Recent Activity
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Jason Cordova joined Team Ella
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Nick Viles created and joined Team Ella
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Our Supporters
- Anonymous Great job, Nick! (& Jason, too!) February 2025 $500.00
- Juan Jose Francisco Diez Hi Nick , this is Juan , Gravotech France , I hope you are well . I send you all my support, strength , good vibes and good wishes for your princess. February 2025 $50.00
- Jose Lazoff January 2025 $50.00
- Deborah Cordova Go Team Ella! January 2025 $50.00
- Andrew/Jerica Miller/Delcour January 2025 $50.00
- Anonymous Go Team Ella! November 2024 $1,000.00
- Anonymous Great job, Nick! (& Jason, too!) February 2025 $500.00
- Anonymous October 2024 $500.00
- Patty Moore Go Nick! January 2025 $250.00
- Billy & Sarah Viles November 2024 $250.00
Team Ella's Fundraising Page
Please help Jason & Nick support Ella and Girl Power 2 Cure in their efforts to raise funds for research for Rett Syndrome.
Rett Syndrome is a debilitating neurological disorder that predominantly affects females but can affect boys. It is the leading genetic cause of severe impairment in girls, brought on by a single gene mutation that leads to underproduction of an important brain protein.
Kids are born “normal,” but without the protein, begin to lose acquired skills between 1 and 3 years old. Many lose their ability speak, walk or use their hands, and depend on their families for every part of their day. Complications include seizures, sudden death in their sleep and scoliosis.
Despite their physical disabilities, girls and boys with Rett Syndrome are believed to be functioning mentally at a much higher level than previously thought. Amidst the mass confusion in their central nervous systems, they are smart, strong, and waiting bravely for us to unlock the door to their recovery.
Today, there is no cure. But Rett Syndrome is CURABLE! Research has proven once protein levels are back to normal levels, symptoms subside.