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What Are Your Biggest Concerns When You Transition To A New Doctor
We are researching medical facilities and insurance options so that my son can transition from pediatric to adult care sometime this year. My biggest worry is the risk of the new doctors having a different approach to how to treat my son. He is 5 years post transplant and for over the past 2 he has been stable and doing well. I would really be hesitant to change any of his treatments, dosages, etc., unless there was a real solid reason for it. But I know doctors have different approaches and opinions and I’m concerned that with this transition we might be facing changes to treatment. Hopefully I’m worrying over nothing and this won’t happen.
What has been your experience when switching to a different doctor or when transitioning from pediatric to adult? How similar or different was the new doctor compared to you former one and how did that effect you?
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