In November 2024, my life changed dramatically when I became seriously ill with Lyme disease and mast cell activation syndrome (MCAS). Since then, I’ve struggled daily with severe reactions—sometimes my throat closes up, and there are days I can barely function or care for my four children. The treatments and supplements my body needs aren’t covered by insurance, leaving me to pay out of pocket for every doctor’s visit, protocol, and supplement. I’ve found a doctor who specializes in alternative medicine for Lyme, and I’m hopeful that with the right support, I can begin to eat without fear and work toward remission. Every step forward is a challenge, but these treatments are my best hope for regaining my health and being present for my family.

This journey has been even harder because my 9-year-old daughter, Olivia, is also battling Lyme disease. Trying to heal myself while caring for her has been overwhelming, both emotionally and financially. My husband is our sole provider, and the cost of our treatments is a heavy burden on our family. We’re doing everything we can to maintain our lives while facing thousands of dollars in medical expenses that insurance won’t touch.

Your support would mean the world to us. It would lift a huge weight from my husband’s shoulders and give me peace of mind as a mother, knowing I can get the help we both need. With your help, we hope to move forward, regain our health, and return to a normal, happy life together.