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I was Dx in 1998 with SPMS. It quickly deteriorate and am now wheel-chair bound since 2004. I lost use of my right arm/hand 2008. I am stable now; thanks for my taking of LDN since 2008 (at least it is what I believe). You can see my full story here: http://algisj.com Feel free to contact me directl...

There we go. The fundraiser has been set. I know you guys have your own to care about; but if you could spare the price of a beer for me I will be your Buddy forever... And if you can't please forward this message to all peoples you may. Thank you heaps. The whole process will be reported here and o...

China Beijing PuHua: ~30KUS$
Swiss Medica Serbia/Moscow: ~28KUS$

I applied both and will decide after we make the budget.

Thanks Notasperfectasyou; useful reading.

Be well; all,


Algis

Sorry hijacking the post; but I have been taking LDN for years now and I am convinced it is it that stopped my progression. I had no relapse for over 8 years taking LDN 5.5mg at night each day. I got an MRI last February and have no new lesion since 2008 and no active inflammation. Thanks to Aletha ...

That's a win, isn't it? Congrats. :) Thanks Cece; I give credit to LDN; it is the only reason it could happen (tho I can't prove it). I have never been in a position to finance CCSVI and now will try to fund a MSCT at a Beijing hospital (see Stem Cells Board) in order to try to regain some function...

Thank you Doctor. I will make an educated research and will talk with Mr.Yang; head of the R&D Center; with whom I have good relation.

I will keep you informed if that is agreeable with you; but in PM not to pollute the thread.

Good day to you;

Algis

I am glad to see all of you still here. Personally the progress of the disease seems to have stopped. For years I had no relapse, tho I also don't regain any lost function. @Doctor Sclafani: do you recall we once talk about a marker in the blood that peak when a thrombosis start forming? I searched ...

Is this thread dead? Do you still here Doctor?

Cheers all;

Algis

Because I am curious; I sent a request to them. For me; it would be 25K€; 12 days at Moscow Clinic (?)

@Seeva: It is in Serbia (Belgrade), cheers Buddy.

http://www.startstemcells.com/stem-cell ... edure.html

Thanks NHE, glad to see you here; been a long time, I was researching a lot and someone has to take the plunge...

I have been accepted for a MSCT treatment at PuHua Hospital in Beijing, China. I am collecting the funds (35KUS$). I will keep the news coming in this thread.

Cheers,

Algis

As few of you knows; I'm living in Asia and can't get a hand on many medicines over here. I have a friend traveling to NYC shortly and she would bring me back 4-AP from a knowned CPharma. Can anyone tell me where they buy their 4-AP in Compound pharmacy?? Multiple addresses would be welcome as my fr...

Thanks Buddy, pretty informative

Hi Fellow MS'ers I am not new here nor with MS (Dx 1998 MSSP actually EDSS ~8~) I reside since almost 30 years in a country (Taiwan) where the welfare for foreigners (I am Belgian) is unavailable. Therefore and in order for me to discuss with the social service locally; I'd need a list or a link of ...