Day 88, Thursday Nov. 19
While each new day is much like the last, monotony doesn't seem to be the correct term for Jeff's routine. It indicates boredom, an affliction Jeff is not fighting.
Each day he is tested to perfect the things he is learning. He practices skills that he may be using for the rest of his earthly life. His mind is busy trying to find ways to make his condition less of a burden for himself and others.
When Jeff's physical restrictions present a roadblock in his progress, he finds a way around them. He has a way of thinking outside the box to accomplish the things he wants done. Watching him in occupational therapy can be pretty entertaining when he gets creative to complete a task.
In therapy today Jeff and Annette spent extra time working on car transfers. Annette is especially nervous to have these skills down before going home. They do such a great job even if it isn't perfect each time. Time and practice will help them gain the confidence they need.
After discussing the standing chair with Natalie yesterday, of course Jeff wanted to try it! They are thinking it may be a good way to help prevent muscle atrophy in Jeff's legs also.
"Look! I'm standing!"
We are so grateful to live in a day and age with so many wonderful medical advances and options for our dad. All of the adaptive equipment he has to help him live a normal life... It's just incredible.
They also worked on stretching today. They tried different ways in the hopes of preventing the dreaded autonomic dysreflexia. What they discovered is that Jeff does better when he's on his side verses when he's on his back.
Only a handful of days and our dad will be coming home! We are so full of gratitude for everyone's overwhelming love and support. Thank you all for your acts of kindness and service as we struggle each day to come to terms with this change. We feel your prayers and your love building us up in our time of need.
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