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An MS Caregiver Needs Stem Cell Information from those with firsthand knowledge

Posted Dec 24 2009 12:00am
Stuart,

I appreciate what you are doing. My wife is quadriplegic, on a ventilator due to MS. Bedridden for 15 years.

I have hopes for stem cells and other possible cures. When I went to the site concerning the experiences in China with stem cell therapy, I noticed a pattern: generally enthusiastic praise for the treatment during and a few weeks after, followed by no further comments or a rare negative one on lack of progressw. The big improvements were to come within a few months and seem not to have occurred. We need to know the unvarnished truth, even if that diminishes the likelihood of a placebo effect.


Now I see other treatments being covered with a similar pattern: early this and early that.
Follow ups are needed!


Douglas W. Cooper, Ph. D.
Walden, NY
Click to view their family webpage: http://tinyurl.com/mfyh47
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email Douglas at: dwcooper05@yahoo.com
or leave a comment on this blog site posting ( not on the facebook page that this will also appear)
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