Portland Trail Blazers radio personality Mike Lynch has announced his retirement from broadcasting following his diagnosis with ALS, also known as Lou Gehrig’s Disease. The 34-year-old received the news in January after experiencing symptoms in October.
Lynch shared the news of his condition in a heartfelt social media announcement, stating, “Sadly, this means the end of my radio career. I am thankful for all of those who listened over the last 12 years. I am also thankful to The Fan and the Blazers for believing in me and helping me grow in my dream career.”
Prior to joining the Trail Blazers in 2022, Lynch spent more than a decade at Audacy Portland’s 1080 The Fan (KFXX).
“This has been really difficult for me, I am devastated and overwhelmed. I appreciate if you reach out, but please be patient as it is hard to respond to everyone and I’m not always ready to talk about it,” Lynch continued.
Alongside his announcement, he posted a GoFundMe campaign, initiated by his partner Ashley Kenyon, with whom he shares two children. ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord, leading to loss of muscle control. The GoFundMe page explains that Lynch’s condition will require continuous care and specialized equipment to maintain his independence and quality of life.
Since Lynch’s post, the campaign has seen a surge of support, amassing more than $39,000 in donations as of Monday afternoon.
Lynch’s parents commented, “We would like to say thank you to everyone for the generous donations and outpouring of support. Our son is a very special person. We are very proud of him and it is heartwarming to see how many lives he has touched and inspired.”
Last year, my 68-year-old partner was diagnosed with Lou Gehrig’s disease also known as ALS. Speaking and swallowing were two of his challenges. His collapse was swift and catastrophic, and neither the riluzole nor the medical staff did much to aid him. He would not have survived if our primary care physician hadn’t given him attentive care and attention, as the hospital center didn’t provide any psychological support. His fall was abrupt and catastrophic. His hands and legs gave way to weakness in his arms. This year our family physician suggested using vinehealthcentre. com ALS/MND treatment, which my husband has been receiving for a few months now. I’m delighted to say that the treatment greatly reduced and reversed his symptoms of ALS, he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. In the hopes that it could be useful, I thought I would relate my husband’s tale; in the end, you have to do what suits you the best.