Who we are

WE ARE A NON-PROFIT ORGANIZATION UNITING AND SUPPORTING PEOPLE
WITH RARE DISEASE OF HEAD AND NECK arteriovenous malformation (AVM).

By the name AVMinority we want to stress out the uniqueness and rareness of head and neck AVM disease which deserves the same attention as other serious diseases despite its low (minor) occurrence.

We are trying to improve quality of life of people suffering with head and neck AVM. We are also trying to increase public and specialists awareness about this disease. We hope this web site will provide additional information also to people with AVM in other areas or with other vessel anomaly.

Information, opinions and recommendations available on this web site are considered only as another source of knowledge. These information should not substitute any professional medical advice or recommendation. One should not act only following information gained on this web site but should consult with medical professional.