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SM Voices

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

  • Kim Lepine Finding community within online platforms

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  • Kim Lepine To Epi or not to Epi, that is the question

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  • Tara Keith Bidding a tearful goodbye to a life-changing clinical trial

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  • Tara Keith Becoming the guide I wish I’d had on my rare disease journey

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  • Tara Keith Is it age, or SM? Getting older with a rare disease

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  • Kim Lepine How I learned that estrogen can affect SM symptoms

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  • Tara Keith My care can be costly. I just learned there are grants to help

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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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