Join me in Fundraising for SMCI!

I’ve raised $6500 in 24 hours — imagine what we could raise if you all joined in?
This is my Crowdrise fundraiser for the Solve ME/CFS Initiative. You can join my team by hitting the “fundraise for this campaign” button. That’s it. You don’t have to create any content, or write anything. Just join the team, and share with the link with your network.
I created a short video that I hope will help patients explain our complex disease in a simple way to friends and family, and get them on board.
SMCI has done great work supporting patients for 27 years. Recently, Carole Head has spearheaded conversations in Washington DC. So they are helping not only with research but also with lobbying at the highest levels. We just made a step with the NIH but must keep pushing — supporting SMCI right now is an important part of that.
JOIN THE CAMPAIGN

Facebook
Twitter
WhatsApp
Email

1 thought on “Join me in Fundraising for SMCI!”

  1. The tally is $8100 now. Please do join in, and share the fundraiser with your network! Xo Elle 🙂

Comments are closed.

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