Tell Congress to Increase ME Funding

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Have you always wanted to email your Congressmen/ women about ME/CFS but don’t know what to say? Or maybe you’re too sick to draft a letter? We’ve made it easy for you!

Write your local representative

1. Go to www.contactingthecongress.org
and enter your address to find out who your Congressmen/women are.
2. Click on the “Contact Form” links.
3. Fill out the webforms by copying and pasting from the sample letter below. You can also add a paragraph with your ME/CFS story, to make it more personal.
4. If you don’t receive a reply, call their office to follow up!
5. Tell your friends and family to contact their Congressmen/women, too! It could be their Christmas, Hanukkah, or birthday gift to you!
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Dear Senator/ Representative,
I am writing to you as a constituent and deeply concerned citizen. I need you to be a champion in Congress for the severely debilitating, chronic, neuro-immune disease Myalgic Encephalomyelitis (ME), also known as Chronic Fatigue Syndrome (CFS). ME/CFS patients are too sick to advocate for themselves. So, despite recent media attention, this condition doesn’t have the widespread awareness that other severe diseases do. That’s why political action on ME/CFS patients’ behalf is so vital. Specifically, I need your help to increase National Institutes of Health (NIH) funding and to modify Department of Health and Human Services (HHS) diagnostic criteria for this horrific disease.
An estimated one million Americans suffer from ME/CFS, a long-term disease that primarily targets young, previously healthy adults from diverse ethnic and socioeconomic backgrounds. The disease is so severe; it renders a quarter of its patients bedbound and unable to care for themselves. More than half are disabled and can’t work, attend school, or participate in daily life activities. ME/CFS patients do not spontaneously recover. The U.S. Institute of Medicine (IOM) calls patients with ME/CFS “more functionally impaired than those with type 2 diabetes, congestive heart failure, [or] multiple sclerosis.” Doctors familiar with both AIDS and ME/CFS say they’d rather have AIDS. The Centers for Disease Control (CDC) estimates ME/CFS’s annual burden on the U.S. economy to be $17-24 billion. However, the NIH consistently places ME/CFS at the rock bottom of its budget, with barely $5 million/year. This is less than the NIH allocates for hay fever, and is nowhere near its allocation for other similarly burdensome diseases:
– ME/CFS: About $5 per patient per year in NIH funding ($5 million in 2015)
– Multiple Sclerosis (MS): About $250 per patient ($103 million in 2015)
– HIV/AIDS: About $2,500 per patient ($3 billion in 2015)
As a result, ME/CFS still has no known cause, no FDA-approved treatment, and no cure. The lack of progress in ME/CFS research over the past 50 years is appalling, and is reflected in the absence of a standard of care for ME/CFS or even a knowledgeable response from most medical practitioners when encountering these patients and their families.
The NIH has responded to past requests for increased funding by saying that few researchers are interested in studying ME/CFS. However, there are currently Nobel Laureates, several members of the National Academy of Sciences, biochemists, biophysicists, geneticists, immunologists, neuroscientists, experts in public health and infectious disease, epidemiologists, and physicians who are eager and ready to study ME/CFS, if adequate funding were available. Many of these researchers have written an open letter to U.S. senators to express their interest and enthusiasm. The letter also notes that there is widespread agreement, both inside and outside the U.S. Government, on the imperative of dramatically increasing ME/CFS research resources.
Recently, NIH has stated that it hopes its renewed focus and efforts on ME/CFS will lead to more research funding. However, new NIH announcements have not included any additional money. NIH has also said that it can’t increase ME/CFS funding because it doesn’t set specific budgets for individual disorders. Yet, the NIH does set specific budgets for its Centers and Institutes, including its Cancer Institute, Institute of Diabetes & Digestive & Kidney Diseases, Institute of Arthritis & Musculoskeletal & Skin Diseases, etc. The NIH also issues RFAs with specific budget commitments, and it develops internal Institute concepts and initiatives with specific budget estimates. The problem is that ME/CFS is not part of this budget planning process. ME/CFS doesn’t have a “home” institute or center, and it hasn’t had a new RFA in over 10 years. Accordingly, these deficiencies need to be corrected if NIH is to realize its “hope” of increased ME/CFS funding.
To move the science forward on ME/CFS, the disease also needs well-defined diagnostic criteria. HHS’s Chronic Fatigue Syndrome Advisory Committee (CFSAC), ME/CFS medical experts, ME/CFS patients, their advocates, and their families have entreated the HHS to strike its current, overly-broad ME/CFS diagnostic criteria in favor of the well-defined, globally-accepted Canadian Consensus Criteria (CCC), which was established in 2003 by a team of international ME/CFS medical experts. The International Association of Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis (IACFS/ME), the field’s professional organization, has officially endorsed and adopted the CCC standards, as have at least 50 ME/CFS medical experts, almost 200 ME/CFS advocates, and more than 6,000 patients. The 2011 International Consensus Criteria (ICC) revision is also well-established and alternatively acceptable.
In conclusion, as a deeply concerned citizen and your constituent, I strongly urge you to use your powers and direct HHS to:
