Grants and Respite: Supporting Families in the Moments That Matter Most.

Grants represent our promise to reduce the financial strain that so often accompanies an FTD diagnosis. Caregiving is costly—emotionally, physically, and financially. Through targeted grants, we aim to provide relief where it’s most needed: caregiving assistance, adaptive equipment, therapeutic services, travel for medical appointments, and other necessities that help families breathe a little easier. These grants are an investment in dignity, stability, and access. They acknowledge the reality that support isn’t just emotional—it’s practical. And sometimes, a bit of financial assistance can change the trajectory of a family’s week, month, or year.

Respite is the restorative counterpart. Care partners often carry the weight of FTD around the clock, with few opportunities to pause, recharge, or simply be human. Respite programs offer a lifeline. Whether through short-term care, community resources, or structured breaks, we help families reclaim essential moments of rest. Respite is not a luxury—it’s a necessity. It strengthens caregivers, preserves their well-being, and ultimately improves care for their loved ones. Our commitment to respite honors the truth that healing and sustainability require time, space, and breath.

Together, grants and respite embody our belief that supporting the FTD community means meeting families exactly where they are—emotionally, financially, and physically. These pillars ensure that our work extends far beyond raising awareness, creating education, or sharing stories. It reaches into the lived, everyday experience of caregiving and says: You are not alone.

Because when families are supported—and when caregivers can rest—the entire community grows stronger.