Chose Copaxone, but now dithering, got a question about it please

I would certainly entertain the idea of a pill Noel. Are you in the process of getting a dx? Are you waiting to see a neuro? My mobility has been getting slowly much worse over about 2 years? Relapses were leaving me more & more affected, the disability is progressing & not showing any recovery after a relapse now. Neuropathic pain is now 1 of my main problems, constant leg pains. I am waiting to see a pain neurologist to have a nerve stimulator implanted in my spine. Tracey

Seen him last january and he told me it was classic ms. Seeing him this August but have been given the options of all the key drugs. And im dithering big time. My ms nurse has told me to wait till I see him. Half on me says just start now. First scan I had 5 lesions 3 old two active that was just before xmas. Second scan was end of jan 17 and I had two mild new ones. So yes thats ms. Although he hasnt dx me yet. He wants me to start, he wanted me to start dmd last november. If I do he wont dx untill he has no choice. But right now hes holding off. Mines really mild so far. My god I pray it stays like it. Its like the biggest grey cloud in the world. But for some reason I feel confident…

Hi Noel,

Lovely post thanks mate!

The Asia thing is not really my idea, LOL! It is for next August, and it’s my wife’s 40th, and so I’m turning it into a bit of a “Sorry I Got MS” thing :slight_smile:

She is deciding where we’re going. I’m OK with it so long as there’s luxury and a fair amount of alcohol.

I don’t imagine my wife is going to pick one or two of the more exotic places you’ve suggested, but who knows?

Now I’m resigned to going though, it’s getting easier to think of getting there.

Cheers for your input, plus the other posters too.

Good luck all, cheers!

Nev