Caregiving can feel heavy, but it’s not all bad. Even on the hardest days, there are moments of joy, connection, and laughter that remind me why this journey is worth it. For me, one of those moments came unexpectedly, years after my mom stopped playing cards with her friends. It…

Caregiving is one of the most emotionally demanding roles I’ve ever taken on. And as someone living with Multiple Sclerosis (MS), it’s more than just an emotional burden—it’s a physical one, too. Stress isn’t just something I feel; it’s something I see reflected in my symptoms. Fatigue, brain fog, muscle…