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Re: USCSF study

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No, never heard of it. But I'd do it if approached. ~*~Hugs~*~ ~*~Akiba~*~ -- USCSF study I got a phone call yesterday from USCSF about a study. They are sending me a kit to have my blood drawn at my local lab, then the lab will mail it back to them. The woman I talked to said they are taking 3,000 samples at USCSF and then collecting additional samples from around the country. She said their goal is 10,000 blood samples from MSers. She said the goal is to identify the genes for MS. She also mentioned they think MS is genetic and environmental.Is anyone else doing this? Sharonjoin me on Facebook:Sharon Mars wobbletowalkThis email is a natural hand ma de product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects.

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No, never heard of it. But I'd do it if approached. ~*~Hugs~*~ ~*~Akiba~*~ -- USCSF study I got a phone call yesterday from USCSF about a study. They are sending me a kit to have my blood drawn at my local lab, then the lab will mail it back to them. The woman I talked to said they are taking 3,000 samples at USCSF and then collecting additional samples from around the country. She said their goal is 10,000 blood samples from MSers. She said the goal is to identify the genes for MS. She also mentioned they think MS is genetic and environmental.Is anyone else doing this? Sharonjoin me on Facebook:Sharon Mars wobbletowalkThis email is a natural hand ma de product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects.

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No, never heard of it. But I'd do it if approached. ~*~Hugs~*~ ~*~Akiba~*~ -- USCSF study I got a phone call yesterday from USCSF about a study. They are sending me a kit to have my blood drawn at my local lab, then the lab will mail it back to them. The woman I talked to said they are taking 3,000 samples at USCSF and then collecting additional samples from around the country. She said their goal is 10,000 blood samples from MSers. She said the goal is to identify the genes for MS. She also mentioned they think MS is genetic and environmental.Is anyone else doing this? Sharonjoin me on Facebook:Sharon Mars wobbletowalkThis email is a natural hand ma de product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects.

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Not sure, but my doctor has sent my blood off to the mayo clinic several times.  The first time was when I was hospitalized, it was to check if I had a rare form of MS (malignantly progressive) which was negative.The other times was for ??

Jolie

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Not sure, but my doctor has sent my blood off to the mayo clinic several times.  The first time was when I was hospitalized, it was to check if I had a rare form of MS (malignantly progressive) which was negative.The other times was for ??

Jolie

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Not sure, but my doctor has sent my blood off to the mayo clinic several times.  The first time was when I was hospitalized, it was to check if I had a rare form of MS (malignantly progressive) which was negative.The other times was for ??

Jolie

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I wasn't invited.. but I do see my neuro in Feb.. and he's usually in on

the studies of different things.. maybe he'll ask me then?

HUGS

|)onna

Sharon wrote:

>

>

> I got a phone call yesterday from USCSF about a study. They are

> sending me a kit to have my blood drawn at my local lab, then the lab

> will mail it back to them. The woman I talked to said they are taking

> 3,000 samples at USCSF and then collecting additional samples from

> around the country. She said their goal is 10,000 blood samples from

> MSers. She said the goal is to identify the genes for MS. She also

> mentioned they think MS is genetic and environmental.

>

> Is anyone else doing this?

>

> Sharon

> join me on Facebook:

> Sharon Mars

> wobbletowalk@...

> This email is a natural hand made product. The slight variations in

> spelling and grammar enhance its individual character and beauty and

> in no way are to be considered flaws or defects.

>

>

>

>

>

>

>

>

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Share on other sites

http://www.ucsfhealth.org/adult/cgi-bin/nihctSearchAction.cgiThis is all that I could find.Love,nTo: MSersLife Sent: Wed, January 27, 2010 7:42:12 PMSubject: Re: USCSF study

I wasn't invited.. but I do see my neuro in Feb.. and he's usually in on

the studies of different things.. maybe he'll ask me then?

HUGS

|)onna

Sharon wrote:

>

>

> I got a phone call yesterday from USCSF about a study. They are

> sending me a kit to have my blood drawn at my local lab, then the lab

> will mail it back to them. The woman I talked to said they are taking

> 3,000 samples at USCSF and then collecting additional samples from

> around the country. She said their goal is 10,000 blood samples from

> MSers. She said the goal is to identify the genes for MS. She also

> mentioned they think MS is genetic and environmental.

>

> Is anyone else doing this?

>

> Sharon

> join me on Facebook:

> Sharon Mars

> wobbletowalk@ yahoo.com

> This email is a natural hand made product. The slight variations in

> spelling and grammar enhance its individual character and beauty and

> in no way are to be considered flaws or defects.

>

>

>

>

>

>

>

>

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