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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.

Transcript

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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More videos

The psychological impact of FA treatment fatigue
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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