I have been a part of the Sturge-Weber Foundation for 5 years.  Through thick and thin they do their best to continue critical research and improve treatments for this rare disease.  SWS affects babies and is a non-hereditary disease causing a large birthmark, seizures and glaucoma.

These children and their families need our help, so please consider joining me in fundraising or just provide a small donation.  Thank you for visiting my page!