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Well Being

Mom calls out 'dirtbag drivers' like her son after he killed five people drunk driving

drunk drivers, you choose, melissa macguinness

Mother speaks out about drunk driving.

This article originally appeared on September 13, 2019


Losing a child is a pain that many of us simply cannot comprehend. Given how much mothers and fathers love their sons and daughters, we can only begin to imagine how much pain they would feel when something terrible happens to their children. But for Melissa Hayes-McGuinness, a mom from Australia, the pain is even greater.

Her son, Jordan, died in a car crash in December 2012 at the age of 18. As did five other people who were unfortunate enough to cross Jordan when he was drink and drug driving at high speeds down a Gold Coast highway following a Christmas party. The five victims were sitting in a broken-down car waiting for help when Jordan collided with them at speeds of up to 87 miles per hour.

The sheer force of the crash caused the parked car to burst into flames. The only survivor was the 16-year-old driver of the parked car, who had to climb over his friends to escape the burning vehicle and suffered from severe burns and a head injury that still affects his memory to this day.

Among those killed in the parked car were a 20 and 23-year-old, their 15-month-old girl was orphaned. The other victims were 16, 17, and 18.


SOURCE: YOU CHOOSE / MELISSA MCGUINNESS

As you can imagine, Melissa has to deal with unimaginable grief on a daily basis. Not only for her son, but for those he killed, and those they left behind. But thankfully, Melissa has found a way to channel that grief positively. Every year, she travels across Australia speaking to teenagers about road safety. As part of her talks, she reads an incredibly powerful speech which she calls "Jordan's confession."

Her speech reads, in part:

"I would give anything that night to have just hit a tree and not left this horrendous legacy," Melissa begins. "Those kids didn't deserve what happened to them. In truth, I guess I did."

"I screwed up and paid the ultimate price. What I did was unforgivable," McGuinness continues, speaking on behalf of her son and addressing the orphaned girl, "I'm the reason you'll never see your mummy and daddy [again]."

Throughout the speech, Melissa shows photos of her son, including on his last day of school. Then, the photos changed to a news clip of the accident, showing blue flashing lights and twisted metal.

"Jordan was smart. Jordan was funny. Jordan was a great person, but none of that means anything now. None of it," McGuinness continues to tell the teenagers sitting in silence before her, many of whom are usually crying at this point.

"That's because he defined himself by his choices that night. He shaped a terrible and permanent legacy for himself, his family and his victims' families because he chose to drink, smoke [marijuana] and speed down that highway."

"And everything he did before that just pales in comparison."

"As much as there are hundreds of reasons to be proud of Jordan... he died in shame," his mother tells them, "This is how he's going to be remembered. There's no getting around that.

"My husband and I did not raise him to think that drink or drug driving was acceptable behavior, yet I stand up here as the mother of a kid responsible for the death of four kids from drinking and drug driving."

"Think of all the good stuff that you've done. Think of all the effort you've put into your life. Think of all the effort people who have loved you put into your life. And imagine all of that being wiped out by one stupid choice. Because that's the brutal reality of what happens."

"I still love Jordan profoundly, I miss him terribly... but this can't be sugarcoated. He defined himself permanently by his actions that night.

"There are accidents and there are choices. Jordan didn't have an accident that night. That's what happened to his victims. Jordan made a choice."

SOURCE: YOU CHOOSE / MELISSA MCGUINNESS

Melissa affectionately calls the teenagers she's talking to, particularly boys, "dirtbags." Why? Because they often think they're "ten foot tall and bullet-proof."

Following the death of her son and his victims, Melissa started the You Choose - Youth Road Safety campaign. It teaches young drivers about the devastating, life-long consequences of being reckless behind the wheel.

Melissa knew that most teenagers won't learn anything through a lecture, so instead, she channels her own grief by telling her own story.

"I'm not lecturing them about right or wrong, I'm demonstrating through actual lived experience what it's like to be on the receiving-end of what I was," Melissa told Yahoo News.

"I show them a clip from Jordan's memorial ceremony and I ask them to imagine while they're watching it what it might be like if their family was in the same predicament that my family's [going through]."

"But pretty much just taking them on this entire grief journey from where it started—as the excited teenager about to start his life to the horrible accident through one stupid choice one night. Then what it looked like for everybody else involved."

"The thing with... Jordan is he's relatable because he's just like any other kid there that's sitting in that auditorium... and I'm also relatable as the mum."

