Young Adult Support Group for those with ME/CFS, FM, Lyme, Long COVID, and Chronic Illness - Summer Session
- Details
- Last Updated: 04 June 2023 04 June 2023
Young Adult Support Group for those with ME/CFS, FM, Lyme, Long COVID, and Chronic Illness - Summer Session
NEW TIMES! Join us on Monday nights @ 7pm and Wednesday afternoons @ 3:30pm!
This drop-in Virtual Support Group is interactive and provides a safe space for patients to share stories and experiences, ask questions, and offer one another support.
In an effort to streamline the registration process, we are offering one registration for the entire Summer Session. Once registered, you are welcome to attend as many meetings as you like.
Summer Session Dates:
Monday, June 12th, @ 7:00 P.M. ET
Wednesday, June 28th @ 3:30 P.M. ET
Monday, July 10th, @ 7:00 P.M. ET
Wednesday, July 26th @ 3:30 P.M. ET
Monday, August 14th, @ 7:00 P.M. ET
Wednesday, August 30th @ 3:30 P.M. ET
Please Note: Due to professional licensing issues, you must be a Massachusetts resident to attend this group.
| REGISTER FOR THE YOUNG ADULT GROUP - SUMMER SESSION |
2023-5 May Newsletter
- Details
- Last Updated: 08 May 2023 08 May 2023
In this month's newsletter:
- Upcoming Events
- MA Bridges Illuminated for World ME Day - May 11
- Massachusetts Long COVID Commission
- Millions Missing Protest - May 12th
- Advocacy Week Recap
- Newsworthy Events and Links
- Lyme Disease Awareness
2023-4 April Newsletter
- Details
- Last Updated: 10 April 2023 10 April 2023
In this month's newsletter:
- Upcoming Events
- 2023 Health Needs Assessment Community Listening Forum
- Our Letter to RECOVER Clinical Trials
- Re-post: MassHealth Renewals
- Newsworthy Events and Links
- Member Spotlight: Julie Bach
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.