Girl Power 2 Cure is a nonprofit organization leading a movement to end Rett Syndrome, a severe neurological disorder that primarily affects girls but does affect boys as well.
The Power of Education Students with complex needs, like those with Rett Syndrome, can progress and excel when educators utilize the appropriate tools, technology and learning techniques. Technology and a comprehensive understanding of the needs of these students...
The resolve and determination of just about every Rett Syndrome family I meet is remarkable. As we draw near the end of 2019, we see our mission to help families #RiseAboveRett fulfilled in so many ways, each and every day. You are our inspiration.Disney Princess,...
To Those Facing Loss, We see you. We know the holidays are a glaring reminder of what should be there but isn’t. All that remains is a gaping hole of what once was. Your child, your grandchild, your sibling, your best friend, your hero, your warrior. You may want to...
We didn’t realize it then, but our journey with Rett Syndrome began on my 33rd birthday. Tori Leigh Krauskopf was born on the 21st of February, 1998. Another 10 or so minutes and she wouldn’t have been the best birthday present I have ever received. She is the...
Halloween is this week, which can be exciting as well as give you feelings of hesitation. How can my child participate? How are they supposed to hold their candy bag or say “Trick or Treat” without being able to use their hands or speak? What if other kids bump my...
My daughter Skylar and I started our Rett journey on August 21, 2004, that is a day that I will always remember. Our story is probably pretty similar to many others. When I got the news that Skylar had Rett Syndrome and I began to read about it, the heartache,...
The holidays are coming up, which means that many of us may be thinking about gift ideas for our loved ones. With the help from our greater Rett Syndrome community, Girl Power 2 Cure has compiled a list of gift ideas for this holiday season and beyond! We hope you...
Imagine getting your Rett Girls socks, AFO’s and shoes on and skipping a step? No shoe laces to tie! Check out these great lock laces! Tons of great colors too! NO-TIE LACING SYSTEM: Turn any pair of lace-up tennis shoes into slip-on sneakers. LOCK LACES are the...
Come join us for the 6th Annual Swingin' 4 Rett on Saturday, November 2nd! The evening will include SWING Dance Lessons, Bake Sale, Glow Dancing and a Garden of Hope! Fun for the WHOLE family! Fighting Rett Syndrome One Dance at a Time! Tickets are only $12 each and...
(February 20-23, 2020, Walt Disney World® Resort - Orlando, FL) 2020 will be the 9th year Team GP2C will be part of the magical Disney Princess Half Marathon Weekend. This weekend is filled with great events, camaraderie and hope. Sorry, we have sold out of the...
We’d like nothing more than for you to join us in our fight to cure Rett Syndrome and free girls around the world who are trapped in their bodies.
You are the difference! Your financial support fuels our mission to work fearlessly to see Rett Syndrome become the first curable neurological disorder.
We have lots of goodies and support materials in our GP2C store for Rett families and supporters. Check it out and maybe snag a few things.
