Forum

my testimony for the PPMS

There are no approved treatments for PPMS. I think it’s enough to know the MS society if we wan’t to know the developments in the world,

I’ve opted not to take anything for 2 years (this was the last Endoxan (french) but it did nothing). I atends advances in research (for 10 years already !)
Careful we are all different with our MS

I’am severely disabled but the life don’t stop here,

Watch my WEB TV on YOUTUBE and reseaxch MrKINKIN93 or http://www.youtube.com/user/MrKINKIN93?feature=mhee

because we are technically well supported if things go wrong

Hi, watched your film… very good!.. even though I don’t speak French so couldn’t understand it!

Good to hear your positive attitude… and welcome to the forum.

Pat x

I learnt my French from a man named Del Trotter. I’m a bit of a linguist; speak about 3 languages fluently, Giberish, Double Dutch; Rubbish but haven’t quite mastered my French oh and English.

George