WHEN Darren Lundy popped out to get some milk and cigarettes on May 12th 2018, there was no reason for his wife Sarah to be worried.
But that fateful evening more than eight years ago soon turned their lives upside down when the beloved dad-of-three never returned home.
Sarah met Darren in 2004 when both were in their thirties and quickly realised she had found the person she wanted to spend her life with Credit: The Widowed Collective
their fairytale story was crushed when Darren was diagnosed with multiple sclerosis Credit: The Widowed Collective
The following was an agonising ordeal – one filled with phone calls, desperate searches and agonising uncertainty, as Sarah tried to hold everything together for their young son Charlie, nine, and stepchildren Jake, 31, and Elliss, 33.
Then, three days later, Darren was, unfortunately, found dead in his car – he had at the age of 50.
“When he was found, everything changed forever. The hardest thing I have ever done was tell my nine-year-old son that his dad wasn’t coming home,” Sarah, 57, from , said.
“As a parent, every instinct you have is to protect your child from pain, but in that moment I was the person delivering the worst news he would ever hear. Watching your child’s heart break in front of you is something that never leaves you.”
Sarah with her son Charlie, who is nine Credit: The Widowed Collective
Without life insurance and with a child depending on her, Sarah returned to work just four weeks after Darren’s death Credit: The Widowed Collective
Although the year before, in 2017, Darren was experiencing serious difficulties, he appeared to have improved and Sarah believed the family had weathered the worst.
Instead, Darren had quietly made a different decision and his body was later found in his vehicle in a hospital car park. Grief-stricken Sarah believes her dear husband had gone because he did not want his family to be the ones who found him.
Sarah met Darren in 2004 when both were in their thirties and quickly realised she had found the person she wanted to spend her life with. At the time, she had never imagined herself getting married and had not planned on becoming a parent.
Darren already had two young children and, together, they began building a life that felt full of possibility and hope.
But their fairytale story was crushed just six months later when Darren was diagnosed with multiple sclerosis – an autoimmune condition that affects the brain and spinal cord.
The disease, which can cause fatigue, pins and needles, numbness or burning, problems with eyesight, memory and thinking problems, and walking difficulties, is thought to affect more than 150,000 people in the UK, according to Multiple Sclerosis Trust .
Every week around 135 more people are diagnosed with this lifelong condition, which can also lead to muscle stiffness and spasms, bladder and bowel problems, and sexual difficulties.
At the moment, although there are treatments to treat the symptoms, there is no cure for multiple sclerosis.
How to get help
EVERY 90 minutes in the UK a life is lost to suicide
It doesn’t discriminate, touching the lives of people in every corner of society – from the homeless and unemployed to builders and doctors, reality stars and footballers.
It’s the biggest killer of people under the age of 35, more deadly than cancer and car crashes.
And men are three times more likely to take their own life than women.
Yet it’s rarely spoken of, a taboo that threatens to continue its deadly rampage unless we all stop and take notice, now.
If you, or anyone you know, needs help dealing with mental health problems, the following organisations provide support:
- CALM, www.thecalmzone.net , 0800 585 858
- Heads Together, www.headstogether.org.uk
- HUMEN www.wearehumen.org
- Mind, www.mind.org.uk , 0300 123 3393
- Papyrus, www.papyrus-uk.org , 0800 068 41 41
- Samaritans, www.samaritans.org , 116 123
Determined not to let the disease define him, Darren continued working as a heating and ventilation engineer in schools and hospitals across the North West.
Proud, hardworking and fiercely independent, he rarely wanted to discuss his condition and preferred to focus on living life as normally as possible. The couple later married and welcomed their son, Charlie.
However, as the years passed, Darren’s condition became increasingly severe, gradually robbing him of his mobility, independence and confidence.
One by one, like a line of dominoes, the dad-of-three lost almost everything. He struggled to walk, lost fine motor skills, found everyday tasks increasingly difficult, experienced short-term memory loss, and became more isolated as his condition worsened.
But Sarah didn’t just have to be there for her husband. As the disease progressed, Sarah, who works as a marketing director, found herself taking on growing responsibilities both financially and practically as she supported Darren and cared for their family.
Sarah said: “When we met, Darren was funny, capable, hardworking and full of life. We genuinely believed we could face whatever Multiple Sclerosis threw at us because we faced everything together.
“Over time, though, the disease changed every aspect of our lives. The man who had always looked after everyone else gradually lost the ability to do so many of the things most people take for granted.
“Multiple Sclerosis doesn’t just affect the person who is diagnosed, it affects relationships, finances, family life, mental health and the future you thought you were going to have.
“We were still each other’s person and we still loved each other deeply, but our relationship changed. I became a carer as well as a wife, and that was incredibly difficult for both of us.”
By 2017, Darren’s physical health had deteriorated significantly and he was experiencing serious mental health difficulties linked to the progression of his illness. Sarah spent months living with the constant fear that she might lose him as mental health crisis teams became involved in his care and every day felt uncertain.
When Darren appeared to improve, Sarah believed the family had weathered the worst. Instead, Darren had quietly made a different decision, and on the evening of 12th May 2018, he left home telling Sarah he was going out for milk and cigarettes.
That was the last time the family ever saw him alive.
“The days that Darren was missing were the most traumatic days of our lives. Every time the phone rang, my heart stopped, and every knock on the door filled us with dread,” Sarah painfully recalled.
“Part of me knew what had happened, but hope is an incredibly powerful thing. You convince yourself there must be another explanation and that somehow they’re going to walk back through the front door.”
The period that followed was consumed by shock, and survival. While trying to process the loss of her husband, Sarah was also faced with the dark realities of widowhood. There was a to organise, official procedures to navigate, an inquest still to come, and a young son who needed stability and reassurance during the most difficult period of his life.
Without life insurance and with a child depending on her, Sarah returned to work just four weeks after Darren’s death.
For Sarah, looking back, she says one of the most difficult aspects of widowhood was realising how quickly support can disappear.
Sarah said: “People are incredibly kind when someone dies and I will always be grateful for that support. The reality, however, is that life naturally moves forward for everybody else while your grief comes with you into every new day.
“Many assume that because time has passed, you’re okay. The truth is that widowhood changes you forever, and there are moments years later when you still need support, but people stop asking how you are because they think you’ve moved on.
“Grief is often seen as the hardest part, but what nobody prepares you for is the moment everyone else’s life starts returning to normal while yours never can. The cards stop arriving, the messages become less frequent, and the phone stops ringing, but you’re still carrying the same loss every single day.
“That feeling of being forgotten is something so many widows and widowers experience, which is exactly why this campaign matters.”
She continued: “My advice to anyone facing widowhood is to reach out, even when every instinct tells you not to. Finding people who truly understand doesn’t take away the pain, but it reminds you that you don’t have to carry it alone.”
Sarah is now a board member of The Widowed Collective and credits the organisation with helping her connect with others who truly understand life after loss.
The Widowed Collective provides free peer-to-peer support for people who have lost a life partner. Through its online community, practical guidance, events and lived-experience support network, the organisation helps widows and widowers navigate life after loss and find connection with others who understand.
For more information about the #WidowedAndForgotten campaign, or to join The Widowed Collective for free, visit www.TheWidowedCollective.com .



