Okay, I can see that was of no help.
What if we try to hear from anyone who has been put on cortisone or other steroid by there lyme doctor.
Instead of the debating and giving opinions.
Has anyone ever heard of Lyme induced polymyalgia rhumatica?
auto immune conditions do develop and accupunture is great but it may be not enough.
Instead of creating a debate over steroids here maybe it would be best of help
for anyone who is on cortisone or other type steroids to weigh in here with their experience.
So here...Mystery. for me I was in your similar position and would like to hear more about
your condition.
I am on hydrocortisone..20 to 30 mg daily. by my LLMD.
I was for 2 yrs on 20mg of prednisone in 2007- 2009. NOT by an LLMD.
by a rhumatologist for polymyalgia .. I later found out that it was lyme induced. As soon as I found out it was lyme disease I had been dealing with half my life I tried to get off the steroids best I coould.
have you checked your ACTH levels?
I would like to hear about
your treatment and any other people who are
in this position.
I am definitley NOT recommending steroids for anyone but your story seems like you have investigated and I'm sure tried everything else.
Post Edited (bucci) : 11/11/2011 11:29:55 AM (GMT-7)