A few days after welcoming our sweet baby girl, Ivy Rose, into the world, our lives changed in an instant. Ivy was diagnosed with Spinal Muscular Atrophy (SMA), a rare genetic neuromuscular condition that affects muscle strength and movement.

Nothing prepares you to hear news like that about your child. Since her diagnosis, our days have quickly filled with specialist appointments, physical therapy, medications, insurance coordination, and learning an entirely new medical world.

The good news is that SMA treatments and therapies have come incredibly far in recent years, and we are so hopeful for Ivy’s future.

As we navigate this journey, we are facing rapidly growing medical expenses, time away from work, physical & occupational therapy costs, and the many unexpected needs that come with caring for a child with a rare condition. We created this fundraiser to help ease some of that financial burden so we can focus fully on Ivy and her care.

If you feel led to support our family, whether through donating, sharing this page, or simply keeping Ivy in your prayers, we are deeply grateful. Every act of kindness means more to us than we can express.

Thank you for loving our girl already. We truly believe she has a beautiful story ahead of her.