HI Kaylasdad
I am also new to this site and really find it to be a great place!
I am so sorry about your daughter and I remember very well when our daughter was dx at age 2yrs old. Very difficult time. Every one is different but we have an 18 yr old daughter who is doing great. Only hospitalized once last year, is a cross country runner (started at a 13 min/mile...down to a 7min/mile!) , is very active in school, has lots of friends and is on her way to college this August on an academic scholarship. She does do nebs and enzymes and has sinus issues. The advice you were given so far is excellent. Dont see her as "CF", enjoy her every day and realize you are in a world right now that has come a long way in the management. When I went to nursing school (about 20 yrs ago) our text books said CF average life span was 5...that has changed quite a bit..now I believe it is 36 and I feel that will just keep moving up!
These are very special people...kids with CF seem to be very compassionate individuals. I know our daughter is really an incredible person and people comment on her to a point it brings me to tears (good ones!!). She plans on going into the medical field and so much of that comes from her personal experiences with CF. So as much as I hate to admit...even with CF....some good always come out of the bad. <img src="i/expressions/face-icon-small-smile.gif" border="0">
Hang in there, take good care...she is beautiful
JW212
I am also new to this site and really find it to be a great place!
I am so sorry about your daughter and I remember very well when our daughter was dx at age 2yrs old. Very difficult time. Every one is different but we have an 18 yr old daughter who is doing great. Only hospitalized once last year, is a cross country runner (started at a 13 min/mile...down to a 7min/mile!) , is very active in school, has lots of friends and is on her way to college this August on an academic scholarship. She does do nebs and enzymes and has sinus issues. The advice you were given so far is excellent. Dont see her as "CF", enjoy her every day and realize you are in a world right now that has come a long way in the management. When I went to nursing school (about 20 yrs ago) our text books said CF average life span was 5...that has changed quite a bit..now I believe it is 36 and I feel that will just keep moving up!
These are very special people...kids with CF seem to be very compassionate individuals. I know our daughter is really an incredible person and people comment on her to a point it brings me to tears (good ones!!). She plans on going into the medical field and so much of that comes from her personal experiences with CF. So as much as I hate to admit...even with CF....some good always come out of the bad. <img src="i/expressions/face-icon-small-smile.gif" border="0">
Hang in there, take good care...she is beautiful
JW212