COVID-19 and Long haul COVID Resources

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Browse News: United States

Photo of US ME/CFS Clinician website. Blue Banner with title at top and a question that reads What is ME/CFS?

All Doctors Should Go To This Website For ME Information!

We are thrilled to share that The US ME/CFS Clinician Coalition has launched a beautiful website to provide clinicians with expert information on the diagnosis and management of myalgic encephalomyelitis/ chronic fatigue syndrome (ME/CFS). The website includes the basics of clinical management, diagnosis and management, comorbid conditions, and resources on ...

#MEAction New York Co-Hosts Free Webinar for Clinicians on September 30th!

#MEAction NY is co-sponsoring a free CME webinar Wednesday, September 30th, 2020 and we need to share widely so clinicians can know to register! DATE: Wednesday, September 30, 2020 12:00-1:00 EST Topic: Post-Viral Syndrome and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): What Every Clinician Needs to Know Speaker: David Kaufman, MD, ...
mayo clinic building

Mayo Clinic Removes GET and CBT from CFS Webpage

The Mayo Clinic recently removed harmful recommendations of Graded Exercise Therapy (GET) and Cognitive Behavioral Therapy (CBT) for myalgic encephalomyelitis (ME) from their website, a win for people with ME and their families. The site still contains problematic language and misleading information, but this recent change could help many individuals ...
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Join Our Community Debrief Meeting about the NIH this Wed.

Join us this Wednesday for a community meeting to debrief about last week's NIH Interagency ME/CFS Working Group meeting, and to discuss where we go from here. Join the call this Wednesday, Aug. 19th at 3pm ET / 12pm PT. The meeting was quite something. At the last minute, Jaime ...
researcher in lab examines chemical compounds

Report Part 2: NIH lacks coordinated response for long COVID research

The NIH is shaping research initiatives to study the long-term consequences of COVID-19 (long COVID), but it lacks the coordinated, outcomes-focused strategy necessary to deliver biomarkers and treatments to the people who need them. Editor’s note: This is part of a series on what the NIH is (and isn’t) doing ...
health technician with blood tubes in the clinical lab

Report Part 1: NIH is not advancing ME/CFS research

The NIH is doing little to expedite a coordinated, outcomes-focused plan for ME/CFS research, an enormous missed opportunity in the era of COVID-19. Editor’s note: This is part of a report series on what the NIH is (and isn’t) doing for ME/CFS and long COVID research. For our Report Summary ...
Birds-eye view of crowd encircling around empty space where NIH logo is

Report Summary: What NIH is (and isn’t) doing for ME/CFS & long COVID research

As more and more COVID-19 survivors report disabling, multi-system symptoms lasting months on end, the National Institutes of Health (NIH) is finally beginning to openly acknowledge the serious health risks ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) poses to the public. In the past couple of weeks, Dr. Anthony Fauci, Director of ...

National Disability Voter Registration Week

National Disability Voter Registration WeekJuly 13-17, 2020 #MEAction is excited to participate in National Disability Voter Registration Week! Let’s get people with ME and all people with disabilities registered to vote, educated about this year’s election, and prepared to cast our ballots!We have gathered resources to help make it as ...

Dr. Anthony Fauci says that post-covid syndrome “is highly suggestive of myalgic encephalomyelitis”

This article was updated on July 27, 2020 to reflect Dr. Anthony Fauci's repeated statements on this topic. Dr. Anthony Fauci is repeatedly warning the public that Covid-19 patients are at risk of developing myalgic encephalomyelitis (ME) and chronic fatigue syndrome (CFS) after being infected with the virus. As of ...

ADA 30th Anniversary–Stories Wanted

The 30th of the anniversary of the American Disability Act (ADA) is fast approaching--July 26th. As a way to celebrate this momentous occasion, we are looking to share stories of how the ADA has positively impacted the lives of people with ME.We want to honor those who fought hard to ...