Pegi Young, 66, Musician Who Started a School for Disabled, Dies

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Pegi Young, a late-blossoming folk-rock musician who was a founder of a school for children with severe physical and speech impairments, like her son from her marriage to the singer-songwriter Neil Young, a performer at its many star-studded benefit concerts, died on Tuesday in Mountain View, Calif. She was 66.

Her brother Paul Morton said the cause was cancer.

By the early 1980s, Ms. Young had grown frustrated with the special education programs available for her son, Ben, who was born with cerebral palsy in 1978. She began thinking about starting a school to better address his needs and those of other children who had largely lost the ability to speak.

That inspiration led in 1987 to the Bridge School, an innovative institution in Hillsborough, Calif., that has since achieved global reach. Ms. Young founded it with the speech and language pathologist Marilyn Buzolich and Jim Forderer, who had adopted many special-needs children.

At the school, about 17 miles south of San Francisco, children from ages 3 to 12 use augmentative and alternative communication techniques, including speech generators and manual communication boards, to help them articulate their thoughts and prepare to complete their educations in their local school districts.

Vicki R. Casella, the executive director, said in a telephone interview that Ms. Young had a “determination to ensure that children like Ben have the opportunity to become active participants in their communities.”

Dr. Buzolich added that Ms. Young’s experience as the parent of a child with special needs had been critical to the school.

“Professionals often diss parental input, but the parent sees the whole child,” Dr. Buzolich said by telephone. “You can imagine the parents at the Bridge School saying to themselves, ‘She understands me, she knows what it’s like, she’s been there.’ ”

The school runs an international teacher training program; implements its curriculum in developing countries; organizes conferences; and conducts research to measure the effectiveness of its educational strategies.

“I take a tremendous amount of satisfaction with the knowledge that we’re changing lives for the better,” Ms. Young said in 2017 in an interview with AXS, a ticketing website. “It’s truly having a global impact.”

Continue onto the New York Times to read the complete article.

SPAN Program provides specialized health care for adults with special needs

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two adults with special needs laughing together

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Regardless of age or health history, taking care of yourself and forming strong healthy habits is one of the most important things you can do. Achieving wellness looks different for all of us, but may be especially challenging for those with disabilities or special needs. Thankfully, some medical professionals have the expertise and compassion to help adults in this situation.

Dually certified in pediatrics and internal medicine, Laura Gaffney, MD, has dedicated her career to caring for adults with special needs. She started the Special Pediatric-to-Adult Need program, or SPAN, at AdventHealth Medical Group Primary Care at Shawnee Mission. The SPAN program is the only primary care program in the Kansas City area for adults with special needs including Down syndrome, autism, cerebral palsy and genetic disorders. It was Dr. Gaffney’s relationship with her mother and grandmother that prompted her to establish the SPAN program.

“My mom had multiple sclerosis and was in a wheelchair,” said Dr. Gaffney. “I felt like she did not get the care she deserved. People would often treat her as if she had impaired intellectual ability, yet she was a pharmacist. Also, my grandmother was a librarian for children with special needs.”

As the medical director of SPAN, Dr. Gaffney has built a team that provides comprehensive, patient-focused care for adults with a chronic condition that persists from childhood to adulthood. The SPAN program offers these patients a consistent and reliable medical home with same-day appointments.

“There are few primary care clinics in the United States for adults with a variety of overlapping needs,” said Dr. Gaffney. “We work to ensure our clinic meets the needs of this unique group.”

Dr. Gaffney and her team will see a patient’s family members and caregivers, which provides an integrated approach to care and a better understanding of the social and emotional needs of the patient. They also have social workers on hand and provide diabetes education. In addition, the clinic features an exam bed that lowers to 14 inches allowing easy transfers and the ability to weigh a patient up to 450 pounds.

“These are ways we are providing whole-person care to adults with special needs,” said Dr. Gaffney. “We have also identified dentists, physical therapists and other specialists who are interested in caring for people with special needs and doing it with respect.”

Dr. Gaffney describes herself as a curious and empathic person. These traits coupled with her background as an internal medicine and pediatric physician give her a unique perspective allowing her to provide excellent medical care for patients with special needs.

