Kevin's Healing Journey: Week 5 after Hyprocure Surgery

Thursday, June 5, 2014

Week 5 after Hyprocure Surgery

NO more big, heavy, clunky, hot boots to wear. Kevin has NEW SHOES and is STANDING, on average 10 seconds 20X day. He is standing much better on his right foot and will favor his left foot. And Oh My Goodness, is he getting TALL, the first time I stood next to him while he was standing took me by surprise.

Kevin is sleeping in his OWN room and bed. This means I get to sleep with the ceiling fan on again and I can wake up early to walk and do some yoga. And while we are talking about me, I am finally strong enough (after my surgery) to carry Kevin up the steps. But I will admit that I kind of miss my snuggler, but we snuggle before bed now.

Thanks to a good friend,
Kevin likes his new Thomas the Train bed comforter.

Kevin is also Gravity Free in the garage…will share pictures or video very soon.

AND THE SUPER SUIT ARRIVED…will share pictures or video very soon.

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My Blog

This blog was created to keep our family and friends updated on Kevin's healing journey. It is also our hope that others may find this blog to give help and hope to other delayed kids.

About Kevin

They told us Kevin would never walk or talk. But with lots of prayers, hard work, and extra hands, he began walking when he was four years old and we continue to have faith and hope as we wait patiently for his speech to develop. Kevin is now eight years old. He is diagnosed with Cerebral Palsy due to a brain-injury he had before birth that was caused by a stroke. In 2006, before Kevin was 2 years old, we found Glenn Doman’s book "What To Do About Your Brain-Injured Child" that had answers to help children with special needs and developmental delays. We began an individualized home treatment program for Kevin immediately and have been dedicated to our program ever since. We spent three years with the Doman family at The Institutes for the Achievement of Human Potential (IAHP) and now we are with Matthew and Carol Newell at The Family Hope Center (FHC). Twice a year we return to Philadelphia where Kevin receives a neurological evaluation to determine the progress he has made in the last six months. Then they provide us with an individualized, program that puts me in charge to help Kevin develop and reach his fullest potential.

Do You Know a Delayed Child?

The best recommendation we can give to another parent with a special needs or developmentally delayed child (brain-injured, brain-damaged, mentally retarded, mentally deficient, cerebral-palsied, epileptic, autistic, athetoid, hyperactive, attention deficit disordered, developmentally delayed, or down's) is to read Glenn Doman's book What To Do About Your Brain-Injured Child and/or Dr. Coralee Thompson and Dr. Philip Maffetone's book Healthy Brains, Healthy Children. By simply reading these books, you will gain valuable information to help your child which will begin to unlock the potential your child has. And best of all you will learn that there are other options to helping your child that you can do yourself. We would also highly recommend attending the parent course at FHC or IAHP. To read how our journey began and the successful progress Kevin has had refer to the January 2010 blog archive.