Couverture de Rarely Normal

Rarely Normal

Rarely Normal

De : Katelyn Nugent and Lindsay Weekes
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 An exploration of the profound journey of loss, from the enduring power of love, to the unexpected moments of laughter, and everything in between. Join us for candid conversations, led by a child-loss mom and the incredible community that has supported her since day one. We’ll delve deep into the unique perspective and heartfelt advice of caregivers, friends, family, and the child-loss community. Together, we unlock the raw and complex experience of loss through the shared stories of resilience, love, and the healing strength that emerges.Katelyn Nugent and Lindsay Weekes Sciences sociales
Épisodes
  • Episode 64: Dr. Paige Ryan | Pediatric Physical Therapist & Caregiver Coach

    Episode 64: Dr. Paige Ryan | Pediatric Physical Therapist & Caregiver Coach
    Mar 3 2026

    What a treat for our listeners, to have Dr. Ryan in the studio. Her work with medically complex children, providing support for patients, but also the whole family, via her caregiver coaching. Her work fills a much needed gap in the community and her commitment is infectious.


    https://www.foundationfirstpt.com
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    46 min
  • Episode 63: Jasmine Newson | Grief

    Episode 63: Jasmine Newson | Grief
    Feb 17 2026

    Saddie Baddies unite! This week, we talk about all the facets of grief with Jasmine, who started her grief journey after the death of her father. This open and vulnerable conversation shows how universal grief is, how important it is to find a tribe, and how critical is to 'feel the feels.'

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    1 h et 10 min
  • Episode 62: Kim Bradley | Type 4 Laryngeal Cleft

    Episode 62: Kim Bradley | Type 4 Laryngeal Cleft
    Feb 3 2026

    This week, Kim Bradley shares her journey being a rare disease mom. Her daughter Laelynn (which is means 'flower of hope'), has faced 100's of surgeries and continues to shine a light of love. We discuss everything from Laelynn's day-to-day care, parenting a big family, PCA (patient care assistant) and the need for rare disease parents to rely on their tribe!
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    42 min
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