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Everyone that has personal experience with Dr. L in Michigan, could you please let me know your thoughts.
I'd like to know what protocols he typically follows.
Does he follow Dr B's protocol?
Does he treat with multiple high dose antibiotics?
Does he treat co-infections at the same time?
How often do you have to go and see him?
Does he test for the co-infections or does he go by symptoms/ clinical assesments?
All informatino and opinions are appreciated Thanks
-------------------- 10/10 EIA 1.4+, 41 (IGG), 23 (IGM) Bitten over 20 years ago. Currently not treating, looking for a Dr who will work with my insurance lol.
More muscular, cognitive, nerve issues than joints. Facial droop and blurred vision. Posts: 323 | From Michigan | Registered: Apr 2011
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I just joined today and am looking for a doctor. I am not diagnosed. Who is doctor L.?
Posts: 2 | From Michigan | Registered: May 2011
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We don't use doctors full names on the discussion boards.
I am fairly new myself. I just started treatment last week. I've had Lyme for a long time though.
Do you have a lyme literate medical doctor (LLMD) that you are seeing?
If you are looking for one you should post a new topic under seeking a doctor and make sure to put the state in the heading.
And Welcome!
Laura
-------------------- 10/10 EIA 1.4+, 41 (IGG), 23 (IGM) Bitten over 20 years ago. Currently not treating, looking for a Dr who will work with my insurance lol.
More muscular, cognitive, nerve issues than joints. Facial droop and blurred vision. Posts: 323 | From Michigan | Registered: Apr 2011
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