
Brooke Tasi's Fundraising Page

ABOUT AAV Project and Other Research
With funds raised from the AHC Foundation, we will support AAV gene therapy and other research related to the project. We believe a path has been identified to a viable permanent treatment: gene therapy. The gene therapy we propose will involve inserting a functional copy of the ATP1A3 gene into a virus (an adeno-associated virus or AAV) that has been stripped of its harmful payload and its ability to reproduce. The virus will then be injected into the cerebrospinal fluid and will carry the functional gene to the cells in the brain that are failing. By delivering additional functional copies of the gene, we should be able to rescue those cells, and treat the disease permanently.
Learn more about the project here.
Supporters | |||
Name | Date | Amount | Comments |
Elizabete Baia-DaSilva | 02/27/2019 | $25.00 | Susie Teixeira | 02/27/2019 | $50.00 | We love you Brooke xoxo | Anonymous Friend | 02/26/2019 | $100.00 | We Love You! | Lori Mihalov | 02/26/2019 | $50.00 | Happy to help find a cure for you Brooke! | Shannon B | 02/26/2019 | $25.00 | positive vibes ❤️ | Yvonne Rocco | 02/26/2019 | $25.00 | From Anna Marina Accumanno, matched by Prudential and Verizon, total amount donated $100 |
Total | $275.00 |