Mom of twins with Down syndrome shuts down critics

Mom Defends Her Rare Twin Girls With Down Syndrome After Cruel Comments Online

While twin births have become more common over the years, they are still considered relatively rare. Between 1980 and 2018, the chances of having twins increased significantly, yet only around 33 out of every 1,000 births result in twins.

Identical twins are even rarer, occurring in only about three or four births per 1,000.

So when 23-year-old Savannah Combs learned she was pregnant with identical twin girls, it already felt incredibly special. Then doctors revealed something even more uncommon — both babies had Down syndrome.

For Savannah and her husband, Justin Ackerman, the news brought strong emotions and uncertainty. They understood that some people would judge their daughters because of the diagnosis.

But to Savannah, the girls were simply extraordinary.

“It’s very rare what they have, but they’ve been my little gems,”

Savannah, who lives in Middleburg, Florida, began documenting life with her daughters on TikTok after giving birth. Her honest and emotional videos quickly attracted thousands of followers who were inspired by her family’s journey.

In one of her posts, Savannah revealed that some people encouraged her to terminate the pregnancy after learning about the babies’ condition.

Doctors warned her that the twins might not survive.

Still, she chose to continue the pregnancy and give her daughters every possible chance at life.

“Every appointment they were alive was a blessing to me,”

she explained.

At the time Savannah received the diagnosis, her husband was away attending boot camp. As the pregnancy progressed, complications developed, and at 29 weeks she was admitted to the hospital.

On May 12, 2021, Savannah gave birth to her twin daughters, Kennadi Rue and Mckenli Ackerman.

Because they arrived nearly two months early, the babies spent several weeks in the NICU before finally being healthy enough to go home.

Savannah later explained that the twins are known as “mono di” twins, meaning they had separate amniotic sacs but shared the same placenta.

“Mo di twins as it is, it’s like very rare. And then you throw Down syndrome on top of it, it’s like one in 2 million,”

she said.

Despite their rare condition, Savannah wants people to understand that her daughters are no different from other children.

“They have feelings. They have a beating heart. They know how to talk. They know how to do things you do. They will get there,”

she explained.

She acknowledged that some developmental milestones may take longer, but she believes her daughters are determined and full of joy.

“I’ve learned these kids are feisty little things and happy little things.”

As Kennadi and Mckenli continue growing, Savannah regularly shares updates online, showing their progress and celebrating every achievement along the way.

Her message has remained consistent from the beginning.

“I’m going to let them know that they’re just like us and they’re going to get there as long as they put their minds to it.”

Unfortunately, not every response online has been supportive.

Savannah has faced cruel and insensitive comments from strangers criticizing her daughters and questioning her decision to keep the pregnancy.

One comment in particular deeply shocked many people.

“I wouldn’t want those babies; if mine came out like that, they would be straight up for adoption,”

one user wrote.

Savannah responded with calm strength and compassion.

“I said, good thing they weren’t born to you and were born to me. God knew what he was doing by giving these babies to the right parents who would love them regardless.”

Her response quickly resonated with thousands online, many praising her love, patience, and devotion as a mother.

Today, Savannah continues using social media to share the reality of raising children with Down syndrome while also challenging harmful stereotypes and encouraging kindness.

Kennadi and Mckenli’s story has touched countless people because it reminds others that every child deserves love, support, and the opportunity to thrive.

To Savannah, her daughters are not defined by a diagnosis.

They are simply her precious little girls — joyful, strong, and deeply loved.

Mod

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