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
There's big news associated with an announcement from Taysha Gene Therapies. Please see the full announcement at the link here and some selected excerpts that I've highlighted after the link. Click here for the full announcement Excerpted highlights: Taysha...
Dear GP2C & Rett University Communities, Keeping you informed! Here are some recent articles regarding work funded by our friends at Rett Syndrome Research Trust, and other companies investigating Rett-related research: In Editing RNA, Researchers See...
The Disney Princess Half Marathon weekend has become an annual holiday in my family. The calendar is booked a year in advance. No one questions what I will be doing during the weeks leading up our reunion with Team GP2C in Orlando. What is it about this one weekend...
By: Jennifer English Hiya pals! We are the English family, and we started our journey with Rett Syndrome three years ago this month. Our youngest daughter Charlie was diagnosed in September 2018, after almost a year of searching for answers. The diagnosis came with...
As we are all focused on staying home for the time being we wanted to provide you with some fun activities to do with your loved ones! We have chosen a handful of products that we feel may prove useful in keeping your loved ones engaged and learning in the next few...
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...
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.
