Does anyone know where this clinic is and it any information about it? Thank you
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genetic ms clinic is California
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UCSF is doing MS genetics research with a dedicated lab. My consulting neurologist, Dr. Hauser, has been in the forefront of this research. Here is a link to a recent write about Dr. Hauser winning the Charcot Award for his research in MS genetics.
http://www.msif.org/global-ms-news/m...sclerosis.aspx
Here is the link from the MS Society discussing the UCSF Genetics Study and how to participate.
[url[/url]
http://www.nationalmssociety.org/res...ies/index.aspx
I hope this is what you were looking for.
**Moderator's Note - the url given wasn't correct, so I added the one I think you meant. Seasha**
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Originally posted by polopuppy View PostUCSF is doing MS genetics research with a dedicated lab. My consulting neurologist, Dr. Hauser, has been in the forefront of this research. Here is a link to a recent write about Dr. Hauser winning the Charcot Award for his research in MS genetics.
http://www.msif.org/global-ms-news/m...sclerosis.aspx
Here is the link from the MS Society discussing the UCSF Genetics Study and how to participate.
[url[/url]
http://www.nationalmssociety.org/res...ies/index.aspx
I hope this is what you were looking for.
**Moderator's Note - the url given wasn't correct, so I added the one I think you meant. Seasha**Tawanda
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Diagnosed with Multiple Sclerosis 2004; First sign of trouble: 1994
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My mom and I participated in the big UCSF study. It's not a clinic though, they just want your blood and history.
We're also giving our DNA to or new doc in Irvine. It's not geared specifically toward multi-generational MS, they just want our blood for studying the genetics of MS, not our specific cases.Aitch - Writer, historian, wondermom. First symptoms in my teens, DX'd in my twenties, disabled in my thirties. Still the luckiest girl in the world.
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Not trying to take over your thread, just want to add info for the MSers who want to do good!
For those interested in donating organs/body after death, I have found out that the Mellen Center at the Cleveland Clinic are always accepting MS brains.
Weird subject for some, I know. I am trying to make lemonade w the lemon disease I've been given. What if it was my brain that helped cure MS for future generations?Dx 3/4/12. Tec X 2 as of 7/7/13
Weebles wobble and occasionally they DO fall down!
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Originally posted by suziq38 View PostHi What is the name of your doctor in Irvine?
I live close to Irvine.
Thanks
suziAitch - Writer, historian, wondermom. First symptoms in my teens, DX'd in my twenties, disabled in my thirties. Still the luckiest girl in the world.
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