Hi Everyone, Looking for Lymies who went to the Mayo for treatment and had a bad experience??? Please post your story. It's for Channel 4 news
Posted by NP40 (Member # 6711) on :
I'll kick this up as there's loads of people here who've been "Mayo'd". Do a search for a thread entitled the "Alligator Pit", lot's of "Hold the Mayo" stories in there.
Posted by timaca (Member # 6911) on :
Mayo Clinic in AZ was not able to diagnose me. Saw an internal medicine doctor, 2 rheumatologists, and a neurologist.
Then I ended up (finally) at Columbia Univ. Medical Center. Dr. F even mentioned in his written report on me that I had been seen by the specialists at Mayo.
The news channel can PM me if they want to. I'd love to get the word out about how lyme is misdiagnosed...especially at places like Mayo Clinic.