May is the ALS Awareness
Month
May 2006
Al is having more difficulty with all his upper
body. speech and swallowing . He has stopped
driving because his arms are so weak and he hardly
has any grip. This is very sad because driving is
such an independent thing to loose. His neck and
shoulders are a lot weaker so he sits often in a
comfy chair with a high back so he can rest
everything. He needs to sit in chairs with arms
even at the dining room table to rest his arms. He
chokes all the time on everything including his
saliva. We have gone to the doctor to find out
about him having a feeding tube put in, etc but he
still isn't sure that's what he wants to do. He is
still feeding himself but his arms are very shaky,
weak and he chews really slow. He is very
self-conscious so he no longer wants to eat out in
restaurants. His speech is very difficult to
understand but most people can catch a word or two
of what he is saying. He needs more help with his
shower, shaving and getting dressed. He gets spasms
in different parts of his body especially his
stomach and legs but he can still walk well. He
talks about getting on his boat the "HAZ" this
summer so with help from family and friends we are
going to get it ready to do a little lobstering. He
is the happiest when he is on the boat or at hunting
camp so we try to keep him going.
We did get away again this winter into a warmer
climate. Al does better in the warm weather. We
visited with our neice, Debbie, in Jupiter, FL for a
few weeks then with Al's sister Janie and Jim(Tommy)
in Hosston, LA . We did a road trip visiting
friends and family along the way. It was difficult
for Al at times but he felt worth the trip. Thank
you Lord for watching over us and bringing us home
safe. It was wonderful visiting with everyone.
I am the optimistic one who wants him to do
everything he can to stay alive. The choice is his
so I need to respect this. I feel there is a lot of
research being done for ALS/Motor Neuron Diseases so
finding a cure is near. When Al was diagnosed they
said they thought there would be a cure in 8 to 10
years. He has been diagnosed 7 years this December.
Thank you, from the bottom of our heart, to all our
family and friends for all you continued love,
support and prayers to help us get throught this
devastating illness. We send all our love, Al &
Gloria