“I have been trained to understand genetic, developmental and intellectual issues and how those change as people age,” said Dr. Gaffney. “People with genetic diseases, neurologic diversity and cerebral palsy are living longer lives and there are few physicians that are willing and educationally able to care for this group.”

Click here to read the full article on Shawnee Mission Post.

The Tourette’s community is livid over the ‘TikTok tics’ media frenzy

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The Tourette’s community is livid over the ‘TikTok tics’ media frenzy

By Jessica Lucas, Input

Last month, a Wall Street Journal article titled “Teen Girls Are Developing Tics. Doctors Say TikTok Could Be a Factor” went viral on social media.

The piece reported a rise in young women presenting with symptoms of Tourette syndrome, a widely misunderstood neurological disorder that impacts roughly 0.6 percent of children and causes people to experience tics — involuntary and repetitive movements or sounds.

The Journal cited “a spate of recent medical journal articles,” in which doctors claim many girls with unexplained tics “had been watching videos of TikTok influencers who said they had Tourette syndrome.” The piece, which featured two teenage girls who linked their tics to TikTok, said that pediatric movement-disorder centers across the U.S. had reported “an influx of teen girls with similar tics.”

“PEOPLE automatically think we’re doing things for ATTENTION, or that there’s NO WAY that Tourette syndrome can be REAL.”
The article acknowledged that the “TikTok tics” epidemic was anecdotal and even quoted an academic who cast doubt on TikTok being the root cause of this phenomenon. “There are some kids who watch social media and develop tics and some who don’t have any access to social media and develop tics,” Dr. Joseph McGuire of Johns Hopkins University Tourette’s Center told the paper. “I think there are a lot of contributing factors, including anxiety, depression, and stress.”

But the headline was damaging enough. And it was worsened by subsequent coverage: Buzzfeed, the New York Post, People, and Business Insider ran with the story — all without any input from the Tourette’s community itself, which has been horrified by the press frenzy.

Ben Brown, host of the Tourette’s Podcast, has been deeply perturbed, as have his listeners. “There’s a lot of frustration. Some people are just livid,” says Brown, who is 41 and based in North Carolina. He was diagnosed with Tourette syndrome at the age of five, but lived a “closeted” life with the condition while he worked as a photojournalist. Brown “came out” with Tourette’s when he launched his podcast in 2018.

“Now we have scientists who are saying things we know from experience are just not safe,” Brown says. He and many others living with Tourette syndrome fear the current rhetoric around TikTok tics could further stigmatize Tourette’s, especially for young women.

Britney Wolf is a 31-year-old Tourette’s campaigner from Ohio. “People automatically think we’re doing things for attention, or that there’s no way that Tourette syndrome can be real,” says Wolf, who was diagnosed with Tourette’s at the age of seven. She interviews people with the condition on her YouTube channel in a bid to challenge stereotypes. “There’s already so many of these people trying to tear us down,” she says, “and articles like this give them more fuel to start claiming that all advocates are faking it.”

Jaleesa Jenkins, a 24-year-old Tourette’s YouTuber from California, is most frustrated by the suggestion that Tourette-like symptoms can be “caught” through platforms like TikTok. “The idea is really oversimplified and really stigmatizing,” she says. “It’s just not true. It makes people afraid, suspicious, or scared to be around us.”

It seems that the recent press attention has undone years of campaigning. “People with Tourette syndrome have worked hard for a very long time to feel understood — particularly for people to understand that tics aren’t voluntary or done for attention,” says Dr. Christine Conelea. The clinical practitioner and researcher is an assistant professor of the Department of Psychiatry and Behavioral Sciences at the University of Minnesota and has worked with Tourette’s patients for 15 years. “I worry that those who are doing advocacy on social media spaces will be questioned and targeted.”

Wolf finds the situation heartbreaking. “So many people have told me how much they have learned about Tourette’s because of people online,” she says. “It felt like we were finally getting somewhere. Now it feels like we’re being pulled back.”

Click here to read the full article on Input.

