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SM Voices

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

  • Tara Keith The power of words and a heart full of love: What I learned from my sister

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  • Tara Keith Even after 25 years, I’m still learning about my indolent SM

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  • Olivia Banks How my dog helps me navigate my systemic mastocytosis diagnosis

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  • Tara Keith Think visiting Disney with a rare disease is too hard? Here’s my tips to make it happen

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  • Olivia Banks Free versus costly medical care: My experience with both

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  • Tara Keith The cost of canceling plans: Feeling shamed when I need support the most

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  • Olivia Banks Traveling with systemic mastocytosis: My tried-and-true tricks

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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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