jim Jordan (R-Ohio), along with Sens. Mike Crapo (R-Idaho), John Cornyn (R-Texas), Lindsey Graham (R-S.C.),  John Thune (R-S.D.), Roger Wicker (R-Miss.), Jim Risch (R-Idaho), John Hoeven (R-N.D.), Mike Lee (R-Utah), Tim Scott (R-S.C.), Ted Cruz (R-Texas), Deb Fischer (R-Neb.), Shelley Moore Capito (R-W.Va.), James Lankford (R-Okla.), Steve Daines (R-Mont.), Dan Sullivan (R-Alaska), John Kennedy (R-La.), Marsha Blackburn (R-Tenn.), Kevin Cramer (R-N.D.), Mike Braun (R-Ind.), Josh Hawley (R-Mo.), Rick Scott (R-Fla.), Roger Marshall (R-Kans.), Tommy Tuberville (R-Ala.), Markwayne Mullin (R-Okla.), Katie Britt (R-Ala.) and Pete Ricketts (R-Neb.).

    Additional co-signers in the House include Reps. Tom McLintock (R-Ca.), Matt Gaetz (R-Fla.), Andy Biggs (R-Ariz.), Chip Roy (R-Texas), Dan Bishop (R-N.C.), Scott Fitzgerald (R-Wis.), Cliff Bentz (R-Ore.), Ben Cline (R-Va.), Barry Moore (R-Ala.), Russell Fry (R-S.C.), Harriet Hageman (R-Wyo.), Wesley Hunt (R-Texas), Laurel Lee (R-Fla.) and Michael Rulli (R-Ohio).

    -30-

    MIL OSI USA News

  • MIL-OSI Australia: $2.1 million to help boost cancer research in NSW

    Source: New South Wales Ministerial News

    Published: 24 September 2024

    Released by: Minister for Medical Research


    Coinciding with World Cancer Research Day today, the NSW Government is committing $2.1 million in research grant funding to support the work of the state’s cancer researchers, including world-renowned Professors Georgina Long AO and Paul Timpson.

    Co-Australian of the Year Professor Long and the team at Melanoma Institute Australia and The University of Sydney have been awarded almost $700,000 for an imaging system that will allow researchers to better visualise and understand tumour cell interactions across various cancer types, via the Cancer Institute NSW funding.

    It is hoped an improved understanding of the tumour microenvironment will assist with cancer diagnosis and treatment.

    Professor Timpson and the team at the Garvan Institute of Medical Research were awarded almost $700,000 to purchase a system that will provide unprecedented insights into cell-to-cell interactions, treatment responses and cancer dormancy to enable more effective treatment for cancers, including pancreatic, breast, and prostate cancer.

    Three clinical trials grants, valued at $250,000 each, have also been funded to support projects focused on improving access to cancer clinical trials, including:

    • The Building Capacity in Cancer Clinical Trials across Maridulu Budyari Gumal project aims to address enrolment challenges in clinical trials by targeting populations with lower trial participation rates. This includes socioeconomic disadvantaged, culturally and linguistically diverse and rural and regional communities.
    • The Sydney Cancer Partners Clinical Trials Support project aims to increase recruitment from priority populations to trials, including Aboriginal, culturally and linguistically diverse and LGBITQ communities.
    • Targeted Cancer Clinical Trials Support for Regional NSW project aims to deliver targeted initiatives such as increased trial sites and education and training to boost clinical trial participation across the Central Coast, Hunter, New England, Mid North Coast and Northern NSW areas.

    The NSW Government, through Cancer Institute NSW, is one of the largest funders of cancer research in NSW, having invested more than $470 million in the past 20 years across nearly 100 competitive research awards and grants.

    Minister for Medical Research David Harris said:

    “Targeted research is vital to delivering better treatments and interventions that reduce the impact of cancer and ultimately save lives.

    “Our researchers strive every day to improve the lives of people in NSW and across the world, and we’re proud to invest in them to continue their work and help improve cancer outcomes for all.”

