ourcarolinelily blogspot.com

Making our way through Rett Syndrome

My name is Marta and I am Caroline Lily

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LINKS TO WEB SITE

Kate Foundation for Rett Syndrome Research

Kate Foundation for Rett Syndrome Research. Monday, November 18, 2013.

About Us Rett Girl

Take a look around! We have a ton to share with you! And please share with us! Everything here is hopefully something that will help your little girl fight a stronger fight against Rett Syndrome. Girl Power 2 Cure items. Gluten and Dairy Free Recipes. Welcome to Rett Girl! .

Special Mommy x 2 Living life with Rett Syndrome, Down Syndrome, Autism and LOTS of love, laughter, learning to adapt.

Living life with Rett Syndrome, Down Syndrome, Autism and LOTS of love, laughter, and learning to adapt. How do I explain? July 22, 2015.

Along for the Ride

The story of the Foster family and their journey with Rett Syndrome. Monday, April 28, 2014. We go way, way back. Back to the age of tight rolled jeans and Bel Biv Devoe. Tape decks and big bangs. Passing notes and first boyfriends. Baby showers and birthday parties.

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Making our way through Rett Syndrome

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My name is Marta and I am Caroline Lily

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This web page ourcarolinelily.blogspot.com states the following, "Making our way through Rett Syndrome." We saw that the webpage said " My name is Marta and I am Caroline Lilys mother." It also said " In June 2011, at 17 months, Caroline was diagnosed with Rett Syndrome. The Road to the Diagnosis. Friday, August 11, 2017. Do I wish Caroline were a typical child? Do I wish Caroline were a typical child? This is a question Ive been asking myself since she was diagnosed in 2011. The answer is yes . Youre probably wondering how I could possibly include a no in my answer. Last, do I wish for a cure? The prot."

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