1. Fund biomedical research for ME/CFS in the amount of $250 million, which is commensurate with similarly burdensome diseases;
2. Establish authority for researching ME/CFS within the National Institute of Neurological Disorders and Stroke (NINDS), which currently leads the Trans-NIH ME/CFS Working Group;
3. Issue a new RFA that sets aside a significant amount of funding for new ME/CFS research; and
4. Endorse the well-defined, globally-accepted Canadian Consensus Criteria (CCC) for U.S. ME/CFS diagnosis and research.
By taking these four critical steps, you will eliminate the greatest obstacles to finding an ME/CFS cure and thereby significantly ease the enormous physical and economic burden of ME/CFS on millions of American patients and family members.
Thank you for your attention. I look forward to your response on this matter.
=============================
Recent media coverage of ME/CFS:
11/3/15 Business Insider: What is Chronic Fatigue Syndrome?
http://www.businessinsider.com/what-is-chronic-fatigue-syndrome-2015-11
November 2015 Oprah Magazine: Chronic Fatigue Syndrome Finally Gets its Due
http://linkis.com/www.oprah.com/health/Gnq0K
10/8/15 The Atlantic: Chronic Fatigue Patients Push for an Elusive Cure
http://www.theatlantic.com/health/archive/2015/10/chronic-fatigue-patients-push-for-an-elusive-cure/409534/
10/5/15 The Washington Post: With His Son Terribly Ill, a Top Scientist Takes on Chronic Fatigue Syndrome
https://www.washingtonpost.com/national/health-science/with-his-son-terribly-ill-a-top-scientist-takes-on-chronic-fatigue-syndrome/2015/10/05/c5d6189c-4041-11e5-8d45-d815146f81fa_story.html
8/17/15 Science Magazine: Lobbyists Seek New Funds for Chronic Fatigue Syndrome Research
http://news.sciencemag.org/biology/2015/08/lobbyists-seek-250-million-new-funds-chronic-fatigue-syndrome-research
=========================
Doctors speak out about ME/CFS:
“[ME/CFS] is one of the most disabling diseases that I care for, far exceeding HIV disease except for the terminal stages.”—Dr. Daniel Peterson, doctor and researcher
“[An ME/CFS patient] feels effectively the same every day as an AIDS patient feels two months before death; the only difference is that the symptoms can go on for never-ending decades.” —Prof. Mark Loveless, Head of the AIDS and ME/CFS Clinic at Oregon Health Sciences University
“Although [ME/CFS sufferers] are ill with a debilitating flu-like illness every day of their lives, neighbors and even friends and family insist they look “just fine.” It’s an unfortunate fact that our culture has yet to accept the harsh reality of chronic disease; often, its ravages are invisible to the naked eye. ”—Dr. David Bell, ME/CFS clinician and researcher
“If I had to choose between the two illnesses [HIV and ME/CFS], I would rather have HIV… My HIV patients for the most part are hale and hearty thanks to decades of research and billions of dollars. Many of my ME/CFS patients, on the other hand, are terribly ill and… experience a level of disability equal to that of patients with late-stage AIDS and patients undergoing chemotherapy… ME/CFS, which impacts a million people in the United States alone, has had a small fraction of the research dollars directed towards it.”—Dr. Nancy Klimas, AIDS and ME/CFS researcher and clinician
“We’ve documented, as have others, that the level of functional impairment in people who suffer from CFS is comparable to multiple sclerosis, AIDS, end-stage renal failure, chronic obstructive pulmonary disease.”– Dr. William Reeves, former CDC Chief of Viral Diseases Branch
================================
Researchers’ Open Letter to U.S. Senators:
August 17, 2015
Dear Senator,
We the undersigned scientists are writing to express our interest and enthusiasm for researching myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), a common and disabling illness long ignored by our nation’s health agencies.
Many of us have had a very difficult time securing adequate funding. Others have been unable to determine even how to apply for funding, as no institute within the NIH has responsibility for researching ME/CFS. The NIH has responded to requests for increased funding by stating that few researchers are interested in studying the illness.
On the contrary there are Nobel Laureates, several members of the National Academy of Sciences, biochemists, biophysicists, geneticists, immunologists, neuroscientists, experts in public health and infectious disease, epidemiologists, and physicians eager and ready to study this disease, were adequate funding made available. The undersigned are just some of those researchers.
We have so much to learn and large studies are needed to understand how to help patients regain their health. With societal costs in the tens of billions of dollars each year, an infusion of government funding could quickly repay that investment.
Currently, ME/CFS is massively underfunded compared to other diseases of similar severity and number of patients. The NIH allocates just $5 million per year to study this illness, which affects between 836,000 and 2.5 million Americans. Patients suffering from ME/CFS deserve funding proportional to and commensurate with other diseases with similar patient populations. The Institute of Medicine, a special HHS advisory committee, and a recent NIH appointed Expert panel all agree: It is imperative to increase research funding for ME/CFS.
If invited to apply for NIH funding via a new Request for Applications (RFA), we would eagerly submit grant proposals.
Sincerely,
Linda Tannenbaum, Executive Director
Open Medicine Foundation
Ronald W. Davis, Professor of Biochemistry and Genetics, Stanford University School of
Medicine, Member of the National Academy of Sciences
 
