You (and anyone else you want to invite) is invited to my virtual #MillionsMissing Day of Change.

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What we need is if you are:

* a person with CFS/ME
please consider taking a photo of yourself or your shoes with one of the posters (http://millionsmissing.meaction.net/wp-content/uploads/2018/04/18_MEAction_Poster_V2_LOWkf.pdf) or with your own sign/note (can be handwritten).

Some ideas of things to include in your sign/note:
– A message directed at the target of your country’s protest (in the U.S., that would be NIH director, Francis Collins);
– Your location – #CanYouSeeMEnow in San Diego, CA;
– Our hashtags – #CanYouSeeMEnow, #MECFS and #MillionsMissing
* a family member or a friend of someone with CFS - hold up a note letting people know how you miss them. We miss you - we miss being with you, talking to you, being a part of the family.

AND then post the photo on my event https://www.facebook.com/events/902263099954183/ - you don't need to go anywhere :)
 
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Great news! The Open Medicine Foundation https://www.omf.ngo/ is co-sponsoring this #MillionsMissing Day of Action with me! The mission of the Open Medicine Foundation is to:

* Invest in accelerating collaborative medical research to find effective treatments and diagnostic markers for ME/CFS and related chronic complex diseases.

* Keep the community informed by disseminating information on current research projects and results

* Bring together thought leaders from around the world to brainstorm and set up targeted initiatives to tackle difficult-to-treat diseases

* Encourage and engage the patient community to take an active role in their own healthcare

https://www.omf.ngo/donate-to-the-end-mecfs-project/