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Girl Power 2 Cure | Rett Syndrome Resources and Information | Girl Power 2 Cure

Rett syndrome is a rare, severe neurological disorder that affects mostly girls. Girl Power 2 Cure is a nonprofit dedicated to supporting Rett families.

http://www.girlpower2cure.org/

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Girl Power 2 Cure

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Girl Power 2 Cure

Ingrid Harding

28891 B●●●●●●●s Court

Ferna●●●●●Beach , Florida, 32034

US

1.90●●●●2628
in●●●●@girlpower2cure.org

View this contact

Girl Power 2 Cure

Ingrid Harding

28891 B●●●●●●●s Court

Ferna●●●●●Beach , Florida, 32034

US

1.90●●●●2628
in●●●●@girlpower2cure.org

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Rett syndrome is a rare, severe neurological disorder that affects mostly girls. Girl Power 2 Cure is a nonprofit dedicated to supporting Rett families.
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Girl Power 2 Cure | Rett Syndrome Resources and Information | Girl Power 2 Cure | girlpower2cure.org Reviews

https://girlpower2cure.org

Rett syndrome is a rare, severe neurological disorder that affects mostly girls. Girl Power 2 Cure is a nonprofit dedicated to supporting Rett families.

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Support our mission to cure Rett Syndrome – GP2C Shop

GP2C Shop Sign in. More categories ›. More featured ›. Hair Tie / Wristband Pack. Music Activity and Therapy Guide. Girl Power 2 Cure, Inc. 626 S 8th Street. Amelia Island, FL 32034.

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Girl Power 2 Cure - Let's Cure Rett Syndrome Together

What is Rett Syndrome? Story of the week. Remember me for 2 weeks. Uncheck if on a shared computer. ]. Don't have an account? Or, sign in with. Sign in with Facebook. Sign in with Twitter. Powered by Z2 Systems. What is Rett Syndrome. Story of the Week. Sitefinity ASP.NET CMS.

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Our Sites | Rett Syndrome Resources

https://www.girlpower2cure.org/who-we-are/our-sites.aspx

What is Rett Syndrome? What is Rett Syndrome? GirlPower2Cure.org is our central website. We also run two other sites.be sure to check them out! Dress Up 2 Cure is our annual fundraiser that takes place throughout the month of April. Why April? April is Autism Awareness Month.and Rett Syndrome is the most physically disabling of the autism spectrum disorders. April is also SPRING! Visit www.dressup2cure.org]. Visit www.rettgirl.org]. What is Rett Syndrome. Story of the Week. Sitefinity ASP.NET CMS.

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What We Do - Our Mission to Cure Rett Syndrome at Girl Power 2 Cure

https://www.girlpower2cure.org/what-we-do/overview.aspx

What is Rett Syndrome? What is Rett Syndrome. Story of the Week. Sitefinity ASP.NET CMS.

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What is Rett Syndrome?

https://www.girlpower2cure.org/who-we-are/rett-syndrome.aspx

What is Rett Syndrome? What is Rett Syndrome? What is Rett Syndrome? Debilitating neurological (movement) disorder that predominantly affects females. Baby girls are born "normal" but begin to lose acquired skills between the ages of 1-3 years old. Caused by a single gene mutation that leads to underproduction of an important brain protein. The leading genetic cause of severe impairment in girls - most cannot speak, walk or use their hands. As prevalent as Cystic Fibrosis, ALS and Huntington's. Amidst th...

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The Purple Card - Rett Syndrome Awareness

https://www.girlpower2cure.org/how-to-help/thepurplecard.aspx

What is Rett Syndrome? You'll never know the power of the purple card until you try! It is a great way to share your Rett Syndrome story anywhere! Imagine, you won't have to explain all about it in front of your daughter ever again! TRUE STORY: (see more PURPLE CARD stories below). So, we stopped trying to call it a business card, or a Rett card, or an awareness card. it is now just THE PURPLE CARD. BONUS: If you sign up for a free web page on Girl Power 2 Cure ( see examples. GET YOUR CARDS TODAY! I don...