Local Teen Clings To Hope Almost A Decade After Epilepsy Diagnosis

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Local Teen Clings To Hope Almost A Decade After Epilepsy Diagnosis

By Derrick Stuckly, Brown Wood News

The month of November is known as a time when we gather around the table with our friends and family to celebrate what we are thankful for. But for more than 3.4 million Americans the month of November means so much more. November is Epilepsy Awareness Month.

According to the National Epilepsy foundation 1 in 10 people will have a seizure and 1 in 26 will develop epilepsy during their lifetime.

Ellie Mclver, a 16 year old junior at Santa Anna High school, is 1 in 26.

For most teenagers their list of worries usually involves what they’re going to wear to winter formal, acne, sports, and narrowing down what college they will apply to. But for teenagers like Santa Anna junior Ellie, her list looks a little different. I had the opportunity to get to know Ellie and her mom Brandi as they both courageously shared with me what Ellie’s life has looked like since she was diagnosed with Epilepsy at the tender age of 8.

Ellie was in class her 3rd grade year when she had her first seizure. Tests performed after that seizure led to an epilepsy diagnosis. The epilepsy diagnosis was hard enough for the family but the news only got worse as they would later be told by doctors that Ellie’s seizures were considered irretractable. Ellie explained to me that this means medicine does not work to control her seizures.

Not even a year after her diagnosis Ellie went in for her first major brain surgery. This was a terrifying time for the entire Mclver family. They weren’t even sure this surgery was going to help but with medicine out of the question, this was their only option to try to stop the seizures.

After surgery Ellie’s family walked around cautiously but eventually a week passed, then a month, and before they knew it Ellie had been seizure free for 4 years.

Time went on and as most families do Ellie’s family gathered around the table for Thanksgiving in 2018 when family members noticed Ellie was “zoned out.” For any other teen this is a pretty normal occurrence but for Ellie this indicated a seizure. After 4 years Ellie was experiencing a focal seizure which meant she was no longer seizure free. Her seizures progressively got worse after this occurance. In September of 2019 Ellie’s family had a hard time pulling her out of a seizure and they had to call an ambulance. Once again Ellie had no choice but to undergo another brain surgery. This time the surgery was unsuccessful, she was still having seizures.

Ellie is 16 now and she knows she is facing more complex brain surgeries in hopes that one day she will be completely seizure free. Ellie is not fearful for what is ahead; she is ready to head into battle to do what she needs to do so she can have more freedom. With that, I asked her if there are things are she’s had to overcome because of epilepsy that other teens her age haven’t had to deal with. She said, “The hardest thing is that I can’t get my drivers license!” She also went on to say, “I miss a lot of school because after a seizure it can take a few hours or even days to recover so I feel like I’m always playing catch up.” I was amazed to learn that even though she is forced to play catch up Ellie’s resilience and urge to be great outweighs the task of that catch up. She told me she is the president of their FFA chapter, she plays clarinet in the high school band, and she takes dual credit classes. She did have to give up playing high school sports because the stress was more than her brain would physically allow her to handle.

Although Ellie has had to give some things up and she has a lot to manage and figure out, she still expressed little concern for herself and more concern for her friends. She shared with me that her friends have never seen her have a seizure and she hopes they never do. She said, “but they do see a lot of side effects from my medication. My medications can be hard to regulate so sometimes I seem “high”, and I have tons of “brain fog.” She said her teachers and friends are great at knowing when she isn’t doing okay, and they do all they can to help support her.

Ellie’s mom Brandi confirmed this by saying, “Ellie has a huge support group and so many people praying for her every day. She gets notes from people in our church, other churches, and several cards a month from a sweet group of ladies that don’t even live in our town.” Brandi went on to say that Ellie calls these things her ‘fan mail” and the encouragement makes a huge difference on this journey.

I asked Brandi what it has been like to watch her daughter battle epilepsy for more than half of her life and I was so inspired by her when she said, ‘Ellie has handled every obstacle in her path with grace and although it has been heart wrenching to watch her go through all that she has, Ellie has never lost faith, so how could I?”

Ellie continued to share her faith and confidence in God when she said “When things get tough, I cling to the verse 2 Timothy 1:7, which reads, “God hasn’t given us the spirit of fear but of power, love, and a sound mind.”

