People who’ve had their families upended by DNA websites reveal what happened.

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People who’ve had their families upended by DNA websites reveal what happened.

According to Divorce Statistics, 2% to 3% of all children are born out of infidelity and most of these children are unknowingly raised by men who are not their biological fathers.

These days, with the availability of so many DNA websites like 23andMe and Ancestry, a lot of people are discovering things that maybe they didn't really want.

A viral post on the askReddit forum asked how these new websites have affected families — "People whose families have been destroyed by 23andme and other DNA sequencing services, what went down?"

Here are the best responses to the question:

1. Finding family

“I’ve been searching for my father my whole life and through 23andme I just found a half-brother, finally answering the question. Our father is unfortunately passed, but we’re meeting in person in April.

A couple weeks after we found each other we were also contacted by another half-sister.”

2. Inconclusive

“My brother got our whole family 23andMe kits for Christmas last year. Everyone did the swab and got their results back which showed how we’re all related and yada yada yada, but my results came back inconclusive. 23andMe sent me a new kit to do it again and THAT one also came back inconclusive. So the company sent me an email basically saying I can never do it again probably because I’m using a bunch of resources with no results.

Anyway now my family says I don’t have any human DNA and that I must be a lizard. They make lizard sounds when I’m around and I am ashamed.”

3. What are the chances?

“Kind of the opposite. I found out I have an older sister, apparently my dad was being a little promiscuous lol. RIP old man. And she also shares my birthday, what are the chances?!”

4. He didn’t know

“I just got off the phone with my newly found bio dad. My mom died in 1980, my dad in 2012. I logged Friday in to AncestryDNA to get my results from their Black Friday sale. It said that this person in NC was my father, no doubt. Turns out it was my moms boyfriend before my dad came along. I have no idea if anyone knew. My newly found father certainly didn’t.”

5. Neanderthal

“I discovered that I have some of the highest known Neanderthal DNA, more than 99% users and over 4% of my total DNA. 3 tests submitted and a flight provided to a university in Australia for a testing. Was cool at first, and then not.

It bothered my wife a bit at first thanks to watching a couple documentaries.”

6. No one ever told them

“Not me, but one of my bar regulars did the test with her older sister. Turns out not only are they not related to each other, but both of them are adopted. And, their adoptive parents are both dead. And, their entire extended family knew the whole time but no one ever told them.”

7. Scandalous

“My 75-year-old grandmother just found out her dad was not her real dad. Turns out her mom had an affair with the family doctor and never told a single soul. Not only did she find out her family doctor was her real dad (the one who birthed not only her but also all of her own children) but turns out this family doctor was sleeping with a lot his patients.

She now has a bunch of new half sisters and brothers, some of them knew who their real dad was and some of them didn’t. My great grandmother was quite the secret keeper.”

8. White mystery

“My dad turned out not to be my dad. So the basic 23andMe family surprise I guess? Also found out that my heritage can best be described as white mystery.”

9. Pissed

“When my birth mom was pregnant with me she was too ashamed to admit who my father was. She was too young to be a mom and so she gave me to my current parents when I was born.(they were 10 years older than her and already had a kid) I love my parents and couldn’t care who my birth father was but I wanted to see what I was made of.

Everyone was pretty pissed when we found out my dad was my birth dad.”

10. At least three

“Not destroyed, it just confirmed what we already knew that there was more than one Father between 5 siblings. At least three as it turned out.”

11. Holier than thou

“Spouse found out his dad wasn’t his dad. His judgmental holier than thou Catholic mom had some explaining to do. He lost an immense amount of respect for her, especially when the bio dad tried to reach out to him. She is still in contact with the married man she had an affair with over 4 decades ago. He refuses to speak to him and has limited contact with her.”

12. Dreading the future

“My grandpa passed away from Alzheimer’s, so my family uploaded our raw DNA to another site to see if any of us have the same genes that make it likely for any of the rest of us to have it as well. Luckily most of us didn’t have the gene my grandpa had, but my uncles have it. So while my immediate family knows we’ve got average chances, my poor uncles are probably dreading the future.”

13. Oh, Papa

“Ours was backwards. A French lady messaged my mom and said she thought they shared a father. Very believable because Papa was a proven whore. Sure enough she did a 23andMe and sure enough papa is a great big slut. Rest in peace.”

