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Why constant communication matters for FA patients

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Patient autonomy

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Christina Cordaro, who lives in Pennsylvania, was diagnosed with Friedreich’s ataxia (FA) in 2011 at the age of 21. She explains that ongoing communication — beyond yearly checkups — helps patients feel supported, informed, and truly connected to their care.

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I think it’s important to always be in constant communication with the patient, instead of leaving it just for the yearly checkup.

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Just having constant, open discussion — whether through a hospital portal, emails, phone calls, or text messages — always being in the loop.

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Choosing to adhere to tough FA treatments, or opt out
Staying positive and proactive while living with FA
Taking time with treatment decisions in FA
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