Multiple Sclerosis...Uprising (please pass video along)

we need to press the issue of finding a cure for this disease, i am tired of living day to day not knowing if i will be able to walk or not

Category:

Nonprofits & Activism

Tags:

• multiple
• sclerosis
• cure
• now
• research
• blog

[ChrisPlugged]

Hey dude. There are many cool groups meeting up regularly who are able to share thoughts in a similar position. It's sometimes nice to remember that there are others you can connect with & who also need a connection.

Do this for me. Search either online or through local centers for groups who do meet up. If they aren't for you, then form your own local body, then raise awareness. A project like this would not only motivate others, but you could also descover some things within yourself. go hard

[Lakalmbach]

Hi, Have you heard of a 35% food-grade hydrogen peroxide regimen? It must be diluted to 3% before internal use. There's a lot of info about this if you look it up. It must be food-grade, not the off-the-shelf stuff. You need to do it exactly right, so get someone to help you. I'm going to try it, if I can find the right stuff, probably online, like Amazon, or H2O2. Then I'm going to try it on my sister, she has MS.

[wheelori814]

Hey man, im sorry you have to go through this. I have a friend also who is going through it. I was just wondering if you have tried the water cure? Was also wondering if you have changed your diet to whole organic foods? I dont know if it will help, but if you can detox your body it might at least help with some of the pain.

[abeautifullie733]

I completely feel your passion! I am working on my own to help spread MS awareness in my area and nationally. I currently run internet groups and websites online dedicated to my brother who has had Primary Progressive MS since 1995. We need to get the word out about MS, No one knows about MS, We do not have a face, we do not have a pink ribbon. We are not Jerry's Kids.. Best of luck to you and you are making an impact by having your opinions up. I will spread along your words.

[FerRamirez2009]

Please check Doc. , Paolo Zamboni he have the solution whith "The Liberation Treatment".

[andie221]

Hey there, know how you feel. We have 18,000 here in Australia and we are often overlooked and forgotten...lots of high profile campaigns for cures for all sorts. With MS the ignorance, confusion, lack of education out there and the stigma or "fear" this disease causes. People have no idea. Frustrating is not the word for it cause it stops so much.I'm angry yes!

As a guinea pig on a trial for us all I guess I'm doing my bit to send this disease back to the hell from which it came!

[MSVlogSupport]

I added this to favorites on the volgs channel. I too always wonder why there is so much more coverage in other countries. I do have hope that something will be done with our own health care reform, I did a 3 part topic on it. Check it out and tell me what you think.

Andrea

[dmplaura]

There's good and bad to be had in the US medical system. It seems that a lot depends on how fortunate you are to be born in XXX State, versus YYY State.

The biggest challenge right now in the US that I see, medical marijuana. Why is this not a commonly accepted pain medication yet? Come on, this is 2009, nearly 2010. It's been legal for this purpose in Canada since 2001 and the gov. hasn't pulled it here.

Get the relief for us while we wait for the cure.

[lovingfatalist]

P.S. The MS Society over here isn't so great anyway. Personally, they only increase my feeling of loneliness. They only seem to care about raising money and 'awareness', and offer very little tangible support.

I could be bitter about this, but choose not to be. No doubt they do their best. And bitterness helps nobody, least of all myself.

So, I mostly find the community support I need in books - Barbellion and Heine, for sure, plus others. These video blogs help too.

Keep your chin up friend ;-)

[lovingfatalist]

Well, I feel your pain, and thanks for posting this, but I don't agree.

Maybe your 'purpose' helps you. (In my experience, Americans always need a purpose.) But I think you're banging your head against a brick wall.

There's no cure. You and I are both gonna die with MS - and that's ok, for me. Worse things happen at sea, as they say.

Don't depend on others - you'll usually be disappointed. Find the strength within...

But I must say - I'm glad I live in the UK. Your health system looks screwed.