Canada AVM Survivors Discussions (9)

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AVM specialists?

I am just wondering if anyone from Canada has an actual AVM specialist... or if there are any in the States. I know Winnipeg is the center…

Started by Emily K

4 on Friday
Reply by Matthew Dubins

Where in Canada are we all?

I live in the Okanagan, BC just outside of Kelowna.

Started by Lianne

53 May 12
Reply by Karla

calgary vascular clinic

HiI was wondering if anyone has been to the vascular clinic in Calgary, or if any one with an avm outside of the brain has been treated in…

Started by patricia

2 Feb 13
Reply by patricia

Ontario Disability Support Program

I was wondering if anyone has been succesful in getting disability benefits from your province?

Started by GinaL

2 Feb 2
Reply by Neil

Anyone here from Niagara? Or been to Toronto Western Hospital?

Started by GinaL

22 Feb 1
Reply by Stephanie

second opinion

Is anyone here from Winnipeg? I am wondering about getting a second opinion, but I am not sure how to go about that. Any ideas?

Started by Emily K

3 Jan 30
Reply by Starr Tze

Uterine AVM?

Has anyone else on this site experienced an AVM in their uterus? I was just diagnosed and I need some advice.

Started by honeybeeB

4 Sep 23, 2011
Reply by Doris

Neurosurgeons for Africa

Dear Canada AVM Survivors: iRapidConsult is working with the Canadian Red Cross to support the people in the Horn of Africa. 100% of the mo…

Started by Starr Tze

0 Sep 20, 2011

where we all live

I live in Terrace B.C. just outside of Kitimat 56clicks

Started by Josi Summerfelt

2 Apr 13, 2011
Reply by Lesli Kauffman

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Counting Down The Days...

Posted by Sam on May 27, 2012 at 3:30pm 0 Comments

I'm counting down the days!!! At the end of June 2012 i have to go to the hospital for another Angio.

Hope to hear good news, that the Embolization and 2 Gamma Knife treatments where succesfull and that after 7 years of fighting the AVM is…

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What up with my ear???

Posted by kristi on May 26, 2012 at 3:17pm 3 Comments

I had a bruit when I had the AVM. It was there all my life. I guess everyone hears it at some point but as an "AVMer" mine was ALWAYS present. We became friends:)

My bruit was my connection to my heart, so I always thought (when I never…

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MRI or angio?

Posted by stephanie on May 26, 2012 at 1:24pm 4 Comments

Click here to visit my latest blog post. If anyone could shed some light on the conclusiveness of MRI and angio, it would be great! The surgeon…

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Stage one complete

Posted by existentialmom on May 25, 2012 at 4:48pm 2 Comments

Merlin came through the first gamma knife well, and we are scheduling stage 2 in August. Her treatment time was 152 minutes! No side effects yet.

We are relieved, but holding our breath against the next 3 months, 6 months, 1 year, 3 years,…

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Thank you

Posted by Cat D on May 25, 2012 at 3:14pm 2 Comments

I only got accepted to this site yesterday and already I feel at home. I hope that this will be good for me and my mom who also was accepted yesterday. We both have been through a lot in the…

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May 2012 AVMSurvivors Community Newsletter

Posted by Ben Munoz on May 25, 2012 at 9:14am 0 Comments

Dear Friends and Family of AVMSurvivors,

We are so excited we cannot wait to tell you about how our organization is growing, so we’ll go straight at it. We are please to tell you that collectively our patient…

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10 days post surgery for my brother

Posted by DsSis on May 25, 2012 at 12:37am 5 Comments

David's surgery was May 14th and today, May 24th, we had a series of wonderful things happen.

1) I finally got to see my brother walk (with the assistance of his wonderful physio) - he made two rounds of the hospital ward...I was the last…

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"Executive Function Disorder"

Posted by Hiro on May 23, 2012 at 8:50pm 10 Comments

I had the neurologist appointment on Monday, and he diagnosed me with "Executive Dysfunction Syndrome" that he thinks stemmed from some sort of damage to my left frontal lobe during/after my surgery (that was where my 3 AVMs were), contributing…

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