[voodidit]

As most of you know i have been diagnosed with MS. I was just wondering if anyone else in the Village has this problem and if they have any favorite sites that visit where I can get more info. I have found some good sites but I want to find everything I can.

 

[Darlene]

I don't have any web sites for you Angie, I just wanted to let you know that I'm here for you to help in any way I can. :heartsm:
My Bil (who I am not close with anymore because he and his wife turned into goofball wierdos) has MS. One of the things that he noticed is that when he was overtired or pushed himself too much he had more problems. Take it as easy as you can.:hugz:

 

[nealy]

I personally don't have MS. But I wanted to say that we are here for you, and you will be in my thoughts. My friend from high school's Dh was diagnosed with MS three years ago he was only 24. He is doing wonderfully, they do the walk for the cure every year now. Lot's of new discoveries and treatments out there. (((hugs))).


Nealy

 

[homesteadmamma]

Sweetie, I don't have MS either, but I want you to know I'm here for you too. If you want to vent or just talk, pm me anytime. I know what its like to live with an illness. I've had fibromyalgia for almost 7 years now.

Know that you are much loved here. :hugz:

 

[voodidit]

Thanks everyone! CJ I have Fibro too and Chronic Pain Syndrome, i"m just falling apart..lol.

 

[SewCrafty]

Angie, I don't have MS either, but my sister does.

The only website I can think of offhand is Montel's. It is http://www.montelms.org/ There is additional MS Resources and Help in getting treatment on his site. I haven't been there in a while and alot of new things have been added.

:hugz:

 

[captclearance]

I'm here for you too Angie !!!!!!!!!!!

 

[frugalmel]

hugs sweetie! (hugs)

 

[Heather]

Sending hugs to you and saying a prayer!!

Does your hospital have a support group? Maybe they would have a package of information with sites, organizations etc. :smball:

 

[Missy]

sending you great big hugs. I have been researching this topic because of some undiagnosed problems my docs seem top never be able to pin down the causes of. so armed with this (and other research) i am going to see my doc thge 14th of May and see what we can come up with to get me towards getting help for my symptoms. here are some of the sites i have come up with so far:

http://www.healthtalk.com/msen/091301/index.html
http://www.msaa.com/
http://www.nmss.org/