Rarely Normal
Rarely Normal
Katelyn Nugent and Lindsay Weekes
Episode 61: Shawna Wanemacher Camilleri | Microcephaly Capillary Malformation Syndrome
53 minutes Posted Nov 17, 2025 at 11:41 pm.
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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/