Choc_marg
<font color=darkorchid>Don't let him rent space in
- Joined
- Jul 13, 2005
- Messages
- 425
Background:
DS5 was born with severe kidney reflux. After a year of tests & hope that he would grow out of it (he didn't), he had reimplantation surgery. That appeared to work for awhile, but his kidneys never completely healed. They have always been enlarged. So after more tests, it turns out that his bladder doesn't communicate with his brain and he was holding 3 times the amount of urine that a normal kid his age should be holding. The bladder couldn't hold it all, so it was backing up into his kidneys again. There was no neurological reason why (no spial cord injury & no spina bifida - confirmed with a spinal MRI). At this point, the docs (we got a second opinion) think that because of the severity of the reflux, his bladder never learned how to sense that it was full.
So, this past summer, he had a pretty intense surgery to enlarge his bladder by using a section of his colon and to create a channel (using his appendix) that connects his bladder with a stoma (button shaped opening) in his abdomen. So the only way he can drain his bladder is through a catheter placed through the stoma. This has to be done every 4 hours. Apparently the insurance policy that DHs company has does not cover "incontinance supplies". So, we have been denied insurance coverage for the catheters, but have been told that we can appeal for the insurance to bend the rules.
We have already sent a letter from the doc about the medical necessity. That was part of the initial inquiry that was denied. Now, we have to send our own letter to start the formal appeal.
Does anyone have any ideas on what to say? What works? What doesn't? Any experiences would be greatly appreciated. The medical stress this summer was enough for us. We really want to get this resolved so that we can get back to our lives.
TIA - Teena
DS5 was born with severe kidney reflux. After a year of tests & hope that he would grow out of it (he didn't), he had reimplantation surgery. That appeared to work for awhile, but his kidneys never completely healed. They have always been enlarged. So after more tests, it turns out that his bladder doesn't communicate with his brain and he was holding 3 times the amount of urine that a normal kid his age should be holding. The bladder couldn't hold it all, so it was backing up into his kidneys again. There was no neurological reason why (no spial cord injury & no spina bifida - confirmed with a spinal MRI). At this point, the docs (we got a second opinion) think that because of the severity of the reflux, his bladder never learned how to sense that it was full.
So, this past summer, he had a pretty intense surgery to enlarge his bladder by using a section of his colon and to create a channel (using his appendix) that connects his bladder with a stoma (button shaped opening) in his abdomen. So the only way he can drain his bladder is through a catheter placed through the stoma. This has to be done every 4 hours. Apparently the insurance policy that DHs company has does not cover "incontinance supplies". So, we have been denied insurance coverage for the catheters, but have been told that we can appeal for the insurance to bend the rules.
We have already sent a letter from the doc about the medical necessity. That was part of the initial inquiry that was denied. Now, we have to send our own letter to start the formal appeal.
Does anyone have any ideas on what to say? What works? What doesn't? Any experiences would be greatly appreciated. The medical stress this summer was enough for us. We really want to get this resolved so that we can get back to our lives.
TIA - Teena
