Building community is an essential part of the mission of Angioma Alliance. Angioma Alliance offers a number of opportunities for getting to know others with cavernous angioma in order to share information and support.
We host a Community Forum that has a bulletin board format. This is the most active section of our website. On the Community Forum, individuals describe their experiences, share their questions, and even organize face-to-face get-togethers. The forum is available in English, Spanish, and French.
Our Blog provides up-to-date announcements of Angioma Alliance happenings and greater depth on stories we may have covered in the newsletter. Subscribe to the RSS feed of the blog or leave a comment if you feel moved.
We have developed a Peer Support program for new individuals to obtain one-on-one information and support from folks who have been with Angioma Alliance for some time.
Choose Member Stories to read about other's experiences with cavernous angiomas and please consider submitting your own.
We provide links to Angioma Alliance Facebook, YouTube and Twitter pages.
Finally, we provide a link to Archives of the posts from the Community Forum that was in use through September, 2010.