"[Through Jordan they're shown] this great kid that made this one stupid choice that could be any of those kids. Any of them."

Melissa says her talks are so powerful because she's the "perpetrator's mother."

The guilt of her son's actions have weighed so heavily on Melissa that she often felt like she "didn't have a right to grieve her son".

"Those kids were innocent kids, they were doing nothing wrong and my son behaved 100 percent irresponsibly and was completely responsible for their deaths."

SOURCE: YOU CHOOSE / MELISSA MCGUINNESS

Each time Melissa talks to a group of kids, it gets a little easier for her. It gets easier to watch footage from the crash, and somehow, it gets easier to watch footage of Jordan's then 10-year-old sister breaking down at the memorial service.

But one thing doesn't change. The reaction from the kids she's speaking to. Melissa says that no matter the type of school or the age of the kids, with very little encouragement, the kids always swarm her with hugs at the end of her speech. In most instances, she says, the instigator is usually the "biggest dirtbag in the room"

"I have a remarkable story to tell. It's the worst story. And I feel really compelled to share that with teenage kids," she told 9now.

"This is what is left behind: Here is the mum that has to attend your funeral, has to pick up the pieces. That car can become your own coffin."

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Three women, three MS journeys: How multiple sclerosis looks different for everyone

Gina, Nathalie and Helga share their reactions to being diagnosed with MS and how they stay informed and positive in the face of ever-changing symptoms.

Courtesy of Sanofi

Helga, Nathalie and Gina all have MS, and their experiences show how differently the disease can manifest.

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It’s been 155 years since neurologist Jean-Martin Charcot gave the first lecture on a mysterious progressive illness he called “multiple sclerosis.” Since then, we’ve learned a lot. We know MS causes the immune system to attack healthy tissue, including damaging the brain and spinal cord. Resulting symptoms can be debilitating and include fatigue, blurred vision, memory problems and weakness. Huge advancements in our understanding of MS and its underlying causes, as well as treatment advances, have been made in the past few decades, but MS remains a complex and unpredictable reality for the 2.8 million+ people diagnosed around the world.

Ironically, the only real constant for people living with MS is change. There’s no set pattern or standard progression of the disease, so each person’s experience is unique. Some people with MS have mild symptoms that worsen slowly but sometimes improve, while others can have severe symptoms that drastically alter their daily lives.

All people with MS share some things in common, however, such as the need to stay informed on the ever-evolving research, find various lines of support and try to remain hopeful as they continue living with the disease.

To better understand what navigating life with MS really looks like, three women shared their MS stories with us. Their journeys demonstrate how MS can look different for different people and interestingly, how the language used to talk about the disease can greatly impact how people understand their realities.

woman with horse, woman riding horseGina loves riding her horse, Benita.Courtesy of Sanofi

Gina—Hamburg, Germany (diagnosed with relapsing multiple sclerosis in 2017)

When her youngest son was 4 months old, Gina started having problems with her eye. She’d soon learn she was experiencing optic neuritis—her first symptom of MS.

“Immediately after the diagnosis, I looked up facts on MS because I didn’t know anything about it,” Gina says. “And as soon as I knew what could really happen with this disease, I actually got scared.”

As her family’s primary income provider, she worried about how MS would impact her ability to work as a writer and editor. Her family was afraid she was going to end up in a wheelchair. However, for now, Gina’s MS is managed well enough that she still works full-time and is able to be active.

“When I tell somebody that I have MS, they often don't believe me the first time because I don't fulfill any stereotypes,” she says.

Overwhelmed by negative perspectives on living with MS, Gina sought support in the online MS community, which she found to be much more positive.

“I think it’s important to use as many positive words as you can when talking about MS.” It’s important to be realistic while also conveying hope, she says. “MS is an insidious disease that can cause many bad symptoms…that can be frightening, and you can't gloss over it, either.”

To give back to the online community that helped her so much, Gina started a blog to share her story and help others trying to learn about their diagnosis.

Though she deals with fatigue and cognitive dysfunction sometimes, Gina stays active swimming, biking, riding horses and playing with her sons, who are now 11 and 6.

Cognitive dysfunction is common in MS, with over half of people affected. It can impact memory, attention, planning, and word-finding. As with many aspects of MS, some people experience mild changes, while others face more challenges.

