Join Team Solve – Fundraising for ME/CFS Research

Share on facebook
Share on twitter
Share on email

Join TeamSolve and help us Solve ME/CFS

It will take more than people with ME/CFS to achieve a world free of ME/CFS. It will take a committed team of many rallying together to effect change – Families, loved ones and friends coming together to make a difference and fund progress.

If someone you love is impacted by ME/CFS, then you can help. Join TeamSolve and help us Solve ME/CFS.

 

What is Team Solve?

Team Solve is the grassroots community fundraising program at the Solve ME/CFS Initiative. Team Solve members worldwide are invited to turn their passions and interests into unique fundraising events that will bring us closer to a world without ME/CFS. If you have been looking for a way to support someone you love that has this devastating disease, Team Solve DIY Fundraising may be your answer. Regardless of your personal means to give, anyone can help us Solve ME/CFS by joining Team Solve to fundraise!
 

Why Join Us?

As a Team Solve member, you join with your ME/CFS community to become a dedicated game-changer for all those impacted by ME/CFS. Whether it’s flipping pancakes, hosting a party with a purpose or leveraging your favorite hobby for fundraising, Team Solve members are passionate about transforming their interests into opportunities to raise funds and awareness for ME/CFS research. The timing is all up to you. You set the date, determine the schedule and work at your own pace, with materials to support your efforts and plans.
 

By signing up for Team Solve, you can:
  • Access and manage a personal fundraising page through Crowdrise
  • Be part of the growing grassroots movement
  • Have access to Team Solve materials
  • Access to our sample fundraising materials such as our official Team Solve logos
  • Leverage your circle of friends to help Solve ME/CFS!

Visit www.SolveCFS.org/Fundraising to get started today!

Share on facebook
Facebook
Share on twitter
Twitter
Share on whatsapp
WhatsApp
Share on google
Google+
Share on email
Email

Leave a Comment

Your email address will not be published. Required fields are marked *

Latest News

Sign petition To Fix ME/CFS tracking In US!

In August, we shared with you that we and six other ME/CFS organizations had submitted a proposal to the National Center of Health Statistics (NCHS) to fix the coding of ME/CFS in the US International Classification of Diseases (ICD-10-CM). Today, we are writing with an update on that proposal and asking that you sign the

Read More »

NICE announces roundtable event to ensure implementation of ME/CFS guideline

NICE announced today that it will hold a roundtable in September as the next step in the publication of the ME/CFS guideline. The roundtable will include representatives from patient organisations and charities, relevant professional societies, NHS England and NHS Improvement, NICE and the guideline committee. It aims to, “better understand the issues raised and determine

Read More »

#MEAction & 6 ME Orgs Call for CDC to Change How it Tracks ME/CFS

Together with six other organizations, we have submitted a proposal to the National Center for Health Statistics (NCHS) to add myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) to the neurological chapter of the International Classification of Diseases (ICD-10-CM).  Today, ME/CFS does not exist in the US ICD-10-CM. Instead,  most US doctors assign the code for chronic fatigue

Read More »

Help keep our work going

We rely on donations from people like you to keep fighting for equality for people with ME.

Donate

Get actions alerts and news direct to your inbox

You can choose what you want to be kept up to date on.

Subscribe
Scroll to Top