Advocacy Win! Disability Partnerships Make a Difference for People with ME

The National Institutes of Health (NIH) announced they will designate people with disabilities as a population with health disparities. This is a win that could have a large impact on people with ME and the millions of people with disabilities across the country. 

“This designation recognizes the importance and need for research advances to improve our understanding of the complexities leading to disparate health outcomes and multilevel interventions,” said Dr. Pérez-Stable. “Toward this effort,National Institutes on Minority Health and Health Disparities and other NIH institutes launched a new research program to better understand the health disparities faced by people with disabilities who are also part of other populations designated as having health disparities.”

We fought for this because the National Institutes on Minority Health and Health Disparities previously rejected the recommendation to recognize people with disabilities as a “health disparity population” within the NIH. 

The letter, co-authored by Dr. Bonnielin Swenor, Director of The Johns Hopkins Disability Health Research Center, and Dr. Jae Kennedy, Professor of Community and Behavioral Health, WSU College of Medicine, explained the value of this proposal:

“Designating people with disabilities as an NIH health disparity population is more than a semantic exercise – centers, offices, and institutes across the NIH use these categories to develop research concepts and FOAs, particularly in the domain of health disparities research. They are also used to target training support and development funds for NIH employees and extramural grantees. Including people with disabilities is therefore essential to the broader health equity goals of the NIH and the US Department of Health and Human Services.”

Many grants at NIH focus on “health disparities populations”. More than one disability researcher has met with a program officer at NIH to see if their research idea was eligible for a specific grant, only to be turned away because their research was on disability– until now.

HHS Secretary Xavier Becerra stated, “Research to understand the barriers and unmet needs faced by people with disabilities, and to develop effective interventions to address them, is needed. This designation will help to improve access to healthcare and health outcomes for all people.” For us, that means that the NIH will be faced with examining the barriers people with ME have faced for decades. 

#MEAction signed on to support this effort brought forth by disability rights groups. This type of win is why aligning with our broader disability community has a positive impact for all. 

Thank you for all of you who continue to support #MEAction, disability advocacy, and our broader chronic illness community. This gives us more power to fight for people with ME each and every day. 

Facebook
Twitter
WhatsApp
Email

Latest News

#MillionsMissing Week is Here: #TeachMETreatME in Action!

We are excited to announce the kick-off of #MillionsMissing 2024 – our ongoing campaign to Teach ME and Treat ME by educating medical providers across our nation’s hospital systems and medical schools about myalgic encephalomyelitis (ME).  Throughout the spring, summer and fall, #MEAction teams are hosting 13 medical education events to encourage medical providers to

Read More »

#MEAction’s Jaime Seltzer Selected for TIME100 Health 2024

We are thrilled to share with you that Jaime Seltzer, #MEAction’s Scientific Director, has been selected for TIME100 Health 2024, TIME’s new annual list of 100 individuals who most influenced global health this year! This is a huge honor based on years of work fighting for equity for people with ME.  We intimately know the

Read More »
white rectangle with the words: Interview with Author Lauren Saikkonen in black font. There is an image of her book cover, Invisible Illness on the left hand side. And a photo of Lauren on the right hand side. Lauren is wearing a red sweater and is smiling at the camera.

Interview With Lauren Saikkonen – Author of Invisible Illness: Coming of Age, Chronic Illness, and a Mother’s Will to Survive

#MEAction is once again thrilled to share a new book, Invisible Illness: Coming of Age, Chronic Illness, and a Mother’s Will to Survive, with you by author Lauren Saikkonen! This book is an autobiography that covers Lauren’s entire life, but heavily focuses on her battle with Ehlers-Danlos syndrome, ME, and fibromyalgia.  You can purchase this

Read More »
Scroll to Top