Jennifer Brea – Find support
Jennifer Brea
  • Blog
  • Home
  • My Story
  • Unrest Unrest VR
  • #MEAction
  • Speaking
  • Contact

Jennifer Brea

  • Blog/
  • Home/
  • My Story/
  • Filmmaking/
    • Unrest
    • Unrest VR
  • Activism/
    • #MEAction
  • Speaking/
  • Contact/

Jennifer Brea

Health activist, filmmaker

Find support

Jennifer Brea

  • Blog/
  • Home/
  • My Story/
  • Filmmaking/
    • Unrest
    • Unrest VR
  • Activism/
    • #MEAction
  • Speaking/
  • Contact/
 

FIND SUPPORT

I think I may have ME or Chronic Fatigue Syndrome. How do I get diagnosed?


It can be difficult to find a doctor who specializes ME. Here is a list of specialists in the US, Canada, UK, Europe, and Australia.

The most important thing is to find a doctor who is open. The IACFS/ME Clinical Care primer is a useful tool to start a discussion with your doctor. Click here and see page 11.

You can also join: #MEAction Facebook Group for Undiagnosed Patients

My Patient Match – a forum and tool to track symptoms and treatments, it matches you with patients who have similar symptoms to you, even if you don't yet have a diagnosis.

I know that I have ME or Chronic Fatigue Syndrome, but I am looking for advice. Where can I go for help?

If you already have a diagnosis but are looking to find a new doctor, seek advice, or become more engaged with the patient community, here are a few resources:

#MEAction New Patient Facebook Group

#MEAction Support Groups – Connect with other ME patients.

My Patient Match – A forum and tool to track symptoms and treatments, it matches you with patients who have similar symptoms to you.

Phoenix Rising – The largest ME/CFS discussion forum on the web, covering a wide range of topics from advocacy to treatment to patient support.