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#1 | |||
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Junior Member
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News just out, a province in Canada is going to back clinical studies for the liberation treatment!Saskatchewan's premier announced today!Saskatchewan has the highest cases of M.S. in Canada.Increasing pressure from M.S. sufferers have moved the premier "No one in this province who doesn't know someone who is fighting this"The province will pay for studies into this!|My thought's finally some movement in this direction thanks to all in Saskatchewan...Maybe this will move the neurologist's to think in a different direction.Because going down this road has produced very little result's if any...
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#2 | |||
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Junior Member
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![]() keeping all fingers,toes and any other loose parts crossed
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DX:June 2007 Plasmapheresis:2007 Cyclophosphamide :07/08 Rebif 44 :2008 -09 Copaxone: 2009 ongoing atypical RRMS NEVER assume! I may not look sick but you should see my brain! . . “The thing that is really hard, and really amazing, is giving up on being perfect and beginning the work of becoming yourself.” Anna Quindlen(American Author, Journalist) |
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#3 | ||
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Junior Member
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I love Sask's Government! They are becoming more and more a positive force for that province.
The ubc ms clinic in BC is supposed to be doing studies as well, but I haven't heard anything so far? Any one else? |
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#4 | |||
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Member
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I've thought about pursuing CCVSI. However, when I've weighed the benefit/risk factors, I've decided that it's not worth it at this point.
My MS Specialist says that, except for study trials, it's starting to be pretty much shut down in the US, as two people have had serious complications. One procedure triggered death, resulting from a brain aneurysm, and another, who had a heart attack, survived. I still support the concept of research, and the right of people to choose to participate in it. However, my choice, at this point, is not to. ~ Faith
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aka MamaBug Symptoms since 01/2002; Dx with MS: 10/2003; Back in limbo, then re-dx w/ MS: 07/2008 Betaseron 11/2003-08/2008; Copaxone 09/2008-present Began receiving SSDI 11/2008 |
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#5 | |||
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Junior Member
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More New's the premier of Ontario Dalton Mcginty announced that Ontario has to wait for more proof that the liberation treatment works..Before the province commits goverment money.If a heart patient has any blockages they are fixed but not M.S. patients.Lucky for me and my family we live in Ontario.
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#6 | |||
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Magnate
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Quote:
WHY? I can only imagine pressure from the higher powers, and the almighty buck. ![]() ~vent~ ![]()
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2004 to present - Trigeminal Neuralgia 2007 to present - Burning Mouth Syndrome March 2008 - Multiple Sclerosis DX 05/2008 - Relapse 05/2008 to 02/2009 - Copaxone 10/2011 - Relapse - Optic Neuritis developed 9/2012 - Relapse - Balance issues 1 sided 8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax) April 7/14 - Raynaud's Syndrome DX |
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"Thanks for this!" says: | Lady (08-09-2010) |
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#7 | |||
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Member
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Quote:
Here are some links to studies that cast doubt on Zamboni's theories: http://online.wsj.com/article/SB1000...155710380.html http://online.wsj.com/article/SB1000...55710380.html" ~ Faith
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aka MamaBug Symptoms since 01/2002; Dx with MS: 10/2003; Back in limbo, then re-dx w/ MS: 07/2008 Betaseron 11/2003-08/2008; Copaxone 09/2008-present Began receiving SSDI 11/2008 |
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#8 | ||
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Junior Member
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Quote:
I also understand our fellow MS'ers like my brother who are cycling with attack after attack needing to action if there is any hope. I just wish they would allow the angioplasty here in North America so we know are folks don't have to go out of the country. And I would also like to know if there is any progress on a venous stent. Angiotech in Vancouver here, invented the first artery stent, I wonder if they are doing anything. If I can I will look into it next week for us. |
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#9 | |||
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Member
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Angiotech needs a ring from you sw8689 Monday. And please get reason why (if any) how Vein/Artery vari stent wise other then more oxygen & pressure.
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#10 | ||
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Junior Member
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Going to try...
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