Dear Friend,

It is time for our annual funds appeal.  We need your donations to continue supporting people with ME/CFS and FM in Massachusetts and beyond. We had a busy 2020 building our support group program and improving our provider referral process, among other projects, and we have big plans for 2021. Please support us by becoming a member or donating now! Read on for more details about our 2020 activities, our 2021 plans, and why you should give today.

You know how devastating living with ME/CFS and FM can be, and the toll it takes on individuals and families. Now imagine living through COVID-19 but never really “recovering,” instead experiencing debilitating exhaustion after taking a shower or washing the dinner dishes, being unable to read or count change, experiencing disturbed sleep, intermittent sore throat and fever, and unremitting muscle pain. Your doctor says you have recovered and should go back to work or prescribes an exercise program. You are not well enough to go back to work, and any exertion makes your symptoms worse. Many COVID “long-haulers” may develop ME/CFS. Where do they turn?

The Massachusetts ME/CFS & FM Association has been here to help for over 35 years. Today, in the midst of the COVID-19 pandemic, we have made significant investments in our support group and provider referral programs, and have gone 100% virtual, making our services and programs available to more people.

In 2020, we:

But we can, we must, do more - and, with your help, we will. Looking to the future, your generous gift will:

Our funding comes from generous, committed, individual donors like you. Could you become a member or donate now to help us kick-start our expanded programs in 2021?

Your support for the vision we share inspires our volunteers to continue their hard work on behalf of all people living with ME/CFS and Fibromyalgia, adding tremendous value to the wonderful work of our professional staff.  But we need to grow to secure the Association’s future to serve a new group of post-COVID patients with ME/CFS-like symptoms. Your generous gift will help create the world we all want: a world where all who live with these devastating conditions live in dignity, community, and better health; a world where ME/CFS and Fibromyalgia are better understood and there are pathways to a cure.

Please make your gift now. You will help so many patients, like Carol, be able to live life to the fullest again.

With gratitude,                              

Leah Williams                 Charmian Proskauer

President                        Past President

P.S. DID YOU KNOW? In 2020, taxpayers who don't itemize deductions may take a charitable deduction of up to $300 for cash contributions made in 2020 to qualifying organizations.

P.P.S. Would you make yours a monthly gift? Just $12, $18, or $25 a month would make a world of difference!

P.P.P.S! Other ways to give – Contact Us for more information