Rarely Normal

Rarely Normal

By Katelyn Nugent and Lindsay WeekesSociety & Culture
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Rarely Normal episodes

  • Episode 31: Jamie Day | Medium

    What a fascinating conversation! This week, we welcome Jamie Day to the studio. We leaned all about mediumship and what it's like to 'engage;' with those who have past and discussed how she harnesses her 'gift' to support others on their grief journey. Thank you Jamie for shining a light on the things we cannot see.

    38 min
  • Episode 30: Marissa Curcuru | Autism Spectrum Disorder (ASD)

    We welcomed Marissa Curcuru to the studio this week to talk about Autism Spectrum Disorder (ASD) and her experience with her son Nolan. Her perspective is powerful and she's committed to paying it forward by supporting others with their ASD journey, She even writing a children's book to help normalize the disorder - check out Unique You See (https://www.amazon.com/Unique-You-See-Marissa-Curcuru/dp/B09YHBG8GD)

    56 min
  • Episode 29: Marybeth Ellis | Child Loss

    This week, we welcome Marybeth Ellis in the studio. Her raw, authentic and loving perspective on child loss is palpable. We're honored she shared her daughter Sidney with us and are in awe of her ability to give back to her community, and be a beacon of hope and love, in her name.


    #childloss

    54 min
  • Episode 27: Tracy Dixon-Salazar | Lennox-Gastaut Syndrome (LGS)

    It was an honor and a pleasure to have Tracy in the studio this week. Not only is she a rare disease parent (her daughter has Lennox-Gastaut Syndrome), but she's the Executive Director of The LGS Foundation, a neuroscientist, geneticist, and patient advocate. We all should be more like Tracey and her daughter Savannah!

    1 hr 3 min
  • Episode 26: Keri Cote | Smith-Magenis Syndrome (SMS)

    We welcome a unique and special guest this week to the studio. She's a physician but also a parent with child who has a rare disease. Keri comes to talk to us abut her beautiful son Tatum, who has Smith-Magenis Syndrome (SMS). We talk about listening to your gut, finding the right community and creating balance.

    54 min
  • Episode 25: Gwen Maesano | Vestibular Schwannoma

    What a ride! We welcomed Gwen, a true survivor, to the studio this week to share her journey with a vestibular schwannoma in her brain. What a story of resilience and the power of the human spirit. A good life lesson on learning to listening to your body!

    1 hr 6 min
  • Episode 24: Kate Manacek | Micro Preemie/Prematurity

    Kate Manacek is back in the studio - this time to share her story and journey to motherhood for the second time, with a micro preemie. Her daughter Ellie was born at 27 weeks and spent the first 6 months of her life in the NICU. Ellie has taught Kate, her family and loved ones the power of love, resilience, and strength.

    1 hr 4 min
  • Episode 22: Jillian Arnold | ASMD

    We're kicking off Season 2 with Jillian Arnold. It was an honor to have her in the studio sharing her love and life with her two incredible kids - Roman and Stella. Both have ASMD (Acid sphingomyelinase deficiency) and her story is definitely one to share! Her perspective on rare disease is so unique and powerful.

    52 min

About Rarely Normal

From the publisher's feed

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…

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