Re: LDN & Multiple Sclerosis

[Guest guest]

I`m so sorry to hear about this Art - I guess we have to remember that LDN

doesnt make anyone invincible. It also helps to remind all those men here with

MS (my husband being one) that it is thought that it hits them harder in the

long run. I think the uncertainly is one of the worst things - just not being

able to predict where you`ll be medically at any given time, as far as mobility

and general levels of health.

It`s hard to find the balance of not giving MS " the power " to rule your life but

still not live in denial and to heed warning signs of disease progression.

Hope the Copaxone and the IV kicks the exacerbation squarely in the ass!

Bev

-- In low dose naltrexone , " art_ldn " <rtee54@...> wrote:

>

> For you new MS people if you want to chat here or via private email.

>

> Last week I had two IV Solumedrol treatments in an attempt to quiet down an

exacerbation I have ignored for a long time. Not a smart move. I am stubborn and

full of pride. Maybe a case of falling blindly in love with a medication -

meaning LDN. I have also restarted Copaxone. Still taking 4.5mgs LDN every night

at midnight and plan on continuing. MS is a disease females get more than males

so maybe I am being hit harder than most. Figures. We will see what happens. Ya

gotta do what ya gotta do.

>

> Don't let anyone tell you differently - MS Sucks!

>

> Art

>

> My MS/LDN story/1988 - 2009

> http://tinyurl.com/mejs2t

> --

>