The Massachusetts ME/CFS & FM Association, a 501(c)3 founded in 1985, exists to meet the needs of patients with ME (Myalgic Encephalomyelitis), CFS (Chronic Fatigue Syndrome) or FM (Fibromyalgia), their families and loved ones. The Massachusetts ME/CFS & FM Association works to educate health-care providers and the general public regarding these severely-disabling physical illnesses. We also support patients and their families and advocate for more effective treatment and research.
- Last Updated: 26 April 2018 26 April 2018
The entire Massachusetts Congressional delegation (two Senators and all nine Representatives) signed a statement of support for ME/CFS patients which was shown on the occasion of the screening of the documentary film “Unrest” on November 12, 2017 at the Regent Theatre in Arlington, MA. Our delegation's support for patients with ME/CFS was projected on the big screen at the event, which was attended by more than 360 healthcare professionals, ME/CFS patients, families, and supporters from Massachusetts and New England (VT, ME, CT, RI). We were proud to announce that Massachusetts is the first state that has had such a statement from every member of its congressional delegation.
- Last Updated: 05 December 2017 05 December 2017
Our special showing of the Sundance award-winning documentary, UNREST, by Jennifer Brea on Sunday, November 12, 2017 at the Regent Theatre in Arlington, MA was a huge success, thanks to our many volunteers who organized the event, our many co-sponsors who promoted the event, and the more than 360 people who attended, including many health care professionals and researchers.
- The event was packed! The UNREST production team believes our event was the most well-attended community-organized screening of Unrest ever held in the country.
- Support from Elected Officials: The joint statement of support from the entire Massachusetts Congressional Delegation, read aloud at the event, will be a role model for other states to follow. We hope you and your friends will sign this digital "Thank you" card to the MA Congressional Delegation (click the button "ADD Kudo/Image/Video.")
- Panel/Video: Our panel moderator, Deborah Becker, WBUR (NPR’s Boston station) senior correspondent/host, and our panelists, Mary Dimmock (ME Advocate), Michael VanElzakker (ME Researcher), Kiki Zeldes (ME Patient and Women’s Health Advocate) and Lisa Hall (Healthcare Professional), did a wonderful job sharing their perspectives and fielding audience questions for 45 minutes. Video of the opening remarks, panel discussion and audience Q&A is now online to share with others. This awareness-raising video is available to be shown on local cable TV stations in New England and the entire US. If you can help by asking your local cable station to air it, please contact us.
- 19 co-sponsoring organizations: Government, healthcare, academic, disability, ME/CFS, religious, arts, and women's organizations co-sponsored our event (all are listed here). They included the MA Department of Public Health and the Division of Women's Health at Brigham and Women's Hospital. This was the most diversely-sponsored ME/CFS event ever held.
UNREST is a moving and beautiful film and an excellent way to raise awareness about this devastating disease that impacts an estimated 28,000 people in Massachusetts and 1 to 2.5 million in the US. We invite you to help us continue to raise awareness about ME/CFS in the medical and healthcare community. Are you available to discuss bringing UNREST to your institution? If so, please contact us.
New Guide: Additionally check out this MEAction Best Practices Guide for how to organize larger, impactful UNREST events. They used our successful event as their case study.
- Last Updated: 03 September 2017 03 September 2017
A support group member in another state, herself a long-time ME/CFS advocate, recently remarked that no one in her support group seemed interested to hear about advocacy activities. Their concerns were with sharing their symptoms and getting ideas from others on how to treat them, where to find knowledgeable doctors, and finding support in the group – all legitimate and powerful concerns, totally appropriate for members of a support group. Still, she wondered, why aren’t more ME/CFS patients interested in what other patients and family members (advocates) are doing to bring more public and government awareness and funding to their disease?
- Last Updated: 11 August 2017 11 August 2017
Save the Date! – Nov 4, 2017
The Association’s annual public lecture will be held on Saturday, Nov. 4, 2017, at Newton Wellesley Hospital. Our speaker this year is Linda Tannenbaum from the Open Medicine Foundation, where some very exciting research is underway.
Mark your calendar now. More details will follow!
Research Symposium at Stanford THIS SATURDAY will be live-streamed!
COMMUNITY SYMPOSIUM at Stanford University (on behalf of Open Medicine Foundation)
We are pleased to announce that the Community Symposium on the Molecular Basis of ME/CFS at Stanford University on Saturday, August 12th will be live-streamed. The event will begin at 9:00 AM Pacific Time and will conclude at 5:00 PM Pacific Time. Patients, parents, researchers, clinicians, family and friends are invited to register to watch all or part of the program from anywhere in the world via live-stream.
