When Phil Green, a husband and father to four children, was diagnosed with ALS in 2018, he decided he was going to dedicate his life to advocating for other people and families affected by the disease. It’s something he believes his life prior to diagnosis had prepared him to do, so there was no question or doubt that he would do everything in his power to make a difference.
“To me, I was still the same person that I had always been,” Phil says as he recounts the day he first had to ask for help buttoning up his shirt. “Suddenly, I felt like I was the only person in the world that was diagnosed. I didn’t know anyone who had ALS and there wasn’t much information to help me and my family better understand what was going to happen to me. The first thing we did was try to figure out what treatments were available to slow down the disease, and we found that there were limited options.”
ALS, which stands for amyotrophic lateral sclerosis (also known as Lou Gehrig’s disease), eventually robs people of their ability to walk, talk, swallow and breathe. Phil’s diagnosis hasn’t stopped him from becoming an avid advocate and ally to make the ALS community’s voice heard loud and clear. Phil is one of thousands aiming to spark conversations about ALS with hopes that progress can be made to better understand and treat the disease.
Over the last three years, Phil has been actively supporting many other people with ALS and their caregivers throughout their journeys, hoping to make as big a difference as he can, while he can. Phil is also on the boards of various ALS organizations across the country. For example, a former football player at the University of Washington, Phil is on Team Gleason’s Board of Directors, which is a nonprofit founded by former New Orleans Saints player, Steve Gleason, and also part of the patient-led organization, I AM ALS. What’s needed, he says, is more attention to the disease, research and funds to bring new treatment options forward. Currently, there is no cure for ALS.
ALS is a relentlessly progressive neurodegenerative disease. For reasons that are not well understood in people with ALS, the motor neurons that allow the brain to communicate with muscles throughout the body begin to deteriorate. People with ALS experience a loss of muscle control, and ultimately, death. Many individuals suffer from significant symptoms and impaired ability to function independently as early as six months from diagnosis or 18 months from symptom onset.
“From my point of view, the more people that know about ALS and how uniquely cruel it is, the more support we can get for broader funding and more compassion for the disease,” Phil explains. “I feel like too many people are just okay with us progressing and dying because the disease has mystified scientists. The more researchers we can have focused on the mechanisms of the disease and the identification of biomarkers, the greater the chance of actually moving forward in a disease that historically has not seen much knowledge gain.”
Phil has had a lasting impact on many touched by ALS, including people with the disease, caregivers, researchers and regulatory authorities. He has even impacted those with no connection to ALS until they met him. Take Dan White, for example, who befriended Phil when they bonded over their love of sports. Almost a decade later, when Phil and others in the ALS community began to raise awareness for ALS through Amylyx Pharmaceutical’s INKEDforALS.com campaign by stamping temporary tattoos on themselves, Dan took it to the next level and tattooed the symbol on his arm — for life.
Reflecting on the decision he made one year ago, Dan shared, “I did it for many reasons, the primary one being selfish. I wanted to see the symbol every day because even if I felt I was having a bad day, I could look down and remember that my day is not so bad. My friend has been dealt a much worse hand in life, and he’s making the most out of it. The world needs to know that people as strong as Phil exist.”
Phil and Dan ask that others join in to help shine a light on ALS so that we can be a step closer to advancing the science and potentially disrupting the disease’s course.
“It’s unacceptable that when Lou Gehrig made a speech 80 years ago, he felt we would be able to cure this in his lifetime. We need to move at what we call the ‘ALS clock’ and help save the people living with the disease today.”
ALS remains a devastating disease, but some researchers believe this is a hopeful and exciting time in ALS research with many promising clinical trials and investigational products being tested at a faster pace than ever.
“I really enjoy doing what I do,” Phil says. “The level of satisfaction that comes with using my voice to help drive initiatives that the ALS community really need would not have been possible if I didn’t receive an ALS diagnosis.”
An unmet need continues to exist in ALS, but advocates like Phil continue to spark meaningful conversations that inspire hope and have the potential to lead to life-changing advances.
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