MrMDM2007's channel

Not sure what all of you are bitching about, looks good to me. All of you haters are BBQ snobs.

Mrmdm

Hi Tom,

I've been on Tysabri for 2 years and JC virus Positive. I'm not clear on the figures you mention, since my understanding is that the risk of PML is more than 1/1000 for us but not what you mentioned. Please clarify your risk calculations.

I've started taking Tysabri every 6 weeks now....

This movie looks very bad-ass! I want to see it for sure.

Hi Vern,

Thanks. I'm still on Tysabri, and feeling really well. (The heat is kicking my butt though..) Still limping around, but other than that I'm okay.

I'm now part of the "Stratify 2" study regarding PML, the JC Virus & Tysabri.

The first step is seeing if I have the JC Virus. I'm expect...

Hey Vern,

You look great!! Thanks for the posting and looking forward to your Wife's perspective.

I stopped my Ampyra since I felt lke crap when I was taking it. Still on Tysabri.

Thanks,

Dave

Hi Judy,

I posted a get well comment for Angela on her PML Post.

I've been on Tysabri for 1 yr. I feel your anger on Tysabri being "bad" but there are lots of people using this drug, like me, that are VERY HAPPY on it. I've heard a bunch of good things from many people on Tysabri not to ment...

Hi Vern,

I've been on Tysabri since early this year, and will not change to another medicine either. I've never felt (since my dx) as good as I've felt on Tysabri not to mention NOT having to deal with ANY shots and bad side effects.

Thanks as always.

Dave

excellent...that's it....nothing else I can say.

I just did training on getting back on a sit top, just like the video. It's actually easier than I expected. You need a wetsuit in the ocean or you increase the odds of freezing prior to getting back on. Even with a wetsuit, it was very cold in Northern Ca, ocean water. thx for the video.

Hi Wanda,

No I have not been tested for CCSVI. I'm on Tysabri, and seem to be doing good/okay but my MS is worse each year. I have a foot movement issue (foot drop) so sometimes I cannot walk totally normal, but I still get around. Im 39 and got dx'd 2 years ago. I try to stay positve.

I wi...

Where is your family or friends? Can they come and visit you? Turn on the lights. I feel really bad for you. I hope that somehow youtube alows you some interaction.

I have MS too, and I know that getting light and being in touch with people is the most important thing.

Dave

Hello Kelli and Others,

I've been on Ty for 8 months. What is important for all MS people to remember is that MS is progressive, period. Since we all are progressing in some fashion, it's going to occur whether you are on drug A or drug B. The hope is that the progression slows down to the p...

Very Good for everyone....especially if you are handicapped. thx for posting. Dave