Life with CMS a parents perspective
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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.
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.
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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Life with CMS a parents perspective. Saturday, June 11, 2011. The roller coaster has been his moving from house to house and I mean friends houses not mine or his dads. After a year, he has finally settled back in with his dad. I am still trying to push him to finish his highschool degree on line, but it looks like a GED is going to be his way to go.when he eventually realizes he needs to have something to move on in life. The Adoption Journey of Baby King. Links to this post. Saturday, May 1, 2010.CONTENT
This web page lifewithcms.blogspot.com states the following, "Life with CMS a parents perspective." We saw that the webpage said " Saturday, June 11, 2011." It also said " The roller coaster has been his moving from house to house and I mean friends houses not mine or his dads. After a year, he has finally settled back in with his dad. I am still trying to push him to finish his highschool degree on line, but it looks like a GED is going to be his way to go. when he eventually realizes he needs to have something to move on in life. The Adoption Journey of Baby King. Saturday, May 1, 2010."SEEK SIMILAR DOMAINS
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Friday, January 20, 2012.