My name is Angelo Oliva, and three years ago I was diagnosed with Spinocerebellar Ataxia (SCA) — a progressive neurological disorder that affects coordination, balance, walking, and speech. SCA is a very rare disease, affecting only 1 to 5 in every 100,000 people. It has slowly taken away abilities I depended on every day, and it has changed my life in ways I never imagined.

I have a family of five: my wife of 33 years and our three wonderful daughters, who have been my greatest support through this journey. Before SCA, I was very athletic and extremely outgoing. I received a full-ride NCAA college scholarship for athletics. I loved hiking, mountain biking, playing soccer and basketball, avidly skiing, and being active with my three daughters. I lived for those moments.

One day, while having lunch with my brother-in-law, I turned to him and asked, “Did you hear that? I just slurred my words.” At the time, I didn’t think much of it. But about a week later, I found myself unable to speak clearly to my clients. That’s when I knew something wasn’t right. I sought medical attention immediately, fearing the worst — even ALS. The neurologist performed an MRI, EKG, and extensive blood work. I also underwent genetic testing at Stanford University, which came back inconclusive. After seeking a second opinion, Dr. Williams at Sutter Health Neurology diagnosed me with Spinocerebellar Ataxia (SCA) — a very rare condition with no known cure, leaving stem cell therapy as one of the few hopeful options for slowing its progression.

Doctors still do not fully understand the cause of SCA, so those of us living with it must advocate for ourselves and pursue every possible option. I am also following the Medical Medium protocol, a clean eating approach my wife has practiced for years, to support my health in every way I can.

The hardest part has been losing the simple joys I once took for granted. I can’t even throw a football anymore. One day, my middle daughter asked, “Why are you throwing everything on the ground, Dad?” It’s moments like these that remind me how much this disease has taken — not just from me, but from my family as well.

For my entire adult life, I cared for seniors through my senior care business. Serving others has always been at the heart of who I am. When my 10-year franchise renewal came up, it became clear that I could no longer run the business due to my health. I ultimately gave it back to the franchisor at a significant loss. Letting go of something I built and loved was incredibly difficult.

This diagnosis has also created serious financial stress for my family. Despite my experience and qualifications, I struggle to secure employment. Although disability discrimination is not supposed to happen, the reality can feel very different. We are doing everything we can to stay in our home and keep up with growing medical bills and everyday expenses.

Because SCA is progressive, I am now seeking all options of stem cell treatment, which has shown promise in potentially slowing progression and improving symptoms. The cost of the procedure, along with travel and recovery expenses, is significant. Your generosity will help cover essential living expenses, pay medical bills, and support my children’s education during this challenging time.

I am reaching out to my football fraternity, the seniors I have always looked out for, and all my friends and community. Your support and encouragement mean the world to me. Any contribution, no matter the size, will help me take the next step in my journey.

Thank you for standing with me and giving my family hope for a better future.

With gratitude,

Angelo