A baby with a rare skin disorder is born after an urgent C-section by medical professionals.

Throughout the nine months of pregnancy, a mother’s heart is filled with anticipation, excitement, and a hint of doubt. When an expecting parent gives birth, they all want the child to be healthy and happy. Regretfully, our expectations are not always met by the way things work out.

Jennie Wilklow, of Highland, New York, was looking forward to meeting her daughter. Jennie and her spouse were overcome with happiness the moment they held their baby.

After multiple ultrasounds and check-ups with the physician, the results consistently showed a healthy baby.

This assurance put their minds at rest, and they had no idea that their darling Anna would be born with a disease that would permanently alter their lives.

At 34 weeks, Jennie had a C-section to deliver Anna. She peered into Anna’s eyes when the physicians placed the baby in her arms and felt an overwhelming sense of love.

Everything was going fine with their cute little one. However, Jennie couldn’t help but feel apprehensive about her husband when he came to visit her.

Jennie told Cafe Mom, “My husband’s silence scared me.” I pressed him for additional information as the doctor was leaving the room, and he just sat there looking shocked. With remorse, he added, “It’s bad.”

Upon meeting her gaze, her spouse said, “Jennie, she has the most beautiful soul.” Jennie did not know what such terms meant at the moment. Her mind was racing, but she had no idea what was wrong.

Anna suffered from an uncommon disease known as harlequin ichthyosis, which showed up as thick, severely fractured diamond-shaped plates. Jennie said to Cafe Mom shortly after giving birth, “Her delicate skin hardened as they desperately tried to help her.”

The dramatic splitting that followed the hardening left her slathered in open wounds throughout her body.”Anna prevailed despite the physicians’ concerns about her prognosis. She was quite beautiful,” Jennie proudly declared.

Unfortunately, there is no known cure for harlequin ichthyosis. The treatment involves regular showering and thorough skin moisturization, which takes consistent effort. I used to bathe her for hours every few hours, slathering her in Vaseline.

It might not seem like much, but it was one of the things I struggled with the most. I had visualized all the amazing clothes my child would have,” Jennie said.

She set up the “harlequin diva” Instagram page and started posting images of Anna there in an effort to raise awareness of this illness. Through her articles, she sheds light on the challenges faced by parents of children with harlequin ichthyosis on a daily basis.

“Anna won many people’s hearts and is the pinnacle of perfection in its purest form.” She has a natural capacity to carry out these mundane tasks. The world celebrates with us every time we achieve a new milestone, Jennie said to Cafe Mom.She went on, “I now realize that my love for my daughter is the reason Anna was given to me.” Because we were destined to be together, we will work together to redefine what true beauty means to the world.

In addition to being beautiful in her own right, Anna is fortunate to have parents who will stop at nothing to ensure that she has a happy existence.

Let’s help spread the news about Anna’s story by inviting our friends and family to read this article on Facebook. Despite our differences, we can work together to raise awareness of and respect for the incredible beauty and power that each individual holds.

Florida mom gives birth to rare set of identical twins with Down syndrome

Identical twins are a miracle all by themselves. Births like this happen three or four times in 1000.

Savannah Combs, a first time mother, learned she was carrying twins. She and her husband were overjoyed by the thought of welcoming two babies.

Everything went well with the pregnancy and the couple learned they were expecting girls. However, they also learned that their identical twins both had Down Syndrome. The news came as a shock at first, but Savannah, 23, soon realized that the condition only meant that her girls would be super special. She didn’t mind they would be born with the syndrome. Of course, she was aware that there would be people who wouldn’t accept her bundles of joy, but that didn’t concern her a great deal.

“It’s very rare what they have, but they’ve been my little gems,” the proud mother told News4JAX.

Once the girls were born, Savannah and her husband Justin decided to share their journey on TikTok. The two tiny beauties, Kennadi Rue and Mckenli gained a number of followers on the social media where Savannah posted about each of the milestones they reached.

In one of the videos she shared on TikTok, Savannah revealed how doctors advised her to terminate her pregnancy because the chances of her girls to survive were slim, but she decided to give them a fighting chance. As it turned out, she did the right thing. ”Every [prenatal] appointment they were alive was a blessing to me,” Savannah explained.

They were born five weeks prematurely and had to spend some time at the NICU. Today, they are nine months old and thriving. In fact, they are just like any other baby out there.

“They’re called mono di twins, meaning that they had their own sacs, but they shared the same placenta, meaning that they were going to be identical,” Savannah explained.

“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.”

“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 added. “Like I said, it may be a step behind but they’re going to do it. I’ve learned these kids are feisty little things and happy little things.”

She loves showing the world that having Down Syndrome doesn’t necessarily mean the life of those people is in any way affected negatively.

“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.”

Of course, there are always those who post negative comments and judge Savannah for keeping her babies.

”I wouldn’t want those babies; if mine came out like that, they would be straight up for adoption,” one person wrote under one of the videos. However, this mother had just the right answer for the mean person. “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,” Savannah replied.

These girls are truly happy for having a mom like Savannah who wants to raise awareness about Down Syndrome and teach the world that those who have it can lead a happy and fulfilling lives, just like her two beautiful angels.

For more on this family’s beautiful life story go to the video below.

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