NorthernRedneck
Well-known member
I was contemplating posting this since last week but decided to as an awareness.
Here's the background info. My dad's cousin was born with congenital heart disease. His heart was deformed and flipped over completely on the right side of his chest when he was born. He saw several different specialists all at an early age who all told his parents the same thing. That he would only live till he was 12-13 yrs old. His parents brought him to a different specialist when he was 7. That specialist informed them that at age 12, he would need a pacemaker. They brought him back when he was 12 to have his first pacemaker installed. The doctor told them at that time that he would most likely live to 35-41yrs old. His entire life involved trip after trip to Toronto to a special clinic. In recent years, the tube going from his stomach to his intestines became blocked. His body basically made itself a new tube going to his intestines. He was informed recently that he would never be able to eat solid foods again and would have to remain on IV for the remainder of his life. He had become weak. There was a chance though that he would be able to undergo surgery to correct this but there was no guarantee it would work. He returned home a few weeks ago from yet another trip to specialists to rest up and become stronger. His heart finally gave out on him two weeks ago. He lived to be 43. I was at his funeral last week as I knew him and his family well.
So my message from this is that if you know someone with this disease, there is a chance at a longer life. Don't give up hope.
Here's the background info. My dad's cousin was born with congenital heart disease. His heart was deformed and flipped over completely on the right side of his chest when he was born. He saw several different specialists all at an early age who all told his parents the same thing. That he would only live till he was 12-13 yrs old. His parents brought him to a different specialist when he was 7. That specialist informed them that at age 12, he would need a pacemaker. They brought him back when he was 12 to have his first pacemaker installed. The doctor told them at that time that he would most likely live to 35-41yrs old. His entire life involved trip after trip to Toronto to a special clinic. In recent years, the tube going from his stomach to his intestines became blocked. His body basically made itself a new tube going to his intestines. He was informed recently that he would never be able to eat solid foods again and would have to remain on IV for the remainder of his life. He had become weak. There was a chance though that he would be able to undergo surgery to correct this but there was no guarantee it would work. He returned home a few weeks ago from yet another trip to specialists to rest up and become stronger. His heart finally gave out on him two weeks ago. He lived to be 43. I was at his funeral last week as I knew him and his family well.
So my message from this is that if you know someone with this disease, there is a chance at a longer life. Don't give up hope.