It Goes Without Saying

In this episode, Cass sits down with Dr. Seyedan to discuss the hardships faced by students living with Lyme disease. School and the teenage years are hard enough, but when you add in a chronic invisible illness, it can become almost unbearable. Dr. Seyedan is on a mission to educate the world so that young people with Lyme disease are able to get the education and socialization of their peers, despite living in constant pain.

Last fall, my neurological Lyme symptoms came back with a vengeance. Brain fog, fatigue, memory issues, periodic paralysis and full body seizures became my daily routine. I fell into a deep depression that I tried to hide from everyone, even myself. I am finally on the other side and wanted to share what has been happening in hope that this will help those who have been through/are going through something similar. The journey is not over yet, but, for once, I am hopeful for the future.

In this episode, Cass is joined by her chicks--Abby, Hannah and Kerry. These girls bonded over growing up with Lyme disease and have stood by each other for the last 11 years. Follow along as they discuss how they met, what growing up with one another was like and a whole lot more.

In this special episode, Cass celebrates one year since her hysterectomy. She dives deep into the why behind the surgery, what the surgery entailed and how her recovery has been.

In this episode, Cass is joined by the magnificent Emma Maxwell (known online as Endometriosis Em). Emma shares her story with endo and how Endometriosis Em came to be. The gals talk about how the healthcare system fails women when it comes to their menstrual health and how the endo community bands together to support one another in the best ways. Follow Emma on Instagram and Tik Tok @endometriosisem!