severedisabilitykid blogspot.com

life with a severely disabled child

Life with a severely disabled child. The title explains it all, doesnt it? Thursday, July 17, 2014. I wont be writing at this blog any longer. Its just not working for me anymore. My life is changing and I am moving on. I think I may end up blogging elsewhere but with a new focus.maybe, maybe not. However, I do have some last words here. Parenting and caring for a child. Ahand to deal with it! Their people, is what makes a nation strong, vibrant and influential on the world stage. And in glowing terms.

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LINKS TO WEB SITE

Single Dad Disabled Daughter

The drive to his residential facility is about two hours, it makes for a long day. A long, horrible day. The law says that every child with a disability is to be educated as much as possible with their non-disabled peers. Blessed is the True Judge.

the early birdies Updates on our 28- weeker preemie twins and raising a child with cerebral palsy

Updates on our 28- weeker preemie twins and raising a child with cerebral palsy.

Helping Kai Play

Monday, October 10, 2011. Birthday and walk around 5 years old. These were my goals for Kai. Kai was going to crawl and walk. I was sure of it. He was just going to be farther behind the curve than most kids. We began weekly therapy visits and I worked with Kai every day I could.

in my eyeslife with Cerebral Palsy removing the fence around social barriers one post at a time.

Removing the fence around social barriers one post at a time. Why I blog without a name. Enter your email address to follow this blog and receive notifications of new posts by email. Music Therapy and other useful info.

Daniels Gift

Whatever their gifts or limitations, people are all bound together by a common humanity. Wednesday, January 14, 2015. The lecturer was a guy in his thirties with autism.

No More Ashley Xs Say NO to Growth Attenuation

A misguided choice for all parents of children with severe disabilities. Wednesday, September 25, 2013. Who is taking care of Ashley? Hoping to point out the deep flaws in thinking and information that exist in what the parents have put forth. I will look at them more carefully afterward.

The Socially Inappropriate Mom

Tuesday, March 31, 2015. So, what does this tell us? No Will we move to transfusion dependency? Bone marrow .

Lessons From Joey

Joey was born with hypotonia and as he has grown he has also been diagnosed as Failure to Thrive and with Hypotonic Cerebral Palsy. 5 years old he functions at a 7-8 month-old level in almost every way. Despite his challenges Joey teaches us something new every day and has changed our lives for the better. Wednesday, April 21, 2010. This is the first therapist. We still have a long way to go to feeding independence as he is not fe.

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life with a severely disabled child

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Life with a severely disabled child. The title explains it all, doesnt it? Thursday, July 17, 2014. I wont be writing at this blog any longer. Its just not working for me anymore. My life is changing and I am moving on. I think I may end up blogging elsewhere but with a new focus.maybe, maybe not. However, I do have some last words here. Parenting and caring for a child. Ahand to deal with it! Their people, is what makes a nation strong, vibrant and influential on the world stage. And in glowing terms.

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This web page severedisabilitykid.blogspot.com states the following, "Life with a severely disabled child." We saw that the webpage said " The title explains it all, doesnt it? Thursday, July 17, 2014." It also said " I wont be writing at this blog any longer. Its just not working for me anymore. My life is changing and I am moving on. I think I may end up blogging elsewhere but with a new focus. However, I do have some last words here. Parenting and caring for a child. Ahand to deal with it! Their people, is what makes a nation strong, vibrant and influential on the world stage."

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