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Girl Power 2 Cure, Inc. - Girls Helping Girls Fight Rett Syndrome

https://www.girlpower2cure.org/Home

What is Rett Syndrome? Welcome to our website! GP2C has been helping girls and families suffering from. Now we are taking our flower and our fight out into the world! We need YOUR POWER now! Disney Princess Race Weekend. We are here for your girls and your families. Want to keep up with the research. Need special equipment recommendations? Looking for a doctor familiar with Rett? Looking for iPad apps your daughter can access? We want to help! Help us by sponsoring or hosting a Garden of Hope!

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Five Things Friday 4/17 – jen with one n

https://jenwithonenblog.wordpress.com/2015/04/17/five-things-friday-417

5 Seconds of Fame. Running Records and Goals. Jen with one n. Five Things Friday 4/17. April 17, 2015. April 17, 2015. On Sunday, I got to volunteer at the Red Coyote Running and Fitness. Water stop for the Redbud Classic. The Redbud is one of OKC’s biggest races with a great after party, but when you volunteer with Red Coyote, the party starts at the water stop! Volunteering at the Redbud Classic with Red Coyote! Post race selfie with some of my buds! 2 “Speed” run. And we had great, cool weather! Stay ...

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My Music | Inspired By Love

https://spiritdances.wordpress.com/my-music

This is my piano music. It is played by my friend and music therapist Karen Bohnert. My hands won’t allow me to play my songs, but the notes are all mine. It takes me about a year to complete each song. I have completed eight songs since I began composing in 2000. I will add a new song when I am able. My Dad helps me put my songs here. To hear some of my songs Click Here to Listen. Karen wrote this information so you would know how I compose my songs with her. Karly’s Composing Process. January 28, 2010.

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Remembering Karly’s Life | Inspired By Love

https://spiritdances.wordpress.com/2012/10/05/1746

Remembering Karly’s Life. October 5, 2012 · Filed under Uncategorized. October 4th, in “Karly’s Spiritdances Garden”. This is the view from the chair Karly sat on in her garden the last few months of her life. October is Rett Syndrome Awarenss month. As Karly’s mom, I know how much she struggled throughout her life and ultimately died as a result of the many complications that Rett Syndrome created in her body. These are her some of her last written words:. I miss hearing her typing. With much gratitude,.

spiritdances.wordpress.com spiritdances.wordpress.com

The Invitation | Inspired By Love

https://spiritdances.wordpress.com/2012/08/20/the-invitation

August 20, 2012 · Filed under Companion Horse. Karly’s precious little hands. She was so determined to share her thoughts with us, then eventually the world after we found a way for her to communicate at age 10. As Karly’s health declined, she asked me to post this poem she wrote, after she passed. Her beautiful heart and spirit continued to guide us right to the end of her days. She leaves behind an enormous hole in our hearts and lives. Lois Swope-Karly’s Mom. Becomes a distant memory. February 17, 2012.

spiritdances.wordpress.com spiritdances.wordpress.com

Karly’s Memorial Service | Inspired By Love

https://spiritdances.wordpress.com/2012/09/17/karlys-memorial-service

Karly’s Memorial Service. September 17, 2012 · Filed under Uncategorized. Thank you to the hundreds who came from all over the country to join us in loving and remembering Karly. She brought so much light into the world and we feel her loss so deeply. She often told us over the past 12 years to remember, “the day I die will be the best day! I n a 2010 chapel talk Karly prepared for other adults living with physical disabilities, she said:. With great love, Lois (Karly’s Mom). 9 Responses so far ». Concer...

