Kenneth Mitchell, the Canadian actor🐎 who is best known for his roles inꦉ the television series "Star Trek: Discovery" and the Marvel film "Captain Marvel," passed away on Saturday at the age of 49. He had been battling amyotrophic lateral sclerosis (ALS) for over five years.
Mitchell's family shared the news on his social media accounts, stating that he had lived with the debilitating neurological disease for more than five years. Despite his diagnosis in 2018, Mitchell's dedication to his craft never wavered. He continued to work, inspiring others with his resilience and leaving behind a leg๊acy of diverse and memorable roles💛 across film and television.
Audiences first encountered Mitchell in various television shows, including "Miracle," where he portrayed a hockey player, and the post-apocalyptic drama "Jericho," where he held a leading role as Eric Green. He also appeared in several other prominent series like "NCIS✨," "Grey's Anatomy," and "Criminal Minds," showcasing his versatility and talent.
In 2017, Mitchell joined "Star Trek" universe, portraying the Klingon warriors Kol, Kol-Sha, and Tenavik in "Star Trek: Discovery." He later voiced characters in "Star Trek: Lower Decks," further solidifying his place in the beloved sci-fi franchise. Beyond his captivating screen presence, Mitchell was known for his strong work ethic and dedi💟cation to understanding his characters. In a 2017 interview with StarTrek.com, he expressed his desire to challenge viewers' perspectives on the Klingons, stating, "Whether someone is good or bad is all about perspective, and it's about understanding that culture."
Mitchell's final years were marked by both personal challenges and continued artistic commitment. He continued to act, prioritizing time with his wife, actress Susan May Pratt, and their children Lilah and Kallum. He even adapted his work, turning down 👍a lead role that required relocation for his family and working with the creators of "Nancy Drew" to ensure his participation despite his physical limitations.
What is ALS?
Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. These nerve cells, called moto⛎r neurons, are responsible for sending messages from the brain to the muscles, controlling voluntary movements like walking, talking, swallowing, a🍷nd breathing.
In ALS, these motor ne🐈urons gradually deteriorate and die, leading to:
1. Muscle weakness: This is the first and most prominent symptom🧔, typically starting in the limbs and progressing to other muscle groups.
2. Muscle atrophy: As the muscles are no longer receiving signals from the brain, they beඣgin to waste away and shrink.
3. Muscle twitching (fasciculations): These are in💃voluntary muscle contractions that can be visible under the skin.
4. Difficulty speaking (dysarthria): The muscles involved in speech become weak, making it sl🐈urred or difficult to understand.
5. Difficulty swallowing (dysphagia): This can lead to malnutrition and dehydration.
6. Difficulty breathing: Eventually, the muscles controlling respira𒈔tion become affecte🌞d, requiring the use of a ventilator.
While the exact cause of ALS remains unkꦇnown, several factors are believed to contribute to its development, including:
Genetics: About 10% of AL♍S cases are considered familial, ꦇmeaning they run in families due to specific gene mutations.
Environmental factors: Exposure to certain toxins or environmental fac🐼tors may increase the risk.
Abnormal protein buildup: Clumps of proteins called TDP-43 accumulate in the motor n𝓡eurons, contributing to th♔eir damage and dysfunction.
Unfortunately, there is no cure for ALS. However, several treatment options can ♚help m♚anage symptoms and improve quality of life, including:
Medications, Physical ther🍷apy, Occupational ther🌳apy, Speech therapy, and Respiratory therapy.
ALS is a progressive and fatal disease. The average life expectancy aft🌼er diagnosis is 3-5 years, although some individuals may live longer with proper care and support.
