truckin4tucker
New member
Tucker went in for his 3 months check-up today and on the way home, had asked lots of questions about his CF. At first he asked, "Mom, how much longer will I have CF?" It broke my heart to hear him ask that. At first I didn't know quite how to respond, but I figured it was best to be honest with him. So I told him he will have it for the rest of his life unless a cure can be found.
I went on to explain to him that is why his dad and I do so many fundraising things, so we can raise lots of money to help researchers find a cure for CF. He then asked "How much money do they need to get rid of my CF?" That was a tough question to answer. I just replied, "Lots and lots". Then he just kept saying "Why do I have CF? I don't want to have CF anymore!". With tears in my eyes I replied, "I know honey. I wish you didn't have CF either. I wish I could make it go away, but I can't. God just made you extra, extra special!" Do any of you parents out there have any other advice or input as to how to handle questions like this? Any input would be much appreciated. He is at that age (6 y.o.) where he is beginning to ask more and more questions about his CF, and I just figure it is best to be short and fairly direct with my answers. I don't want to "sugar coat" anything about his disease really. I don't think that is fair to him.
There are so many days that go by where I kind of forget about him having CF. But then there are days like today that smack me in the face and remind me he DOES have CF. My heart aches for him! Thanks for letting me vent.
I went on to explain to him that is why his dad and I do so many fundraising things, so we can raise lots of money to help researchers find a cure for CF. He then asked "How much money do they need to get rid of my CF?" That was a tough question to answer. I just replied, "Lots and lots". Then he just kept saying "Why do I have CF? I don't want to have CF anymore!". With tears in my eyes I replied, "I know honey. I wish you didn't have CF either. I wish I could make it go away, but I can't. God just made you extra, extra special!" Do any of you parents out there have any other advice or input as to how to handle questions like this? Any input would be much appreciated. He is at that age (6 y.o.) where he is beginning to ask more and more questions about his CF, and I just figure it is best to be short and fairly direct with my answers. I don't want to "sugar coat" anything about his disease really. I don't think that is fair to him.
There are so many days that go by where I kind of forget about him having CF. But then there are days like today that smack me in the face and remind me he DOES have CF. My heart aches for him! Thanks for letting me vent.