Gina says that while there’s still a lot of education about MS needed, she feels positive about the future of MS because there’s so much research being done.

woman in wheelchair holding medal, woman rowingNathalie is an award-winning rower with multiple international titles.Courtesy of Sanofi

Nathalie — Pennes Mirabeau, France (diagnosed with relapsing-remitting multiple sclerosis in 2002)

Nathalie was a teenager and a competitive athlete when she noticed her first symptoms of MS, but it would take four years of “limbo” before she was diagnosed.

“Ultimately, the diagnosis was more of a relief, than a shock,” she says. “Because when you have signs and you don’t know why, it’s worse than knowing, in the end, what you have.”

However, learning more about the disease—and the realities of disease progression—scared her.

“That glimpse of the future was direct and traumatic,” she says. Her neurologist explained that the disease evolves differently for everyone, and her situation might end up being serious or very mild. So, she decided to stop comparing herself to others with MS.

She said to herself, “We’ll see what happens, and you’ll manage it bit by bit.”

By 2005, Nathalie’s MS had progressed to the point of needing a wheelchair. However, that has not dampened her competitive spirit.

Nathalie began her international rowing career in 2009 and has won multiple world titles, including two Paralympic medals—silver in London and bronze in Tokyo. Now, at 42, she still trains 11 times a week. Fatigue can be a problem, and sometimes hard workouts leave her with muscle stiffness and shaking, but she credits her ongoing sports career for helping her feel in tune with her body’s signals.

“Over the years, I’ve learned to listen to my body, letting my body guide when I need to stop and take breaks,” she says.

Nathalie explains that she used to only look backwards because of the initial shock of her diagnosis. In time, she stopped thinking about what she couldn’t do anymore and focused on her future. She now lives in the following mindset: “Even when doors close, don’t miss out on those that open.” Instead of focusing on what she can’t do, she focuses on the opportunities she still has. Right now, this includes her training for the 2024 Paralympic Games in Paris, where she will compete for another rowing medal.

“I only go forward,” she says. “Well, I try, anyway…It’s easy to say, it’s not always easy to do. But that’s what I try to do.”

woman exiting water after swimming, woman with great daneHelga's Great Dane has become a helpful and beloved companion.Courtesy of Sanofi

Helga—Johannesburg, South Africa (diagnosed with relapsing multiple sclerosis in 2010)

When Helga first started having balance issues and numbness in her feet, she chalked it up to her training as a runner. But when the numbness moved to her face, she knew something was wrong. She never guessed it was MS.

“When I was diagnosed, I felt completely overwhelmed and clueless,” Helga says. “I felt that I had nowhere near enough information. I did not know anything about the disease…I had no idea that it was going to be a process of continually monitoring and adjusting your lifestyle.”

In the beginning, Helga’s symptoms developed slowly, and she didn’t appear ill to others. She was even able to run for a few years after her diagnosis, but she couldn’t do marathons anymore, and she began to fall frequently due to balance issues and right-foot dragging. Then her cognition issues became more problematic, especially in her job as a trainer in a printing company.

“My executive function, decision-making and short-term memory were affected to the point that I was eventually medically unfit for work,” she says. She stopped working in 2017.

However, she didn’t stop living life. Even though she could no longer run, she continued to swim competitively. She got a Great Dane puppy and trained him as a service dog to help her walk. She also serves as vice chair of the patient support organization Multiple Sclerosis South Africa, and she advises others who have been diagnosed to join a patient advocacy group as soon as possible to get reliable information and meet others with MS.

Helga says she is “hopeful” about the future of MS. “I must say that I am so grateful that we have all the new medications available, because my life would not be the same if it wasn't for that,” she adds.

Part of how she manages her MS is by looking at the positives.

“If I could tell the world one thing about MS, it would be that MS is an incurable disease of the nervous system, but it's also the greatest teacher of valuing your health, family, friends, and managing change in your life,” she says. “My life is diversified in a way that I never, ever thought it would, and MS has been honestly the greatest teacher.”

Each MS journey is unique – with each person impacted experiencing different struggles, successes, and feelings as they manage this unpredictable disease. But the common thread is clear – there is a critical need for information, support, and hope. We are proud to participate in World MS Day and share these incredible stories of living life while living with MS. To learn more about MS, go to https://www.sanofi.com/why-words-really-matter-when-it-comes-to-multiple-sclerosis.

MAT-GLB-2301642-v1.0-05/2023

This article was sponsored by Sanofi. Participants were compensated when applicable.

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