Young people with Sickle Cell Disease often wonder, "Why me? Why do I have to have this disease?"
These questions often lead to anger, despair and resentment. This resentment often leads to non-acceptance of their illness and to ignoring the need to take care of themselves.
Death amoung young people who are in transition from childhood care to adult (self-managed) care is entirely too high.
These young people in transition need our support, love and encouragement. They also need to see examples of older adults "living" with Sickle Cell Disease and living well despite the difficulties.
Here's some help and resources:
Teen Health - Childrens National Medical Center Transition Education
Teen Health - KidsHealth.Org - Transitioning Your Medical Care
Pyschosocial Help - New Jersey Department of Health
Living with your teen - North Carolina Department of Health
Nice post you got here.
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