Webinar: Dr. Levine and Montoya to discuss developments in ME/CFS research

On Thursday, April 20, Solve ME/CFS Initiative (SMCI)‘s research webinar series will be a double feature with Dr. Susan Levine and Dr. Jose Montoya at 10 a.m. PT/ 1 p.m. ET.
Dr. Levine is founder of the Medical Office of Susan M. Levine, MD. Over the last two decades, Dr. Levine has collaborated with other clinicians and researchers, co-authored a `Manual for Physicians’, a primer for internists about the care of CFS patients, and is currently serving on the Federal Advisory Committee for CFS.
Dr. Montoya is a professor of medicine, Division of Infectious Diseases, at Stanford University Medical Center and head of the Stanford Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Initiative.
Both Dr. Levine and Montoya are members of the SMCI Research Advisory Council.
Doctors Levine and Montoya will update the community on recent work and key developments in the ME/CFS field.
To register for this free webinar, go here.
 
 
 
Dr. Susan Levine.jpgDr. Montoya.jpeg
 

Facebook
Twitter
WhatsApp
Email

Latest News

Facets of ME: Temperature Dysregulation

Welcome to June’s #FacetsOfME! Facets of ME is an educational feature where we dive into a particular aspect (or facet) of ME and explore it more in depth. This month we are focusing on temperature dysregulation- heat and cold intolerance. It is surprising how difficult this symptom can be to manage until you experience it.

Read More »

Dept. of Labor Updates Information on ME/CFS for Workers, Employers

The U.S. Department of Labor’s Office of Disability Employment Policy (ODEP) has updated the information on ME/CFS provided at its Job Accommodation Network website to align with the most current CDC guidance. This action will help workers and employers find accurate information on ME/CFS and combat stigma and improve workplace outcomes. At #MEAction’s recent meeting

Read More »

#MillionsMissing: 7 Days in Self Portraits with ME/CFS

After taking #MEAction’s photography workshop with photographer Lucia Doynel for #MillionsMissing, Terra Dumont produced these stunning photos as a glimpse into her life as someone living with ME/CFS. Terra spread this experience over 7 days, focusing on a different theme each day. See her wonderful work and accompanying commentary below. Click on any of the

Read More »

Help keep our work going

We rely on donations from people like you to keep fighting for equality for people with ME.

Donate

Get actions alerts and news direct to your inbox

You can choose what you want to be kept up to date on.

Subscribe
Scroll to Top