It is without a doubt that even at such a young age with such a tough diagnosis Ellie has power, love, and a sound mind about her. People who don’t know Ellie would never know that she currently takes 3 medications that must be administered on a strict schedule, they don’t know how often her family must make the drive to Fort Worth to be seen and monitored by her neurosurgeon, and they don’t know that sometimes she suffers in pain and in a fog. Her radiant smile would surely tell you otherwise.

Click here to read the full article on Brown Wood News.

The first IRONMAN with Down syndrome turns his winning moment into a growing movement for inclusion

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The first IRONMAN with Down syndrome races forward for inclusion

By Julia M. Chan, CNN

Chris Nikic’s journey to becoming an elite athlete began with a single step. What kept him going was a single recipe for success: get “1 percent better” every day.

“One percent — stick with that goal,” Chris says. “If you stick with that goal, (you) can succeed and be a successful person.”

Last fall, Chris showed the world the power of small but consistent improvement, setting a Guinness World Record as the first athlete with Down syndrome to complete an IRONMAN triathlon: a 2.4-mile swim followed by a 112-mile bicycle ride, ending with a 26.2-mile marathon. But crossing that finish line was only the beginning.

Now, the 22-year-old Special Olympics Champion Ambassador from the Orlando area is on a mission to promote inclusion and highlight human potential.

Early hurdles

From birth, Chris faced a number of cognitive, physical, and sensory challenges, according to his mother, Trish Nikic. He underwent open-heart surgery at five months old and years of therapy to help with things like eating, speech, and balance.

Perhaps the biggest obstacle he encountered, though, was how other people perceived him.

“People treated me different,” Chris recalls. “They were telling me that I can’t do that or can’t do this.”

When Chris was eight, he and his family found a supportive and welcoming community in Special Olympics Florida. Inspired by his athletic older sister, Chris eagerly took to sports like basketball, golf, and track.

Their true benefits went beyond exercise for the growing boy. Athletics “gave him an opportunity to be socially included with others,” Chris’ father, Nik Nikic says.

Leveling up

As Chris got older, he became more sedentary while recovering from a series of ear surgeries. After Special Olympics Florida launched its triathlon program in 2018, Chris’ parents encouraged him to try it to get in shape and have fun.

“The first time he ever did a sprint with Special Olympics, he came in dead last,” Trish says. “But you know what? Chris was happy.”

Chris soon outgrew his first triathlon coach. Dan Grieb, the captain of a local triathlon club, came on board to help take Chris to the next level. In a year and a half of training, Chris went from the couch to a sprint 14-mile triathlon.

Chris set his sights on a half IRONMAN race scheduled for May 2020. When Covid-19 forced organizers to scrap the official event, Chris and his team held their own race. CNN affiliate Spectrum News 13 followed Chris’ journey, ultimately ending with him qualifying to compete in the full IRONMAN competition in Panama City.

Click here to read the full article on CNN.

Next Big Thing: ‘Eternals’ Star Lauren Ridloff on Becoming Marvel’s First Deaf Superhero

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“I’m hoping that more people are going to be able to dream bigger,” says Lauren Ridloff of playing the first deaf superhero in a Marvel film. COURTESY OF ERIK CARTER

BY ABBEY WHITE, The Hollywood Reporter.

Being a superhero wasn’t part of Lauren Ridloff’s plan. The Eternals star wanted to be a children’s book author before an American Sign Language tutoring gig for the director of Broadway’s Children of a Lesser God led to a starring role in the show’s revival.

Theater, she says, is a “much more natural and inviting medium for deaf actors,” and the production came fully staffed with a toolbox ready to support its deaf and hearing artists. But coming off that critically praised performance in 2018, Ridloff wasn’t sure she wanted to keep acting. TV and movies weren’t a place she had seen herself represented growing up, instilling the idea that it couldn’t be part of her dream.

Yet, after scoring The Walking Dead as her first TV role, Ridloff found herself in demand. Now, she’s set to star in the Chloé Zhao-directed Marvel movie that will take her and deaf representation to marvelous new heights when it releases on Nov. 5.

