We talk about child and disability shaming (especially through children’s books) as well as parent shaming.
In this mini-episode, Jessica discusses paying for treatments for the medical conditions of her children and the lack of public/government funding.
We discuss what kind of research we did to know who to go to with our concerns about our children, and what type of doctors we went to in order to receive diagnosis for our children.
We talk about the different experiences we had noticing things were atypical with each kid, and what the push was to take the leap and get them evaluated.
In this episode, we introduce who we are and why we named our podcast FUBAR.