annamarymacdonald blogspot.com

The MacDonald Family

Thursday, September 5, 2013. Quest for a Cure 2013! Were walking again to CURE Rett Syndrome! Come on out and join Annies A-Team on Sunday, Oct. 6 , 10am at the beautiful Inglenook Park in Southfield! Its a great morning and dont worry it wont take up your entire Sunday, just a couple hours to show your support for our little hero Annie! If you cant make it, you can always support Annies A-Team by donating online HERE. 156,000 is needed by December 2013 to fund this project. Ben Philpots la.

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Alexandra or another Rett

Please excuse all spelling and grammatical mistakes, my mom first language is French, but she loves to express herself in English. Saturday, November 29, 2014. Sunday, March 30, 2014. My eyes are my way of speaking. They reflect my soul, my being and what I want to say. Tuesday, January 14, 2014. Monday, September 23, 2013. In May 2012 we contacted Make a Wish. Had a fun party for her, we are all flying to France June 21st. Late story and Make a Wish! .

dear little leah

Sunday, May 26, 2013. Sure, you like your ribbons and pink polka dot attire. But you also like your biking gear. Love you and your wild side,.

Lifes What You Make It

A journey of our crazy life that I would not trade for anything! Friday, September 23, 2011. I am officially a Tough Mudder. I feared the Mudder! Well actually, Matt went to .

Girl Power 2 Cure

Wednesday, December 21, 2016. 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.

life at mannchester estate

These pages share our journey of adoption, parenting, and raising three kiddos with a wide range of special needs. Sunday, February 25, 2018. On this day, six years ago, our daughter coded. I wrote about it here. Focusing on the here and now though, it makes the pain feel a little less.

My Silent Angels Fight

The 4 Stages of RS. Monday, November 16, 2015. She has worked with over 300 Rett girls to teach them how to communicate. Also teaching them how to read and write as well as teaching the parents and school the best way to teach us and help us learn. Next video continues with the conversation.

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! .

Rett Syndrome News

Create your own video slideshow. A new video channel on YouTube.

Indian Rett Syndrome Foundation

This blog is to raise global awareness of Rett syndrome. Please join and share this blog with everyone. Monday, June 29, 2015. 8 Million For Research and Two Clinical Trials. Is publishing this finding today. You may be asking yourself, why does this matter? .

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The MacDonald Family

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Thursday, September 5, 2013. Quest for a Cure 2013! Were walking again to CURE Rett Syndrome! Come on out and join Annies A-Team on Sunday, Oct. 6 , 10am at the beautiful Inglenook Park in Southfield! Its a great morning and dont worry it wont take up your entire Sunday, just a couple hours to show your support for our little hero Annie! If you cant make it, you can always support Annies A-Team by donating online HERE. 156,000 is needed by December 2013 to fund this project. Ben Philpots la.

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This web page annamarymacdonald.blogspot.com states the following, "Thursday, September 5, 2013." We saw that the webpage said " Quest for a Cure 2013! Were walking again to CURE Rett Syndrome! Come on out and join Annies A-Team on Sunday, Oct." It also said " 6 , 10am at the beautiful Inglenook Park in Southfield! Its a great morning and dont worry it wont take up your entire Sunday, just a couple hours to show your support for our little hero Annie! If you cant make it, you can always support Annies A-Team by donating online HERE. 156,000 is needed by December 2013 to fund this project."

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