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Jessica Lynn

  • This Mother Has Fought for Three Years to Find Answers for Her Undiagnosed Son – Can You Help?
    September 8, 2026

    This Mother Has Fought for Three Years to Find Answers for Her Undiagnosed Son – Can You Help?

    Jessica Lynn
  • CAMP4 Therapeutics’ CMO Yuri Maricich Describes Push to Deliver the First SYNGAP1 Treatment
    August 24, 2026

    CAMP4 Therapeutics’ CMO Yuri Maricich Describes Push to Deliver the First SYNGAP1 Treatment

    Jessica Lynn
  • AI-Driven Patient Detection Surfaces Approximately 1,200 Likely-Undiagnosed GEP-NET Patients in UK Primary Care
    June 30, 2026

    AI-Driven Patient Detection Surfaces Approximately 1,200 Likely-Undiagnosed GEP-NET Patients in UK Primary Care

    Jessica Lynn
  • Machine Learning Maps and Discovers Clinical Endpoints in Pompe Disease Using Real-World Data
    June 8, 2026

    Machine Learning Maps and Discovers Clinical Endpoints in Pompe Disease Using Real-World Data

    Jessica Lynn
  • Tisento Therapeutics’ Chad Glasser Discusses PRIZM Trial, Zagociguat Development for MELAS
    April 29, 2026

    Tisento Therapeutics’ Chad Glasser Discusses PRIZM Trial, Zagociguat Development for MELAS

    Jessica Lynn
  • Multiple Conditions and a Mission to Stop the Stigma: Sammy’s Story
    April 7, 2026

    Multiple Conditions and a Mission to Stop the Stigma: Sammy’s Story

    Jessica Lynn
  • “Not Defined By His Disability:” What Bennett Has Taught His Family About Spinal Muscular Atrophy
    April 7, 2026

    “Not Defined By His Disability:” What Bennett Has Taught His Family About Spinal Muscular Atrophy

    Jessica Lynn
  • SURVEY: The Rare Disease Diagnostic Odyssey
    March 23, 2026

    SURVEY: The Rare Disease Diagnostic Odyssey

    Jessica Lynn
  • My Immune System Attacks My Liver — and Nobody Knows Why: Katherine’s Autoimmune Hepatitis Story
    March 20, 2026

    My Immune System Attacks My Liver — and Nobody Knows Why: Katherine’s Autoimmune Hepatitis Story

    Jessica Lynn
  • “Spinal Muscular Atrophy Is Not Our Whole Story”: How One Family Navigated Two SMA Diagnoses and Found Hope
    March 18, 2026

    “Spinal Muscular Atrophy Is Not Our Whole Story”: How One Family Navigated Two SMA Diagnoses and Found Hope

    Jessica Lynn
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Rareatives is a patient-led publication where the unique stories of the rare disease community become headline news. We’re flipping the script on rare diseases. Not just awareness — action. Your story could spark the next big change. Ready to rewrite the narrative?

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