During her transition from stage to screen, Ridloff says she’s felt like she wanted to prove she’s easy to work with, something that has led to her not always advocating for what she needed as an actor. But being on this massive Marvel production full of A-listers who “know exactly what they want” helped change her outlook.

Ahead of The Eternals’ anticipated release, The Hollywood Reporter spoke to Ridloff about her journey from stage to screen, how working on a blockbuster as an emerging actor changed her perception of self-advocacy on set, and why the Eternals cast wasn’t sure what to expect in the final cut.

Your journey to acting was a bit of being in the right place at the right time. Before that Broadway break-out, what were your acting ambitions and how have those changed?

My goal growing up was to write a book. That’s why I studied English and creative writing in college, and that is a big reason I started teaching. I wanted to write children’s books. I felt that the best way to understand how a child thinks in their mind is to be with them all day. So I started teaching because of that. I didn’t dream of acting. I didn’t want to pursue acting. I had some acting experience — your basic high school play, or I was a part of a performance group in college, a dance group. I just didn’t see enough people on the screen like myself. Every once in a while, like maybe Marlee Matlin, I saw on the big screen, and then years went by, and you would see somebody appear on one episode of a TV show or another episode there. Acting on Broadway came so completely as a surprise to me. It wasn’t part of my plan.

And, yes, absolutely, my goals have changed since I’ve gotten into acting. When I was on Broadway, my manager was interested in pursuing and looking for other projects, and I told him to then I didn’t know if I wanted to continue acting. Maybe this was just a one-time thing. I wasn’t even sure if it was my thing. But then, when I saw the theater audience full night after night, and I saw the lines forming at the back door, I realized that my classroom just got a lot bigger. I made a bigger impact here. It seems like I can act, and I enjoy the opportunity to fully immerse myself in a character, which is very connected to reading and writing. When you write, you need to drop into that character and how it represents itself on the page. So I felt like it was a very natural leap into acting because of that.

Click here to read the full article on The Hollywood Reporter.

Disability Advocate Chelsie Hill Has the *Best* Advice for Fending Off Fitness Class Intimidation

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Chelsie Hill seated on a wheel chair in front of a pool with yellow digital background surrounding her

By Zoe Weiner, Well + Good

When Chelsie Hill was in a car accident at age 17, her “whole world was flipped upside down,” she says. A spinal cord injury left her paralyzed from the waist down, but as a lifelong dancer, she refused to let the fact that she was in a wheelchair get in the way of her passion. So two years later, in 2012, she started a wheelchair dance team called “The Rollettes.”

Hill connected with a group of women through social media who, like her, were in wheelchairs and wanted to dance. “I wanted to meet girls like me and find friends… I wanted to just feel a sense of normalcy, and feel like I wasn’t the only person in my community or in the world who got in the car with a drunk driver or became paralyzed,” she says. “When you’re by yourself and you’re alone and you’re trying to figure out life, it can be very lonely—it can feel like you’re the only one. And for me, being around these girls helped me gain a sense of confidence that I never thought I would ever get.”

In the near-decade since the Rollettes conception, the group has performed all over the world, introduced the “Boundless Babes Society” mentorship program to connect women and girls living with a range of disabilities, and grown its platform to increase visibility for people with disabilities. “I have so many little ones who come to Rollettes Experience and they look on TV and they don’t see anybody like themselves,” says Hill. “And so for us, representation and education are the two biggest things that we’re very passionate about in every way.”

Hill’s role as the team choreographer has given her the opportunity to take the dance moves she loved when she was younger and make them accessible to people with differing abilities. “I love going to dance classes and adopting the choreography from an able-bodied choreographer to make it work for me,” she says. “That’s when I get the most creative, because I am forced to do moves that my body naturally wouldn’t know how to do… but I can translate them in a way that looks similar because my body is used to all of the moves from when I was a little girl. That’s kind of the advantage I have as a wheelchair dancer: I know how all these moves are as an [able-bodied person], so I just make them work for what my ability is now.”

