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Know the Difference: Homocystinuria Versus Hyper-Homocystinemia.
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A: I can communicate independently with my medical team during visits.
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A: I feel comfortable speaking with my doctors and asking questions without my parent or caregiver.
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A: I decide who I want information shared with (family, friends etc.).
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A: I know how to contact various medical professionals (Primary, Genetics team, specialist).
A: I can set up doctor appointments and blood draws.
A: I meet independently with my medical team during my visits.
A: I know whom to contact for non-urgent needs (refills, questions, etc.).
A: I am comfortable making major medical decisions.
A: I can provide a summary of my medical history (such as dates and types of surgeries, family history, allergies and medications).
A: I know my rights to keep my health information private.
A: I can get myself to doctor appointments.
A: I know who my various medical providers are and their roles in my health.
A: I remember to implement new procedures and follow up items from doctors.
A: I know how to get your medical records if needed.
A: I have an up-to-date medical summary, either printed or digital.
A: I know how to fill out medical forms.
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