Category Tag: fundraiser

#SockItToMECFS with BHC’s new fundraising challenge!

/ by / 2 Comments
Bateman Horne Center launches the #SockItToMECFS Challenge. Wear your wildest and wackiest socks to raise awareness and funds for advancing ME/CFS diagnosis and care. Challenge your friends to do the same ...

#MillionsMissing Crafts Competition

/ by / 2 Comments
#MillionsMissing Crafts Competition We want to have fun while we work for equal treatment for ME sufferers! Win prizes! Submit photos and pattern of a crochet - or knitting project with the #MillionMissing logo. ( Also with a picture of the finished product). We pick three winners receiving a prize ...

Join the MILLIONSMISSING Chicago Protest/Day of Action

/ by / 0 Comment
The Chicago protest #MillionsMissing will feature talks by Dr. Leonard Jason, Dr. Marcie Zinn, well-known epidemiologists; Carol Head, of Solve ME/CFS; Barbara Morrison; ME/CFS patients; and families and friends. It will take place at the James Thompson Center, 100 W. Randolph St, Chicago between 11:30am-12:30pm. Please click below to attend, learn more ...

Help Cure My Husband Please

/ by / 0 Comment
I have had M.E. for years now, unable to work. My 19 year old daughter is unemployed, pregnant and living at home looking for a job. My husband was just put in the hospital for 2 days and told he needed his colon removed, an ileostomy, and a second surgery ...

Join the #MillionsMissing fundraising team!

/ by / 7 Comments
With the help of our community’s ingenuity, strength, and indomitable spirit, #MEAction has: Spearheaded a petition to release the PACE trial data, garnering over 12,000 signatures.  This was presented in the recent FOI request to release PACE data as evidence of peaceful patient involvement Launched the worldwide protest #MillionsMissing in ...

Help fund CII’s ME/CFS Monster Study: Microbes, Immunity, & Complex Data

/ by / 5 Comments
Columbia University - Center for Infection and Immunity has seriously upped the ante on the initial microbe discovery project in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Their impressive, rigorous new study could point the way to diagnostic tests, and even treatments – but first they need the funds to complete the work ...

ME in Poland: Help me raise awareness & funding all across the EU

/ by / 1 Comment
Hi, I'm Mike Harley from the UK, and for the last 18 months I've been raising awareness and funds for the biomedical research charity Invest In ME. One of my best friends has had ME for over 10 years and over the last 2 years I've met a number of ...

Send Dr. Ron Davis a 75th birthday message!

/ by / 2 Comments
The Open Medicine Foundation (OMF) is inviting patients and supporters to send Dr. Ron Davis a message for his birthday and a donation to support his End ME/CFS Project. The OMF said that the messages would be compiled into a “massive card” that would be presented to him. Dr. Davis, of Stanford ...

Solve ME/CFS Initiative Update

/ by / 0 Comment
Last year was a pivotal point in the battle against ME/CFS. Game-changing reports from the Institute of Medicine and the National Institutes of Health’s Pathways to Prevention Workshop delivered long awaited public credibility for our disease. The federal ME/CFS landscape has shifted, and there is newfound openness and awareness among ...

Donate to the Bateman Horne Center Capacity Campaign – Wings to Fly!

/ by / 0 Comment
The Bateman Horne Center (BHC) - uniquely positioned to create collaborations between amazing, well-qualified patients and stellar research partners - has an urgent need to increase capacity in order to see patients and grow the research program. Investigators are seeking access to our patient population more and more, yet due ...
Menu