Stem Cell Therapies

Discuss stem cells, adult and embryonic, and their therapeutic potential for MS here.

Stem Cell Therapies

Postby StemHope » Fri May 23, 2008 9:50 am

I spent less than 20k in Thailand, here is the letter I sent them when I got home.

Thank you for the medical care that I received during the stem cell procedure in Bangkok, Thailand. The doctors were the highest professional level. The science was advance. Your team's gentleness and care made it much easier than I experienced in any other medical or hospital facility outside Thailand.

I must admit that at first I had doubt. However, I am surprise of the advance knowledge and the professionalism of the doctor team and the wonderful hospital facility. I will definitely recommend this to my friends. I am sure to come back to additional treatment that are available in Thailand. But, unfortunately not yet in my country.

If you are considering going to get treatment overseas for Stem Cells I would be happy to point you in the right dirrection. My Dr was Dr Narong and he is known all over the world. Good Luck
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Postby mrhodes40 » Fri May 23, 2008 11:50 am

Isn't the internet interesting? Now we are getting a BRAND NEW member, someone who has never been here before appearing to give us a testimonial about Thailandese treatment.

This person is obviously a non native English speaker, most likely Dr N himself.

Dr N confess it is you and tallk to us honestly about your approach! We don't go for deception
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Postby StemHope » Mon May 26, 2008 11:44 am

Hi Friend I assure you I am no Dr. I wonder if you know what it is like to have receive a gift you never thought possible. If I use my first post to express my gratitude and extend this gift and it reaches one other person and I get provoked by you, then I guess I made a mistake of what this area was actually for. Otherwise, I am from Orlando Fl born and raised I live in Metro West about 10 min away from Universal Studios Orlando. Also if I was a Dr I would certainly be recommending this same miracle to everyone I ever met, but A.D.D. would not let me sit through any class but Lunch>>>have a good one BUDDY :wink:
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Postby Frank » Sat May 31, 2008 4:27 am

Hi StemHope,

if you really had these great kind of experience please share some more information about it.

What kind of stem cell therapy (SCT) did you get?
Did it improve some of your symptoms? What symptoms and in which way did they improve?
How long did you have these symptoms before SCT?
What type of MS are you (RR, SP, PP), when have you been diagnosed, what kind of therapy have you tried before SCT, how old are you, male or female.

Thanks
--Frank
Treatment: Gilenya since 01/2011, CCSVI both IJV ballooned 09/2010, Tysabri stopped after 24 Infusions and positive JCV antibody test, after LDN, ABX Wheldon Regime for 1 year.
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Postby DIM » Sat May 31, 2008 8:54 am

Frank just saw your signature, would you mind to tell me please why you stopped LDN, have you had bad experience with it, no good results, MS progression, what exactly?
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Postby Frank » Sat May 31, 2008 3:20 pm

Hi DIM,

I wanted to give LDN a try because some people had really good results with significant improvements.
For me LDN didnt do much. I did not notice any improvements and apart from the temporary sideeffects at the beginning (mostly sleeping problems) I always noticed an unpleasent muscle stiffnes in the mornings.
It wasnt a big deal but I really took more drugs than I would like to, so after half a year or so I deceided that I didnt want to use it anymore.
If you have further questions, just let me know...

--Frank
Treatment: Gilenya since 01/2011, CCSVI both IJV ballooned 09/2010, Tysabri stopped after 24 Infusions and positive JCV antibody test, after LDN, ABX Wheldon Regime for 1 year.
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Postby DIM » Tue Jun 03, 2008 9:11 am

So no positive nor negative results Frank (except the morning stiffnes) you just wanted to change drug!
Do you have a pre and after-LDN MRI scan for comparison?
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Postby Frank » Tue Jun 03, 2008 5:01 pm

Yes I have regular MRIs, but I think the latest negative change was in 10/2006 (one lesion got bigger).
So there also was no change in MRI before-, compared to after LDN.

--Frank
Treatment: Gilenya since 01/2011, CCSVI both IJV ballooned 09/2010, Tysabri stopped after 24 Infusions and positive JCV antibody test, after LDN, ABX Wheldon Regime for 1 year.
Frank
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Posts: 543
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