Marion’s daughter, Sarah, was diagnosed with a rare form of Leukemia at 14 years old. Together, with the rest of their family, they faced the rollercoaster of treatment, relapse, stem cell transplant

The mama you are meeting today is not only full of hope for her child, but for all of our children. Danielle is a mother of two girls, one who has a rare disease called Feingold Syndrome. Not only is

This is your warning: There is no real point to this 4AM Bonus Content.  We try to talk about Holiday shopping and somehow end up chatting about the EICU.  (Elf Intensive Care Unit… Duh…)  Links and r

This ride y’all… it’s a crazy one. A lot of us somehow ended up on a path we never expected to be on.  It can be dark and cold, scary and lonely.  But it can also be bright and warm, encouraging and f

This 4AM STARTED as a traditional When Autumn Comes episode but Suz and Diane got side tracked talking about pie and… well now it’s 4AM.  Links and resources: Follow Suz: Follow Di: Join the conver

Meet Stacie! Mama to Lainey and Calvin.  Lainey has a rare genetic disease that can make their day-to-day lives incredibly unpredictable due to her main symptom, recurring attacks of paralysis that ca

It has been over a month since Suz and Di saw each other.  Today they are reconnecting for the first time and chatting about so many things. Suz shares the details about botox and Lorelei’s Wishbeads

Today we are sharing a conversation that Diane and I recorded on a whim after a friend sent me a text about her mixed emotions about her daughter’s recent IEP meeting.  We chat about struggles with th

Meet Megan!  She is a sister with a lot of siblings, three of which are disabled.  We are pretty sure Megan is a unicorn example of a sister but we are hopeful there are more out there like her.  Mega

For the first time ever, Suz and Di meet IN PERSON.  They share a bit about their time together and we quickly realize that they are much better at recording separately than together. Sorry for the no