    NSW Chief Cancer Officer and CEO Cancer Institute NSW, Professor Tracey O’Brien AM said:

    “While significant progress has been made in understanding and treating cancer, it remains the leading cause of death in NSW with sadly one in two people set to be diagnosed with the disease in their lifetime.

    “Investing in and accelerating research and innovation is key to improving our understanding of a disease that continues to devastate communities across NSW.”

    Professor Georgina Long AO said:

    “Technologies that provide a clear large-scale and detailed view of tumours and enable us to see how cells interact with each other are critical to move the cancer field forward.

    “The imaging system, called the Phenolmager HT 2.0, which we have been able to purchase through the research equipment grant, provides the ability to better understand tumour cell interactions.

    “This will enable researchers at Melanoma Institute Australia and The University of Sydney to bridge cancer research to clinical use and ultimately deliver more effective cancer treatments.”

    Professor Paul Timpson said:

    “The cutting-edge Akoya-PhenoCycler Fusion system will concurrently detect and visualise 100 proteins, providing unprecedented insights into cell-to-cell interactions, chemotherapy and immunotherapy responses, cancer dormancy, and novel therapies for cancers like pancreatic, breast, and prostate cancer.

    “Proteins drive functional outcomes within cells, and constitute drug targets, yet existing technologies do not accurately reflect protein activity at a specific location or time.”

    MIL OSI News

  • MIL-OSI USA: In White Plains, Gillibrand Announces Legislation to Address Epidemic of Traumatic Brain Injuries in Service Members and Veterans

    US Senate News:

    Source: United States Senator for New York Kirsten Gillibrand

    Following a disturbing report showing that service members are sustaining crippling traumatic brain injuries as a result of firing their own weapons, U.S. Senator Kirsten Gillibrand visited the Westchester County Michaelian Office Building in White Plains to announce legislation to address traumatic brain injuries among service members and veterans. 

    Service members who regularly fire heavy weapons are at increased risk of brain injury as a result of repeated exposure to explosions or blasts from their own weapons and explosives – otherwise known as blast overpressure. These brain injuries can cause depression, anxiety, cognitive problems, hallucinations, panic attacks, violent outbursts, suicidal tendencies, psychiatric disorders, dementia, and a variety of other serious health problems. At least a dozen Navy SEALs who have died by suicide over the past decade were later found to have suffered blast injuries, and many more service members have complained of health issues after blast exposure. Despite this, the Pentagon has struggled to properly investigate the impact of blast overpressure, effectively track the prevalence of blast overpressure-related injuries, or offer appropriate care to service members and veterans. Gillibrand is calling for more research and better treatment for those affected.

    Gillibrand was joined by Westchester Deputy County Executive Ken Jenkins, New York State Assemblyman Chris Burdick, City of White Plains Mayor Thomas Roach, Westchester County Board of Legislators Chairman Vedat Gashi, Director of the Westchester County Veterans Service Agency Ronald Tocci, City of Mount Vernon Director of Veteran’s Services Andrea Molina, and local veterans.

    After repeatedly being exposed to blasts from their own weapons during both training and combat, our service members are sustaining severe and crippling brain trauma,” said Senator Gillibrand. “This bill will require the DoD to investigate the prevalence and causes of these brain injuries; to track each service member’s exposure to blasts; and to help service members access care. This is a critical bill and I look forward to getting it passed in the NDAA.” 

    “With research showing an increased risk of traumatic brain injuries for our service members who regularly fire off heavy weapons, it is imperative we work together at all levels of government to start addressing the health implications they are being exposed to from the blasts of their own weapons. We know that doing so can truly save lives as blast overpressure has already been linked to the development of suicidal inclinations and cognitive issues,” said New York State Senate Majority Leader Andrea Stewart-Cousins. “The Blast Overpressure Safety Act will provide tools to investigate the scope and root causes of TBIs while also tracking service members’ exposure to blasts. The act will also promote access to care. I highly commend Senator Gillibrand for introducing this proactive piece of legislation, and I look forward to continuing to collaborate on initiatives to further protect our active service members and veterans who put their lives on the line to protect us.”

