sorry for the multiple responses...i just came on the forum briefly to see if by chance there is a dr in fl who took ins and luckily there is but he is so far...if he needs to see me often it won;t...
but the fact remains that in order to be able to do any protocol completely i need to be closer to family who are in florida and NY..ny not an option due to the cold and cost so florida is it....
i have to plead the 5th about some of the az drs...i have seen both of them..also know alot of people who went to envita and the dr associated with them and spent thousands and didn't get well but...
someone said florida is horrible for lyme...is it because of the weather, i,e humidity, rain? or because of the lack of drs?? i am from az and we are beyond limited with drs here but i must say..the...
it seems that alot of people see dr c and he is beswt in florida so i might have to find a way there..a bus or something...
thnks...yes i did try to pm but it said not available??? then again maybe it is my lyme brain ;(...
it is not allowing me to private message you??? can you pm me? thanks!!...
My current dr studied closely with him and he follows alot of the same protocols but i know he takes no insurance...just wondering if anyone has seen him and your experiences...i know he does alot...
I am moving to south florida (sunrise area) to be closer to family...i am in need of a dr WHO TAKES INSURANCE..I CANNOT STRESS THIS ENOUGH...i know people want to help me others the best care...