Rarely Normal
Rarely Normal
Katelyn Nugent and Lindsay Weekes
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.
Episode 69: Andrea Lessard | Stillborn
[Trigger warning for expecting moms]We're so grateful to have Andrea in the studio this week to talk about her daughter Emory and her experience with her stillbirth. Andrea's perspective on loss, love, and her ability to continue to celebrate Emery's life is nothing short of awe-inspiring. Her daughter, Emery Grace has taught her the power of grief and is inspiring Andrea's approach to life.
May 25
55 min
Episode 68: Ashley Hopkins-Shack | Anxiety
Excited to have Ashley in the studio to help us discuss different forms of anxiety and unpack solutions. From cognitive restructuring to the power of journaling and identifying patterns, we loved this open and authentic episode Buy the Journal: https://a.co/d/0akrFLSU Website: https://fourprogress.com/
Apr 27
52 min
Episode 67: Amy Patterson | OCD + ADHD
Adult diagnoses are often not discussed, which is exactly why our conversation with Amy is so critical. She wasn't diagnosed with ADHD until adulthood (thanks to her determination!) and not until she became a mom, that she was diagnosed with OCD. We hope this episodes inspires others to seek medical testing and intervention, no matter the age!Check out her blogs:Facebook page:  https://www.facebook.com/61588540267695/Blog on systems thinking: https://meanwhile.ghost.io/
Apr 13
57 min
Episode 66: Kelsey Stanczyk | Child Loss
We couldn't be more grateful to Kelsey for sharing her daughter Stella with us. She's fearless and strong, beyond measure. Her work in the Courageous Parents Network is paying it forward to other parents and families dealing with child loss and we're honored to have her join the podcast and share her perspective on love and loss.https://courageousparentsnetwork.org/
Mar 30
55 min
Episode 65: Lolita Jones | ALD (Adrenoleukodystrophy)
We're beyond grateful to Lolita for sharing her son Michael's journey with ALD. From discovery to treatment, to his day-to-day care, we're in awe her of love and compassion for others. We even love how his sisters are getting into the medical field - inspired my Michael.https://www.aldalliance.org/https://www.hopkinsmedicine.org/health/conditions-and-diseases/adrenoleukodystrophy
Mar 16
51 min
Episode 64: Dr. Paige Ryan | Pediatric Physical Therapist & Caregiver Coach
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
Mar 3
45 min
Episode 63: Jasmine Newson | Grief
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.'
Feb 17
1 hr 10 min
Episode 62: Kim Bradley | Type 4 Laryngeal Cleft
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!
Feb 3
42 min
Episode 61: Shawna Wanemacher Camilleri | Microcephaly Capillary Malformation Syndrome
We're honored to welcome Shawna to the studio this week to talk about her son Keenan and his journey with Microcephaly Capillary Malformation Syndrome. From seizers to surgeries and seeing specialists in two states, their strength is palpable. Now Shawna is paying it forward by creating counseling and support for bereaved parents with Keenan's Caring Konnections and raising money for epilepsy.https://www.caringkonnections.com/https://www.instagram.com/keenans_caring_konnections/
Nov 17, 2025
53 min
Episode 60: Ashley Fisher | Spiritual Guide
What a pleasure it was this week, to connect with Ashley about her connection to loss. Her ability to apply experiences being a Reiki Master, reading tarot cards, working in hospice, and studying astrology and signs, means she has an incredibly interesting POV on life, dealth, and everything in between. Check her out at ashleypagehealing.com
Nov 11, 2025
1 hr 8 min
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