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Liberation Treatment on MS 

By: geraldine murphy 
Date: 14/12/09 
Why not get the word out to all MS people in Canada and their families and get the Venous doppler tests started we cannot wait. I've had MS for 14 yrs and have been fighting it all this time; I'm not walking now, I've never had pain, incontinence or fatigue enough to give up. I knit and find it to be great therapy where I can drown out what goes on around me here in the nursing home. I'm a very strong person with a family willing to help in any way & a careing husband wanting me to be successful in my appointment on Feb. 1st. 

Comments

From Tom Brewer 
On January 05, 2010 
yes, let us get the word out. I'm hearing some "professionals: think this does not hold water. Let us ensure our researchers have open minds. My fear is some cant see the tree's for the forest. I'm 64, male and cant walk without a walker! Fatigue takes me down quickly. We live with expensive drugs that help some [not me] and keep filling the pockets of drug companies. The drug companies have not been able to "cure" the disease but we pay them dearly. If Dr. Zamboni's procedure helps let us get on with the task of helping those we can.... the same way drugs have helped others! 
From jen 
On January 14, 2010 
Geraldine.....are you getting the Venous dropples test on Feb 1st? If so, where? 
From Jodi Johnston 
On January 19, 2010 
I sufer from MS that they say it looks like on my MRI that it has been there for a couple of centuries. Explains a lot! I want to know where I can get the treatment or tests at least. 
 

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