
Only weeks after Millie Smith and Lewis Cann learned they were having twin baby girls, they learned that only one would survive.
On April 30, after 30 weeks of a high-risk pregnancy, Smith delivered identical twins, Callie and Skye, the latter who lived only three hours.
Later in neonatal intensive care unit (NICU), Callie slept without her sister in the incubator, with her loving and grieving parents watching over her. In the unit with other babies, an overwhelmed mom of healthy newborn twins innocently told Smith that she was “so lucky” to not have two babies.
Crushed by the words, the new mom couldn’t find the words to explain her loss. Then, she realized that Skye’s legacy was to help other families who lose a child, and it came in the form of a purple butterfly.
In November 2015 Millie Smith and partner Lewis Cann found out they were having their first Child. Smith, who has twins in the family, said she had a “gut feeling” about having a duo and 10 weeks later, doctors confirmed she was expecting identical twin girls.
Less than two weeks after the excitement of knowing they would double the children in their home, the British couple were devastated to learn that one of their babies had a fatal condition and wouldn’t survive after birth.
“During the scan, the doctor didn’t say anything. I was very excited and loved seeing the little babies, but she was silent. Both Lewis and I immediately knew there must be a problem,” Smith said.
Doctors shared the news that one of the babies had anencephaly, which according to the Centers for Disease Control and Prevention (CDC) affects about one in 4,600 babies across the U.S. It’s a serious birth defect where a baby is born without parts of the brain and skull, and “almost all babies born with anencephaly will die shortly after birth.”
Knowing that one baby would die soon after birth, and that there were risks involved for their other baby, the couple decided to move forward with the extremely high-risk pregnancy.
Over the next several months, Smith and Cann named their twins Skye and Callie. “We knew that Skye needed to have a name before she was born,” Smith said. “Knowing she would only survive for seconds or minutes, I wanted her to be named during that time.”
The meaning behind “Skye,” she explained “was somewhere we knew she would always be, that we could look up at the sky and remember our baby.”
When Smith went into labor after only 30 weeks on April 30, she needed an emergency C-section. To help navigate the loss, the couple had a “bereavement midwife” during the birth, and they were put I a special room the called the “Daisy Room,” where families can spend time with a baby before and after she/he passes.
“When the girls were born, they both cried. This was a huge moment, as we were told that Skye would not make a noise or move,” said Smith, who was thankful to have three hours with Skye before she died. “We were cuddling Skye when she passed away. This was the worst moment in our lives. I have never ever felt heartbreak like that before. But I am proud that she fought for so long to spend time with us.”
Born premature, Callie had to stay in NICU while she gained some strength and also in the unit were three other sets of twin.
“Most of the nurses were aware of what had happened, but as time passed, people stopped talking about Skye. After about four weeks, everyone acted as though nothing had happened, meaning the families around me had no idea about our situation,” Smith recalled.
One morning, a stressed mother whose twins were also in NICU, harmlessly said to Smith that she was “so lucky” to not have twins.
“None of the other parents knew what had happened or anything about Skye. The comment was completely innocent and more out of humor…They weren’t to know that I did at one point have two.” Smith continued, “But the comment nearly broke me. I ran out [of] the room in tears and they had no idea why. I didn’t have the heart to tell them what had happened. A simple sticker would have avoided that entire situation.”
It was in that moment Smith realized she had to create something that would speak for parents who had just lost a baby, ensuring the misunderstanding never happens again.
She designed a poster for the NICU explaining both hospital personnel and visitors that any incubator with a purple butterfly on it means that one or more babies, in a set of multiples were lost.
“I chose butterflies, as I felt it was fitting to remember the babies that flew away, the color purple because it is suitable for both boys or girls,” said Smith.
The purple butterfly concept–now under the Skye High Foundation–has spread to hospitals in several countries around the world.
Callie is now a lively, happy seven-year-old, and twin’s memory lives in purple butterfly cards along with other initiatives to help families with babies like Skye all over the world. The purple butterflies now come in numerous forms, like ornaments, cards, blankets, stuffed animals and more.
“Ultimately I will never be able to stop this from happening but the more support groups we can set up and put things in place like the stickers the better it will be. It’s the hardest thing anyone has to deal with,” Smith said.
Parents’ Love Drives Them to Remove Daughter’s Birthmark

Parents go above and above for their kids in order to assist and safeguard them. Celine Casey, a British woman, took an exceptional step for her daughter Vienna Brookshaw. Vienna, who was born in April 2021, had a birthmark between her eyebrows on her forehead.

Congenital melanocytic nevus (CMN), the birthmark, didn’t present any health issues, but Casey was concerned about the emotional effects it would have on Vienna as she got older.
An Uncommon Illness
A rare disorder known as congenital melanocytic nevus (CMN) occurs when a baby is born with a harmless cluster of pigment cells. These cells have the capacity to proliferate along with the child. Fearing that Vienna would grow to hate her parents, Casey went straight to the physicians to discuss her choices for having the birthmark removed, worried about the difficulties her daughter might encounter later on.
“We cherish every moment of Vienna’s journey and eagerly await the day she can express her own thoughts,” said Vienna’s mother, Casey, who is immensely compassionate. We would always and forever love her, birthmark or not.
The Need to Be Accepted
Casey was inspired to have Vienna’s birthmark removed because her infant seemed uncomfortable with people staring at her. Vienna was handled differently than other babies, which made her even more determined to pursue the removal.
Overcoming Difficulties
When Casey first requested the operation, the National Health Service (NHS) turned him down because they said it was more cosmetic than necessary for his medical well-being. Unfazed, Casey launched a crowdfunding effort to secure the required sum of money from kind donors. The campaign raised an incredible $52,000 in just one day. Unfortunately, they still need an extra $27,000 for the procedure because of higher hospital expenses during the COVID-19 pandemic.
In an attempt to raise additional funds, they went back to GoFundMe to pay for Vienna’s birthmark removal procedure. “Everyone has insecurities about their body,” said Casey. We perceived it differently, even though the doctor assured us that it wouldn’t currently affect Vienna’s mental health. Little ones are sensitive and pick up on these things, especially when they begin school at age three.
A Pathway to Recovery
Vienna’s birthmark has been successfully removed, and she is now a healthy two-year-old with just a tiny scar remaining on her forehead. Casey frequently remarks on her newborn girl’s extreme beauty while providing regular updates on her daughter’s recuperation.

The concerned parents went so far as to fly to London to have the surgeon confirm that the little scar was healing. Vienna had already undergone three operations and therapies, so they wanted to make sure she wouldn’t need any more. Fortunately, she is well at the moment and doesn’t need any more medical attention.
Vienna’s Promising Future
We send little Vienna our warmest regards. We wish her a lifetime of health and pleasure as she grows up. Do not hesitate to tell others about her inspirational tale!
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