Neurology Now writes about CFS

Neurology Now on CFS

Neurology Now recently posted an article targeted at neurologists with the headline “Beyond Tired: Is chronic fatigue syndrome a real medical condition? Yes, according to a report from the Institute of Medicine, which urges physicians to treat it accordingly.”  The piece is primarily focused on the IOM report and its suggested diagnostic criteria. It is useful to read to understand what some medical professionals are being told about the IOM report and about diagnosing and treating CFS.

Dr. Sabin says the IOM’s proposed diagnostic criteria is “a simplification [of the condition], perhaps,” but one that clarifies the core symptoms and makes it easier to diagnose. He also thinks the report will draw attention to CFS, and he is happy that it confirms that the syndrome causes real suffering and should not be dismissed by doctors.
As the chair of the US Federal Advisory Committee on CFS, which is responsible for evaluating and implementing the IOM report, Dr. Levine says there is still debate about whether other common symptoms of CFS, such as viral infections, muscle and joint pain, and swollen lymph glands, should be included as part of the diagnostic criteria. Otherwise, she thinks the panel’s proposed criteria are a good start.
Dr. Berger adds that he believes too many people whose only symptom is fatigue are diagnosed with CFS. He thinks that physicians should apply the new diagnostic criteria for CFS strictly, and if their patients don’t satisfy them in full, they should look elsewhere for underlying causes.

Read the entire article
 

Facebook
Twitter
WhatsApp
Email

1 thought on “Neurology Now writes about CFS”

  1. In the article, Dr. Berger talks about 1 of 3 patients end up with an MS diagnoses. If that was even true, how about the other 2. Dr. Berger in my personal experience was extremely dismissive. How does a patient break that barrier, especially when they have waited for an appointment for 6 months with a so called ” leading expert” and get shut down and dismissed. Where do we go from there?

Comments are closed.

Latest News

a blue square image that features waves as the background. The 2025 #MillionsMissing logo at the top. followed by the words, Why We're sending out an SOS. A life preserver is in the bottom right corner and the meaction logo is in the bottom left corner.

Why We’re Sending out an SOS this #MillionsMissing

On May 12th, #MEAction and the #MillionsMissing are sending out an SOS to Congress to Save our Support Systems. Save our Science. Save Our Society.  HERE’S WHY: Healthcare, research funding and accessibility were already incredibly fragile for people with myalgic encephalomyelitis (ME), Long Covid and the disability communities. Now, we are seeing constant threats to

Read More »

Writers Guild Initiative Writing Workshops: Apply Today

#MEAction is excited to announce we are partnering with the Writers Guild Initiative (WGI) again to offer creative writing workshops for people with ME and Long COVID**. WGI has graciously donated their time to offer these writer workshops through personal mentorship with the writers of the #MEAction community! The workshops consist of three sessions during

Read More »
Purple rectangle. on the left: image of the book cover for Nobody's Empire. On the right the words: Virtual Interview + Q&A with Stuart Murdoch. MEAction logo on the bottom corner.

Virtual Interview + Q&A with Stuart Murdoch

Stuart Murdoch, from the band Belle and Sabastian, will be interviewed by #MEAction Minnesota’s State Chapter Leader, Terri L Wilder, about his recently released novel, Nobody’s Empire, on Saturday, April 19th at 1pm ET/6pm BST. We hope you join us for this virtual event to learn more about his debut novel. Tickets are available for

Read More »