Last year, at just nine months old, our daughter Magnolia was diagnosed with Langerhans cell histiocytosis (LCH), a rare disease we had never even heard of until it became part of our family’s story.

Since then, Lola has endured scans, procedures, countless appointments, steroid treatments, and a year of oral chemotherapy. She has faced all of it with the biggest personality packed into the tiniest body and now we’re turning every step of her story into something bigger.

Miles for Magnolia is our way of honoring Lola while raising money for the Histiocytosis Association. These funds help support critical research, better treatments, resources for families, and hopefully, one day a cure.

If you’d like to help, you can:

• Donate: Every amount, big or small, moves us closer to our goal.
• Share: Help us tell more people about LCH and why this research matters.
• Join our team: Walk or run alongside us in honor of our feisty girl.

We never imagined this would be our family’s story. But we have been carried by a community that continues to show up for Lola again and again.

Every mile is for Magnolia. Every donation is for a future where no family has to learn about histiocytosis because their baby was diagnosed with it.

Thank you for loving our girl and standing beside our family. ?