This Is MS Multiple Sclerosis Knowledge & Support Community

Indeed, CureOrBust...indeed. I would never expect nothing more than I get, in just 2 days after the first lp. As I told to relatives and friends who asked me, I suppose I have to follow up my self for, at least six months...and maybe it will require more time and time, even more than 6 months. Probl...

What can I say...I'm at Vienna airport after one and a half day after my first infusion. I'll tell you what : I don't know how many cells have been transplanted to me (guess there should be a very exact number of it, right), no one was so kind to tell me how things are going to proceed, now, chemo o...

The greatest problem, I think, it's turning mesenchimal treating into a drug. Slavin itself said it would take to much researching time and it would be costing billions of dollars, and every patient is responding too differently. But if you have drugs companies against, I guess you wouldn't go too f...

I was still Relapsing Remitting form, when I took the ccsvi "liberation" treatment. I was so stupid that I believed to be safe, after the ccsvi treatment, and I stop the therapy I was following, with copaxone. Now I've turned into secondary progressive and I can hardly walk in normal way, ...

This was the first message I received from dr.Slavin secretary, Ruth Grunblaum. It's in italian, copy and paste it into google translator, I know its just for bad translating, but just to get the idea...

grazie per aver contattato il nostro centro. CTCI Le allego un formulario da compilare e rispedire per sapere se e' possibile trattare il caso nel nostro centro. In caso positivo eccole alcune informazioni sul trattamento: Si tratta di venire qui a Tel Aviv per un consulto col professor Slavin e per...

Well, being my same bone marrow cells, at this moment I didn't take any immunosoppression, any chemio.I guess chemio was required if it was cells coming from someone else's.

I've done yesterday my 1st MSCT infusion, the "soup" was prepared since june, with my bone marrow blood under supervision of Slavin in Tel Aviv, and the reinfusion was in Vienna, yesterday, at "dr.Kleef klinic". I don't care about blocking relapses, the way I care for repairing d...

I'm really afraid every single patient, me included, has asked himself the very same question,dude! In my country (Italy) every years they say "damn...we've founded, in maximum 5 years there will be a revolutionary solution to face off against ms...you'll see!" ...problem is that more then...

I am still able to walk but things are getting worst and worst. I need some pratical result, NOW.....for me, the ones like me and everyone in world who'fighting against this F*****G disease.....fountain of great money for the medical companies! I wish to take my kindest regards and a very warm greet...

Top of the morning, everyone, I'm Andrew, I'm 38 from Italy and I am a secondary progressive form MS patient with more then 25 years of fighting experience against our desease.Yesterday I've taken my first bone marrow mesenchimal stem cells infusion, I am following dr.Slavin's program. This has cost...