    New York State Senator Shelley B. Mayer said, “I am honored to join Senator Gillibrand in showing our steadfast support for our veterans, both abroad and when they return home. Traumatic brain injuries can be life altering and early assessment is critical to ensure that veterans have the resources and support they need to continue living life to the fullest. As a state and nation, we must do better to support our veterans.”

    “I am very pleased to see Senator Gillibrand’s support for the Blast Overpressure Safety Act,” said New York State Assemblymember Chris Burdick. “This is a great step in taking care of our active service members and veterans, who have already sacrificed so much for our country. As a society we are making progress in addressing traumatic brain injuries in sports, so it is not only appropriate but crucial that we also make progress concerning those who are putting their lives on the line for our democracy.”

    Westchester County Executive George Latimer said, “The brave men and women who serve our country deserve comprehensive care for the injuries they endure in the line of duty – that is the very least that we owe them. Traumatic brain injuries caused by blast overpressure are devastating and all too common, yet we’ve seen a lack of sufficient research and support for those affected. I applaud Senator Gillibrand’s outstanding leadership on this legislation. It is a critical step toward ensuring those we send to the front lines receive the care and understanding they need to heal.”

    “Our service members have sacrificed so much for our country, and it is our responsibility to ensure they receive the highest level of care when they return home,” said Westchester Deputy County Executive Ken Jenkins. “The effects of blast overpressure are a silent threat, leading to traumatic brain injuries that can severely impact their quality of life. Senator Gillibrand’s legislation is a vital move towards better understanding, tracking, and treating these injuries.”

    Specifically, the Blast Overpressure Safety Act would: 

    1. Mandate regular neurocognitive assessments over a service member’s career, including a baseline neurocognitive assessment before training. 
    2. Create blast overpressure exposure and TBI logs for all service members.
    3. Increase transparency regarding blast overpressure safety in the weapons acquisition process. DoD must consider the minimization of blast overpressure during the acquisition process, require contracting entities to provide blast overpressure safety data, and publish blast overpressure safety data for weapons systems and its plans to better protect service members from in-use weapons systems. 
    4. Improve data on concussive and subconcussive brain injuries service members sustain. This includes information on discharges related to and medical providers trained in these injuries, as well as efforts with allies and partners to better address these injuries. 
    5. Enhance efforts to mitigate exposure and help service members access care. This includes retaliation protections for those who seek care; modifying existing weapons system to reduce blast exposure; updating and making publicly available blast overpressure thresholds and creating a waiver system for exceeding these thresholds; training high-risk service members to help them recognize exposure symptoms and creating strategies to mitigate their risk; and expanding the types of technologies in the Warfighter Brain Health Initiative pilot blast monitoring program. 
    6. Support service member treatment by establishing a Special Operations Comprehensive Brain Health and Trauma program, making the National Intrepid Center of Excellence (NICoE) a program of record and requiring DoD to provide child care services to those seeking treatment there, and mandating training for medical and training personnel on blast overpressure and exposure and TBI. 

    MIL OSI USA News

  • MIL-OSI USA: Sen. Marshall Joins Grassley and Bicameral Colleagues in Calling Out Abuses in the Biden-Harris Unaccompanied Migrant Children Program

    US Senate News:

    Source: United States Senator for Kansas Roger Marshall

    Washington, D.C. – U.S. Senator Roger Marshall, M.D. joined Sen. Chuck Grassley (R-Iowa) and bicameral Republican colleagues in a letter urging President Joe Biden and Vice President Kamala Harris to work with Congress to root out abuses in their administration’s unaccompanied migrant children program and stop the Department of Health and Human Services (HHS)’s cover-up of the crisis. HHS has failed to comply with two out of three Department of Homeland Security (DHS) subpoenas and other information requests issued amid its investigation into more than 100 suspicious sponsors identified.
    Program Abuse
    More than 500,000 unaccompanied migrant children have crossed the southwest border under the Biden-Harris administration, while cartel trafficking activity surged an estimated 2,500 percent. Amid this crisis, the lawmakers note that the Biden-Harris administration limited background checks for sponsors of unaccompanied children, cut back on familial DNA testing at the border and decreased information sharing with law enforcement.
    Seeking Solutions
    The lawmakers are urging Biden and Harris to “make changes to [their] policies and procedures” in order to “end this public safety crisis.” They are specifically calling on the Biden-Harris administration to enhance information sharing with law enforcement and Congress, fully cooperate with DHS’s child exploitation investigation and thoroughly respond to all congressional oversight requests.
    “[The Biden-Harris HHS] must stop its cover-up and cooperate with law enforcement and Congress to end this crisis and protect unaccompanied children and the American people,” the lawmakers concluded.
    Read the full letter HERE.

