Kevin's Healing Journey: February 26

Friday, February 26, 2016

February 26

Here we are again...February 26. Kevin's walking anniversary from 2009. He was four years old and had worked so hard for 2 1/2 years before taking those first steps. I never thought we would still be where we are today. I am thankful for the walking that Kevin can do but it's hard for me not to worry about his walking future.

Open the Little Orange Book.

Jesus Calling by Sarah Young - a daily devotional

February 26

I am leading you, STEP BY STEP, through your life. Hold my hand in trusting dependence, letting Me guide you through this day. Your future looks uncertain and feels flimsy - even precarious. That is how it should be. Secret things belong to the Lord, and future things are secret things. When you try to figure out the future, you are grasping at things that are Mine. This, like all forms of worry, is an act of rebellion: doubting My promises to care for you.
Whenever you find yourself worrying about the future, repent and return to Me. I WILL SHOW YOU THE NEXT STEP FORWARD, AND THE ONE AFTER THAT, AND THE ONE AFTER THAT. Relax and enjoy the journey in My Presence, trusting Me to open up the way before you as you go.

Ok, I get it. But I might forget. So remind me when I do.
Read and Repeat.

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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.