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If you come from a blended family, these real-life accounts will hit home.

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Every family is different. Every family is special.

That's something we hear often. Whether it's written in children's books or on TV shows, the message that every family is unique is something that's become ingrained in us.

What makes a family a family, though? For a long time, we were taught that it was just a biological bond — that the people you're born to are the people you belong to for a lifetime.


Of course, now we know that's just one kind of family. It's one small part of a much bigger picture.

[rebelmouse-image 19397764 dam="1" original_size="700x467" caption="Photo by Vasile Tiplea/Unsplash" expand=1]Photo by Vasile Tiplea/Unsplash

Today, more and more people are members of blended families.

According to the US Census Bureau, over 50 percent of families in America consist of people who are re-married or re-coupled. More than 1300 step-families come together every day. Recent statistics also show that more than 135,000 children are adopted every year in America.

These family members may not all share biological bonds, but they share something just as important: love.

[rebelmouse-image 19397765 dam="1" original_size="700x467" caption="Photo by rawpixel/Unsplash" expand=1]Photo by rawpixel/Unsplash

While being part of a blended family can be as rewarding as every primetime TV show makes it out to be, it can also be a challenge. But we often don't talk about the realities of what it's like to be a member of such a unit.  

That's why Sean Anders, writer and director of the upcoming movie "Instant Family" wanted to make something that was different and real.

Anders and his wife are the parents of three children who they adopted in 2013 who also happen to be the inspiration for Anders' film.

"I wanted to tell a more complete story that doesn't shy away from the tragedy or the trauma, but also really gets into the laughs, and the love, and the joy involved as well," he says of the new film.

"We hit upon the idea of adoption exactly like it happens in the movie. I made that same joke to my wife, that I was feeling like I was gonna be too old of a dad, and she said  'Why don't we just adopt a five year old? It'll be like I got started five years ago.' I was totally kidding. But, she took it seriously enough to get us moving down the road." Anders was on board, but could never have anticipated the challenges, or the rewards for that matter.

"You go through this really awkward time where you have these people in your house who, you're supposed to be their parents, and you don't love them. And they don't love you. You don't even know each other yet. You go through some really difficult transitional times, but you also get this amazing experience of getting to fall in love with your kids."

We wanted to know more about what it's like to come from a blended family.  So we asked. Real people answered.

Here are 5 people's true stories of the ups, downs, and life-changing experiences that being part of a blended family brings.

1. Krista Ball was raised by her grandparents, and learned family are the people who accept you for who you are.

"I was adopted as an infant by my maternal grandparents. Children being raised by other family members was fairly common where I grew up (Newfoundland, Canada), so I didn't feel isolated or weird. My teens were tough, though, as I went through a lot of identity issues. I wondered why my biological mother gave me up, but kept her other children.

"As an adult, I absolutely understand those kinds of decisions and I feel no malice or ill-will. It was the best decision for her in that time and place. But I didn't have the tools to understand that at fifteen. I didn't know my biological father's identity until I was in my 30s."

"Family is such a strange thing. I think it's the people who teach you things, who accept you the way you are, and who try to do what's best for you. Mom and Dad (her grandparents) are my family, and I am fiercely protective of them. There is a kind of connection that is beyond simple genetics and shared last names. I was given the best possible life for me. As I get older, I am so grateful for that. Whatever struggles I had as a teenager were worth it, in the long run."

2. Courtney Lipsham is a step-daughter and became a step-mother three years ago at 19-years-old. As such, she thought she knew what to expect. She didn't.

[rebelmouse-image 19397766 dam="1" original_size="750x563" caption="Photo by Sestrjevitovschii Ina on Unsplash." expand=1]Photo by Sestrjevitovschii Ina on Unsplash.

"I come from a blended family and I’ve always had my step-mum around since I was young. I don’t actually remember a time when we weren’t a blended family. When I met my partner I had false hope in the fact that I’d grown up in a blended family fine, so taking on becoming a part of his would be easy, which is quite a misconception I’ve heard among step-parents.

