Tags: MA, recommendation
Some history:
We were treated by PBR at Mass General in 1992 by a Dr. Kjellberg, who was one of the pioneers in using PBR to treat AVMs. He spent a lot of time overseas, conducting testing on animals to see how to perfect PBR. He seemed like a nice man, and looked like Santa Claus with his beard. We received a short cryptic letter several months after treatment, saying Dr K would not be able to keep us as patients (no explanation).
With such a unique name, and the internet coming online, I searched the Boston papers and found Dr. K's obit! He died from cancer, and although I initially wondered about radiation exposure, I was enlightened by a young Dr who had worked with him--Dr. K chain smoked, which is what I suspect got him.
The DR that emerged as MGH's AVM guru following Dr. K was none other that Dr. Ogilivy. I have not met, nor spoken with him.
One of the first peer to peer support groups online was coordinated by Dr (sorry, forgot his name)at MGH. When it first started, it was pretty state of the art. I was a mod with them and it had several hundred following online. It was cumbersome by standards of this website.
When Ben's site began, the volume on the MGH dried up. They were supportive of posting Ben's links at their site. IIRC, they shut it down about a year after Ben's came online.
At the time, MGH was the ONLY place to go for things like we all come here for now.
Best wishes,
Ron, KS
Glad you told us about your MGH story, Ron...I always wondered why your wife didn't continue with her PBR. AND Ben did tell me how our Network took over from the MGH's Group. Thanks for sharing.
Permalink Reply by Holly on November 6, 2011 at 3:05pm
Permalink Reply by secrockett@verizon.net on January 29, 2012 at 4:03pm do you have a cerebral avm?? we live in western mass and really are having a hard time with anyone who can help. they always say "that is huge", but say there is nothing they can do. my husband just lays in bed on pain meds for weeks and months on end......he cannot alleviate the pain even w/fentanyl patches and oxc's. he just wants to die from the pain. any suggestions???
secrockett, my AVM was on my left temporal lobe. The best doctors in our area are in Boston...Have you been to any of them yet? I totally believe in second, third and fourth opinions. If you need any further information, please reply back to me.

Permalink Reply by Janaran on March 31, 2012 at 2:21pm In Boston, I swear by the staff at Brigham and Women's hospital. I was under the care of Dr. Ebon Alexander, in neuro-surgery. But, I'm in Virginia, now, and I don't know if he's even there, still.
Permalink Reply by jacquelyn wheeler on April 1, 2012 at 12:15pm I'm with you... Mass General
made me an AVM survivor as well!
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Posted by Sam on May 27, 2012 at 3:30pm 0 Comments 0 Likes
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…
Posted by kristi on May 26, 2012 at 3:17pm 3 Comments 0 Likes
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…
Posted by stephanie on May 26, 2012 at 1:24pm 4 Comments 0 Likes
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…
ContinuePosted by existentialmom on May 25, 2012 at 4:48pm 2 Comments 0 Likes
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,…
ContinuePosted by Cat D on May 25, 2012 at 3:14pm 2 Comments 2 Likes
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…
ContinuePosted by Ben Munoz on May 25, 2012 at 9:14am 0 Comments 2 Likes
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…
ContinuePosted by DsSis on May 25, 2012 at 12:37am 5 Comments 2 Likes
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…
Posted by Hiro on May 23, 2012 at 8:50pm 10 Comments 0 Likes
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…
ContinueOctober 11, 2011 at 6pm to October 10, 2012 at 7pm – Some where with good Coffee
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