Letter to Burwell and Collins Demands Funding Equality

Author:

Uniting the ME/CFS community is not easy, but it has never been more important than right now. One thing we all agree on is the urgent need for vastly increased funding at the National Institutes of Health, our nation’s scientific research machine. When two federally funded reports told NIH that there was an “urgent need” to invest in ME/CFS research, a number of advocates seized the opportunity to push even harder for substantive change.
Among the efforts, a recent one was aimed at demonstrating consensus among advocacy groups on a platform of immediate next steps toward full funding at NIH. I worked with many ME/CFS advocacy organizations to fashion a 5-point platform for next steps at NIH and, with endorsement of a broad set of groups, sent it to Secretary of Health Burwell and NIH Director Collins in September.
The 1-page platform builds on engagement by patients, experts and advocates since the release of the IOM and P2P reports. Last spring, more than 500 patients and caregivers sent emails to Secretary Burwell and Director Collins highlighting the “urgent need for research” validated by both panels, calling on them for equal funding. CFSAC, with significant input from advocates, made recommendations to operationalize the IOM report and much more. SolveMECFS hosted a Congressional Briefing with Morgan Fairchild, among other things, and advocates engaged meaningfully with the Senate Appropriations Committee after it zeroed the minuscule funds earmarked to CFS in the CDC budget. MEAction is a welcome new force in catalyzing patient engagement.
The confluence of the two federal reports, the results of the Lipkin/Hornig immune studies, and numerous powerful media stories have created a demand for change that that has rarely been seen before.
I believe it is important to demonstrate our unity, to show the Secretary and NIH at every turn that we are united in our goal of equal funding for the science that can diagnose, treat and cure our disease. The more we act in concert, the more we will achieve.
Editor’s note: We at #MEAction believe in empowering a diversity of views and strategies within the movement. However, there is a strong consensus around the goals of Courtney Miller’s letter and so when she approached us about adding our support, we put the letter to a vote of all registered users of #MEAction. 57 users participated and support for the letter was nearly unanimous.

Facebook
Twitter
WhatsApp
Email

3 thoughts on “Letter to Burwell and Collins Demands Funding Equality”

  1. Please add Chronic Fatigue Syndrome Research Center at Stanford University to the groups signing.

  2. Thanks, Janet and Pat. I will add your organizations. Thank you as well for all you do. Janet, the Post story about your son was very well done from the outside, heartbreaking though it is. Wishing you all better days.
    Courtney

Comments are closed.

Latest News

black rectangle with white squiggles in the background. red bubbles and honeycomb in the corners. in the middle a red box that reads: #MEAction & the Mayo Clinic awarded the Sigma 2024 American Nurses Credentialing Center Evidence-Based Practice Implementation Grant. #MEAction logo in the bottom right hand corner

#MEAction & Mayo Clinic Projects Continue – New Grant Awarded

Given the rapidly changing landscape at the federal level, we recognize that the road ahead may bring some changes for patient advocacy. Even in this evolving environment, we’re excited to share some positive news: #MEAction and the Mayo Clinic have been awarded the Sigma 2024 American Nurses Credentialing Center Evidence-Based Practice Implementation Grant awarded by

Read More »

You’re Invited: The Beth Mazur Innovation Prize Fundraiser

You are cordially invited to The Beth Mazur Innovation Prize Fundraiser on Wednesday, November 13th at 2pm PST/5pm EST. Beth Mazur, who co-founded #MEAction was a kind and compassionate human being. She cared deeply about the ME and the Long COVID communities. She also cared deeply about innovation, new creative ways to solve problems that

Read More »
rectangle image with a purpleish marble background. In the center is a blue square with the words a very modified movement class - nov 15th-. the #MEAction logo and nourish therapeutic yoga logo at the bottom.

A Very Modified Movement Class on 11/15

Join #MEAction for our final very modified movement class of the year on Friday, November 15th at 11am PST/2pm EST/7pm GMT. This class has been crafted specifically for people with ME. This 30 minute class will be hosted virtually. We are, once again, thrilled to partner with Shannon Williams-Bramburger of Nourish Therapeutic Yoga, who has

Read More »
Scroll to Top