About This Site
Cavernous Angioma Information
Genetics of Cavernous Angioma
Questions to Ask Your Doctor
glossary
Community Forum Instructions
Community Forum
Chat Information
List Server Information
Your Stories
Support Contacts
Newsletter
Family Conference
press room
Research Funding
Genetic Non-discrimination
Genetic Testing
Diagnostic Imaging
Brainstem Cavernous Angioma
Hemorrhage
Radiosurgery
Spinal Cavernous Angioma
Temporal Lobe Epilepsy
Venous Angioma
Preparing for Surgery
Things for the Hospital
Caregiver Information
Emotional Support
Rehabilitation
Cognitive Changes
Vocational Rehabilitation
Pregnancy & cavernous angioma
Children with cavernous angioma
Cavernous Angioma and School
Patient Tissue/DNA Bank & Registry
US Studies
International Studies
General Resources
Disability Resources
Financial/Insurance Resources
About Angioma Alliance
Mission and Vision
Board of Directors
Scientific Advisory Board
Volunteer Opportunities
Financial Statements
Angioma Alliance Product Store
IGive
Bookstore
Make a Donation
Angioma Alliance
 

Angioma Alliance is a non-profit patient-directed health organization created by people affected with cavernous angiomas (cerebral cavernous malformations). Our mission is to inform and support people affected by cavernous angiomas while facilitating improved diagnosis and management of the illness through education and research. Our activities are monitored closely by a scientific advisory board comprised of leading cerebrovascular neurosurgeons, neuro-geneticists, and neurologists.

The individuals you see scrolling at the top of this page are all affected by cavernous angiomas. Cavernous angiomas in the brain and spine do not discriminate: people of any age can be faced with symptoms that may include seizures, chronic pain, and physical or cognitive deficits similar to those caused by strokes.

Our website provides:

  • Information about the illness with in-depth articles on topics of special interest
  • A quarterly newsletter providing timely information about cavernous angioma
  • Networking and support resources
  • Ways people can become involved and help drive research

Angioma Alliance does the following:

  • sponsors national patient conferences
  • hosts a DNA/Tissue Bank and Patient Registry to support research
  • distributes patient education materials to neurosurgeons, neurologists, and genetics professionals
  • sponsors scientific workshops that bring together the research community
  • sponsors an annual Neurology Residents’ Award to increase physician education and improve patient care
  • works with the National institutes of Health and other government agencies to support cavernous angioma research
  • works with the media to increase public awareness of the illness
  • supports the formation of independent international cavernous angioma support organizations

View our video about Cavernous Angioma and Children.

You can help our activities by sending donations to:
Angioma Alliance
142 W. York Street
Suite 708
Norfolk, VA 23510-2015
USA

Or donate using a credit card with our Paypal connection.


Paypal's low cost to us means that more of your contribution can go directly toward the work of Angioma Alliance. We are a non-profit 501(c)3 tax exempt organization. All contributions are tax deductible.