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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » feedback on Dr. H. in Boston

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Author Topic: feedback on Dr. H. in Boston
heartof14k
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Has anyone seen Dr. H in Boston? I have CFIDS/FMS for about 10 years and have just been diagnosed (IgeneX and CDC IgM positive) with Lyme, and possibly Erlichiosis (1:80) I'd like any feedback. I think I may need iv's for 4+months. Thanx for any info or suggestions on who to see. I would travel anywhere for the best approach. I have BCBS PPO.
14k
Posts: 51 | From Boston, Ma. | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
bettyg
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anyone?
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22dreams
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Heartof14K,

I don't know of a lyme-literate "Dr. H" in Boston itself.

Perhaps responses would be more forthcoming if you indicate the region?

i.e. Dr. H in either "Boston-MetroWest" or "Central Massachusetts". Just a thought.....
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jtavares76
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I see a Dr. H in western massachusetts...is this the one you are looking for feedback on?
JT
Posts: 72 | From Massachusetts | Registered: Feb 2009  |  IP: Logged | Report this post to a Moderator
   

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