CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
I didn't think it was too harsh. And I don't think it's "dodgy" ground at all to suggest this disease suck. I have MS, and it sucks. I don't spend my days feeling sorry for myself or whining but the fact of the matter is having MS fucking sucks. And as anyone with MS knows many of us walk around with "invisible" symptoms, I know myself I tend to just smile & deal with it because what else can I do. But I think because of these things MS does tend to get overlooked when it comes 2 ppl being aware
Somehow effective in a morbid sort of way... And not limited to any one nation. MS lives on this planet. I have MS and really- If it wasn't for the MS Society of Canada Chapter in my local community, life really would be hell- They gave me hope!
Wasn't there a much more recent motor neurone disease ad that was very similar and also walked the dodgy ground of "this condition really fucking sucks"? I shall link here if I find it.
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CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Gregmills007 11 months ago
...so maybe we need to get more harsh and less " my life with MS is fine" to get ppls attention. JMHO
TheAleeMac 1 year ago
I didn't think it was too harsh. And I don't think it's "dodgy" ground at all to suggest this disease suck. I have MS, and it sucks. I don't spend my days feeling sorry for myself or whining but the fact of the matter is having MS fucking sucks. And as anyone with MS knows many of us walk around with "invisible" symptoms, I know myself I tend to just smile & deal with it because what else can I do. But I think because of these things MS does tend to get overlooked when it comes 2 ppl being aware
TheAleeMac 1 year ago 4
a hope in hell.
i can imagine people with MS not asking them for help, thinking:
helping us only when we die... bloody get your arse off.
moksheebs 1 year ago
this Video is a Joke! they look after them selves no one else!
gekiryudojo 1 year ago
Diagnosed RRMS in 2003. I'm now in a wheelchair.
But I am also the MonSter MS fears.
May God bless you for sharing this.
mooseasaurusrex 2 years ago
Somehow effective in a morbid sort of way... And not limited to any one nation. MS lives on this planet. I have MS and really- If it wasn't for the MS Society of Canada Chapter in my local community, life really would be hell- They gave me hope!
pgwalknroll 2 years ago
...or your penis!
Duvmasta 2 years ago
Many thanks for posting
StopUnumNow 2 years ago
Wasn't there a much more recent motor neurone disease ad that was very similar and also walked the dodgy ground of "this condition really fucking sucks"? I shall link here if I find it.
emmascribbles 2 years ago
Yeah, that does seem awfully harsh, especially the tagline.
electrogeek77 2 years ago