Where do you turn when you've been told you have a rare disease, but you've never even heard of an AVM?

Who will help you sift through the new neuro-jargon, the types of clinicians, and the ever-growing stress of your aneurysm or AVM diagnosis?

How do ensure your child receives the best neurological care when she's too young or in too much pain to explain how she's feeling?

How can one person/family affect change in this vast community?

These are but a few of the many questions patients and families face when dealing with vascular malformations of the brain like aneurysm or AVM. Those at The Aneurysm and AVM Foundation (TAAF) dare to answer these questions.  They serve a growing community in need of hope by raising awareness, providing resources and education, and dedicating funds to the research of these life-threatening diseases, and I have joined their team for TAAFWalk 2022, their 17th Annual Aneurysm and AVM Awareness Walk held on September 18th.

Please help me support TAAF by making a donation through my page. The process is fast, easy and secure. Thanks so much for your support... and please don't forget to send this page to any friends you think might be interested in donating!