Andreas M. Kogelnik, Physician, Scientist,
Founder and Director of the Open Medicine Institute
Susan Levine, MD Researcher and Clinician, Private Practice New York, New York Visiting
Fellow, Cornell University Ithaca, New York
Peter C. Rowe, MD, Professor of Pediatrics, Director, Pediatric Chronic Fatigue Clinic, Johns
Hopkins Children’s Center, Maryland
Alan R. Light, PhD, Professor, Department of Anesthesiology and Department of Neurobiology
and Anatomy, University of Utah, Salt Lake City, Utah
Kathleen C. Light, PhD, Researcher, Professor, Department of Anesthesiology, University of
Utah School of Medicine, Salt Lake City, Utah
Zaher Nahle, Phd, MPA, Vice President for Research and Scientific Programs, Solve ME/CFS
Initiative, California
Leonard A. Jason, PhD Professor of Psychology DePaul University Chicago, Illinois
Derek Enlander, MD, MRCS, LRCP Attending Physician Mount Sinai Medical Center, New York ME CFS Center, Mount Sinai School of Medicine New York, New York
David L. Kaufman, MD, Medical Director, Open Medicine Institute, California
Staci Stevens, MA, Exercise Physiologist, Founder of Workwell Foundation, California
Jared Stevens, BS, Clinical Coordinator, Workwell Foundation, California
Dorothy Hudig, PhD, Professor of Immunology, Department of Microbiology and Immunology,
University of Nevada School of Medicine Reno, NV
Patrick O. McGowan, PhD, Assistant Professor, University of Toronto Scarborough Centre for Environmental Epigenetics and Development (CEED) Department of Biological Sciences Cell and Systems Biology, Psychology, Physiology Toronto ON
Jarred Younger, PhD, Associate Professor, Departments of Psychology, Anesthesiology, and Rheumatology, University of Alabama at Birmingham
David Maughan, PhD, Professor of Molecular Physiology & Biophysics, Emeritus, University of Vermont School of Medicine Burlington, VT
Lucinda Bateman, MD, Medical Director at Bateman Horne Center, Salt Lake City, UT
Isabel Barao-Silvestre, PhD, Assistant Professor, School of Medicine, University of Nevada, Reno

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1 thought on “Tell Congress to Increase ME Funding”

  1. My RE: Line included – “NIH $2B More In Funding – ME/CFS – Researchers Ready To Submit RFAs”
    This was my paragraph at very beginning.
    I MAY HAVE WRITTEN BEFORE BUT NOW I HAVE A NEW CONCERN IN REGARDS TO ME/CFS~GETTING MY DISEASE FUNDED WITH THE $2B MORE AWARDED TO NIH. AT THE BOTTOM ARE NAMES OF RESEARCHERS INTERESTED IN SUBMITTING RFAs. RESEARCHERS ARE VERY, VERY INTERESTED IN RESEARCHING THIS DISEASE.

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