A Vasculitis, Autoimmune anonymous support group with information on diagnosis, treatment, symptoms, along with personal stories and experiences with Vasculitis, Autoimmune. You're not alone.
Stories
No forum posts yet. Be a star and start a topic. The shy ones will thank you. |
These snippets show some of the most common themes mentioned in this experience's stories:
- "CNSV happens when the immune system attacks the body and mistakenly identifies the blood cells in the brain and / or the spinal cord as the enemy..."
- "When I was 17, I was diagnosed with children's Primary Angiitis of the Central Nervous System cPACNS , also known as primary central nervous system vasculitis PCNSV ...."
- "I hope to raise awareness about my rare illness, provide hope to other people who live with an illness, and express how I live my life now with this invisible illness..."
50% of people who have this experience are in their twenties, 25% are in their sixties, and 25% are in their thirties. 100% of people who have this experience are women.
Other experience groups that have been combined into this group include: None yet.
Login or Register to get started in seconds.





