Category: Featured actions

Fundraiser: #MillionsMissing needs your help!

On May 25, 2016, #MEAction is sponsoring a community-organized protest at Departments of Health and Human Services (HHS) across the country, and in cities all over the world. As a community, we are bowled over by the response.  The protest started as a single effort in Washington, D.C., but as of today there will be

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Add the Filter your profile pic for #MillionsMissing

Introducing the #MillionsMissing Profile Filter App!  This app was designed to help raise awareness for the millions of people living with Myalgic Encephalomyelitis (ME) and Chronic Fatigue Syndrome (CFS). It lets you add a special theme to any picture you choose so that you can upload it to your social media profiles to show your

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#MillionsMissing: your shoes now have a final destination!

#MillionsMissing now has an address where you can send your shoes! We are asking patients who are unable to make it to the physical protest locations to please donate one pair of shoes to the address below and we will display them in their honor at the Washington, DC protest. You can send a pair of

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Contribute to #May12BlogBomb in 2016!

May 12th Awareness Day is a great day to share a blog post. If you are writing a post, please consider using the tag #May12BlogBomb when you share your post on social media, and, also submitting the blog link for inclusion on the 2016 #May12BlogBomb Link List that will be collated on Sally Burch’s blog Just ME

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10 things you can do for #MillionsMissing with limited spoons

The #MillionsMissing protest is full-steam-ahead: we’re mobilizing in Washington D.C., Seattle, San Fransisco, and Dallas; we’re revving up our engines in other cities all across the United States, our friends in other countries have pitched in, and the enthusiasm has reached an all-time high.  However, if you’re sitting at your computer holding five spoons for

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Put us on the map!

How many of us are out there with ME/CFS? Put yourself on the map so that we can show the world how many of us exist! Put yourself on the map using this website: diseasemaps.org. Simply search for Chronic Fatigue Syndrome/M.E., and then add your information. (Include name or not.) We can prove to our

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