A couple of docs I've seen raised all sorts of cautions about
using Heparin prescribed by my Lyme doc. Have docs gotten some kind of warning about
this? Seems as though it made them EXTREMELY uncomfortable. Maybe it’s just fear around liability or something. Oh, well, it is what it is!
Any good ways to explain it or justify it to an non-LLD??
THANK YOU KINDLY!
Cynthia
Post Edited (Cynthia929) : 10/31/2013 3:48:41 PM (GMT-6)