my testimony for 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

because we are technically well supported if things go wrong