LUID
STATE OF
MIND.

# Episode #63 NO CURE YET! Seven years ago, Kate Cusmano’s life changed forever when she was diagnosed with Multiple Sclerosis. In this deeply personal episode of **LUID State Of Mind**, Kate opens up about what it really means to live with an incurable disease while continuing to build a life filled with love, family, adventure and purpose. For Kate, her world revolves around her two young boys and her incredibly supportive husband, Adrian. They are her motivation, her safe place and the people who remind her that MS doesn’t define who she is. Kate takes us through the reality of living with MS — from her ongoing DMT treatment every six months and the uncertainty that comes with the disease, to one of her biggest daily challenges: **chronic fatigue**. We talk about the things people may not see from the outside and the frustration of having a body that sometimes simply refuses to cooperate. But this isn't a story about limitations. Kate shares her love of travel, including a recent family adventure to Japan, and her aspirations to see more of the world with her family. We also explore her journey with running and what it means to pursue something physically demanding while living with MS. There are challenges, there are difficult days, and there are plenty of unknowns. But there is also laughter, determination, family, adventure and an undeniable desire to keep moving forward. **“No Cure Yet”** is a conversation about living with uncertainty without allowing uncertainty to stop you from living. A story of motherhood, marriage, resilience, running, travel and the simple determination to make the most of the life you have. Because sometimes living a better life isn't about waiting for the perfect circumstances. **It's about getting out there and living it anyway.** 🎙️ **LUID State Of Mind — No Cure Yet with Kate Cusmano**