Three weeks on ldn

[Guest guest]

I have been on ldn for three weeks. I also take avonex, amantidine,

bacllofen,

klonapin and celexa. I have ms for almost 30 years and am in a

wheelchair.

After I took my first few doses (4.5 mg), I noticed the pain in my

butt stopped, I

slept better and some weaknees in my right arm im proved. I have

stopped the

baclofen, celexa and amantidine. The results have not been earth

shattering,

but I realize my ms has been around for quite a while and it will

take some

time for my body to improve signifcantly. I would like any input from

someone who

is in a similar position as me, or any one who can add something.

Thanks,

Gerry

[Guest guest]

Hi Gerry, Welcome! I was on Avonex and then Copaxone, and got off

copaxone and on LDN. If I understand correctly, Avonex and LDN

don't compliment each other....avonex is an immune suppresant and

LDN is an immune system uplifter and regulater. So, just my

oppinion, you might even do better with the ldn, if you drop the

Avonex. since LDN stops the progression of MS, you really don't

need the avonex at all. talk to your doc and see if he/she agrees.

I, like you, have had MS for 30+ yrs and have been thru it all, and

truely empathize with you. The ldn is working for me as it is for

you, not earth shattering, but subtle changes for the better....and

that is something that the abcr's didn't do. I feel better and I

will take all the plusses that ldn has to offer.

I hope this helps and keep us posted as to how the ldn experience is

going for you.

Best Regards

Sally

--- In low dose naltrexone , " gerald " <vze23dyj@v...>

wrote:

> I have been on ldn for three weeks. I also take avonex, amantidine,

> bacllofen,

> klonapin and celexa. I have ms for almost 30 years and am in a

> wheelchair.

> After I took my first few doses (4.5 mg), I noticed the pain in my

> butt stopped, I

> slept better and some weaknees in my right arm im proved. I have

> stopped the

> baclofen, celexa and amantidine. The results have not been earth

> shattering,

> but I realize my ms has been around for quite a while and it will

> take some

> time for my body to improve signifcantly. I would like any input

from

> someone who

> is in a similar position as me, or any one who can add something.

>

> Thanks,

> Gerry