Re: LDN for copaxone users

[Guest guest]

When my husband (PPMS) was slipping fast he was on Avonex. August

2002 his Neuro suggested that if he didn't want to stay on the Avonex

then he should switch to copaxone. I argued with the Neuro that as my

husband was PPMS the CRABS wouldn't work for him anyway .. but the

Neuro insisted something was better than nothing .. and also that he

was very lucky to be on Avonex as he would be much worse without it!

I went crazy!

I asked Dr Bihari at the time what he would do if he were in my

husband's position .. would he personally take copaxone with the LDN?

He said no, he said that if it were him he would just take the LDN ..

he would stop the other drugs ... so my husband did .. and pulled

back a bit and has stabilized. The only other thing he takes is a

calcium based multi vitamin.

All the Best

> > > Do any of you MSers smoke (cigarettes) and how does the cravings

> > for

> > > nicotine change, if at all , whilst you are on LDN?

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> > > Im so anxious to start LDN and report back to you all too. Damn

> > > Doctors not co-operating. grrrrrr

> > >

> > > Friday

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