You'll never know the power of THE PURPLE CARD until you try! These amazing little personalized awareness cards are a great way to share your Rett Syndrome story anytime, anywhere! Imagine never having to explain Rett Syndrome in front of your daughter ever again!
Ever wish you had a place where you could share your daughter's story? A place where friends, family, and co-workers could go to learn more about Rett Syndrome and even make a donation in her honor? Now you can! Sign up for your very own GP2C web page!
[email firstname.lastname@example.org to learn more about starting on your page]
Check out our YouTube channel filled with inspiring Rett Syndrome angels accomplishing AMAZING things. These videos are perfect to share with therapists, teachers, and others who often say "she can't." This is also a place for you to share videos of your daughter as well!
[visit RETT WE CAN!]
Giving our girls "a voice" is a huge priority for us as parents. Thanks to new computer technology, it is now possible to control a computer with just your eyes!
Want to learn more? Have a device and want to network with other families?
You do not want to miss our new Eye Gaze Resource Page which has:
[visit our eye gaze resource page]
We have all seen the videos and stories coming out of the Special Needs world about how awesome the iPad is for kids with disabilities. GP2C families have tried out each recommended app with their daughters to see how it would work with a RettGirl!
[check out our iPad app recommendations]
Keep connected with ALL THINGS Girl Power! Be sure to sign up for our newsletter, friend us on Facebook, follow us on Twitter.....and more!
[click here to connect with GP2C!]
This Q & A session with GP2C founder, Ingrid Harding, for PediaStaff.com is perfect to share with all of the therapists that are or will be a part of your daughter's life!
[read the Q & A]
IEP...the three most intimidating letters of the alphabet! We want to help. We are compiling IEP examples currently used by other girls with Rett Syndrome. Our goal is to help you through the IEP process as well as provide you a place to share your daughter's IEP with other parents.
[visit our IEP bank]
Wouldn't you love a beautiful way to honor your daughter throughout your community and raise money for research that will bring her a cure?
Plant a Garden of Hope in her honor.
Similar to the March of Dimes, we have paper icons that are signed for a $1 donation. Only we have a flower! Together these flowers create a "Garden of Hope." We will GROW these funds into even more money for research!
[visit our garden page]
EVERY APRIL: This is absolutely the most fun you will ever have fundraising! We want to encourage ALL Rett Syndrome familes to sign up for a team. We will provide you with all the help you will need! So join us! Get Silly. Spread Hope. Cure Rett Syndrome!
The Power of Music. The Power of Girls. The Power 2 Cure.
Hundreds of girls worldwide are enjoying the amazing music on the GP2C music CD, make especially for girls with Rett Syndrome. Is your daughter? We hope so! We also want to share some great therapy activities that go along with each of the songs.
[download the cd from cdbaby.com]
Need some information in Spanish?
We have a few pages translated to help!
Meet other girls who are battling Rett Syndrome and connect with their families!
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