Megan and Ashley talk to Cliff Gorski, director of communications for the United Mitochondrial Disease Foundation! The UMDF is the largest organization dedicated to fighting mitochondrial diseases! Visit umdf.org for more info.
This is a podcast for families and friends of children with Mitochondrial Diseases. Two moms of Mito kids sharing support and resources and building community.
mitopodcast.com
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Episode #9 - Stephanie from Sunshine Ranch Therapeutic Riding!
Megan and Ashley talk to one of their favorite people - Stephanie from Sunshine Ranch Therapeutic Riding! Stephanie has been providing horse therapy riding services to children - including mito kids - for over 8 years. This is Megan's son Troy's favorite physical therapy and he has been riding with Stephanie for 5 years. Please visit sunshineranchriding.org/ for more information about this wonderful non-profit!
This is a podcast for families and friends of children with Mitochondrial Diseases. Two moms of Mito kids sharing support and resources and building community.
Subscribe on the Apple Podcast app!
Listen on Google Podcasts.
Like us @ Facebook.com/mitopodcast
This is a podcast for families and friends of children with Mitochondrial Diseases. Two moms of Mito kids sharing support and resources and building community.
Subscribe on the Apple Podcast app!
Listen on Google Podcasts.
Like us @ Facebook.com/mitopodcast
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Episode #8 - Quarantine Life
Megan and Ashley talk about day to day life with Mito kids and how it is similar and different during the current COVID-19 pandemic.
This is a podcast for families and friends of children with Mitochondrial Diseases. Two moms of Mito kids sharing support and resources and building community.
Subscribe on the Apple Podcast app!
Listen on Google Podcasts.
Like us @ Facebook.com/mitopodcast
This is a podcast for families and friends of children with Mitochondrial Diseases. Two moms of Mito kids sharing support and resources and building community.
Subscribe on the Apple Podcast app!
Listen on Google Podcasts.
Like us @ Facebook.com/mitopodcast
~ No comments: ~
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Megan and Ashley have a great talk with April ("ChronicallyApril), who was diagnosed as an adult with a mitochondrial disease. She is ...
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Ashley and Megan talk to Sebastien of the Flowering Hope Foundation. His son, Jagger, has Leigh Syndrome, a mitochondrial disease. Sebastien...
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Megan and Ashley are back after a little break! A quick update about what's been going on in their lives. Happy New Year! The Mito Podca...
Episode #54 - Grieving the life you had planned
In this episode, Megan and Ashley continue to talk about grief. Specifically - grieving the life you had planned before your child was diagn...
