We attended a seminar at our local hospital and it was suggested that we have a Living Will for our son who has Cystic Fibrosis since he will be 18 in April. They will be asking for a copy with each admission he may have.
Does your child have one? If so, how did you approach the subject with them, without frightening them?
We were considering have our son's social worker talk with all of us together at a future visit to the CF Center as a start.
We have talked earlier this year when there was the debate with the Florida woman on life support between husband and her parents, asking him what his thoughts on the subject but nothing decisive.
Does your child have one? If so, how did you approach the subject with them, without frightening them?
We were considering have our son's social worker talk with all of us together at a future visit to the CF Center as a start.
We have talked earlier this year when there was the debate with the Florida woman on life support between husband and her parents, asking him what his thoughts on the subject but nothing decisive.