Amy from Floyo Travel is opening up and sharing all of her tips and tricks when it comes to communication while on vacation. We talk about communication for our nonverbal children, but also communication roles as parents and caregivers. Topics discussed that you do not want to miss: Links and resources: Make sure you hit…
This week Amy from Floyo Travel is sharing tips and tricks for cruise ship travel. She is also talking about traveling as a family with special dietary needs. Join her and Suz as they continue the When Summer Comes Series. We are keeping these episodes short and sweet, and packed full of travel tips for…
Amy from Floyo Travel is joining Suz for our When Summer Comes Series. We are keeping these episodes short and sweet, and packed full of travel tips for medically complex, disabled families. This week Amy is sharing travel tips related to mobility needs of families like ours. Topics discussed that you do not want to…
Amy from Floyo Travel is joining Suz for our When Autumn Comes – scratch that – When Summer Comes Series. We are keeping these episodes short and sweet, and packed full of travel tips for medically complex, disabled families. This week we are kicking things off by talking about the always important respite. Topics discussed…
I cannot believe we are wrapping up season two of When Autumn Comes. Today is another “solo suz” episode where I talk about a few things that have been weighing heavy on me lately. Y’all know I’m not a huge fan of solo episodes because I definitely prefer talking to someone directly in front of…
Leah is back! Since we last met her, early in season one, she has released her debut memoir, Loving You Big. It is a story of beautiful, loving, chaos that so many of us can relate with and feel comfort in knowing that we are not alone in this journey. Leah and Suz are hosting…
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…
Janice is back! Scroll back and listen to episode 5 called “Quarantine Blessings” to hear her full story. Today we are simply two bereaved medical, special needs moms talking about what has helped our grief journeys and what has not. Trigger warning: this episode is raw, candid and plenty of tears were shed. Topics discussed…
You are about to meet a brave mama who will do whatever it takes to make sure her children are receiving the best care, best support and best adventures they can possibly imagine. Kristy and her husband packed up their family (during a global pandemic) and moved across the country so her son Robbie could…
After her daughter, Nina, passed at 8 years old from Rhabdomyosarcoma (soft tissue cancer) Stephanie continued on, facing waves of grief along with her husband and two other children. 15 years later, Stephanie is now leading grief support groups, helping other parents process the loss of their child(ren). Topics discussed that you do not want…