Guest guest Posted November 6, 2001 Report Share Posted November 6, 2001 When I was in highschool and college I went to Cystic Fibrosis camp every summer as a counselor. We frequently put an extra breathing mask on the child's teddy bear or other stuffed animal. This always helps. Also, pretending to be Darth Vader can work for the boys. Another idea might be to call the respiratory therapy department of a hospital and ask talk with one of the RT's that works with pediatrics - they might have some good ideas. I'm also a firm believer in helping the child to " own " whatever it is that needs to be done. Show your child how to put the mask on himself, and let him play with one. Very soon he will realize how much better he feels with the treatments ... and it will be much easier. Good luck. __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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