    MIL OSI USA News

  • MIL-OSI New Zealand: Child-care centre guidance on Police vetting for workers

    Source: Worksafe New Zealand

    We have updated our guidance on the requirements for vetting workers at limited-attendance child-care centres.

    The new Regulatory Systems (Education) Amendment Act 2024 means updates have been made to the Health and Safety at Work (General Risk and Workplace Management) Regulations 2016 (Regulation 51).

    A key point is that Police vetting must be completed for non-teaching and unregistered employees at unlicensed child-care centres before the person begins work. This vetting must be used to assess any risks to the safety of children. 

    What are limited-attendance child-care centres?

    These are any premises that are:

    • used regularly for the care of three or more children under six years old (not including the children of the persons providing the care) and
    • where the children do not stay for more than two hours per day and
    • where the children’s parents or caregivers are in close proximity to the children, and are able to be contacted and resume responsibility for the children at short notice. 

    For example, a crèche at a gym or shopping mall.

    It does not include being provided with care before or after school.

    Read more information in the fact sheet: What to know when employing or engaging limited-attendance child-care centre workers

    Related information:

    Governance of education sector boosted | Beehive.govt.nz (external link)

    Regulatory Systems (Education) Amendment Act 2024 – Education in New Zealand | Education.govt.nz (external link)

    MIL OSI New Zealand News

  • MIL-OSI New Zealand: Work-related health newsletter – September 2024

    Source: Worksafe New Zealand

    Kia ora koutou and welcome to the September work-related health newsletter. Check out the latest guidance to help you ensure a healthy and safe work environment for you and your workers.

    In this edition:

    • WorkSafe’s priority plans published
    • Updated guidance for working with asbestos
    • New manual tasks screening and risk assessment tools
    • Keeping volunteers healthy and safe
    • Health and safety governance good practice guide
    • ACC levy consultation
    • Upcoming conference.

    Read the full newsletter(external link)

    MIL OSI New Zealand News

  • MIL-OSI United Kingdom: Safe Access Zones

    Source: Scottish Government

    Protected zones around abortion services now in place.

    Protected zones of 200 meters around all abortion services in Scotland are now in place.

    Within these zones, it is now a criminal offence to intentionally or recklessly behave in ways that could influence the decisions of women and staff to access services; impede their access; or otherwise cause alarm, harassment or distress.

    Police Scotland are responsible for enforcing the legislation. People who break the law can be fined up to £10,000, or be given an unlimited fine, depending on the court procedure.

    Determining whether an offence has been committed will be a matter for Police Scotland, the Crown Office and Procurator Fiscal Service and the Courts. Depending on the facts and circumstances of each case, some examples of criminal behaviour may include: approaching someone to try and persuade them not to access abortion services, surrounding people as they try to go in or out of the clinic or hospital, handing out leaflets, religious preaching and silent vigils.

    Minister for Public Health and Women’s Health Jenni Minto said:

    “The introduction of Safe Access Zones is a crucial milestone in protecting women’s abortion rights – no one has the right to interfere in women’s personal medical decisions and the law now makes that abundantly clear.

    “I thank Gillian Mackay and all those involved for their work to progress this legislation. I would like especially recognise the women who showed incredible courage in speaking up and sharing their experiences during the Bill process.

