I'm a 27 year old woman w/ CF and I would have totally, compleltely DIED if this had happened to me in junior high! Ack! Poor daughter!
This thread is fascinating. It makes me realize something that I have been thinking about for years:
What should we do about people who we may not know who then GOOGLE our disease and then read all the morbid and statistically depressing information about it, and come to you with questions about your life expectancy, and such? In my experience, (especially in high school) when I let a friend know about my disease they always had a freak-out session and went to the library to research about it. Unbeknownst to me, the friends would discuss my disease when I wasn't there. I knew this was out of concern, but high schoolers can be cruel and I felt like I was defenseless against all this gossip.
I didn't know how to handle the situation properly.
I'm wondering if there are any resources out there for teenagers w/CF to take control of their disease and perhaps workshop ways to tell their friends without it sounding like they were under a death sentence. It's not good to have to feel like you have to hide the disease but it's also sometimes WAY SCARIER to disclose the information and deal with the questions, the tears, the fear, and the denial, etc. This would have been great for me when I was in high school. High school is dramatic enough without life-threatening illnesses thrown into the mix!
Now, as an "adult" I am definitely more open about it, but it still remains a major point of privacy! I feel like I'm finally ready to proactively deal with this disease...but I had to "work up to it" by thinking about it for many years. For better or for worse I never had hospitalizations or treatments that forced me to explain it....so it's almost like I conditioned myself to be in denial. Definitely something I continuously am working on.
Good luck and I know your daughter will come out of this fine.
--Welshwitch, 27 w/CF