Pre-registration is required. There is still time to register to watch the program live. Please tell a friend - forward this announcement to share this unique experience with our worldwide community.
Ronald W. Davis (Stanford)
Robert Naviaux (UCSD)
Chris Armstrong (U Melbourne)
Jonas Bergquist (Uppsala U)
Maureen Hanson (Cornell)
Neil McGregor (U Melbourne)
Baldomero Olivera (U Utah)
Mark Davis (Stanford)
Alan Light (U Utah)
Alain Moreau (U Montreal)
Wenzhong Xiao (MGH)
The Symposium will be made available on OMF's YouTube Channel for free or you can order a DVD for $15 (which includes shipping). All orders are due by September 10. Order your DVD today.
For more information, see www.omf.ngo/community-symposium
Tell Congress "Don't defund ME/CFS!"
Urge your Congress people to restore funding for CDC (thanks to Solve ME/CFS Initiative)
Last week, the House Appropriations Subcommittee on Labor-HHS zeroed out the $5.4 million line item for Chronic Fatigue Syndrome at the CDC....again!
Tell your members of congress to restore the funding for ME/CFS for next year’s budget. We cannot abandon the progress we've made so far!
Here's a simple form you can fill out to send a personalized letter directly to your U.S. Senators and Congressperson who will be voting on the 2018 Federal Budget. We want as many letters as possible from as many states as possible! Here’s another chance to make ME/CFS visible to your representatives in D.C. Be sure to personalize your letter by writing a sentence or two about yourself in the “Add a Personal Message” box. Your personal message will appear at the beginning of the letter. To access the form: https://solvecfs.secure.force.com/actions/kwac__takeaction?actionId=AR00009
Action is needed NOW, since the Senate will begin work on the budget as soon as they return in September.
NASA 10-minute Lean Test for Orthostatic Intolerance
Have you been tested for Orthostatic Intolerance?
OI is one of the 5 key symptoms of ME/CFS identified in the Institute of Medicine report. Although it appears to be more common in children and adolescent patients, many adult patients also have this condition but it may not have been recognized. It is treatable! There is a simple test which requires no special equipment that your doctor can do can show if you have OI.
Here’s one patient’s experience with the test. The page has links to more description about the test and complete instructions that you can take to your doctor.
We need your help to identify doctors who can treat ME/CFS and FM patients!
Here’s a note from our Patient Services team. Help finding doctors is our most requested service. We have very few doctors to recommend – we need more names! Please help us by letting us know of any doctor you see who has helped you. They don’t have to be ME/CFS or FM experts, just open-minded, respectful, and willing to learn and work with you to help you feel better. Our focus is on doctors in Massachusetts or surrounding states.
Dear fellow patients, family members and friends,
One of the most important of patient needs is to find physicians and health care providers that are knowledgeable about ME/CFS, fibromyalgia, Lyme Disease, and other associated illnesses.
One of our major services is health care provider referrals. And our primary source for these referrals is the patient community.
We especially need patients and their families to tell us about physicians/health care professionals they've seen who are able to provide diagnosis and treatments.
We are asking for your help. Please click this link: https://www.masscfids.org/provider-recommendation-form to fill-out a questionnaire on health care professionals with whom you've had significant contact. We understand you are sick and may not have a lot of energy at any one time, so go at your own pace. If you can provide feedback on more than one doctor or other provider, please use multiple forms.
We want to assure you that any and all information you provide will be kept strictly confidential and your name will never be associated with the information. Also, we are careful not to overload any one doctor with patient referrals.
We would like to get both positive and negative feedback so that we can help patients obtain the best referrals possible.
By taking a little time, you will be helping patients who need to obtain diagnosis and treatment.
THANK YOU SO MUCH.
Patient Services team, Massachusetts CFIDS/ME & FM Association
This is Part One of our summer newsletter. Part Two will follow shortly and will focus on recent research and advocacy.
More Articles ...
Notice about names
The Massachusetts ME/CFS & FM Association would like to clarify the use of the various acronyms for Chronic Fatigue Syndrome (CFS), Chronic Fatigue & Immune Dysfunction Syndrome (CFIDS) and Myalgic Encephalomyelitis (ME) on this site. When we generate our own articles on the illness, we will refer to it as ME/CFS, the term now generally used in the United States. When we are reporting on someone else’s report, we will use the term they use. The National Institutes of Health (NIH) and other federal agencies, including the CDC, are currently using ME/CFS.
Massachusetts ME/CFS & FM Association changed its name in July, 2018, to reflect this consensus.