#MEAction’s Postcards to Doctors is an Unprecedented Success!

#MEAction’s Postcards to Doctors initiative has been successful beyond our wildest hopes!  Since August 1, we’ve received requests for more than 3,500 postcards from hundreds of individuals and groups.  People from all over the United States have signed up to write to their clinicians asking them to take #MEAction’s CME program – we’ve sent out over 1,400 addresses!  

In order to catch up to this unprecedented response, we’re putting Postcards on hold through the month of September.  

  • If you’ve already sent for addresses and postcards, don’t worry — we’re going to keep working on the orders we’ve already received, and you should get your addresses and postcards this September!  
  • If you haven’t participated in the Postcards initiative, yet, you haven’t missed out on your chance: visit #MEAction for the Postcards re-launch on October 1, when we’ll also be showcasing the art of one of our postcard designers, Lia Pas.  

If you have any additional questions, you can send them to [email protected].

So far we’ve sent postcards to metros like New York City, Los Angeles, and San Francisco, to rural towns in Ohio, Pennsylvania and Maryland; and we’ve ensured our reach is to diverse neighborhoods with historically underserved populations, so that anyone can get diagnosed and treated for ME no matter their background.

It never ceases to amaze me how our community steps up where there is a clear need and puts their collective shoulders to the wheel.  We all have limited energy, but we know — maybe better than healthy individuals, sometimes — where to spend that energy. You’ve spoken with one voice that clinical education is important to you, and we’ll keep fighting for clinical understanding and better care.  

You inspire me so much!  I’ll be thinking of all of you next week at the Stanford conference, and holding that fighting spirit close.

Sincerely,

Jaime

Facebook
Twitter
WhatsApp
Email

Latest News

a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.

Severe ME Artists Project 2024

Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by

Read More »
Light blue square with rainbows in the top left and bottom right corner. In the middle are the words, -Pride is Valid- No Matter How One Celebrates or Experiences It. #MEAction Board Member, Jennifer England, shares her views on Pride. The #MEAction logo in the top right corner.

Pride Is Valid No Matter How One Celebrates or Experiences It

In honor of Pride Month, #MEAction is sharing a heartfelt message from our board member, Jennifer England, about what Pride means to her and her wife who lives with severe ME. My wife and I have both been queer our whole lives, but in the 70s that was the quiet part you didn’t say out

Read More »

Questions to Ask Prospective MPs About ME/CFS

In the next few weeks, candidates will be knocking on doors seeking votes for the upcoming UK Election. It’s important that candidates from all parties are made aware of the challenges facing people with ME and Long Covid. It can be a little daunting to be unprepared so here are some questions you might want

Read More »
Scroll to Top