EP: 88 Celebrating 10 Years Of 'A Song, A City' with Megan Male
Episode description
'P, is for the People both big & small, U, is for the unity that gathers us all. S for Spina Bifida, H for Hydrocephalus. Send a P.U.S.H to the world, never let them get the best of us'
- Celebrating 10 years of 'A Song, A City': The first ever Music Tour across the UK & Europe (2013)
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Hey all!
Welcome back to Season 3 of the PodCast.
This Season kicks off a year long, 10 Year Anniversary, and Celebration, of A Song, A City.
In this Conversation, Danny sits down with Megan Male of St. Catharines, ON, Canada.
June is Spina Bifida & Hydrocephalus Awareness Month across Canada, as well as 50 years of Hydrocephalus Canada, and so we're super excited to sit down with a bunch of friends from across Canada this month.
Megan talks about her journey through getting into, and playing, the DRUMS, as well discovering her diagnosis of Hydrocephalus in 2008, at 21 years old.
She talks about being a nurse today, how living with Hydrocephalus has shaped she works as a nurse, as well as the incredible fact that she works on the same floor as where she spent time during her first surgeries.
Megan gets personal, sharing about her new born daughter Lily, how her family inspires her, as well as some of the current health challenges that she’s been facing.
Megan, you're the absolute best!!
Thank you so, so much for doing all that you do, and we'll see you again soon!
❤️
:)
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The 'P.U.S.H' Project Podcast
(People, United for Spina Bifida, and Hydrocephalus)
A Song, A City
http://www.asongacity.com/podcast