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A dad shares his emotional story of dealing with miscarriage.

'How would we bounce back from this? This wasn’t how things were supposed to go. Not for us.'

"Having children is going to be great! Nine months will fly by, and we’ll be parents. How exciting!" This was our thinking beforeit happened.

It was early August, and my wife and I were trying for our first child. We thought of all the possibilities of names, of the different transformations we could do to our guest room, and of the extra joy that would be present within our lives and in our family’s lives.

Photo via iStock.


We figured that if she ended up getting pregnant, it would work out perfectly: She could go on maternity leave during her summer break (she’s a teacher). So we checked ovulation charts and tried to time everything perfectly. We changed our diets and drank minimal alcohol and caffeine; we wanted everything to be just right.

At first, everything felt perfect.

We started taking the cheap pregnancy tests. Once they started reading positive, we sprung for the higher-end ones just to be sure. Everything was working out just as we had planned: We’d have our summer baby, and my wife would have plenty of time to stay home with the kid.

We hadn’t planned on telling anyone until the first trimester was out of the way since the most risk typically occurs during this time period.

Then we went over to some friends’ house to watch football a couple weeks prior to our "planning to tell" date. They started asking questions once they saw that my wife wasn’t drinking. (She doesn’t drink much anyway, but for her to not even have a glass of wine was odd to them.) So much to our chagrin, we ended up telling them. Then we went home.

We were getting ready for bed that night when it happened.

My wife yelled my name from the bathroom. She came out in tears. Something was wrong. There was blood. We googled it. It might not be that big of a deal, the internet said, but we called the doctor, and she said to come in the next day.

I remember that next day like it was yesterday. I had a job interview for a job that I was really excited about at the exact same time as her appointment. I bombed the interview because I was so nervous. My wife went in, and they took her blood. They did an ultrasound. The baby had a heartbeat, they said, but it was very faint. She would have to get her blood taken again a few days later to compare.

A few days came and went. One of our good friends from out of state was visiting, and we were planning on going to dinner with him. We told him ahead of time about the situation, so he knew that we might receive good or bad news sometime during dinner.

We were nearly finished with dinner when the call came. Things were not good.

They told my wife that it wasn’t a viable pregnancy and there was nothing they could do. She could take pills or let her body do the work. We said goodbye to our friend and went home.

The next week was hard. I remember holding my wife, crying with her. Our dreams, our plans — they were shattered.

Photo via iStock.

How would we bounce back from this? This wasn’t how things were supposed to go. Not for us. I was doing my best to be strong for both of us. This was the worst thing I’d ever been through. I couldn’t imagine what she was feeling. It was hard to eat. Hard to sleep. Hard to function, let alone be strong enough and assure my wife that everything would be OK.  

During the next couple weeks, friends, family, and our church pastors came and prayed with us and sat with us.

People tried to offer us encouragement. Things like "everything happens for a reason" or "it doesn’t make sense now, but it will." None of these things were helpful (other than the people being present with us).

Eventually, we learned how common miscarriages are and how many people experience it throughout their lives. The numbers (10% to 25% of all clinically recognized pregnancies end in miscarriage) were very eye-opening.

No one talks about miscarriage. It’s taboo, but it shouldn’t be. As human beings, we need to talk about these things more openly and grieve together and grow together. Our struggles and our triumphs are what bring us together.

It’s been nearly two years since my wife and I experienced the tragedy of miscarriage.

Reece, our son, is now 11 months old. It’s crazy to think that if we wouldn’t have been through what we had, he wouldn’t be here with us. He is our joy and sunshine every day, but we still mourn the loss of our first child.

But now, I often wonder what I can do to help other people, especially men whose partners are going through this same thing.

Photo via iStock.

As men, we’re often so sure we should be strong that we don’t show emotion. But I will share what I learned in that moment when we got the news: It’s OK to cry. It’s OK to let someone else pick you up.

It’s OK — and helpful — for all of us to be vulnerable. It’s OK to grieve and to mourn when life feels too heavy to bear. We will all become stronger together, and apart, if we let ourselves feel.

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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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