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I saw that as well, and agree, I think its one of the reasons he never moved when he was the GM for the Lions.Hang tough Matt.
On a side note I watched the special with him and interview on his property. That looks like a spectacular piece of property he has.
really sorry for his situation; seems like he's handling things bravelyHis heart is working at 30% capacity and he is on the heart transplant list. Surprised he tried to broadcast this season. That has to take a toll on him.
sorry to hear, this cant be good, always loved him as a player!
Didn't think of that possibility. If so, that would be good news. As I recall, Governor Casey had multiple multiple organ transplant surgery from this. Don't know if, or how long that prolonged his life.Odd, when I saw that I immediately thought, "Hey, maybe this means they matched him up with a donor!"
But I have no idea how that works, anyway. Pretty sure that he would not go public with good or bad news at this point.
Needed: A Heart for a LionOdd, when I saw that I immediately thought, "Hey, maybe this means they matched him up with a donor!"
But I have no idea how that works, anyway. Pretty sure that he would not go public with good or bad news at this point.
If I become the optimist around here, we are all in a world of hurt..Didn't think of that possibility. If so, that would be good news. As I recall, Governor Casey had multiple multiple organ transplant surgery from this. Don't know if, or how long that prolonged his life.
Well, you got me beat in that respect.If I become the optimist around here, we are all in a world of hurt..
If I become the optimist around here, we are all in a world of hurt..
Really jealous of his woodworking tools.Looked like a well organized setup exactly the opposite of my stuff.Wish him only the best.Get well MattHis heart is working at 30% capacity and he is on the heart transplant list. Surprised he tried to broadcast this season. That has to take a toll on him.
I'm sorry to hear that. Sounds like a terrible disease, though I admittedly don't know much about it. Best wishes to Matt and his family, I'm sure he'll give it a hell of a fight.
My father in law has amaloidosis as well and has been to VA hospitals, Penn medical in Philly, and even the Mayo Clinic. He has the type where medicine will theoretically stop the progression but he won’t get his function back. They are trialing new meds that they hope will allow patients to regain some function back.Most cardiologists don't know much about it either. It took a trip to the Mayo Clinic in Jacksonville to find one that finally got the correct diagnosis.