rett family support

great stuff for rett families!

Expand all

rettgirl.org

RettGirl.org is the EVERYTHING RETT SITE created as a resource for Rett Syndrome families. We hope everything on this site helps your RettGirl fight a stronger fight against Rett Syndrome. Check out the product reviews, tips from other families, doctor and therapist listings, and even our own little Rett-"bay" where you can find/sell/donate used items. It is also a place for you to submit your own ideas and products!

[visit rettgirl.org]
the purple card

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!
[see a sample card and order YOURS]
gp2c personal webpage

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!
[see examples on our Meet the Girls page]

[email us to get started on your page]
rett we can on youtube

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!]
eye gaze page and community hub
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:
- the four most popular devices currently being used by other Rett girls
- sample letters of medical necessity (that have worked!)
- a communication "hub" to connect with other families and therapists that are using the devices
[visit our eye gaze resource page]
iPad app recommendations

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]
newsletter, blogs, facebook, twitter

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!]
rett q&a for therapists

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 samples

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]
garden of hope

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]
dress up 2 cure

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!

[visit www.dressup2cure.org]
music cd and therapy guide

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]
GP2C en Espanol

Need some information in Spanish?

We have a few pages translated to help!

[click here]

	home \| contact Who We Are About Us What is Rett Syndrome? Founder's Story The People Our Sites Gp2C en ESPANOL faq Contact Us What We Do Overview Programs and Events Family Support Research Overview How To Help Give Volunteer Host An Event Spread Awareness Share Your Story Shop Sign Sarah's Wall News and Events What's going on? Press Video Newsletter Story of the week Garden of Hope 2011 Gratitude Report Overview Programs and Events Family Support Research Overview rett family support great stuff for rett families! Expand all rettgirl.org RettGirl.org is the EVERYTHING RETT SITE created as a resource for Rett Syndrome families. We hope everything on this site helps your RettGirl fight a stronger fight against Rett Syndrome. Check out the product reviews, tips from other families, doctor and therapist listings, and even our own little Rett-"bay" where you can find/sell/donate used items. It is also a place for you to submit your own ideas and products! [visit rettgirl.org] the purple card 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! [see a sample card and order YOURS] gp2c personal webpage 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! [see examples on our Meet the Girls page] [email us to get started on your page] rett we can on youtube 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!] eye gaze page and community hub 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: the four most popular devices currently being used by other Rett girls sample letters of medical necessity (that have worked!) a communication "hub" to connect with other families and therapists that are using the devices [visit our eye gaze resource page] iPad app recommendations 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] newsletter, blogs, facebook, twitter 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!] rett q&a for therapists 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 samples 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] garden of hope 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] dress up 2 cure 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! [visit www.dressup2cure.org] music cd and therapy guide 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] GP2C en Espanol Need some information in Spanish? We have a few pages translated to help! [click here]
	Who We Are About Us What is Rett Syndrome Founder's Story The People Our Sites FAQ Contact Us What We Do Overview Programs and Events Family Support Research Overview How To Help Give Volunteer Host An Event Spread Awareness Share Your Story Shop Sign Sarah's Wall News / Events What's Going On? Press Video Keep In Touch Story of the Week Garden of Hope Copyright 2010 © Girl Power to Cure. All Rights Reserved. Site Design by Red Fin Group, LLC.