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5 things every new dad should do to crush the first year of fatherhood.

This week, my son had his first birthday. The last year has changed my life a lot, and I believe I have changed as a person too.

It was important to me from the very beginning that I wouldn’t be just the secondary parent. Although we live in the 21st century, it seems we are stuck in roles that are from the 1950s when it comes to parenting.

If you’d like to be an active father and an equal parent, here are a few things I learned throughout my first year as a father that might help you along your way:

1. Start talking early about the details.

Whenever people give a couple the advice to talk with each other, it seems like such a no-brainer. It seems ridiculous to even mention it. But when it comes to parenting and the question of which role you want to take on (and maybe which one you don’t) it is just so important.

I suggest you start talking really early about your ideas, as specifically as possible.

For example: When my wife and I started to discuss our parental leave while she was still pregnant, we realized that we had quite different ideas of “equal.” Only when we talked about how many months I really wanted to stay at home full-time and how much I wanted to reduce work hours after that did we realize that our ideas diverged.

Let’s just split 50/50 or 60/40 or whatever is still very general. But when you start to think about what that actually means, then you’ll have the important discussions. Suddenly it becomes something like this:

Partner 1: “Let’s do the 50/50 model. That means I’ll start work at 9:00 a.m. and leave at 1:00 p.m. Oh, wait a minute, Thursday I usually have a meeting at 9:00 a.m. and one at 3:00 p.m., which I really can’t miss. So I’ll just stay longer that one day. Ah … and maybe sometimes Monday too.”

Partner 2: “So what does that mean? I just work whenever you choose to be available? How am I supposed to plan that at my work? By the way, I need to be at the office Monday morning as well. And I can’t just always go to work at 2:00 p.m.“

That’s the moment when it gets interesting and when the actual discussions start. So stop making general comments and be specific early on. How? Write a plan, draw a sketch, create a shared calendar. Just be sure to be specific.

2. Take as much time off as you can.

When our son was born I stayed at home with my wife for about two months. Throughout the first year, I took another three months off and reduced my work time to 75%. I was lucky to live in Germany at the time I became a father, where it was technically possible to leave my job for up to 12 months while getting partially paid. Not everyone has that option, but I encourage everyone to get as much time at home with the baby as possible. Even if you can't stay home, dialing back your working hours just a little can make a huge difference.

Everything seems so peaceful and quiet before baby's arrival. Soon you'll need every pair of hands. All photos by Manuel Grossmann, used with permission

The first few months, my wife and I were both struggling with the new life, the lack of sleep, and all the new challenges and worries.

When I look at the pictures from those days, I think “Gee, we look terrible.” It is a funny mixture of what seems to be the longest sleepover ever (we were wearing PJs all the time) and the night after a rough party (messy hair, sleepy look…). But besides the fact that this is a time when there is more than enough work for two people, it is also a time that you really don’t want to miss as a father.

During those first weeks, my son and I got to know each other. I learned how to hold him, how to dress him, how to change his nappies (of course), and how to calm him down, etc.

Not everyone has that option, but I encourage everyone to get as much time at home with the baby as possible

I know a lot of fathers who were at home very little during that time or not at all due to work-related travel. In these cases, the learning curve of the mother was just so much steeper than the father’s because the mother was at home all the time.

I’ve met fathers with six-month-old babies who can’t bring their children to bed by themselves, are not able to calm them down during the night, or never stay home alone with them. This is not because fathers are genetically less connected to their child. It is simply the lack of practice that makes fathers feel uncomfortable or that the child has established those routines with the mother alone and gets irritated when suddenly the father tries to do it.

This is the time to create a strong bond between you and your child from day one. It’s not a vacation — there were times when I was tired beyond anything I’d experienced — but it helped me deepen my relationship with my son. Try not to miss that chance!

Parental leave is fun and work at the same time, like preparing and feeding lunch every day.

3. Get organized.

When you really boil it down, your daily routine after your child is born changes because of two major differences: lack of sleep and lack of time. Lack of sleep is something you get used to much quicker than you’d expect. Lack of time is what I found most challenging.

