Hello everyone, my name is Laura Hall, and I’m reaching out on behalf of our family with a heartfelt request for support.

This summer, life took an unexpected turn for our sweet and spirited 5-year-old, Sydel. If you know Sydel, you know she’s vibrant, bold, and such a loving little girl—truly one of a kind. What began as a simple treatment for what we thought was eczema quickly escalated. By late July, Sydel began experiencing leg pain and difficulty walking. On August 3rd, she was admitted to Levine Children’s Hospital, and shortly after, she received the diagnosis: Juvenile Dermatomyositis, a rare autoimmune disease.

True to Sydel’s unique spirit, her case is unlike others and is unique. She and her mom, Grace, have spent most of August in the hospital as doctors work to find the best course of treatment. This will be a long journey—one that may require years of medication and ongoing care. Our once energetic and sassy girl is now facing challenges no child should have to endure, but we remain hopeful and faithful that brighter days are ahead.

We are deeply grateful for the outpouring of love—your prayers, cards, gifts, visits, Sydel Strong shirt purchases, and donations to her Amazon wish list have lifted her spirits. We’ve witnessed God’s grace firsthand, especially when her CK levels dropped significantly last week—a sign of progress and hope.

While insurance thankfully covers medical expenses, the day-to-day costs are adding up. Grace has been unable to work while staying by Sydel’s side, and Caleb continues to juggle work, hospital visits, and caring for their 3-year-old son, Sylas. We’ve created this fundraiser to help ease the financial burden—covering essentials like food at the hospital, gas for travel, and monthly bills during this uncertain time.

If you’re able to contribute, no matter the amount, it would mean the world to us. Thank you for standing with Sydel and our family during this journey. Your kindness and support are truly a blessing.