I am seeking a LLMD in Minnesota but preferrably in the Minneapolis/St. Paul area if there is one.....Thanks!
Posted by LymeXtu (Member # 24590) on :
PM Sent
Posted by Marz (Member # 3446) on :
I should probably check with LymeXtu myself, since I am switching back to my former LLMD in Winona and not sure if I'll stay there.
Just wanted to say if you were recommended a particular one in St Paul who I had switched over to, I would not advise it.
She's a wonderful doctor, but she's limited by insurance eg. she told me my diagnosis is fibromyalgia although she knows I have lyme.
But the big thing is that the max time she can spend with me is 30 min. I will keep her as my PCP since she's sympathetic to lyme and knowledgeable. In 9 months, we've never had time to address lyme.
So I'll pay out of pocket to former LLMD and get an hour exam.
Good luck! I don't understand why MN has such a dearth of LLMDs since our state is becoming endemic.
I'm curious who might have been recommended to you.
Posted by pmonee (Member # 32771) on :