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
Posted by bettyg (Member # 6147) on :
anyone?
Posted by 22dreams (Member # 17846) on :
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.....
Posted by jtavares76 (Member # 19216) on :
I see a Dr. H in western massachusetts...is this the one you are looking for feedback on? JT