Cook Clan vs. ALS: Reflections on 2006
One of the most important things I have learned this year is that each of us have the opportunity to build a legacy. We build it every day with the people we love, the people we work with, our friends, and other random people we encounter. Our legacy is not what we looked like young and thin in those high school pictures with great skin and a heart-shaped face or even what we look like middle aged with little use of our neck and arms. Instead, our legacy is defined by our character and how we represent who we are on the inside. What we remember about Moanie and Papa and everyone that is not with us anymore, is not what they looked like but all the little things that they did and said to shape us.
With ALS, Popi is experiencing all the physical aspects of the disease. He alone knows what it feels like to no longer be able to scratch his nose or to give a big bear hug. But, even though he alone is experiencing the physical side to the disease, he is not alone in the mental and emotional aspect. We each feel it every day. In a way, Popi wasn’t diagnosed with ALS but the Cook family was. We have been forever changed as a family and will walk through each stage of the disease together.
Even though ALS has been the thing that has dominated our year, it has also been a gift to us. It has given us the gift of perspective. We all know that none of us is guaranteed a tomorrow. But, this year we have been given the opportunity to look at life in a whole new way and to really squeeze everything possible out of each experience. 2006 will be remembered as the lemon that we discarded after we squeezed out every drop to make our sweetest lemonade to be served with steak and grilled potatoes and corn on a warm summer’s night spent together.
I hope that we will look back on this year and remember our beach trip—I want to remember the way it felt to see Jonson and Popi walking on the beach together. I hope we will remember the moment that the adoption was final and these boys became our boys once and for all. I hope we remember our RV trip and bumping along the highway napping and chatting together. I hope we will laugh for years to come at the incredible mounds and mounds of stuff accumulated by mom and dad in only 12 years. I think we will look back on this year and our news of Lillie and Jacey and all the other amazing things that have happened and we will remember these things. These things that were each and every one a result of our finding out that we have ALS. I think THIS gift is one that we cannot possibly deserve but one that we have embraced like only the Cook family can.
This is our legacy…our response to our diagnosis of ALS, our reaction to all that has happened and will happen. We have approached it with strong character and a will to make the best of every moment. We have approached this diagnosis together as a united front. We will look back on this and be proud of who we were and the legacy we created in 2006. I hope that we will now set about creating a 2007 that will top even this amazing year. Merry Christmas!


