In January 2016, I was diagnosed with MS—a life-changing moment for me and my loved ones. I endured years of constant nerve pain, but after one failed medication, my doctor secured approval for Lemtrada, which reset my immune system for a fresh start. Today, I’m fortunate to have minimal symptoms, but I know not everyone is as lucky.
Now, I dedicate my story and efforts to helping those still fighting this terrible disease—raising awareness, sharing resources, and offering hope to those who need it most.
