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  • Do you have any creative ways to make treatments feel more exciting and less scary for your child?

    Which treatments are you (or your child) taking on a day to day basis? (Remember, this is a place to talk about personal experiences, but we ask that you do not give medical advice.)

    Eating enough nutrients and calories each day can be challenging for children with CF. Share any tips you have on making sure your child eats enough while they're at school or away from home.

    Are you experiencing pain during intimacy? How is it affecting your relationships? Share any tips/advice! (Remember, this is a place to talk about personal experiences and you’re welcome to suggest products, but no sales or soliciting!)
Viewing 4 topics - 1 through 4 (of 4 total)