In August 2024, I was diagnosed with spindle cell rhabdomyosarcoma, a rare and aggressive cancer. So rare that I am actually the first person with this specific genetic mutation— meaning there is no specific treatment protocol.

Since then, my journey has been filled with surgeries, treatments, and moments of both hope and heartbreak.

I’ve undergone surgery to address the cancer in my leg, and while my recovery from that has been promising, recent scans showed that the cancer has spread to my lungs.

My oncologist has shared that this type of cancer is rarely curable once it has metastasized, and I’ve been given a life expectancy of five years or less.

Despite this, I’m holding on to hope, exploring every possible treatment, and focusing on making meaningful memories with my family.

This diagnosis has made it impossible for me to work full-time. I still have my daughter, Saylor, to care for, and we are facing difficult decisions about selling our home, moving to an apartment, managing medical bills, and adjusting to this new life.

Your support means everything. Donations will help with:

• Covering health insurance costs to ensure I can continue treatment.

• Moving expenses as my family transitions to a more affordable home.

• Everyday living costs as I transition to Social Security Disability.

• Creating joyful memories with Saylor and working through my bucket list.

Whether it’s through a donation or simply sharing my story, your support is a lifeline during this challenging time.

Thank you for walking this journey with me.