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Jackson August Smith: Pool Party at the Trine's

http://jacksonsmith.blogspot.com/2010/03/pool-party-at-trines.html

I am Jackson, I am six years old! I love kindergarten at Carlin Park where my mom teaches! It has been awhile since my mom has posted :( I hope you like keeping up with me and my mommy on this blog! Tuesday, March 30, 2010. Pool Party at the Trine's. Jordan, Ethan and Jackson hanging out poolside! That is a jellybean in Jackson's hand. Yep, that is Jordan on Josh's back and Jackson upside down in the air. Can you tell Jackson is having a good time today? Thank you Mr. and Mrs. Trine! My new cousin Boston.

penniesforerett.blogspot.com penniesforerett.blogspot.com

Pennies for Rett: April 2011

http://penniesforerett.blogspot.com/2011_04_01_archive.html

Pennies for Rett January 2011. Look at all of the pennies I have collected so far! Wednesday, April 6, 2011. My Pennies for Rett Video. Monday, April 4, 2011. I got lots of coins this week at school doing Pennies for Rett! Subscribe to: Posts (Atom). Rett Syndrome on The View 1/28/11. Girl Power 2 Cure. Girl Power 2 Cure. Runner Spotlight: Molly Barker. Quest for a Cure 2013! My Pennies for Rett Video. There was an error in this gadget. Simple theme. Powered by Blogger.

penniesforerett.blogspot.com penniesforerett.blogspot.com

Pennies for Rett: March 2011

http://penniesforerett.blogspot.com/2011_03_01_archive.html

Pennies for Rett January 2011. Look at all of the pennies I have collected so far! Monday, March 7, 2011. Rockin for Rett 2011. I know this is early but I cannot wait for rockin for Rett. My cousin Rachel and I are having a cupcake stand. We are going to even make cupcakes for dogs. pupcakes ha ha. mom is going to e mail Gorge Town cupcakes the DC cupcakes show to see if they will donate something for the auction. I am going to burst. We will definitely get close to curing Rett. Subscribe to: Posts (Atom).

rettgirl.blogspot.com rettgirl.blogspot.com

Rett Girl Blog: Being Avery's Dad

http://rettgirl.blogspot.com/2014/06/being-averys-dad.html

Friday, June 13, 2014. Welcome to our 3rd Annual Salute to Rett Dads! Each day this week leading up to Father's Day, we will share a blog written by a father of a girl suffering from Rett Syndrome. Later in the week we will share a video slideshow of over 100 dads with their beautiful girls. Just because these girls have Rett Syndrome does not mean they are not still "Daddy's Little Girl" . times one million! To all the Rett Dads - thank you for your special role in raising these very special girls.

brooklynbutler.blogspot.com brooklynbutler.blogspot.com

Brooklyn Ashleigh Butler: Professor Adrian Bird

http://brooklynbutler.blogspot.com/2012/02/professor-adrian-bird.html

My name is Brooklyn. I am six years old and I have Rett Syndrome. My mommy works with a wonderful Rett Syndrome organization called Girl Power 2 Cure. Be sure to check it out www.girlpower2cure.org I hope you enjoy this blog.it is filled with stories and pictures of our family's life with Rett Syndrome. Friday, February 17, 2012. Prof Adrian Bird's Speech at Reverse Rett London event. Subscribe to: Post Comments (Atom). Click the picture to visit my brother's blog! Southeastern Rett Syndrome Alliance.

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Wednesday, December 21, 2016. Runner Spotlight: Molly Barker. Molly Barker, Founder Girls on the Run International and The Red Boot Coalition. Team GP2C has a new team member for the Disney Princess Half Marathon in February! Molly Barker is the founder of Girls on the Run International, the program that uses running to empower girls. She will help us power the flower on the course to raise awareness for Rett Syndrome! In addition, we are honored to have her as our guest speaker for our team dinner.

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Girl Power 2 Cure. What is Rett Syndrome? Send us your flower power! Every 90 minutes another girl is born with Rett Syndrome somewhere in the world. Helping means being a supporter, but sometimes it means just being a friend. There is more than hope for a cure, it's backed by research. Learn more about it here. Thank you Girl Power 2 Cure for all your encouragement and for making it fun and easy to spread awareness! She is soo happy for all the community support! Mdash; Jennifer Castro Rett Mom. We’d li...

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