Stuart Murdoch of Belle and Sebastian ME/CFS Interview in L.A.
Stuart Murdoch, lead singer of the indie band Belle and Sebastian, talks to the Solve
September 9, 2015
Stuart Murdoch, lead singer of the indie band Belle and Sebastian, talks to the Solve
Lucinda Bateman, MD, specializes in the diagnosis and management of unexplained chronic fatigue, ME/CFS and fibromyalgia. Having served on the IOM committee that produced the recent report, Beyond ME/CFS: Redefining an Illness, she brings an in-depth, well-informed opinion to the conversation surrounding the IOM report on ME/CFS, the new diagnostic criteria and the proposed name, Systemic Exertion Intolerance Disease (SEID). READ MORE…
IOM Report Released – Recommends New Diagnostic Criteria, Calls for More Research, and Proposes New Disease Name. The report underscores the profound impact that ME/CFS has on the millions who suffer from it worldwide (est. 17 million) and the importance of getting people diagnosed; committee calls for more research funding. READ MORE…
Often those with ME/CFS experience gastrointestinal symptoms. Biomarkers of these symptoms could help to identify subtypes in ME/CFS. Dr. Armin Aledini is using samples from the SolveCFS BioBank™ to look for auto-antibodies against a range of dietary proteins. In this guest blog post he discusses Celiac disease, which is a commonly misdiagnosed condition with symptoms similar to ME/CFS. READ MORE…
On September 18, 2014, Dane B. Cook, Ph.D., Associate Professor of Kinesiology at the University of Wisconsin, Madison and a Solve ME/CFS Initiative 2011 funded investigator, presented our most popular webinar of the year on the system biology approach his team is taking to provide a clear picture as to what causes post-exertional malaise. In this guest post for our blog, Dr. Cook reviews the material presented and tackles the many questions we received from webinar participants.
In this 3rd piece of our three-part blog series Dr. Peter Rowe discusses range of motion in ME/CFS patients.
In the 2nd part of this three-part blog series on physical examination in ME/CFS, Dr. Peter Rowe discusses joint hypermobility. Read More…
The first in a series of blog posts from Dr. Peter Rowe of Johns Hopkins University entitled “Is the physical exam in CFS normal?” Read Part 1 of the series – We are certain that this information will be of great value to both you and your doctor and will clearly illustrate the value of a true physical examination in ME/CFS.
For ME/CFS sufferers, “coming out” to family and friends about their illness can be a tremendous challenge, especially at the holidays, but it is an important piece of the puzzle. We are proud and thankful to work with individuals who are willing to share their story as widely as possible, like Anna Zapp…
September is Pain Awareness Month; we wanted to bring you some resources about managing the pain associated with ME/CFS. For a long time pain was not thought to be a prominent symptom in ME/CFS, but muscle pain, joint pain and headache are common in ME/CFS patients.
By Jennifer Spotila, J.D. for The CFIDS Association of America, 2010 Part One – Unraveling
By Peter C. Rowe, MD, Kevin R. Fontaine, PhD and Rick L. Violand, PT In
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