Re: [LDN_Users] Curiosity about medications...

[Guest guest]

hi raymond -i have never known anyone with ppms to be given any of the 'crab' drugs

all i take is ldn [2ml] as i have neuro muscular leg problems and baclofen [1x10mgx3a day]

good luck

regards/peter/london/ppms

From: RAYMOND <rrunge3@...>LDN_Users Sent: Monday, 25 April 2011, 11:51Subject: [LDN_Users] Curiosity about medications...

Hey everyone, hope you all had a nice Easter holiday. We actually had a tornado move through on Good Friday, luckily no deaths making it a better Good Friday.But anyhow, I'm seeing a new Neuro. I was originally diagnosed with PPMS and put on Rebif. After taking that for 18 months my insurance company said that I wasn't qualified for it. I felt like it was making me worse anyway. So I've been without anything except LDN as of earlier this year.I went see my new Neuro and she diagnosed me as RRMS. I'm confused by that since I've seen no remission. She wants to put me on Copaxone. From other sites and boards, I've read that Copaxone can make some symptoms worse in PPMS. I'm also concerned that there may be some kind of problem taking both, the LDN and the Copaxone.Does anyone have any experience with my situation?Thanks for your help,Ray