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Thanks I will forward that to the neurologist.

@NHE : Well; I know 6 months is too short a time, but... I have no progression nor regression since I started Tecfidera.
As I use to say "At lest I don't get worse"

Thanks all; I'll keep working on it and relate if I find changes,
Cheers, be well all

Thanks for the replies. @Zyklon : yes, SPMS. No much other option over here (Taiwan). I tried Copaxone injections but they makes me very sick with relapses... I was really down and had to stop it. The neurologist chose, he knows me since 1998 and follow my case, I trust him. @NHE thanks :) The probl...

Hi Friends; I am now for 6 months on Tecfidera, and would like to see if now, April 2023; anyone can vouch any improvement due to the med. I have not much side effects which includes rash, occasional diarrhea (lasting 2 days) and red flush that last 2 hours. I am EDSS 8+ and honestly don't feel much...

No Guys; All is fine; just exhausted by physical therapy and how to follow-up. I'll try to catch-up forgive me!

Thank you Guys; thanks ElliotB for suggestion, I might try that.

Cheers

Algis

Updates are coming. The fact is; I have got a darn bad allergy (probably related to the MSCT) and furthermore, the weather here is killing me; we have permanently 36°C with 90%+ humidity, I cant move a finger without sweating half a liter... And for a reason beyond my understanding, TIMS doesn't sen...

Ok; am back home. I have finish updating the blog up to the last day. I will keep reporting there, way more convenient.

All went smooth and well.
Cheers!

Updates still there; few answers are too private so if you dont see in your private email/msg box it means I dont answer those questions ... Usual Q are: Is the foundraiser keep going and if yes why? How is the cost of everyday life there? How are the people? Why chose your daughter and not you wife...

further updates will be placed mostly on the website's blog due to the complexity of the matter throughout ThisisMS and the PRC tecoms

http://algisj.com/wp/

Apologies for delay in reporting; but it is very busy and communications are a darn thing here... The first place I post is in the blog http://algisj.com/wp so if you are eager there is the place to go. Also as it is my server I can put as many pictures as I am pleased. D-DAY The 3rd of July it is....

The dinner organized last Friday was great fun! You can see here:

Report and Pictures on the website!

http://algisj.com/wp/2017/06/24/glory-f ... -luck-pot/

Could you please describe the kind of stem cell therapy you are undergoing or provide a link so I can read about it. Also, why you have chosen this kind of stem cell procedure. (You doubtless have already written about it. Could you direct me to the relevant post?) I assume you are not undergoing c...

D-Day - 18 Time is passing even slower... So eager to be there. We are close to the target in matter of fundraising. We will have a smaller party at a Friend's Restaurant in Taipei and get some more new people registering. We will have no auctions and the meal is very reasonably priced; so it will m...

Prior to the Gala; we had to make a lot of noise. A community magazine was kind enough to publish my story and it helped much to collect and gather people... All our thanks go to Suzan Babcock who donate much time and energy for this to happen. Here is a copy of the article that was given with the &...