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Mayo Minnesota reviews

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Posted 9/1/2017 12:18 AM (GMT 0)
Hi, has anyone been to the Lyme specialists at Mayo Minnesota in 2016 or 2017? Just wondering if it's gotten better from some earlier posts I've read.. Thanks very much!
Posted 9/1/2017 1:08 AM (GMT 0)
Bump
Posted 9/1/2017 1:40 AM (GMT 0)
You're talking about the Mayo Clinic?


I don't know if they have LLMD's there.

And this will bump for more views.
Posted 9/1/2017 2:39 AM (GMT 0)
Your better to just cross them off your list.
Posted 9/1/2017 4:18 PM (GMT 0)
Thanks for the replies. I called yesterday and they said they had Lyme specialists in Minnesota.
Posted 9/1/2017 5:24 PM (GMT 0)

LilyAZ said...
Thanks for the replies. I called yesterday and they said they had Lyme specialists in Minnesota.

They most likely are following the IDSA guidelines.

Do they even treat chronic Lyme?
Posted 9/1/2017 6:37 PM (GMT 0)
But if the Mayo was good for chronic lyme, people from MN, WS and Iowa would go there - they dont for a reason.

All of those state tick/lyme associations advise against the Mayo as they are CDC oriented regardless of their claims. Meaning, you need a bullseye rash, a positive cheap western blot or Elisa and you then get 2wks antibiotics. Maybe 4 at most. They go by what insurance accepts- which is the above.
Posted 9/1/2017 6:39 PM (GMT 0)

astroman said...
But if the Mayo was good for chronic lyme, people from MN, WS and Iowa would go there - they dont for a reason.

All of those state tick/lyme associations advise against the Mayo as they are CDC oriented regardless of their claims. Meaning, you need a bullseye rash, a positive cheap western blot or Elisa and you then get 2wks antibiotics. Maybe 4 at most. They go by what insurance accepts- which is the above.

That's my point - IDSA guidelines...not ILADS.

...and they most likely deny chronic lyme exists.
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