Quote:
Originally Posted by michatki
Hi Ella, I am also Canadian. Just DX with petrosal vein compression of the CN5, and awaiting MVD.
Doctors have not yet referred to TN, only using the phrase spasms.
I have spasms both right-&-left side of my face.
Question: Are there any local support groups in Canada...?
Thx
michatki
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Sorry I did not see this earlier. There is a support group that meets usually once a month in the Thornhill Community center on Bayview and John. The next meeting is Sept 30, 2012 at 9:30 a.m. The person who sends out the emailed notifications is Kathy, her email is
toronto@catna.ca. Please write to her to get further info. I believe they are in the process of arranging their annual TN dinner right now and Dr. Anthony Kauffman from Winnipeg is usually the guest speaker. If you need to reach me I am at
ellacjn@hotmail.com
09-25-2012, 05:19 AM
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