    “The new zones of 200 meters around all abortion services will help ensure women have safe access to healthcare – free from intimidation. This law is about protection for women at a time when many will feel incredibly vulnerable around taking a deeply personal and difficult decision.”

    Background

    Full details of the penalties that apply for committing an offence.

    Full list of the locations of zones:

    University Hospital Crosshouse – Kilmarnock

    Borders General Hospital – Melrose

    Dumfries and Galloway Royal Infirmary

    Galashiels Health Centre

    Oak Tree Family Health Centre – Stranraer

    Queen Margaret Hospital – Dunfermline

    Victoria Hospital – Kirkcaldy

    Forth Valley Royal Hospital – Larbert

    Aberdeen Royal Infirmary

    Aberdeen Community Hospital

    Aberdeen Maternity Hospital

    Dr Gray’s Hospital – Elgin

    Inverclyde Hospital – Greenock

    Royal Alexandra Hospital – Paisley

    Sandyford Sexual Health Clinic – Glasgow

    Princess Royal Maternity Hospital – Glasgow

    Ross Hall – Glasgow

    New Victoria Hospital – Glasgow

    Queen Elizabeth University Hospital – Glasgow

    Stobhill Hospital – Glasgow

    Vale of Leven Hospital – West Dunbartonshire

    Raigmore Hospital – Inverness

    University Hospital Wishaw

    Royal Infirmary Edinburgh

    Chalmers Sexual Health Centre – Edinburgh

    St John’s Hospital – Livingston

    The Balfour – Livingston

    Gilbert Bain Hospital – Lerwick

    Ninewells Hospital – Dundee

    Western Isles Hospital – Stornoway

    MIL OSI United Kingdom

  • MIL-OSI USA: Capito, Colleagues Reintroduce Bill to Crack Down on Illicit Drug Analogues

    US Senate News:

    Source: United States Senator for West Virginia Shelley Moore Capito

    WASHINGTON, D.C. – Last week, U.S. Senator Shelley Moore Capito (R-W.Va.) joined a bipartisan group of colleagues to reintroduce the Stop Importation and Manufacturing of Synthetic Analogues (SIMSA) ActThe legislation is led by U.S. Senators Chuck Grassley (R-Iowa) and Maggie Hassan (D-N.H.).

    Specifically, the SIMSA Act targets deadly drugs that are substantially similar to already-controlled substances, but carefully engineered—often in China or Mexico—to slip into the U.S. undetected.  

    “Preliminary data from the West Virginia Department of Health and Human Resources shows that fentanyl and fentanyl analogues were involved in approximately 82% of all drug overdose deaths in West Virginia in 2023,” Senator Capito said. “These deadly substances are flowing into our communities from China and across our southern border, and criminals know that they can get around existing law by slightly changing the chemical makeup of a drug while still having the same negative effect on the human body. This legislation will allow for law enforcement to crack down on synthetic drugs and save lives.”

    BACKGROUND:

    U.S. law prohibits the unauthorized use of certain controlled substances. However, illicit drug makers and importers circumvent those laws by altering single atoms in controlled substances to create tweaked drugs that are not yet outlawed, but have similar effects on users. Currently, uncontrolled substances must undergo a time-consuming analysis before the Drug Enforcement Administration (DEA) can permanently schedule them. 

    Full text of the bill can be found here.

    MIL OSI USA News

  • MIL-OSI USA: Senator Markey’s Major Alzheimer’s Legislation Passes Through House, Moves to President Biden’s Desk

    US Senate News:

