Heartbreaking news from Barry: A young mother’s sudden passing has opened a crucial discussion on epilepsy care. Megan Gardiner, just 25 and 17 weeks pregnant, tragically passed away due to Sudden Unexpected Death in Epilepsy (SUDEP). Despite suffering frequent, uncontrolled seizures since age 13, Megan and her family were not clearly informed of the specific risks associated with her condition, an inquest revealed.

Megan’s mum, Alison Woolcock, remembers her daughter as a “beautiful, sensitive, kind and funny” soul. She hopes that uncovering what went wrong can help prevent similar tragedies in the future, urging better awareness and support for epilepsy sufferers.
During the inquest, Coroner Kerrie Burge found significant gaps in Megan’s care. Had there been proper risk communication and follow-up support, the outcome might have been different. The court heard from Megan’s family, epilepsy experts, and healthcare professionals, with heartfelt testimony shining a light on the imperative need for consistent and comprehensive patient education and safety measures.

As Megan’s family fights for answers, this case underscores the importance of transparent healthcare communication, especially for those navigating epilepsy during pregnancy. SUDEP Action Caseworker Julia Stirling and solicitor Elaine Macdonald stressed the importance of risk awareness and support, advocating for significant improvements in epilepsy care.
We’re deeply moved by Megan’s story and her family’s courage. Let’s join them in raising awareness, ensuring better outcomes for all living with epilepsy. Share to spread the word and support the call for change. 🌟
