solve mecfs initiative

July 2019 Solve ME Webinar: Disability Insurance for ME/CFS Disability Insurance Attorney Andrew Kantor from Kantor & Kantor, LLP joins us to explain the ins and outs of filing for disability under an ERISA (employer-sponsored) Policy when disabled from ME/CFS. Register for the webinar here...

The Science for ME forum are delighted to talk to Dr Sadie Whittaker from Solve ME/CFS Initiative about Solve's work, in particular their patient registry, related app and biobank, as well as their Ramsay Award programme, that awards grants to fund much needed research into ME/CFS and which, at...

Your Advocacy in Action: Our ME/CFS Senate Resolution is Moving! Thanks to your efforts during ME/CFS Advocacy Week, Senators Markey and Collins will be introducing our resolution recognizing International ME/CFS Awareness Day. This is the last chance to urge your Senator to be a part of this...

Register at https://register.gotowebinar.com/register/6221975071436912643

Copy and paste link https://youtu.be/8WlTkH_Wnsg Quite nice timing. I'm due to, finally, do my Q&A with Sadie later this month, if this video inspires a question you'd like me to ask her then add it to this thread...

https://www.meaction.net/2019/04/11/celebrating-our-wins-for-me/

https://solvecfs.org/smci-ramsay-award-program/

https://solvecfs.org/an-important-update-from-carol-head-at-smci/

ME/CFS Advocacy Week Online Training Part 1: Best Practices for a Successful Advocacy Meeting Wednesday, March 13, 2019 1:00 PM - 2:00 PM EDT//10:00 AM - 11:00 AM PDT Solve ME/CFS Initiative and #MEAction present an online workshop to help you host a successful meeting as part of ME/CFS...

Solve ME/CFS Initiative (SMCI) is hosting our first ever EmPOWER M.E. Roundtable on April 2, 2019 moderated by Board Certified Patient Advocate, Sharon Stevenson, DVM PhD. As part of Advocacy Week in Washington DC, this event is free for all who attend and will also be livestreaming online for...

http://lobby19.solvecfs.org/ ETA: correcting link.

http://go.solvecfs.org/webmail/192652/94324627/24015c72674826bb6afeb2b821c459697133845373a35af1590d299b6891b413

https://medium.com/@rochellejoslyn/2018-me-cfs-research-summary-9fe3f60b2f48 Link to interactive version hosted by Solve, https://solvecfs.org/me-cfs-research-a-year-in-review/

" SolveCFS Published on Dec 12, 2018 At a recent SMCI gathering in Redwood City, Dr. Jose Montoya, a clinician who has fought for people with ME/CFS for nearly two decades, addressed those who suffer from ME/CFS on behalf of all clinicians. Dr. Montoya is a powerful and caring ally, and we were...

https://www.tandfonline.com/doi/full/10.1080/15592294.2018.1549769?scroll=top&needAccess=true Abstract published. Article behind a paywall. Research financed by Solve ME/cfs.

https://solvecfs.secure.force.com/actions/kwac__takeaction?actionId=AR00042&cid=

Station: University of Minnesota / SMCI / YouTube Date: November 13, 2018 WebTV: Item: Medical education ME/CFS-event at the University of Minnesota On November 7, SMCI in partnership with the Minnesota ME/CFS Alliance co-sponsored a medical education event at the University of Minnesota...

Ten organisations ask congress to create legislation for ME/CFS On Friday, November 2nd, #MEAction, the Solve ME/CFS Initiative, and eight other ME/CFS organizations sent a letter to our champions in the House of Representatives – Representatives Eshoo (CA18), Lofgren (CA19), McGovern (MA02)...

Source: Solve ME/CFS Initiative Date: November 29, 2018 Time: 18:00-19:00 UTC URL: https://register.gotowebinar.com/register/5744870584301904899 You + M.E.: A community resource, built by the community -------------------------------------------------------- In 2010, Solve ME/CFS Initiative...