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  • Hear My Voice | Emily Woolf

    Hear My Voice | Emily Woolf

  • Hear My Voice | Tamanika Zinger

    Hear My Voice | Tamanika Zinger

  • Hear My Voice | Megan Woolf

    Hear My Voice | Megan Woolf

  • Hear My Voice | Nell Choi

    Hear My Voice | Nell Choi

  • Hear My Voice | Monica Jones

    Hear My Voice | Monica Jones

  • Hear My Voice | Maggie Kang

    Hear My Voice | Maggie Kang

  • Hear My Voice | Sandra Adda

    Hear My Voice | Sandra Adda

  • Hear My Voice | Shekita Green

    Hear My Voice | Shekita Green

  • Hear My Voice | Heather Sowalla

    Hear My Voice | Heather Sowalla

  • Hear My Voice | Kristin Wiedower

    Hear My Voice | Kristin Wiedower

  • Mysterious and challenging life experience. Living with NMSOD

    My journey began with a non definitive diagnosed illness, I have learned NMSOD mimics other illnesses from lupus to MS. I stayed at many hospitals with the Hope I would be cured. Had tried all types of medications, from morphine to calm me (mind though at ER everyone thought I lost my mind due to…

  • Rare disease has taught me to live one day at a time

    My life changed a few months ago when I heard doctors tell me they had a diagnosis for every weird and unexplained symptom I’ve had in the last 6 months. At some point I felt like I went crazy, because I felt so exhausted, constant headaches, unexplained nausea, some skin rash that was really bothersome,…

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