LDN Is Great But Not Magic

[Guest guest]

I only speak for MS. I take 4.5 mg/day at bedtime (when I go to bed, regardless

of the clock time or where I am on Earth).

I believe Naltrexone is FDA approved in a 50mg/day dose for addictions,

So, obviously at 4.5 mg you'd believe it to be safe (unless you have some

unusual reaction or allergy).

I asked my PCP for a prescription for LDN and he gave it to me and said " well it

can't hurt you " . That was more than 5 years ago and I have not had an

exacerbation since (WHICH MAY HAVE HAPPENED ANYWAY).

I also take Copaxone, paid for by the Chronic Disease fund (www.cdf.org)

I have taken almost all the Interferon drugs and am glad to stop those.

My Neurologist gave me in site as to the real usefulness of the drugs when I

asked why he called me R/R (I thought I was some type of Progressive) He told me

diagnosing me as R/R was the only way to get Betaseron (at the time). That is

also why I don't spend a lot of time worrying about my type of MS (as long as it

is not CP),