Even with decades of experience under her belt, though, Hill is no stranger to the oh-so-relatable experience of entering a dance or workout class and immediately feeling intimidated—something many of us can relate to. “I was always so intimidated to go into any class, especially in Los Angeles with some of the top dancers in the industry, top choreographers and me and my wheelchair rolling in and people looking at me like, ‘What is she doing here? Does she know where she is?'” she says. “So I can totally empathize with that feeling of not feeling like you’re ready.”

Click here to read the full article on Well + Good.

He’s 72, an amputee, and won 6 medals at National Veterans Wheelchair Games

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Patrick Terry is 72, an amputee, and won 6 medals at National Veterans Wheelchair Games

By Jerry Carino, Asbury Park Press

At first, the bad news hit Patrick Terry hard: His right leg would have to be amputated below the knee due to an infection.

“I cried for about half an hour that day, sobbing,” he said.

Then he remembered something a mentor taught him: the Serenity Prayer.

“God, grant me the serenity to accept the things I cannot change, courage to change the things I can, and wisdom to know the difference.”

That was 2009. Terry, a U.S. Navy veteran and longtime Union Beach resident, accepted his condition. Then he sought to make the best of it by participating in adaptive sports. His quest reached an apex last month, when he won six medals — three gold, one silver and two bronze — at the National Veterans Wheelchair Games in New York City.

At age 72.

“My family and the people that know me are proud of me and just overwhelmed that I could do this,” he said.

From addiction to adaptive sports
Originally from Yonkers, N.Y., Terry competed in football and track in high school and enlisted in the Navy in 1969, serving aboard the USS Albany. He later served in the U.S. Navy Reserve and worked for New York City’s Department of Transportation, paving and milling roads.

By 2005, he was in need of help for alcohol and drug addiction. A sponsor in a 12-step recovery program introduced him to the Serenity Prayer.

“That freed me to be the person I am,” Terry said. “I now have 16 years clean and sober. I used to blame everybody else for my problems. The problems, they were with me.”

In 2009 he joined the East Orange Thunder, an adaptive sports team comprised of veterans and founded by Ralph Jones, a recreational therapist with the Veterans Affairs New Jersey Health Care System.

“He picked up on all the adaptive sports quickly,” Jones said. “He’s just a natural athlete.”

Click here to read the full article on Asbury Park Press.

Paralympian Sophia Herzog has a mental health coach and psychologist ‘to get me prepared and healthy’

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Sophia Herzog smiling at the camera

By Cindy Augustine, Yahoo! Life

The Unwind is Yahoo Life’s well-being series in which experts, influencers and celebrities share their approaches to wellness and mental health, from self-care rituals to setting healthy boundaries to the mantras that keep them afloat.

Sophia Herzog may be a Paralympian bound for Tokyo and determined to win a medal in swimming, but in many ways, she’s a lot like her 20-something peers: focused on her future. The Colorado native, who was born with a form of dwarfism, has been steadily training at the Olympic Training Center in Colorado Springs, prepping for the Tokyo games — but she knows she can’t swim forever.

When Herzog, 24, isn’t training or obsessing over her dog, Odie, she’s been thinking about what lies ahead after swimming — and choosing to make her education a priority. As a graduate from DeVry University, an official education provider of Team USA, Herzog was able to get her degree on her own terms (mostly virtual), and showed off her ability to juggle her athletic training and career training.

Herzog will be competing in freestyle, breaststroke and butterfly heats as the Paralympic Games get underway on Tuesday. Before taking off for Tokyo, the athlete caught up with Yahoo Life and shared how she stays focused and mentally prepared.

How do you approach taking care of your mental health?

We saw how much pressure athletes are under from the [Tokyo] Olympics, and I think it’s really important. I have a mental health coach and a psychologist that I work with almost weekly to get me prepared and healthy, just like my gym coach and swim coach. It’s nice to shed a light on the pressure — Olympic superhero athletes are just like every other human.

Aside from being in the pool, what else brings you joy?

We adopted a dog last June, and he’s been [helpful] in disconnecting from swimming. Getting outside and watching him be joyous over the littlest things has been a huge help for me. He’s now my child [laughs], Odie. I’m only 24 years old now and this is what I’ve done professionally for 12 years. I haven’t really experienced life outside of swimming and I’m looking forward to finding what brings me joy — besides my dog.

