We can all connect to school regulations, even though our recollections of school can be both happy and sad. It’s a turbulent time filled with highs and lows.
While some regulations, such as prohibiting jewelry during sporting events, make sense, it seems wasteful of resources and misses educational opportunities for the children engaged to send someone home with excessive makeup or because they brought in a particular soda.
Schools’ stringent policies on children’s appearance frequently conflict with the moments in their lives when they desire to stand out and express themselves.
These regulations may have gone too far for one mother and her kid and may have prevented an 8-year-old boy from receiving a quality education.
Model scouts are drawn to Farouk James of London, England, because of his gorgeous head of hair. He’s done photo sessions in Italy and New York and is currently employed as a child model.
However, his look has only caused problems for him in the classroom; because of the length of his hair, he has been turned down by several schools.
James’s mother, Bonnie Miller, claims that she was informed that her older brother’s hair was too short while he was in school.
According to Bonnie, Farouk’s father is from Ghana, and his parents didn’t cut his hair until he was three years old due to cultural customs.
Bonnie told CBS News, “At that point, he was attached— and so was I, to be honest— with his beautiful hair.” “We only retained the hair.”
The family resides in the UK, where the majority of schools have a regulation prohibiting boys from having long hair, even if girls are permitted to.
According to Bonnie, it is against children’s human rights to have them cut their hair.
His mother Bonnie posted on Instagram, saying, “I will not give up trying to persuade governments to put legislation in place to protect children from these outdated, punishing rules.”
“You reject Farok even though he hasn’t done anything wrong! When his friends are all admitted to the universities he so much wants to attend, he will have to say goodbye to them.
Bonnie even created a Change.org petition to outlaw hair prejudice in the United Kingdom as a result of this circumstance.
Bonnie declared, “We’re assembling a real team and dubbed it the Mane Generation.” “We will battle this until these regulations are altered. And it’s not limited to the United Kingdom; it’s worldwide.
With over a quarter of a million followers, Farouk’s mother runs an Instagram account that highlights his life as a playful boy and child model.
But even with all the love and support he receives on the internet, they continue to get hate mail. Following her discussion of the family’s effort to find a school that will accept Farouk and his hair on the well-known U.K. TV morning show “This Morning,” Bonnie claimed she received a lot of harsh feedback.
Bonnie remarked in May of last year, “This is mental health week, so I’m surprised to be receiving lots of negative comments about Farouk’s hair.”
“Farouk does not keep his hair long at my request, but it is a God-given aspect of him, and he will not cut it to please anyone.”
Bonnie contends that since many schools forbid braids and dreadlocks, the dress codes for boys and girls in schools are antiquated and occasionally discriminatory.
The mother promises that she will never give up on getting acceptance for Farouk, his hair, and all the other kids who face prejudice for wishing to show their identity and cultural background.
Farouk’s hair is an integral part of who he is, and in 2022, it will not be acceptable for those entrusted with our children’s education to reject a child because of the color of their hair. These regulations ought to be outlawed.
If you see a purple butterfly sticker near a newborn, you need to know what it means
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.
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