Well Gracie has been to a pediatric urologist on and off for over a year a half. They never diagnosed her, and refused to even consider that IC was a possiblity because she is only 6 (seven in September, she won't let me for get it). So we have had her on IC treatments since then, but it's not IC. Yeah right. When we moved from Washington back to Michigan I stopped her meds, she was in a full blown remission and family members only argued when they saw her three perscription routine. Well the remssion is over big time. She is back with urgency and frequency, burning, pain and basically a rotten flare kind of feeling. My poor baby was up until 4:30 am last night dealing with a flare. After ditropan, and a warm sitz bath plus lots of hugs I finally got her to sleep.
I hate this disease and I hate the fact that it is soooooooo obvious that something is wrong and docs won't diagnos her because of her age........so what we can only get sick when we turn 18???
Thankfully I had learned a few tricks from this site about how others deal with flares, and since Grace seems to flare differenlty than I do, I am falling back on that knowledge every day. Thanks guys.
I wonder how long before the new research on diganosing kids with IC will be useable to gain treatment for our daughters. Hummmmmmm Lisa
I hate this disease and I hate the fact that it is soooooooo obvious that something is wrong and docs won't diagnos her because of her age........so what we can only get sick when we turn 18???
Thankfully I had learned a few tricks from this site about how others deal with flares, and since Grace seems to flare differenlty than I do, I am falling back on that knowledge every day. Thanks guys.
I wonder how long before the new research on diganosing kids with IC will be useable to gain treatment for our daughters. Hummmmmmm Lisa
Comment