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TK2d Voices

The latest insights and perspectives from people who have lived and struggled with TK2d

Aneesa Gracen Redefining a “good day”: The importance of rest for a child living with TK2d
Aneesa Gracen How chiropractic care supports my child’s TK2d diagnosis
Aneesa Gracen Writing the pages that don’t exist: Why sharing my son’s journey with TK2d matters
Aneesa Gracen Rising up to rare: How my life changed with my son’s diagnosis
Aneesa Gracen Thrown into rare, and finding the puzzle pieces fit

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Rare Disease Companion (RDC) is a network of news and information websites that supports people living with rare diseases. Through accurate, authentic, and compassionate news coverage, feature-length articles, and patient-friendly educational material, RDC provides insights into living with rare diseases at every point along the patient journey.

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