Latest in Solve webinar series

The latest webinars in Solve ME/CFS Initiative’s 2016 series will soon take place, with Dr Jarred Younger speaking on 19 May and Dr Jose Montoya on 16 June.
Dr Younger is Associate Professor in the Departments of Psychology, Anesthesiology and Rheumatology at the University of Alabama at Birmingham, and Director of the Neuroinflammation, Pain and Fatigue Laboratory at the university.
Dr Montoya is Professor of Medicine in the Division of Infectious Diseases at Stanford University Medical Center and head of the Stanford Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Initiative.
The topics of the talks have not been announced but Dr Younger has a special interest in inflammation in ME/CFS, fibromyalgia and Gulf War Syndrome and in rapidly trialing over-the-counter treatments for these conditions; and Dr Montoya focuses on the role that infection and immunity plays in chronic diseases such as ME/CFS.
Recent speakers have included Drs Avindra Nath, Susan Levine, Alan Light, Peter Rowe, Dane Cook and Zaher Nahle.
The hour-long sessions take place at 1 pm US Eastern Time. Patients must pre-register to view the live webinars (here for Dr Younger, here for Dr Montoya) and will receive an email address via which to send questions for the speakers to be answered during the Q&A period of the webinar.
All webinars are recorded and posted to Solve’s website and YouTube channel following the presentation. Details of their past and future presentations can be found here.

Facebook
Twitter
WhatsApp
Email

Latest News

a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.

Severe ME Artists Project 2024

Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by

Read More »
Light blue square with rainbows in the top left and bottom right corner. In the middle are the words, -Pride is Valid- No Matter How One Celebrates or Experiences It. #MEAction Board Member, Jennifer England, shares her views on Pride. The #MEAction logo in the top right corner.

Pride Is Valid No Matter How One Celebrates or Experiences It

In honor of Pride Month, #MEAction is sharing a heartfelt message from our board member, Jennifer England, about what Pride means to her and her wife who lives with severe ME. My wife and I have both been queer our whole lives, but in the 70s that was the quiet part you didn’t say out

Read More »

Questions to Ask Prospective MPs About ME/CFS

In the next few weeks, candidates will be knocking on doors seeking votes for the upcoming UK Election. It’s important that candidates from all parties are made aware of the challenges facing people with ME and Long Covid. It can be a little daunting to be unprepared so here are some questions you might want

Read More »
Scroll to Top