SM Voices
The latest insights and perspectives from people who have lived and struggled with SM
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The cost of canceling plans: Feeling shamed when I need support the most
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Traveling with systemic mastocytosis: My tried-and-true tricks
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I’m living my best life, even if it’s now from the back of the plane
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Finding new hope: My trip to Boston to attend the WODC 2025
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My doctors let me down. Now I’m learning to live with new worries
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Facing a shortage of medication when you need it most