Before our son was born, my wife and I were both very active people. During the day we’d work and meet people for coffee or lunch. In the evening, we’d go out, meet friends, join professional meet-ups, or work on our own projects. Once there is a little human who needs care and attention literally 24 hours a day, your life changes quite dramatically.

I read a really good book that suggested a strict shared calendar for everything. We tried this out and it worked extremely well for us. Our calendar includes work slots, child care slots, and external babysitting. So far so good. What made the real difference is that we added individual free time and couple time as predefined placeholders. We agreed they were equally important to anything else in the calendar. Each of us had one evening per week for ourselves. This allowed us to see friends, go to meet-ups, or whatever. We also made sure to plan in regular date nights for which we would get a babysitter.

If you get organized, you'll both have time for things you enjoy as individuals. I took a print making class.

Without free time for yourself and for you as a couple, you lose a lot of your life and become dissatisfied. This will eventually have an impact on your relationship and the way you interact with your child.

4. Include your child whenever possible.

It seems a lot of people exit the world they used to live in once they become parents. But contrary to popular belief, you actually don’t change completely as a person the moment you become a parent.

Once you get over the first three months, normal life starts to come back if you allow it to. And you’d be surprised how many events you can actually attend with your child. Before our son turned one, my wife and I went to conferences, birthday parties, weddings, and even business meetings!

What I found much harder than actually bringing my son to these events was the idea of doing it. I was simply scared. However, most people are very supportive and happy when you bring your child.

For some of the events, I found it easier to go there with my wife and take turns if necessary.

Give it a try and see what works best for you. Just don’t decline invitations to all the things you still want to do.

5. Get support and ask for help.

It has always seemed odd to let other people do the things that I could do myself. When I became a parent, this attitude changed — a lot. As I said, your daily routine will change dramatically once the little one arrives. Suddenly, individual and couple time as well as sleep will be your most precious resources. Don’t waste them on things you might as well outsource.

One of the first things we did was to get someone to clean our apartment once a week. This saved us so much stress and arguments that I honestly think it was one of the best value for money investments ever.

But there are other things you can outsource. For example, I became a regular customer of services that send pre-packed recipes to your house.

Besides professional help and services, there is, of course, your family. If your family is around, then you’re lucky.

In the beginning I didn’t like the idea of my mum cooking lunch for me — it felt like going back in time and losing my independence. But when she came over with a delicious meal ready to be eaten, all doubts vanished and I was deeply thankful. Often, the small things matter the most. Like my parents or in-laws coming over and taking our son for a short walk in the park while we take a nap. Or my sister-in-law coming over to babysit while we go on a date.

One of the meals my mother brought over.

The thing about help is, it won’t magically appear on your doorstep. Often you’ll need to ask for it. This seems so hard, but once you do, you’ll discover it is worth it. So swallow your pride and ask family and close friends for help.

Believe me, it’s worth it.

The bottom line? Life is a list of priorities.

In my opinion, life is a list of priorities. You can have (pretty much) everything you want — just not everything at the same time. It is easy to find reasons why certain solutions work for others but just not for you. In most of these cases, however, they don’t work for you because you don’t want them bad enough.

Way up on top of my list: my son.

Decide what is important to you. If necessary, put these things on a list and prioritize them. Everything on on the list is either more or less important than something else.

Whatever is on top of your list is a conscious choice. And only you are responsible for it.

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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.

True

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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More Americans are supportive of the LGBTQ community than ever.

There have been numerous high-profile controversies surrounding LGBTQ rights recently that make it appear as though there has been a considerable backlash in acceptance of the LGBTQ community among Americans.

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Clearly, if people are getting riled up over the normalization of LGBTQ culture throughout America, we must be amid a considerable backlash, right? In reality, the truth is the exact opposite.

A new poll by GLAAD has found that non-LGBTQ Americans are more accepting of the LGBTQ community than ever and want them to be treated like everyone else. So, even though there is a loud contingent of political activists pushing back against LGBTQ progress, they don’t seem to significantly impact the growing movement toward acceptance.

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