This Is MS Multiple Sclerosis Community: Knowledge & Support

How many here are members of the Registry? I've read that there are more than 20,000 enrolled. That's pretty impressive. I joined shortly after being diagnosed in 2000.

The reason that I ask is that I just got the latest issue of the MSQR newsletter. So it just got me to thinking

For those who are not familiar with the registry, here's a link to the CMSC-NARCOMS info (Consortium of Multiple Sclerosis Centers)-(North American Research Committee on Multiple Sclerosis)

http://www.mscare.org/patient.cfm?doc_id=64

The newsletter is a quarterly. I find it to be very informative with information on various studies and trials. Being a member of the registry, I get the newsletter for free. I occasionally get questionnaires to answer. That's all

Anyway, like I said, just curious

Cheers

Niko

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"Avoid making irrevocable decisions when tired or hungry." -- Robert Heinlein

Hi Niko,

I must admit that I'm not a member of the registry, I hadn't heard of it until your message was posted. There seems to be plenty on the site to read, so I'll give it a go.

Thanks for raising the point.

All the best,
Chris P

Thanks for the info. Never heard of the registry but I'll give it a try.I like to read everything I can about MS and try to keep up with the latest news. Thanks again! Linda

I'm registered too, Niko.

I love comparing my status every six months. Sometimes I am pleasantly surprised by how "stable" I am, although I find it very difficult to remember to answer the questions about how I'm doing the last month or so, and not the last six months.

The Quarterly is worth it's weight in gold in my opionion as well. You can take it on line or have it mailed to you, which is very good for those with privacy issues. Did you notice how much it would cost to receive the quarterly, if you had to pay for the subscription, as opposed to receiving it free because you fill out the survey? EEK!!!!

Oops, forgot to sign in, so the above comment is mine, Bonnie.

I just realized you can't edit your posts on this board? I must have that wrong, can anyone help me with this question?

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Bonnie

Hi Bonnie,

You should be able to edit your posts... there *should be* a button in the upper right corner of your posts (next to the "quote" button) that says "edit" on it. If there is not, please let us know and we'll make sure there is.

Glad I was curious

Bonnie, you're right about the newsletter being worth it's weight in gold. Very useful info

In the Spring issue, there's a news item from the BBC, there was a British Medical Journal study on stress.
http://news.bbc.co.uk/1/hi/health/3118758.stm

A stress link to MS? Oh yes, I do believe so!
When I first developed symptoms, I was under tremendous stress from work. It was absolutely awful. I resigned before I got the official diagnosis. I felt much better after leaving the job.

I think the stress opened a door for the MS to show itself.

Stress. It's a bad thing

Cheers,

Niko

_________________
"Avoid making irrevocable decisions when tired or hungry." -- Robert Heinlein

I LOVE my Narcoms quarterly magazine. I love the up to date info on the latest clinical trials.

I have to update my info for the registry....just got an e-mail about that.

Take care all........Kim

Greetings all and thanks Niko for the info on the registry. I didn't know about it and have contacted them to send me the info and I'll certainly sign up.



Sharon

Yes, I'm also a big fan of the Quarterly Update... it does seem to have most of the latest info and some things I haven't heard of yet.

The survey doesn't take too long, but sometimes I think they are asking things that I have already answered like when were you diaganosed ( I don't remember anyway -- I just remember the MRI) ... since you keep the same username I don't see why they keep doing that.... but I'll put up with it to keep getting the quarterly update...

=G