This Is MS Multiple Sclerosis Knowledge & Support Community

Hi Keith--welcome!
How great that that you're looking out for your niece! Sounds like she's already on the right track!
There's a great bunch of knowledgable people on this forum, so don't hesitate to post any questions.
Wishing all the best to your niece!

chrishasms wrote:Dr. John Cotboy or Dr. Volmers.

Head neuros st Rocky Mountain MS Center.

Thanks so much, Chris! I'll definitely be looking them up!

First of all, Jack, welcome! You'll definitely find lots of great info, and great people on this forum. I'm sorry about what you're going through--I know how scared you must be. Try to stay as positive as you can--and hopefully you'll get an answer soon. As scary as it is to get a diagnosis for anyt...

Hi there--I unfortunately don't have any info to share, but I just wanted to say I'm sorry this happened to you, and I hope you find a solution soon. Good luck to you!

You might try http://www.msneuroratings.com/ . You have to join to read but it's free! The ratings are reports from real people with MS. Thanks Sparky--I actually joined a while back, hadn't gone on there in a while--so I posted there this morning. I got a couple of names from older posts, and hope...

Hi--just thought I'd post this again in case some one from Denver happens to see it.
Thanks!

Hey Sparky--welcome! It's great to have you here!

Hi everybody!

My husband and I are moving just outside of Denver, CO next month (to Lakewood)--anyone have a referral for a great neurologist in Denver? Thanks in advance!

Thanks so much JL--I really appreciate it!
Have a good week!

Hi Randi! Welcome to the board! I noticed you used a smiling emoticon, even though this is all so very new to you...that's great! Try to stay as positive as you can-- I wish you all the best!

I'm from the US, but nice to meet you, Mandy! Sounds like you have a great attitude--which isn't always easy to maintain! I was dx'd in 2001, but I think I've had it since '96 or '97. I love that you help injured and orphaned animals--that's really wonderful! Take good care, and "see" you ...

lovebug wrote:You can read about it at http://www.neuropathytreatmentgroup.com............I am not sure what to make of it yet.........

It's so hard to know whether to try these things, I know! I'm gonna read about it more.
If you decide to try it, let me know what you think!

jimmylegs wrote:ok supplement regimen update pending, next couple days you'll have the latest, koop

JL--any time is great--take all the time you need


And thanks for the magnesium review, Pointsnorth!

Just saw this--sorry for the late response! I don't know if you've already been diagnosed, or are hoping to be....but I had a defibrillator implanted about six month after my dx, and haven't been able to have an MRI since then.(2001) I can only be treated clinically; so if you absolutely can't have ...

This is the first I've heard of it--I'll definitely look it up. Thanks for passing it on! :-D *--I just saw a couple of links to some reviews/comments about it: http://www.drugs.com/answers/peripheral-neuropathy-has-anyone-tried-neuropathy-415947.html http://neurotalk.psychcentral.com/thread138278.h...