Member blog links now on our site

Discussions of issues related to living with cavernous angiomas

Member blog links now on our site

Postby Connie Lee » Sun Sep 21, 2014 4:11 pm

We've added links to member blogs on our website at http://www.angiomaalliance.org/pages.aspx?content=92

If you have a cavernous angioma blog you'd like added to the list, please message me or list it below.
Connie Lee
President and CEO, Angioma Alliance
17-year-old daughter with CCM3 mutation who has had 4 brain surgeries, T2-L3 spinal fusion
To support Angioma Alliance, visit http://www.Angioma.org/Donate.
User avatar
Connie Lee
Founder, Angioma Alliance
 
Posts: 440
Joined: Sat Sep 25, 2010 2:41 pm
Location: Norfolk, Virginia

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