A support site for people/family/friends dealing with AVM's. If you or a loved one has an AVM, this is the place for you! Lots of wonderful people ready to offer support, information, advice, or anything else you need. I love this group and hope you all join us over there!
Blog with many stories about AVM's.
A new "no-brainer" with an AVM on his cheek.
Cyndi's new blog with her continuing journey...
Camellia's story. Mom's journal detailing the treatments and progress
Baby Nathan's story told by his mom Jaimee. Unfortunately Nathan left us, just shy of his first birthday.
Jaimee's blogs at AVM Survivors Network
Maddy's story. Mom's journal detailing their journey (just started!)
Arie's Story. Link to her mom Jody's first post at AVM Survivors network which details Arie's journey.
Also see her pictures posted on y picture page!
http://www.avmsurvivors.org/profiles/blogs/a-support-finally
Andrew's story. Mom's journal at Caring Bridge. Andrew is on his second round of brain surgery! http://www.caringbridge.org/visit/andrewbrown http://www.avmsurvivors.org/profile/janicebrown If you have a chance, go sign his guestbook. Andrew loves to get new messages, and they are trying to get up to 100,000 signatures!!! Lanie's journal on Caring Bridge, told through her mom Monica. Although there is a new post typed out all by little Lanie herself!!! They just started treatment with Doctor Yakes in July 2009 www.caringbridge.com/visit/lainieisabel The Dahl House. Family blog documented by mom Ashley. Little Gabi also has a facial AVM and is being treated with Doctor Yakes! Very cute little family. http://ashleyedahl.blogspot.com |