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The SM Journey: Seeking

In search of the right diagnosis? Learn the basics of SM and how it is diagnosed.

Diagnosis Seekers
Newly Diagnosed
On Your Way
Long-Term Living

Science Case report: 2 patients without KIT mutations diagnosed with SM
Science Patient diagnosed with SM through routine colonoscopy
Science My 25+ year journey to diagnosis of indolent systemic mastocytosis
Science Case report shows novel disease presentation in SM patient
Science Type 1 interferon autoantibodies not linked to development of SM
Is systemic mastocytosis hereditary?

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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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