alifeforkaitlyn blogspot.com

Kaitlyn Hatchard Spinal Muscular Atrophy-Type 1

Kaitlyn Hatchard Spinal Muscular Atrophy-Type 1. Hello and welcome. My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1. Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, and clear my airway. Tuesday, August 21, 2012. So what can we do about this? Our other biggest battle h.

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LINKS TO WEB SITE

Spinal Muscular Atrophy Canada

Thursday, May 29, 2014. Thursday, February 6, 2014. 15 Things Never to Say to a Special Needs Parent. Dr Darla Clayton, Psy. Founder, Strong as Steel Adaptive Sports. All of the following examples of things not to say come from things that have actually been said to me or other special needs parents.

Our SMA Angels.

The largest on-line source of information and inspiration regarding children dealing with Spinal Muscular Atrophy. Come see their faces, read their stories, remember those who have passed and fight with those who are fighting. If you have difficulty getting into the site, or to skip the intro, enter the site Here. To break out of other frames, click Here. Site best viewed at 800x600 or higher, IE 4. 0 or better, and Java enabling.

Behind a Shoelace a Smile

Wednesday, October 8, 2014. If you know me at all, you know that I draw inspiration from everything. Anything can be inspiration for me to create. Help You Stand SMA Awareness.

The Daily Dakin

Saturday, December 1, 2012. He said he wanted to stay there his whole life, and he asked me to sing our special secret song. He has also been asking me about turning right on red.

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Kaitlyn Hatchard Spinal Muscular Atrophy-Type 1

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Kaitlyn Hatchard Spinal Muscular Atrophy-Type 1. Hello and welcome. My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1. Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, and clear my airway. Tuesday, August 21, 2012. So what can we do about this? Our other biggest battle h.

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This web page alifeforkaitlyn.blogspot.com states the following, "Kaitlyn Hatchard Spinal Muscular Atrophy-Type 1." We saw that the webpage said " My name is Kaitlyn Anne and I have Spinal Muscular Atrophy Type 1." It also said " Children born with SMA 1 gradually lose strength in their nervous systems and die, usually by the age of two. There is no known cure or long-term treatment. SMA not only affects the muscles that help me move, but it also affects those that allow me to breathe, and clear my airway. Tuesday, August 21, 2012. So what can we do about this? Our other biggest battle h."

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