on copaxone

[Guest guest]

Hi gang I am new to this site and am trying to get ldn from my neuro

but have not heard back yet. I got dx in 12-02. Started on Rebif

and it was TERRIBLE I felt like I had the flu 24/7!! Changed to

copaxone with good luck until lately I see to be having more bad

days. Flare for 1 month then ok for a week another flare for a month

etc. I will get ldn somehow and I think I will stop the Copaxone at

first just to see if ldn is working for me and compare otherwise I

won't know whats working and what not. if not then back to

Copaxone. The only fear I have with the ldn is that the abc drug

are to keep the disability away long term not stop the flares. I

know ldn is new but are people stable with no more new symptoms and

if so how long has it been? Have the people on C had better results

on ldn or both combined? Thanks for your help. Off to Disney world

in the morning for 4 days I hope the ms stays in MN.( smile) Jeanie