Tell Congress We Need An ME Champion

Send Llewellyn King’s letter to your Congressional Delegates

Llewellyn King of The White House Chronicle, a long time supporter and fighter for ME patients, has written an article on The Hill’s “Congress Blog”.
>Mr. King’s blog is a plea to members of congress, seeking a “champion” to take on the campaign for ME. The emphasis is on raising awareness about the devastation ME causes and to persuade HHS to fund research for a cure.
With this in mind, MEadvocacy.org has created an easy one click letter for US citizens to send to their congressional representatives.  It contains Llewellyn King’s full blog post.
Help us reach every member of congress!
Fill in your name and US address.  Three letters will be instantly generated and sent to your two senators and house representative.

Facebook
Twitter
WhatsApp
Email

2 thoughts on “Tell Congress We Need An ME Champion”

  1. My daughter Laura, has this horrible disease!! It has been six years!! She is only in her 50’s and has no quality of life!! Please help raise funding for this dibelating illness!

  2. This disease is devastating to young and old and not clearly understood by the medical community. Ignoring it will only lead to more suffering and despair to the persons and families affected by it. Please consider funding for research to discover the cause and cure so that all are able to live with dignity and hope. Thank you. Kathleen Ciani

Comments are closed.

Latest News

Image is a sky blue rectangle, with an image of the #MEAction Maryland's logo that has the words Maryland State Chapter over an image of a lighthouse. On the righthand side if the image are the words, Join #MEAction's Marylans's #HelpMESenator Campaign in black font.

Join #MEAction Maryland’s #HelpMESenator Campaign

We are writing this article to share some exciting news! On Tuesday, September 26, ME advocates delivered copies of the book, The Puzzle Solver, by Tracie White with Ronald W. Davis, PhD, along with information about ME and Long Covid to Senators on the Hill. The books were donated by an individual living with severe ME/CFS in an effort to raise

Read More »
a collection of millionsmisisng pictures featuring people protesting over the years in red shirts and with protest signs. white dashses connect the photos. the words words "the Story of the #MillionsMissing" is in white font in the top lefthand corner with the #MEAction logo there. The words "Coming Soon" is handwriting font is in the top righthand corner.

“#MillionsMissing is our drumbeat”–Preview Party 9/24

RSVP TODAY: We are hosting a preview party for the new, virtual Home of the #MillionsMissing this Sunday, September 24th, at 12 pm PT/ 3 pm ET/ 8 pm BST! RSVP & Get Zoom Link Here We have always had to be creative in telling Our Story – the story of M.E. – to the world

Read More »

JNNP to publish edited rapid response by MEAction UK.

MEAction UK have been in communication with the BMJ and are delighted to announce that the Journal of Neurology, Neurosurgery & Psychiatry (JNNP) are publishing an edited version of our rapid response to  ‘Anomalies in the review process and interpretation of the evidence in the NICE guideline for chronic fatigue syndrome and myalgic encephalomyelitis’. We

Read More »