Just before his death at age 35, Game of Thrones actor Michael Patrick shared a final social media message, saying he had ‘lots planned’ for the future.
Michael Campbell, a well-known actor on television and stage, died on Tuesday at Northern Ireland Hospice. He had been receiving care there for ten days after a three-year struggle with Motor Neurone Disease.
Michael shared an update on his journey with MND, saying it’s been three years since his diagnosis and remains challenging. He and his wife, Nomsheehan, recently spent over a week in the hospital undergoing tests and consulting with doctors.
We discussed the potential risks and what to expect daily after getting a tracheostomy. We covered how life would change after the procedure.
‘In short I’m not going ahead with the tracheostomy.
I was told it would likely take between six and twelve months before I could return home, because they didn’t have enough staff.
We’re incredibly grateful for all the support we’ve received – from the hospital CEO and politicians to our dedicated social workers. Everyone worked tirelessly on this, but unfortunately, we’re still facing a critical staff shortage.
Michael was told by his doctors that he likely had about a year left to live, but unfortunately, he died just a few weeks after receiving that news.
He added that his neurologist believes he probably has around a year to live, though it’s impossible to know for sure. They’re still hopeful that a new drug trial might extend his life.
‘So I don’t want to risk a significant amount of that time being in a hospital bed.
Thank you all so much for your incredibly generous donations to the GoFundMe. Even though I ultimately decided not to have the tracheostomy, the funds will still be used to help cover the costs of specialized care as I navigate the final stages of my life. I’m truly overwhelmed by your kindness.
Despite everything, I’m staying positive and have plenty to look forward to. I was happy to receive a visit from my godson, Micheál, while I’m in the hospital.
It is with a heavy heart that I share the news of Michael’s passing. His wife, Naomi, let us know he passed away peacefully, surrounded by the love of his family and friends. It’s a reminder to cherish those moments with loved ones, and I’m sending my deepest condolences to Naomi and everyone who knew him.
In a social media post, she wrote: ‘Words can’t describe how broken-hearted we are.
Many people have said that Mick inspired everyone he met, not just during his recent illness, but throughout his entire life.
He lived a truly rich and fulfilling life, filled with happiness, a strong spirit, and a contagious laugh. He was a larger-than-life man with bright red hair. We are deeply thankful to everyone who stood by us during the past few years.
After earning a science degree from the University of Cambridge, Michael pursued his passion for acting at Mountview Academy of Theatre Arts in London.
He’s been on TV in shows like Blue Lights, Game of Thrones, Soft Border Patrol, and My Left Nut.
He gained significant recognition for his theatrical work, most notably his award-winning portrayal of Richard III. He performed the role in a wheelchair and received the Judges’ Award at the Stage Awards in January 2025.
Even after being diagnosed, Michael kept acting. He found that performing and writing helped him stay positive by giving him something else to concentrate on besides his illness.
In 2025, he was honored with the Overcoming Adversity Award at the Spirit of Northern Ireland Awards, recognizing his ongoing efforts and support for others following his diagnosis.
The Lyric Theatre Belfast, where Michael regularly performed, paid tribute in a statement.
Jimmy Fay, the executive producer, shared that Mick demonstrated incredible strength and grace after being diagnosed with Motor Neurone Disease (MND). Despite his illness, he continued to work with energy and passion. He even performed his one-man show, ‘My Right Foot,’ on the Lyric stage as recently as last November.
Everyone at the Lyric is deeply saddened by the loss of a truly gifted artist, and we extend our heartfelt sympathy to his wife, Naomi, his mother, sisters, and all who knew and worked with him. His passing is a great loss for our community, but we find comfort in knowing his spirit shines on.
The exact cause of Motor Neurone Disease (MND) remains a mystery, and unfortunately, there are no cures available yet. Doctors currently concentrate on managing the symptoms to improve quality of life.
Approximately 5,000 adults in the UK currently live with this condition, and there’s about a 1 in 300 chance of someone developing it during their life.
The disease causes muscle weakness that gets worse over a few months or years,
The first signs of the condition often involve stiffness or weakness in the hands, legs, and feet, which can lead to frequent tripping. Muscle twitches, spasms, or cramps may also occur.
As motor neuron disease progresses, people often find it increasingly difficult to breathe, swallow, and speak. Ultimately, the condition leads to a loss of movement and the ability to walk.
For roughly half of those diagnosed with this condition, life expectancy is only two to five years after symptoms first appear. Unfortunately, these symptoms often get worse quickly.
Michael is remembered by his wife, Naomi, his mother, Pauline, and his siblings Kate, Maurice, and Hannah. He is also survived by his nephew, Michael.
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2026-04-09 19:49