My name is Sterling Troy Lyman, and I’m 53 years old. I live in Soldotna, Alaska, with my sweetheart and best friend, Char.

My career has been dedicated to working with youth since 1991. In 1998, I founded Triumph Youth Services in Utah, offering foster care, outpatient, and residential treatment services for youth struggling with drug and alcohol abuse, addiction, and behavioral disorders. Today, Triumph Youth Services’ residential treatment centers in Brigham City, Utah, continue to thrive, working with boys aged 12-18 from all over the United States.

Alongside my work, I’ve coached football and baseball for many years, finding great success in both sports. I have a true love for the outdoors, especially hunting and fishing. With four wonderful children and their spouses, whom I am incredibly proud of, my heart belongs to my seven grandchildren.

In 2016, my life of excellent health took a turn when I was diagnosed with Complex Regional Pain Disorder (CRPS), a chronic pain condition that I still battle today. However, that was just the beginning. In August 2019, I received the devastating diagnosis of Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s Disease. Neurologists warned me of its aggressive progression, giving me up to two years to live. But my wife and I refused to accept this outcome. We made a decision to fight and do everything possible to reverse this monstrous disease.

Shortly after my diagnosis, I began honey bee venom therapy, which I continue to undergo every day. Char administers up to 45 bee stings each day, following a special ALS protocol. I also adhere to all the steps outlined by healingals.org, along with various other treatments and regimens.

Unfortunately, treatments for ALS come with a hefty price tag, and the majority are not covered by insurance. Despite the financial strain, my wife, our family, and I are 100% committed to doing everything possible and never giving up. We choose to LiveON!

Living with ALS has been an expensive journey, from costly treatments to purchasing wheelchairs and making our home handicap accessible. To alleviate some of the financial burden, our friends and family have organized fundraisers. Their support means the world to us, and I am incredibly thankful for every donation.

ALS was once considered a rare disease, but sadly, that’s no longer the case. I’ve spent my life savings and sold everything I own to advance research for those fighting alongside me and after me. Together, we can beat this and reverse ALS.