Andy your thread has delivered as always. The duct work looks good. Time to get some heat in the shop so work on the Stude can continue.
I have some understanding of what you are dealing with your wife. My oldest son has DMD (Duchenne Muscular Drystrophy). A very aggressive muscle disease he was born with. We found out by accident when he was 2. The doctor's said he would be wheel chair bound by age 10 and his life expectancy was 20-25 yrs of age.
Truly heart breaking to a couple of new parents to say the least. The good news and silver lining for us is he 11 now and still walking just fine. Each individual is unique and follows there on path. He does have a manual chair that he uses when he gets tired. He can't walk long distances or stand for a very long time. He can't run or jump and has no reflexes so he does fall sometimes but the kid is a fighter and very strong will(like his mother). His mother is the carrier of the gene on the X chromosome. So when we found out we were 5 months pregnant with his brother. We were very lucky he did not get the disease.
Both of them are blessings from God. We live day by day with his disease and my wife is an advocate for research and raising funds helping to find a cure for the disease. It's hard to think about the future for him but I believe God chose our family to have him for the pure reason that we are strong enough to take it on.
Sorry for the long post buy you struck a chord with me and I don't mind sharing this part of my life with you and just to tell you that you being Andy to your wife is all you can do and it sounds like you do a very good job at taking care of her.
Merry Christmas and Happy New Year from Texas!
Bret
I have some understanding of what you are dealing with your wife. My oldest son has DMD (Duchenne Muscular Drystrophy). A very aggressive muscle disease he was born with. We found out by accident when he was 2. The doctor's said he would be wheel chair bound by age 10 and his life expectancy was 20-25 yrs of age.
Truly heart breaking to a couple of new parents to say the least. The good news and silver lining for us is he 11 now and still walking just fine. Each individual is unique and follows there on path. He does have a manual chair that he uses when he gets tired. He can't walk long distances or stand for a very long time. He can't run or jump and has no reflexes so he does fall sometimes but the kid is a fighter and very strong will(like his mother). His mother is the carrier of the gene on the X chromosome. So when we found out we were 5 months pregnant with his brother. We were very lucky he did not get the disease.
Both of them are blessings from God. We live day by day with his disease and my wife is an advocate for research and raising funds helping to find a cure for the disease. It's hard to think about the future for him but I believe God chose our family to have him for the pure reason that we are strong enough to take it on.
Sorry for the long post buy you struck a chord with me and I don't mind sharing this part of my life with you and just to tell you that you being Andy to your wife is all you can do and it sounds like you do a very good job at taking care of her.
Merry Christmas and Happy New Year from Texas!
Bret







I came close to really screwing up.