    Source: United States Senator for Massachusetts Ed Markey
    Then-Representative Markey authored the National Alzheimer’s Project Act in 2011 and the Alzheimer’s Accountability Act in 2014
    Washington (September 23, 2024) – Senator Edward J. Markey (D-Mass.), chair of the Senate Health, Education, Labor and Pensions (HELP) Subcommittee on Primary Health and Retirement Security and founder and co-chair of the Congressional Task Force on Alzheimer’s, applauded passage by the House of Representatives of the National Alzheimer’s Project Act (NAPA) Alzheimer’s Accountability and Investment Act, legislation that would cement and build on the important progress that has been made to prevent and effectively treat Alzheimer’s disease. The National Alzheimer’s Project Act (NAPA) Reauthorization and the Alzheimer’s Accountability and Investment Act (AAIA) now head to President Joe Biden’s desk to be signed into law.  
    “Since my mother was diagnosed with Alzheimer’s in 1985, I have fought to ensure the federal government has the funding, resources, and coordination necessary to find a cure for this disease,” said Senator Markey. “The National Alzheimer’s Plan Act and the Alzheimer’s Accountability Act have transformed our understanding of the disease and its risk factors for more than a decade. But our work is not yet done. Today’s extension of these bills until 2035 is a commitment from Congress that we will not stop fighting until Alzheimer’s is a disease only found in history books. I thank Senator Collins and my colleagues for their support in delivering hope to millions of families just like mine across the country as these two bills head to the President’s desk.”
    “We have made tremendous progress in recent years to boost funding for Alzheimer’s research, which holds great promise to end this disease that has had a devastating effect on millions of Americans and their families,” said Senator Susan Collins, a founder and co-chair of the Congressional Task Force on Alzheimer’s Disease. “These two bills will maintain our momentum and make sure that we do not take our foot off the pedal just as our investments in basic research are beginning to translate into potential new treatments. We must not let Alzheimer’s to be one of the defining diseases of our children’s generation as it has ours.”
    “I know from firsthand experience what a devastating illness Alzheimer’s disease is, as I watched my mother battle with it for a decade before her passing,” said Senator Mark Warner, co-chair of the Congressional Task Force on Alzheimer’s Disease. “While we’ve made great strides in research, there is still so much work to be done to find effective ways to prevent and treat Alzheimer’s. On behalf of the millions of American families who have been touched by Alzheimer’s, I’m glad to see these two bills head to the president’s desk to be signed into law.”
    The NAPA Reauthorization Act — co-led by Senators Ed Markey (D-Mass.), Collins (R-Maine), Mark Warner (D-Va.), Shelley Moore Capito (R-W.Va.),  Jerry Moran (R-Kan.), Bob Menendez (D-N.J.), Lisa Murkowski (R-Alaska), and Debbie Stabenow (D-Mich.) — would reauthorize NAPA through 2035 and modernize the legislation to reflect strides that have been made to understand the disease, such as including a new focus on promoting healthy aging and reducing risk factors. The bill also includes updated language to reduce health disparities for underserved communities, including Black, Brown and disabled communities, who are at increased risk for Alzheimer’s as they age.
    The NAPA Reauthorization Act is endorsed by the Alzheimer’s Association, UsAgainstAlzheimer’s, National Down Syndrobe Society, National Down Syndrome Congress, and LuMind IDSC Foundation.
    The Alzheimer’s Accountability and Investment Act — authored by Senators Markey, Collins, Capito, Warner, Moran, Menendez, Murkowski, and Stabenow — would continue through 2035 a requirement that the Director of the National Institutes of Health submit an annual budget to Congress estimating the funding necessary to fully implement NAPA’s research goals. Only two other areas of biomedical research – cancer and HIV/AIDS – have been the subject of special budget development aimed at speeding discovery.
    The Alzheimer’s Accountability and Investment Act is endorsed by the Alzheimer’s Association and UsAgainstAlzheimer’s.
    Senator Markey is a leader in the fight to find a cure for Alzheimer’s disease and to support family caregivers. In July 2024, Senator Markey applauded the HELP Committee’s passage of Older Americans Act Reauthorization Act of 2024, which included provisions based on his Respite Care And Resources for Everyone (CARE) Act and Convenient Care for Caregivers Act to expand respite care for family caregivers of older adults that need long-term care, including individuals with Alzheimer’s disease and related dementia. Earlier that month, Senator Markey unveiled his “Caring for Caregivers” family caregiving agenda, which included his Convenient Care for Caregivers Act to support family caregivers and individuals with Alzheimer’s receiving health care services at the same time and location to improve health outcomes. As a member of the House of Representatives, Senator Markey founded the bipartisan, bicameral Congressional Task Force on Alzheimer’s to develop a whole-of-government approach to finding a cure for Alzheimer’s. He created the Independence at Home program to provide seniors, including individuals with Alzheimer’s and other dementia, the option to receive primary care in their home. Senator Markey authored the bipartisan Spending Reductions Through Innovations in Therapies (SPRINT) Act, which would encourage drug development for high-cost, chronic health conditions such as Alzheimer’s, the Health Outcomes, Planning and Education (HOPE) Act to improve early detection and diagnoses of Alzheimer’s and support caregivers, and the Alzheimer’s Breakthrough Act, which would require the National Institutes of Health (NIH) work to improve treatment outcomes and engage federal agencies in the effort to combat Alzheimer’s.

