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  • September 19, 2011 at 6:57 pm #305995
    vera
    Participant

    Hi Everyone,

    I am wondering if anyone sees an LLMD here in Minnesota (I’m in the St. Paul/Mpls) area. If you do, would you mind sending me a PM? I just don’t know where to start, and need to see someone that takes insurance. Thanks for any help!

    Lori

    September 20, 2011 at 2:34 pm #359308
    Trudi
    Participant

    I will send you a PM–
    Trudi

    Lyme/RA; AP 4/2008 off and on to 3/2010; past use of quinolones may be the cause of my current problems, (including wheelchair use); all supplements (which can aggravate the condition) were discontinued on 10/14/2012. Am now treating for the homozygous MTHFR 1298 mutation. Off of all pain meds since Spring '14 (was on them for years--doctor is amazed--me too). Back on pain med 1/2017. Reinfected? Frozen shoulder?

    September 20, 2011 at 5:08 pm #359309
    vera
    Participant

    Trudi,

    Thanks for your PM! I didn’t realize until just now you are dealing with Lyme. My heart goes out to you. Many thanks for the info you sent me.

    Lori (Vera)

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