cmsluke blogspot.com

Luke and Congenital Myasthenic Syndrome

Wednesday, May 1, 2013. For Congenital Myasthenic Syndrome. Hi everyone, I wanted to post about a facebook group that is really amazing for us CMSers. Here is the LINK Congenital Myasthenic Facebook GROUP. Please ask to join the group. Its private.but let them know your history and diagnosis and Denise will ADD you. Its up to 453 MEMBERS. WHOOT! Have a great day. In the meantime.Heres a pic of LUKE and Hannah in the bluebonnets. Hes being goofy and sitting in her lap! Andrea The H family. Hes read.

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LINKS TO WEB SITE

Ken and Congenital Myasthenic Syndrome

Monday, February 8, 2010. Much has changed since my last update. I have not smoked cigarettes in over 6 months and have not smoked marijuana in over a year and a half. Monday, December 1, 2008.

Carter Family and Congenital Myasthenic Syndrome

Carter Family and Congenital Myasthenic Syndrome. Wednesday, September 14, 2016. 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. What is normal? September 10, 2015.

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.

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Luke and Congenital Myasthenic Syndrome

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Wednesday, May 1, 2013. For Congenital Myasthenic Syndrome. Hi everyone, I wanted to post about a facebook group that is really amazing for us CMSers. Here is the LINK Congenital Myasthenic Facebook GROUP. Please ask to join the group. Its private.but let them know your history and diagnosis and Denise will ADD you. Its up to 453 MEMBERS. WHOOT! Have a great day. In the meantime.Heres a pic of LUKE and Hannah in the bluebonnets. Hes being goofy and sitting in her lap! Andrea The H family. Hes read.

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This web page cmsluke.blogspot.com states the following, "Wednesday, May 1, 2013." We saw that the webpage said " Hi everyone, I wanted to post about a facebook group that is really amazing for us CMSers." It also said " Here is the LINK Congenital Myasthenic Facebook GROUP. Please ask to join the group. but let them know your history and diagnosis and Denise will ADD you. Its up to 453 MEMBERS. WHOOT! Have a great day. Heres a pic of LUKE and Hannah in the bluebonnets. Hes being goofy and sitting in her lap! Andrea The H family."

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