    MIL OSI USA News

  • MIL-OSI New Zealand: Three cheers for Simon Court

    Source: ACT Party

    The Haps

    ACT MP Todd Stephenson has picked up the End of Life Choice baton. David Seymour’s original bill did not restrict access to people terminal within six months, but he would have had no bill without adding the restriction. That political compromise has meant some of the people who suffer most – especially those with long, slow, degenerative diseases like Motor Neurone Disease – are denied choice and control. Stephenson explains how his new bill would put this compromise right on Q&A, here.

    Three cheers for Simon Court

    The most important thing this Government does in three years may be what’s happening quietly in the background of resource management reform. Last week Court announced, beside Chris Bishop, that the Government is replacing the RMA with two laws based on property rights.

    If you’re a long-term Free Press reader, all of this will sound very familiar. The difference is that this time it is happening. It is now official Government policy with a series of dates by when legislation will be drafted, introduced to Parliament, and passed into law.

    At the heart of New Zealand’s problem is that it’s a beautiful, isolated piece of land. It has a mild climate that beats Canada’s skin-freezing cold or Australia’s blood-boiling heat any day. It’s filled with resources that make it one of the richest per-capita in the world. Climate change will probably actually make New Zealand even better off compared with the rest of the world.

    When a group of people have such a wonderful inheritance, they have two choices. Either make the most of it, or pull up the drawbridge.

    Making the most of it would mean making it easy for each generation to build a home. That would mean making it easy to build the infrastructure that connects homes together, forming towns and cities. It should be easy to farm the land, and extract resources that make human life long and happy (just not while they’re left in the ground).

    This seems like an obvious choice, but enter human nature. For the last few decades, the net result has been pulling up the drawbridge. You can’t do bloody anything, home building has only once reached the levels of the 1970s, when there were only three million people. There are probably more Kiwis working in Australian mines than New Zealand ones.

    The result is a generation who feel hopeless. Born into the best place on the planet where it’s needlessly hard to get a place of your own. Why not vote for a politician who promises to tax the rich? Better still, cut out the middle man, join a gang, and do it yourself. Then there’s those who leave.

    That is the result of the RMA. The simple diagnosis is that it’s a bureaucratic nightmare, but it’s more than that. It is the legislative expression of a people’s desire to enjoy what they have and bugger anyone else.

    The central concept in the RMA is sustainable development, to provide for current generations without taking from future ones. Because nobody knows what future generations want, or what technology they’ll have to achieve it, the best way to achieve this is to do as little as possible, which is pretty much what’s happened.

    Too many people have too many grounds to object to too many activities meaning nothing gets done. It’s not unusual for it to take longer to get permission to do something than to actually do it. The range of criteria Councils must consider under the RMA is everything from climate change (but you already pay under the ETS for whatever you do) to the ‘intrinsic values of ecosystems’ (how can you know them if they’re intrinsic)?

    David Parker’s RMA reforms, replacing it with three acts, introduced a new central concept ‘te oranga o te taiao.’ Nobody knows what that means in the context of resource management decisions. By the time the Courts figured it out, Indonesia would have overtaken us in GDP per capita.

    So that’s gone and the Resource Management Act is being replaced with a law whose central concept is the enjoyment of private property. The starting point is that you have a right to use and develop your own property. The second result is that you have a right to object only if your own property is affected.