"Between issues with the bio mum, families, living far away from his daughter, and the terrible twos, it’s been challenging to say the least. However, being a part of this family is the most rewarding decision I’ve ever made, especially now his daughter is four and we can go on little adventures together. Seeing her come out of herself with bundles of confidence and watching her grow up is a blessing I never imagined!"

"I’m just so proud of her and so proud of the journey we’ve come on as a family."

3. Louis Swingrover's family is even more unique than most blended families. He can't imagine it being any other way.

[rebelmouse-image 19397767 dam="1" original_size="750x500" caption="Photo by Brittany Simuangco on Unsplash." expand=1]Photo by Brittany Simuangco on Unsplash.

Photo of the Swingrover family by Amber Glanville.

"My wife and I have four children-two biological boys, a girl we adopted through the foster care system, and another girl we are currently fostering. It might be the case that blended families in general tend to have some features that are not as common in other kinds of families, but to be honest, I have no idea what those are! I am only aware of what it is like to be a part of my family. It is incredible, innervating, embarrassing, pride-giving, life-giving, depressing and uplifting."

"We have contact with members of our daughter’s family of origin. This means that a distinct kind of extended family is attached to ours, which can be both challenging and rewarding. No other reward in life, however, has the distinct quality that raising an adopted child does. Watching my daughter thrive, and knowing that I played a teeny tiny role of some kind in that is marvelous. But what is more profound to me is the attachment we have formed."

"I will never forget the moment I learned that she would be issued a new birth certificate. It does not list us as the biological parents (our version of the certificate does not include them), it just simply lists as us as her parents, period. From the legal to the relational, I cannot help but marvel at the sheer miracle of her being ours. "

4. Tiffany's new siblings helped heal her relationship with her father.

[rebelmouse-image 19397769 dam="1" original_size="750x1125" caption="Photo by Conner Baker on Unsplash." expand=1]Photo by Conner Baker on Unsplash.

"My parents went through a nasty divorce when I was nineteen which strained me and my younger sister’s relationship with our father for quite some time. When my father reached out a few years later to let me know that he was expecting a child and marrying a woman I’d never met, I was completely caught off guard."

"This woman was not that much older than me, and I was in the midst of planning my own wedding when I received the news. I remember thinking that I was entirely too old to have an infant sibling."

"Five years (and three new siblings) later, I get to be a big sister to these tiny impressionable little humans and I gained an awesome stepmom in the process. As an added bonus, the births of my new siblings brought my father and I back together and our relationship has never been stronger. Their existence forced my father and me to work through our issues to ensure that they do not grow up witnessing the conflict that infiltrated my childhood home."

"One of the best things about being in a blended family is that I get to feel those warm feelings of nostalgia when I see my dad teaching my younger siblings some of the same fun traditions I got to enjoy as a child."

5. Jill Johnson Young has been widowed twice and has three adopted daughters. Their bonds are too strong to ever be broken.

Linda Johnson-Young and Kerry Johnson-Young, Photo courtesy of Jill Johnson-Young.

"One memory, I will never forget was the first night our oldest child, Kerry, was at home with us for good. We'd been visiting her on day visits for weeks while we waited for her to finish her school year. We brought her home the day school ended. "

"That night we bathed her, helped her dress in her little jammies, and brushed her hair. We read stories, said bedtime prayers, made sure she had enough lights on, and kissed her goodnight."

"30 minutes later she came back out of her room, and looked really scared. She said 'I can't sleep. Can I come spend time with you guys?' We took her into our room, and turned on Ann Murray singing 'Can I Have This Dance?' We picked her up and laid her across our arms, holding her like a hammock laying between us, and slowly danced with her while her eyes started to slowly trust us enough to close."

"It's the moment you know your child has decided she is yours, and that remarkable ability to trust big people again after so much trauma. I keep it close to me."

When she's missing my first wife, her mama, Linda, I tell her the story again. All of us wrapped together. A new family that she knew would be hers — we just needed to find her."

There is no right way to be a family. Love, support, and understanding are what truly make the people in your life your closest allies.

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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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