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Has anyone gone to Mayo Clinic to see a CFS specialist?

Visiting Mayo Clinic | Last Active: Sep 20 2:25pm | Replies (26)
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@colleenyoung

Hi, @iamwell, I'm tagging @welchllb @suzanne2 and @uldiver who I believe have been to Mayo Clinic for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). I'm not sure which location.

Will you be moving your care to Rochester?

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Replies to "Hi, @iamwell, I'm tagging @welchllb @suzanne2 and @uldiver who I believe have been to Mayo Clinic..."
suzanne2 | @suzanne2 | Feb 13 10:47pm

I have been to Rochester but they didn't delve into my CFIDS/FM that much. I went mainly for gastrointestinal issues. I have wanted to come back for that but haven't been able to. The people I spoke with seemed to understand my symptoms and the issues I am living with.

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