Raising Awareness of Medical Advancements
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Wanda Baum
- Female
- Warren, MI
- United States
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- I'm from ... (city / state / country)
- Michigan, USA
- I'm Here As ...
- Potential Adult Stem Cell Therapy Patient
- My Diagnosis, My Story ...
- I was diagnosed in 1994 when I was 37 years old. It all started when I was 36 and started having problems with my eyes. After many appointments and many tests the MS was found. I of course was in total denial. Heavens, I could walk and my eyes by this time were fine. I have had only one exacerbation since that time. But as time goes by my symptoms have gone from nothing to confinement to a wheelchair. I can only walk with the help of a walker and maybe one or two steps at a time. I have very little movement in my right leg and foot drop.
- My Family, My Hobbies, My Goal ...
- I have a wonderful and supportive family. I enjoy the computer and I still do some crocheting. I belong to a wonderful MS support group that meets every Friday.
He is so inspiring
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By NATASHA SINGER and DUFF WILSON
Published: December 12, 2009
SOURCE: http://www.nytimes.com/2009/12/13/business/13drug.html?em
MILLIONS of American women in the 1990s were told they could help their bodies ward off major illness by taking menopau…
Hi Everyone,
Have you heard of this. There is research going on in Buffalo right now....
CCSVI in Multiple Sclerosis just google it there is a bunch of stuff on this on Youtube and on Canadian News... The Canadian MS Society is opening up funding…
Hi Everyone,
Have you heard of this. There is research going on in Buffalo right now....
CCSVI in Multiple Sclerosis just google it there is a bunch of stuff on this on Youtube and on Canadian News... The Canadian MS Society is opening up funding…
There are quite a few people here on this site ; Janice Fuller and two that come to mind immediately. There is about 80-100 people from D/FW that have been. Only a fraction of us show up at a monthly meeting but most are interested in talking. On to…
Thanks Preston, that is wonderful to hear. Who else do you know of that has gone to Costa Rica that would not mind discussing the journey with a prospie like me?
I believe they understand it as much as they can. Dr. Neil Riordan, who is the CEO of the clinic, has a very good understanding of what is going on...You can find a number of his papers posted online by searching.. He is a research scientist and dir…
Dear Preston, I have Cerebral Palsy and am on the fence about ASCT. I do not have the terrible fear and pain of a degenerative diisease breathing down my neck as you did; I think that makes the leap of faith a little harder for me, if you know what…
Hey everyone,
I am new here, and seeking information and perspective. I am a 25 yr old male afflicted with moderate Cereral Palsy. I am looking to contact other CP patients (and their loved one) who have gone the ASCT route. I have heard so much mi…
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I've been doing okay ~ thanks for asking :-)