solve mecfs initiative

Ramsay 2018 award recipient https://solvecfs.org/ramsay-2018-meet-professor-theoharis-theoharides-md-phd/

Ramsay 2018 award recipient https://solvecfs.org/ramsay-2018-meet-dr-liz-worthey/

2018 Ramsay Award recipients https://solvecfs.org/ramsay-2018-meet-professor-jonas-blomberg-md-phd-dr-anders-rosen-md-phd/

Source: Solve ME/CFS Initiative Date: October 18, 2018 Time 19:00-20:00 UTC URL: https://register.gotowebinar.com/register/3070787936016442371 Back to School Part 2: Individualized Education Plans (IEPs) for students with ME/CFS in Public Schools...

Good news! The ME/CFS line item at the CDC was funded in the recent budget compromise announced today. Committee report language was included, unedited, from advocacy efforts earlier this year.. You can see SMCI's statement here...

https://solvecfs.org/nih-launches-new-working-group-dedicated-to-me-cfs/

Source: Solve ME/CFS Initiative Date: September 13, 2018 Time: 15:00-16:00 UTC URL: https://register.gotowebinar.com/register/7863577812392103170 Appropriately and Accurately Assessing Symptoms in Patients with ME ---------------------------------------------------------- Join Leonard A...

Pasted as received apart from formatting: Source: Solve ME/CFS Initiative Date: August 30, 2018 Time: 17:00-28:00 UTC URL: https://register.gotowebinar.com/register/141286537318847234 Ref: https://www.youtube.com/user/SolveCFS Back to School Part 1: 504 Education Plans and Medical...

PEM: It's Time to Retire the Term by Pete Hanauer It is long past time to retire the term PEM and replace it with somethingthat accurately reflects what happens to ME/CFS patients after physical or mental exertion and that respects their dignity. We suggest the term Post Exertional Disability...

Hello from the Solve ME/CFS Initiative. We want to share our latest news and research with you, but we also want to respect your space and not spam the forums. In order to do that, we are starting a monthly thread where will we add all of the latest news from SMCI. Throughout the month we plan...

Hi all. I have the chance for an interview with Dr. Sadie Whittaker at some point, so I wondered if you had any questions that you'd like asked? If you do, let me know in a post below. Thanks Andy

https://solvecfs.org/research-highlights-from-2018-so-far-notable-study-developments/

I don´t think this was posted elsewhere.

Hello from the Solve ME/CFS Initiative. We want to share our latest news and research with you, but we also want to respect your space and not spam the forums. In order to do that, we are starting a monthly thread where will we add all of the latest news from SMCI. Throughout the month we plan...

Register for the livestream here, https://register.gotowebinar.com/register/8156426135278094337 I'm sure it will also appear on YouTube shortly afterwards.

We are pleased to introduce our new Chief Scientific Officer Sadie Whittaker, PhD. Dr. Whittaker has many years experience in the biotech industry, clinical development, medical affairs, strategy, advocacy, policy, and communication. She received her PhD in molecular biology at University...

WASHINGTON D.C. – The Solve ME/CFS Initiative (SMCI) announced Tuesday that 102 people with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and their loved ones rallied together in the largest Capitol Hill action for the disease to date. Advocates from across the country called for...

– The Solve ME/CFS Initiative (SMCI) announced Tuesday that it is now accepting applications for the 2018 cycle of its Ramsay Awards program. SMCI is currently seeking researchers who want to make an impact in the field of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) research...