This Is MS Multiple Sclerosis Knowledge & Support Community

Hi all, Just wanted to update. I looked into the MRF but they basically told me that they are more interested in big investors. So,,,I have decided to work with Accelerated Cure Project based on a tip from someone on this website. I would be the first to do a fundraiser for them in Canada, so I am v...

Oh boy...what a great topic! The tears are just rolling reading all your comments. I think I would just breathe again. Like I used to. Without worring. One nice deep breath knowing that I am back in control again. I would spend time with family and friends that cared and just laugh from the bottom o...

How is it that they can modify the vaccine as they go on with the study? How do they know that there won't be dose related side effects for example? wouldn't they be using a different vaccine than the one that was determined to be safe in the last phase?
NN

Crue
Thank you for taking the time to translate. Same to you connib
NN

Hi Brock, I have to say that I totally agree with WW. do not worry yourself with lesion load. I think that it is an awful thing that in the US they have yearly MRI when there is not a damn thing that they can do about the results of them. They sure make money off ppl though. In Canada, we do not hav...

WOW thanx I am really happy about this.
NN

Hi thinkingoutloud,
That's great!!! It's exactly what I need. I will look into it.
NN

Hi Lately I have been feeling like I need to do something in order to make it faster for these researchers to get the money they need to start pumping out the drugs. I wanted to organize a sponsored walk for the myelin Repair foundation. I have actually never done anything like that and don't really...

When I was diagnosed, they didn't even bother finishing the count of my lesions that made me feel like I was a lost cause. the findings just says greater than 10 mostly in the preventricular area. I really have no idea how many I have. My neuro app is coming up so I will ask. The last year has been ...

Hi Broc, I am pretty lucky to have met her. I think that next time I see her I will talk to her about thing. She doesn't come around often though which is too bad. She probably goes to the neurology unit a lot more often. Anyhow, hope she answers your email. If not, You let me know. I know where her...

Hi
Dr. Metz comes to my unit every so often when we have a neurology pt. She is really nice. I have never had enough guts to go up to her and talk about my MS as she seems pretty busy when she is on the unit.
NN

Good luck guys...can't wait until we are rid of this stupid disease.
NN

Hi Karl
Thanx...sounds really interesting.
NN

Harry... Yes...I had to read your post again just so that I can make sense of what is going on. I just do not get why you don't understand the fact that we all know that bad things exist with MS. None of us are ignoring it. Mostly because we can't even if we wanted to. I have no idea why it is so ha...

Yeah...thanx for the stats...like who the heck asked for that? I am about to get married and that makes me feel real good. I knew I should have skipped over HarryZ posts. Goshh. 66, I am sorry about your girlfriend. If she broke up with you because of physical disability, well then that says a lot a...