cmskyla blogspot.com

Carter Family and Congenital Myasthenic Syndrome

Carter Family and Congenital Myasthenic Syndrome. Wednesday, September 14, 2016. Update Freshman Year September 2016 14 yrs. old. Hi friends and family! Just a quick update on Kyla Ann and her journey with CMS. She is a freshman now and I am super proud of the young lady she is becoming. She loves to read, participate in theatre, choir and her youth group. Her transition to high school has been positive and her teachers are awesome! But Im not normal or ordinary. What is normal? September 10, 2015.

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LINKS TO WEB SITE

Luke and Congenital Myasthenic Syndrome

Wednesday, May 1, 2013. Please ask to join the group. but let them know your history and diagnosis and Denise will ADD you. WHOOT! Have a great day.

Humphreys Adventures

Missy now at least 90lbs. Saturday, March 31, 2012. Watch Us Grow as a family. Click here to view this photo book larger. Shutterfly allows you to customize your photo book. Just the way you want. Wednesday, January 11, 2012. Gavin enjoying his 1st Thanksgiving dinner! 1st time to meet two of his cousins. Baby Jaxon and BJ! Gavin with more cousins BJ Tara and Rook. Sitting up and using the big duck! Saturday, January 7, 2012. Watch Us Grow as a .

Landon Warren

Pending a diagnosis and a cure www. Saturday, August 11, 2012. Landon is now at Little Light House. Would love your help in sponsorship to help the school stay open and help all the special kids. Just click on the link and say you will sponsor Landon and they will send you a tax receipt. do? Thursday, July 19, 2012. Thursday, May 3, 2012.

News From the Liminal State

Words from betwixt and between. I am super unreliable when it comes to doing personal blogging stuff. Guess the right ones and you win a cake. 1 my life is pretty boring, and nobody wants to hear about it.

Myaware Kids UK Ireland

Toby, Acetylcholine Receptor Deficiency. Ellen, unknown gene fault. Charlie, unknown gene fault. Bringing families with myasthenia together. Paris to Florence - June 2013.

The Stockman Family

There was an error in this gadget. Osan AFB, South Korea. Carter Family and Congenital Myasthenic Syndrome. Anniversary Trip to San Diego. New name, new website, new blog. Korean - Audio Word of the Day. Friday, December 25, 2009. Saturday, December 19, 2009. Thursday, July 30, 2009. Now we are living in an .

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Carter Family and Congenital Myasthenic Syndrome

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Carter Family and Congenital Myasthenic Syndrome. Wednesday, September 14, 2016. Update Freshman Year September 2016 14 yrs. old. Hi friends and family! Just a quick update on Kyla Ann and her journey with CMS. She is a freshman now and I am super proud of the young lady she is becoming. She loves to read, participate in theatre, choir and her youth group. Her transition to high school has been positive and her teachers are awesome! But Im not normal or ordinary. What is normal? September 10, 2015.

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This web page cmskyla.blogspot.com states the following, "Carter Family and Congenital Myasthenic Syndrome." We saw that the webpage said " Wednesday, September 14, 2016." It also said " Update Freshman Year September 2016 14 yrs. Hi friends and family! Just a quick update on Kyla Ann and her journey with CMS. She is a freshman now and I am super proud of the young lady she is becoming. She loves to read, participate in theatre, choir and her youth group. Her transition to high school has been positive and her teachers are awesome! But Im not normal or ordinary. What is normal? September 10, 2015."

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