Rare Care Chronicles

TANGO2 Research Foundation
  • ٥٫٠ (١)
  • غير ربحي
Rare Care Chronicles

Rare Care Chronicles is a podcast series by the TANGO2 Research Foundation covering many topics including rare disease care, research, and experiences.

الحلقات

  1. ٢٨ ربيع الأول

    "Can We Fix It?" by Kasha Morris

    This is a story about fixing an impossible problem in an unexpected way. Kasha Morris is a retired teacher that co-founded the TANGO2 Research Foundation with her husband Mike in 2018 after a fifteen-year diagnostic journey for their son Ryan. Faced with the reality of a life-limiting ultra rare genetic condition they got to work to help their son. Although TANGO2 was newly discovered, their search would take them back twenty years to uncover some answers in an unexpected place. To learn more, visit ⁠⁠⁠⁠⁠www.tango2research.org⁠⁠⁠⁠⁠. Find us on Facebook: ⁠⁠  / tango2research  ⁠⁠ Find us on X: ⁠⁠  / tango2research  ⁠⁠ Find us on Instagram: ⁠⁠  / tango2researchfoundation  ⁠⁠ Find us on LinkedIn: ⁠⁠  / tango2-research-foundation

    ١٤ من الدقائق

  2. ٩ محرم

    Igniting Hope Through Research

    Listen to Dr. Sam Mackenzie talk about what is happening now behind the scenes and the progress being made with TANGO2 deficiency disorder. About the TANGO2 Research Foundation: Our mission is to lead the way in finding a cure for TANGO2 deficiency disorder. To learn more, visit ⁠⁠⁠⁠www.tango2research.org⁠⁠⁠⁠. Find us on Facebook: ⁠  / tango2research  ⁠ Find us on X: ⁠  / tango2research  ⁠ Find us on Instagram: ⁠  / tango2researchfoundation  ⁠ Find us on LinkedIn: ⁠  / tango2-research-foundation

    ١٦ من الدقائق

  3. ٩ محرم

    Between Hope and Fear

    Between Hope and Fear: Facing a Potential Diagnosis with a New Pregnancy Meet Jake's parents and Erling's dad. Both Jake and Erling live with TANGO2 deficiency disorder (TDD). In anticipating another pregnancy, how did they cope with the fear of a possible TDD diagnosis with their 3rd child? Take a moment and listen to their story and their journeys of hope and fear. About the TANGO2 Research Foundation: Our mission is to lead the way in finding a cure for TANGO2 deficiency disorder. To learn more, visit ⁠⁠⁠⁠www.tango2research.org⁠⁠⁠⁠. Find us on Facebook: ⁠  / tango2research  ⁠ Find us on X: ⁠  / tango2research  ⁠ Find us on Instagram: ⁠  / tango2researchfoundation  ⁠ Find us on LinkedIn: ⁠  / tango2-research-foundation

    ٢٨ من الدقائق

  4. ٩ محرم

    Uncharted Youth: Caregiving in the Teen Years

    John was diagnosed with TANGO2 deficiency disorder when he was a teen. His dad, Cesar joins us to answer questions and share with us what it's like to be a caregiver for teen. About the TANGO2 Research Foundation: Our mission is to lead the way in finding a cure for TANGO2 deficiency disorder. To learn more, visit ⁠⁠⁠www.tango2research.org⁠⁠⁠. Find us on Facebook: ⁠⁠  / tango2research  ⁠⁠ Find us on X: ⁠⁠  / tango2research  ⁠⁠ Find us on Instagram: ⁠⁠  / tango2researchfoundation  ⁠⁠ Find us on LinkedIn: ⁠⁠  / tango2-research-foundation

    ١٥ من الدقائق

  5. ٩ محرم

    Beyond the Diagnosis

    A doctor's Heartfelt Recollection of Heartbreak to Hope. An interview with TANGO2 Research Foundation’s Co-Founder Kasha Morris and Dr. Cheyenne Beach’s experience with TANGO2. They discuss Dr. Beach’s experience with the Morris Family, and what her involvement has meant to her and the community.  About the TANGO2 Research Foundation: Our mission is to lead the way in finding a cure for TANGO2 deficiency disorder. To learn more, visit ⁠⁠⁠www.tango2research.org⁠⁠⁠. Find us on Facebook:   / tango2research   Find us on X:   / tango2research   Find us on Instagram:   / tango2researchfoundation   Find us on LinkedIn:   / tango2-research-foundation

    ٤١ من الدقائق

  6. ٥ محرم

    Nurturing Gratitude: A Journaling Guide for Caregivers

    Amanda Hull is from Suffolk in England. She and husband, Daniel, have three boys; Joe, Sebby and Walter. Sebby is a 13-year-old diagnosed with TANGO2 Deficiency Disorder. Amanda has worked as an Educational Psychologist for the past 18 years, and discusses how to journal as an outlet for caregivers. About the TANGO2 Research Foundation: Our mission is to lead the way in finding a cure for TANGO2 deficiency disorder. To learn more, visit ⁠⁠www.tango2research.org⁠⁠. Find us on Facebook: ⁠  / tango2research  ⁠ Find us on X: ⁠  / tango2research  ⁠ Find us on Instagram: ⁠  / tango2researchfoundation  ⁠ Find us on LinkedIn: ⁠  / tango2-research-foundation

    ٢٩ من الدقائق

  7. ٥ محرم

    Rare Care: Reducing Distress & Embracing Well-Being

    Amanda Hull is from Suffolk in England. She and husband, Daniel, have three boys; Joe, Sebby and Walter. Sebby is a 13-year-old diagnosed with TANGO2 Deficiency Disorder. Amanda has worked as an Educational Psychologist for the past 18 years, and discusses strategies for increased well-being for rare disease caregivers. About the TANGO2 Research Foundation: Our mission is to lead the way in finding a cure for TANGO2 deficiency disorder. To learn more, visit ⁠www.tango2research.org⁠. Find us on Facebook:   / tango2research   Find us on X:   / tango2research   Find us on Instagram:   / tango2researchfoundation   Find us on LinkedIn:   / tango2-research-foundation

    ٤١ من الدقائق

  8. ٥ محرم

    A Doctor's Discovery Ignites a Child's Legacy

    Ann Geffen, Executive Director of the TANGO2 Research Foundation interviews Marcie Lopez (mom to our TANGO2 angel Sammy) and Dr. Seema Lalani. Marcie and Dr. Lalani share their experience on how Dr. Lalani became the first person to recognize TANGO2 deficiency disorder and why she decided to get involved with the Foundation. About the TANGO2 Research Foundation: Our mission is to lead the way in finding a cure for TANGO2 deficiency disorder. To learn more, visit www.tango2research.org. Find us on Facebook:   / tango2research   Find us on X:   / tango2research   Find us on Instagram:   / tango2researchfoundation   Find us on LinkedIn:   / tango2-research-foundation

    ٢٦ من الدقائق
  • ٨ حلقة

التقييمات والمراجعات

حول

Rare Care Chronicles is a podcast series by the TANGO2 Research Foundation covering many topics including rare disease care, research, and experiences.

المعلومات

  • صناع العمل
    TANGO2 Research Foundation
  • سنوات النشاط
    ١٤٤٦ هـ
  • الحلقات
    ٨
  • التقييم
    ملائم
  • حقوق النشر
    © TANGO2 Research Foundation
  • موقع البرنامج على الويب
    Rare Care Chronicles

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