#MEAction U.S. State Chapters have a BIG Vision for ME! Find Out What is Happening in Your State.

#MEAction is fighting to end the crisis of myalgic encephalomyelitis (ME) and create an equitable world for people with ME. We know that we must fight at every level to make this happen. #MEAction U.S. State Chapters are dug in and working to change the landscape of ME in their home states, and create a ripple effect across the U.S.

#MEAction California is fighting to institute a statewide Center of Excellence program to bring treatment and research to its residents, while #MEAction Colorado has undertaken the tedious legwork of asking the international Rotary Club to vote on a resolution for ME.

#MEAction expanded its U.S. State Chapter program this past summer with the ultimate goal to build an advocacy network in all fifty States to more effectively reach our local communities and advocate for national legislation.

Our State Chapter landing pages are now live! Read about the ongoing work, accomplishments and advocacy vision in your State. Get involved in your State’s advocacy efforts, or pass on these links to healthy allies!

ARIZONA  |  CALIFORNIA  |  COLORADO
FLORIDA  |  GEORGIA  |  NEW YORK  |  TEXAS

Our State leaders have BIG ideas! 

In the past few months, we have highlighted the work and vision of our California and Colorado State Chapters.

#MEAction California is fighting to gain legislative support for the State to institute a statewide Centers of Excellence program to train ME specialists, provide treatment for people and conduct research. Activists across the state have already met with 24 state legislators to discuss this initiative, and working with Stanford and the University of California to support the program! Read more.

#MEAction Colorado activist, Jim Lutey, introduced a resolution for ME before the Rotary Club to encourage research, education and funding. He got it passed at his local chapter. Then, he took it to his district chapter, which includes all of Wyoming, north central Colorado, and a bit of Nebraska and Idaho. The district chapter will now submit the resolution to the Rotary International Council on Resolutions with a final vote in November. We hope the Rotary Club will fight as vigorously for ME as they did for the Polo virus! Read more.

#MEAction Colorado is fighting for Rotary International to pass a resolution for ME.

Our State chapters act as laboratories to incubate new ideas for advocacy and outreach: successes in one state can be shared and propagated across the country.

We are thrilled by the dedication of our State Chapters but they need your help, and the support of your network. Get involved today!

Facebook
Twitter
WhatsApp
Email

1 thought on “#MEAction U.S. State Chapters have a BIG Vision for ME! Find Out What is Happening in Your State.”

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