| Researchers around the world are working on a cure RIGHT NOW that will have life-changing consequences for thousands of families worldwide. Rett Syndrome is a neurological genetic disorder that occurs almost exclusively in girls. Most are unable to walk, talk, crawl, or use their hands effectively. With all the amazing research going on we are getting closer to getting these girls back by the day. The only way we are going to get there is if we all rev it up a notch. This is the time to harness the power within you, within your daughter and within your community to knock Rett Syndrome off the face off the planet. Proceeds from our "Girl Power" CD will go directly towards research. Whether or not your little girl has special needs, these songs will inspire her imagination and energize her day. Another great way to help out is to host a "Dress Up 2 Cure" event at your school! We also need girls to get involved with Girl Power 2 Cure through school, church, their favorite girls' club or with friends and mom! Check out the links above to see how you can help! Girls helping girls. Now that's GIRL POWER! Ingrid Harding, Sarah's mom President and Founder Girl Power 2 Cure, Inc. |
NEWS
FLASH!
Rett Syndrome
is reversible!
Read more...
FLASH!
Rett Syndrome
is reversible!
Read more...
| In August 2005, our daughter Sarah was diagnosed with Rett Syndrome, a devastating neurological disorder that only affects girls. Sarah is a brave little girl who inspired this web site. Girl Power 2 Cure, Inc is a 501(c)(3) non-profit organization dedicated to raising funds for research for treatments and a cure for Rett Syndrome. The Foundation will also allocate funds to build and manage an interactive website where girls can learn about Rett Syndrome, and Rett families can find unique resources for their girls. |
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| Sarah's wall of signatures is growing! Join in and submit the name of a special woman or girl in your life: daughter, mom, grandmother, aunt, friend, teacher! Click here to see the wall! |
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