Daniel | Trees

Happy Fathers Day to all the dads out there! This week, instead of having a mom share her story, we invited a dad to the show! Daniel introduces us to his family, he talks about what it feels like to be a rare disease father as he faces the ‘it’s not fair’ moments as well as the waves of grief. Daniel is one of the founders of the Rare Disease Film Festival and the Disorder Channel where they showcase rare stories.  Topics discussed that you do not want to miss: What we felt when we heard our children could be nonverbal Timing throughout the journey “This isn’t fair” vs “why me” mindset Career change for rare Waves of grief  Links and resources: You can watch films on The Disorder Channel with a Roku or Fire Stick Learn more about Disorder Channel: www.thedisordercollection.com Connect with Daniel: www.instagram.com/disorderrarediseasefilms Freebies for you: www.SuzGeoghegan.com/Freebies  Follow us on Facebook: www.facebook.com/WhenAutumnComesPodcast Join the WAC Society to talk about all things pod related: www.facebook.com/WhenAutumnComesSociety Follow us on Instagram: @WhenAutumnComesPodcast Catch up with Suz: @suzgeoghegan on insta Make sure you hit SUBSCRIBE so you don’t miss out on our upcoming stories from other members of our medical and disabled community.  And, if you enjoyed this episode, please leave us a 5 star rating and a review!  Thank You!  

Om Podcasten

We call ourselves the 4am Mom Club because more nights than not, our kids are awake at 4am. We both have very medical, complicated, rare, beautiful children. This is a podcast for medical and disability mamas (and the people who love them) who are facing a life they never expected. We share hope-filled stories of families, all shapes, colors, sizes and abilities, all in different phases of their medically complex or disabled caregiving journey. When Autumn Comes Podcast is a program of the Apricity Hope Project nonprofit. Our mission is to care for caregiver. Learn more at apricityhope.org