    The result is a switch back to the pioneering vision of New Zealand. A nation of people who can instead of a nation of people who are not allowed.

    The law will also make many processes standard. If you have a water treatment plant that spits out water with less than x parts per million of E. Coli, congratulations. You’ve met the standard and can just build it.

    The Government will now listen to an expert advisory group, people with real experience of development, as the law itself is developed for introduction to Parliament. It will be passed before the next election, and New Zealand will have taken a massive step forward to achieving its potential.

    Much of this is owed to Simon Court, one of only two engineers in Parliament (David Seymour is the other one). Court has been working away since he entered Parliament, releasing ACT’s detailed RMA policy in 2022, and making it real in Government. A very good example of how ACT keeps the Government in place, and makes it better.

    MIL OSI New Zealand News

  • MIL-OSI USA: Senator Collins’ Two Bills to Combat Alzheimer’s Head to President’s Desk

    US Senate News:

    Source: United States Senator for Maine Susan Collins
    Washington, D.C. – Today, U.S. Senator Susan Collins applauded the passage by the House of Representatives of two bipartisan bills she authored that would cement and build on the important progress that has been made to prevent and effectively treat Alzheimer’s disease. The National Alzheimer’s Project Act (NAPA) Reauthorization and the Alzheimer’s Accountability and Investment Act (AAIA) now head to the President’s desk to be signed into law.
    “We have made tremendous progress in recent years to boost funding for Alzheimer’s research, which holds great promise to end this disease that has had a devastating effect on millions of Americans and their families,” said Senator Collins, a founder and co-chair of the Congressional Task Force on Alzheimer’s Disease. “These two bills will maintain our momentum and make sure that we do not take our foot off the pedal just as our investments in basic research are beginning to translate into potential new treatments. We must not let Alzheimer’s to be one of the defining diseases of our children’s generation as it has ours.”
    More than six million Americans are living with Alzheimer’s. Alzheimer’s costs our nation an astonishing $360 billion per year, including $231 billion in costs to Medicare and Medicaid. If we continue along this trajectory, Alzheimer’s is projected to claim the minds of 13.8 million seniors by 2060 and nearly surpass $1 trillion in annual costs by 2050. In 2022, family caregivers provided 18 billion hours of unpaid care for loved ones with dementia.
    In 2011, Senator Susan Collins authored the National Alzheimer’s Project Act (NAPA) with then-Senator Evan Bayh (D-IN).  NAPA convened a panel of experts, who created a coordinated strategic national plan to prevent and effectively treat Alzheimer’s disease by 2025. The law is set to expire soon and must be reauthorized to ensure that research investments remain coordinated, and their impact is maximized.
    The NAPA Reauthorization Act would:
    Reauthorize NAPA through 2035 and modernize the legislation to reflect strides that have been made to understand the disease, such as including a new focus on promoting healthy aging and reducing risk factors.
    Update language in recognition of the need to include underserved populations, including individuals with Down syndrome, who are at increased risk for Alzheimer’s as they age.
    This bill is now endorsed by the National Down Syndrome Society, the National Down Syndrome Congress, and LuMind IDSC Foundation.
    The Alzheimer’s Accountability and Investment Act would:
    Continue through 2035 a requirement that the Director of the National Institutes of Health submit an annual budget to Congress estimating the funding necessary to fully implement NAPA’s research goals.
    Only two other areas of biomedical research – cancer and HIV/AIDS – have been the subject of special budget development aimed at speeding discovery.

    Senator Collins authored the NAPA Reauthorization Act with Senator Mark Warner (D-VA) and the Alzheimer’s Accountability and Investment Act with Senator Ed Markey (D-MA). Both bills are cosponsored by Senators Shelley Moore Capito (R-WV), Jerry Moran (R-KS), Lisa Murkowski (R-AK), and Debbie Stabenow (D-MI).
    The NAPA Reauthorization Act and the Alzheimer’s Accountability and Investment Act are endorsed by the Alzheimer’s Association and UsAgainstAlzheimer’s.

    MIL OSI USA News