14. I feel like this probably happens a lot

“I found out I’m not Irish after taking one….I have an Irish tattoo. My mom’s family always bragged about how Irish we were. My life obviously wasn’t destroyed but funny anyways.

It was over twenty years ago, I was 18 and stupid. The tattoo is a nautical compass with a Celtic knot in the middle on my shoulder.”

15. A happy ending

“My story has a rough beginning, but a happy ending. I apologize, this will be a bit lengthy.

I ordered 23andme to try to figure out 'what' I was, not to track down any long lost family members. I had known since I was a teenager that my dad who raised me wasn’t my biological father. I used to ask my mom if I was adopted because I don’t look like anyone in my family.

My mom is almost 100% Irish and my dad (who raised me, he is and always will be my dad) is also Caucasian and I look a bit ethnically ambiguous. Olive (but fair) skin, dark hair, and green eyes; no one else in my family looked like me. My mom finally told me the truth when i was 16.

When I got my report back, I was mostly European by my breakdown, I was still confused. I had several cousins show up, but contacting them didn’t interest me at all. One day I got a notification that I had new relatives and a half sister popped up. This caught me completely off guard and I didn’t know what to do…because I wanted to contact her.

For the first time ever, I wanted to know more. I messaged her, not telling anything about myself, just that if she’d like to know more about me, I would be open with all that I knew. I never got a reply, this kind of broke my heart if I’m being honest, but I accepted that she probably knew nothing of me and that the revelation of my existence may have hurt their family horribly.

A few months later a second cousin popped up and she was shown to be the first cousin of my 'half sister,' this confused me even more. Why was she my second cousin and my half sisters first cousin? She contacted me because she thought I may have answers for her, I told her that I had tried to contact my half sister but heard nothing and apologized for not being able to help her. (Her story is oddly similar to mine.) She also told me that she had communicated briefly with her first cousin, but after bringing me up, she cut off contact with her.

That made me feel horrible. But through our brief interaction, i realized that the three of us were connected through my 'half sisters' maternal blood line. I know my mom is my mom, there’s no question there, so I started thinking, how could this be?..then I realized that my “half sister” was actually my aunt, my biological father’s sister. Half-siblings, aunts and uncles, and grandparents all share 25% of their DNA, all the connections on these websites are based on probability.

I messaged her again and told her that I thought she may be my aunt and I told her more about myself…my birthdate and where I was conceived, and that if she had a brother who was in that area at that time, he was my biological father. She messaged me back in no time. It turns out that my paternal grandfather had passed away years ago and when she got the first message and saw the half sister connection, she assumed her father had a child that none of them knew about. I’m younger than her and her siblings, obviously, so I would have come along after them.

She didn’t contact me because she didn’t want to hurt her mother, and I’m sure she was hurt by this too. I understood, completely. She then went on to tell me that they all knew about me but didn’t want to disrupt my life. She said my biological father never forgot about me…I had always thought I was his dirty little secret. (He and my mother were both married to other people when I was conceived..that’s another long story.)

Anyways, my husband, children, and I have since met them all. I actually have three half siblings that also knew about me. It was so strange to finally meet people who I resemble. I’m a spitting image of my paternal grandmother when she was young, they were all blown away by that. We stay in contact and I couldn’t be happier that I bought the 23andme kit.”

A version of this article was originally published by our partners at Did You Know Facts and was written by Matt Gilligan.

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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 horse Gina 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 rowing Nathalie 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 dane Helga'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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People who’ve had their families upended by DNA websites reveal what happened.

According to Divorce Statistics, 2% to 3% of all children are born out of infidelity and most of these children are unknowingly raised by men who are not their biological fathers.

1. Finding family

2. Inconclusive

3. What are the chances?

4. He didn’t know

5. Neanderthal

6. No one ever told them

7. Scandalous

8. White mystery

9. Pissed

10. At least three

11. Holier than thou

12. Dreading the future

13. Oh, Papa

14. I feel like this probably happens a lot

15. A happy ending

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.

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

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

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

"Imagine telling them that their free unlimited minutes only started after 9:00 and on the weekends."

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