Welcome to Emi's Dream Team Fundraising Page!
Emi suffers from STXBP1, a genetic condition characterized by recurring seizure episodes & difficulty with verbalizing thoughts due its effect both mentally & physically. There is no cure for STXBP1 Disorders. But, we are working hard to change this.
It is the mission of the STXBP1 Foundation to drive & accelerate research efforts.
During STXBP1 Awareness Month we encourage you to donate, and together we will Move to Cure STXBP1!
Thank you in advance for your generous donation to the STXBP1 Foundation, we are thrilled to have you join Emi's Dream Team. Your donation and participation means the world to us and the entire STXBP1 community! Donations directly fund critical research for treatments, therapies, and a cure for STXBP1 disorders.
Buy custom team shirts here:Let’s support Emi by wearing her team shirt!