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05-10-2011, 04:15 PM | #1 | ||
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In Remembrance
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paula "Time is not neutral for those who have pd or for those who will get it." |
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"Thanks for this!" says: | soccertese (05-11-2011) |
05-10-2011, 06:38 PM | #2 | ||
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05-10-2011, 08:28 PM | #3 | ||
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they probably sleep quite comfortably -i guess i don't know European countries' laws. It is apparently legal, or was, but where has therapeutic efficacy been proven? do countries have different rules about experimental treatments: well they obviously do. what were people told that made them think it could be successful.
We only have Freeds fetal cell trial and it helped the one person i know who was in it, but she has since had a DBS and is very dyskinetic. So her fetal cells may be multiplying too much or dying. I do not trust stem cells from another person- there is no reason to yet. We are all too different and stem cells are not like organ transplants. I like my medicine to be synthetic....ha. Seriously tho, has anyone got a good report about being treated at XCell? it's not funny, two little boys died. I hope the brave people who were treated didn't give up their life savings.
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paula "Time is not neutral for those who have pd or for those who will get it." |
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"Thanks for this!" says: | made it up (05-18-2011) |
05-11-2011, 09:41 AM | #4 | |||
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My guess is her fetal cells are dying off because nothing was done to correct the problem before the new cells were implanted.
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"You can't fight City Hall, but you can pee on the steps and run." --Gary North Last edited by GregD; 05-11-2011 at 02:13 PM. |
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05-18-2011, 01:57 PM | #5 | ||
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By using his own stems cells being extracted, cleansed, counted for efficacy, and put back into his spinal column, he has seen so far a 38% reduction in his Parkinsons symptoms. The website listed the names of some of the patients who allowed them to be accessed for comments which we did including our doctor. Plus all their statistics on all the opertions they performed for each disease they treated was on-line and sent to us verified by DRS. in the US. For my husband, and obviously myself, it was a miracle. My husband has reduced his meds by 60% and counting. It takes about a year for the damaged cells to be replaced. We are hoping for a 70% recovery but are more than happy for what has transpired so far. As far as sleeping is concerned, they should sleep well due to the miracles they performed and so do we because of those miracles. *edit* Last edited by Chemar; 05-18-2011 at 02:11 PM. Reason: NeuroTalk Guidelines |
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05-18-2011, 05:07 PM | #6 | ||
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"Thanks for this!" says: | made it up (05-18-2011) |
05-18-2011, 05:31 PM | #7 | ||
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I could probably score 38% better on a test on a good day "on" compared to being off. Can you tell us more? I'm torn between understanding that this clinic is trying to help people and i have advanced pd and fight all the time for speeding up treatments, but even the researchers here say IPS cells are not of therapeutc value yet. So if you see the improvement in your husband and he feels better I'm very happy for you both. is there more you can describe about his improvement? are they providing follow up? or were they before being closed? the best way to get a treatment going is to share what it did to your husband. Convince us and then we'll be hopeful that maybe this is just a regulation problem. best to you,
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paula "Time is not neutral for those who have pd or for those who will get it." |
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"Thanks for this!" says: | VICTORIALOU (05-19-2011) |
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