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MSRC

Last Active: 10th Oct. 07:48 AM
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About Me

MSRC firmly believes that our role is simply to act as a conduit for people to share their thoughts, experience and knowledge. We believe that given sufficient information anyone who visits is capable of making their own decisions appropriate for their lives.

Our MS Discussion Boards at http://msrcsharing.yuku.com/directory are a lively, inspiring and very supportive place to visit, even if you just read what goes on. Our website at http://www.msrc.co.uk has over 3000 pages of information on all aspects of MS for people affected by Multiple Sclerosis.

We hope you will visit them and find them places you want to be.

The MSRC Team.

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MSRC Chatroom Sessions for week commencing 6th October 2008.

We are holding 3 scheduled, moderated chatroom sessions this week in the MSRC Chat Room.

Tuesday 7th, Morning, 10am - 12Noon BST (British Summer Time)

Wednesday 8th, Evening, 8pm - 10pm BST

Thursday 9th, Afternoon, 2pm - 4pm BST

Hope to see you there.

http://www.msrc.co.uk/index.cfm?fuseaction=show&pageid=10

MSRC's cre8Buzz Blog

Family caregiver quality of life in multiple sclerosis among Kuwaitis: a controlled study

BuzzRank 3868

Myelin oligodendrocyte glycoprotein antibodies and multiple sclerosis in healthy young adults

BuzzRank 140

US veterans' Multiple Sclerosis study awaits President's sign-off

BuzzRank 90

High prevalence of multiple sclerosis in area investigated

BuzzRank 89

New blood test could help track progression of Multiple Sclerosis

BuzzRank 98

[View All Blog Posts]

MSRC's Video Gallery

What is Multiple Sclerosis?
BuzzRank 835

Stem Cell Therapy of Multiple Sclerosis: Positive Case Reports
BuzzRank 24

Charlie (Saltpye) talks on how Cannabis helps his leg spasms
BuzzRank 41

Chrystal Gomes at Comedy 54
BuzzRank 48

[View All Videos]

MSRC's Blogs and Sites

The MSRC Website
BuzzRank 52

MSRC MS Discussion Boards
BuzzRank 72

Multiple Sclerosis Resource Centre Facebook Group
BuzzRank 43

Squiffy's House Of Fun - Laughter For Multiple Sclerosis
BuzzRank 85

The Global MS Community
BuzzRank 21

My Friends

Wizzie

kadiprescott

squiffy2

tidesong

Vespula

Sinnaminika

moonwolf

ohegarty

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MSRC's Album

Worldwide MSBuzzRank 6739

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MSRC's Podcast

"The greater the obstacle, the more glory...

[play]

BuzzRank 44

TeamMSRC on the Radio!

[play]

BuzzRank 1

Comedian Jonathan Katz on His Life with MS

[play]

BuzzRank 7

All In The Mind - Programme on Multiple Sclerosis

[play]

BuzzRank 51

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Recent Comments

ResPres said (4 days ago)

Checking out non-profit pages today. Very nice page layout.

Vicki said (21 days ago)

hi! how have you been? i have been sooo busy lately! i wanted to mention this though. a friend of mine's son recently hurt his back very badly. he was out of work for a few weeks and is now having a hard time playing catch. he's registered at modest needs.org which is a website that allows individuals to contribute as much or as little as they can towards his one time debt of $745. they can even give a dollar or less, and the idea is that everyone gives a little bit towards helping. so i'm telling everyone i know on the buzz. if you or anyone you know would be interested you can see his page on their website here: http://www.modestneeds.org/features/ledger/viewapp.asp?mode=upd&rp=l&id=88070&pageno=13&monthno=30&yearno=0 i'm really hoping this will work for him as he is a good kid. and come by my page again, i'm hoping to have information on an all fabric website up soon! -Vicki

dadofdivas said (about 1 month ago)

Just buzzing around to say hello. Like your thoughts and look forward to reading more. Hope you will come by the divadom when you get the chance!

jojo said (about 1 month ago)

I may have been misdiagnosed, but while doing research into neurosarcoidosis I have run across the fact that plasmaphoresis has had really amazing results for M.S. also.

AnnieRob said (about 1 month ago)

Hi there, I see you have been visiting. Would you like to know a secret? I don't talk about it much but, I had (yes HAD) MS, and I do not any more. Docs won't let me say I have 'cured' it as that is apparently impossible. But there it is in a wheelchair for 3 years and dancing at my daughters wedding 2 weeks ago (14 years later. How? I know this is your next question and that is a really long story.

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	The MSRC Website BuzzRank 52
	MSRC MS Discussion Boards BuzzRank 72
	Multiple Sclerosis Resource Centre Facebook Group BuzzRank 43
	Squiffy's House Of Fun - Laughter For Multiple Sclerosis BuzzRank 85
	The Global MS Community BuzzRank 21

MSRC

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Recent Comments

ResPres said (4 days ago)

Vicki said (21 days ago)

dadofdivas said (about 1 month ago)

jojo said (about 1 month ago)

AnnieRob said (about 1 month ago)

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