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!
Youtube- Nikki Lilly- Pretty much the coolest girl with an AVM. You should subscribe!!!
https://www.youtube.com/channel/UC4RH7UBW2_c8qUP2qcF6zmQ
Blog with many stories about AVM's.
http://delorumrex1.blogspot.com/
A "no-brainer" with an AVM on his cheek.
http://sixsentences.blogspot.com/2008/08/avm.html
Cyndi's blog with her journey... (RIP sweet friend)
http://avmjourney.blogspot.com/
Camellia's story. Mom's journal detailing the treatments and progress
http://www.caringbridge.org/visit/camelliaschaner
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
http://www.avmsurvivors.org/profiles/blog/list?user=1atzc36u2222p
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.
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.
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