Click here to read the full article Yahoo! Life.

Midlothian boy born with rare condition gets a special escort on his first day of kindergarten

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Midlothian boy born with rare condition gets a special escort on his first day of kindergarten Batman and Captain Marvel greeted 5-year-old Michael Denison outside his house Monday morning. He got a look inside a police squad car and fire engine before taking off for his first day of school.

By Lori Brown and Shannon Murray, Fox LA

MIDLOTHIAN, Texas – Midlothian police officers and firefighters helped make the first day of kindergarten special for a little boy who is facing some challenges this school year.

Batman and Captain Marvel greeted 5-year-old Michael Denison outside his house Monday morning. He got a look inside a police squad car and fire engine before taking off for his first day of school.

Then at Mountain Peak Elementary, classmates and teachers gave him a warm welcome.

Last week, Michael’s mom, Brittany Denison, made a plea on social media for kids to be kind and asked parents to educate their children about people who are different.

Michael was born with a rare condition called Treacher Collins syndrome. All of the bones in the lower half of his face are smaller than they should be just like the boy Auggie in the movie “Wonder.”

“We’ve had multiple instances where people have used the words scary, monster or weird and that’s really uncomfortable,” she said. “When you’re in a room with Michael for two minutes you understand immediately that he is just the same as every other kid.”

Midlothian’s fire chief said as the story spread on social media, his firefighters knew they wanted to do something to help. So they reached out to the family and school to coordinate the special escort.

“My name is Dale, I am the fire chief,” Dale McCaskill told Michael. “We heard you might be a little nervous going to school your first day so we are going to give you a ride on the fire truck.”

Michael’s mom said when she made that plea on social media she had no idea it would lead to so much support in both the community and from people all across the world.

“To see him smile like that, that was once in a lifetime. That was amazing, unforgettable,” she said after dropping him off for his first day. “He’s an extraordinary kid so I wanted him to have an ordinary year. But I can’t imagine this will be an ordinary year for him anymore. The welcoming experience of the kids being outside, the waves and the smiles, that’s what you want for your kid to be welcomed with open arms.”

She hopes that it creates an even bigger conversation for all families and all students about accepting each other despite differences and standing up for one another.

Click here to read the full article on Fox La.

Photo of Braille-etched Railing at Italian Castle Describing Stunning View Goes Viral

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Braille-etched Railing at Italian Castle

By News 18

Often the internet tends to shine a light on something beautiful and fascinating and a recent photo of a railing on a window in a castle in Italy has gone viral. And it has happened for a good enough reason. Sitting atop a hill that overlooks the Italian city of Naples is the Castel Sant’Elmo (St Elmo Castle) which is a popular tourist haunt.

Hundreds walk up to the top of the castle to enjoy the view but there is yet another attraction on display in the castle. A 92-foot-long piece of stainless steel is attached to the wall fence of the castle of one of its large sized windows and it has a poetic description of the view in Braille. The unique railing was installed by artist Paolo Puddu in 2015 and titled ‘Follow the Shape’ and has been a permanent fixture at the castle since 2017, a report on Ozy.com said. The art had won the fifth edition of the ‘A Work For the Castle’ contest.

Visitors are encouraged to feel the installation wherein they run their hands on the rail and those who can read the Braille script can ‘follow the shape’ on the railing to read the verses from Italian author Giuseppe de Lorenzo’s ‘La terra e l’uomo’ or the ‘The Land and the Man’.

Click here to read the full article on News 18.

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Upcoming Events

  1. City Career Fair
    January 19, 2022 - November 4, 2022
  2. The Small Business Expo–Multiple Event Dates
    February 17, 2022 - December 1, 2022
  3. CSUN Center on Disabilities 2022 Conference
    March 13, 2022 - March 18, 2022

Upcoming Events

  1. City Career Fair
    January 19, 2022 - November 4, 2022
  2. The Small Business Expo–Multiple Event Dates
    February 17, 2022 - December 1, 2022
  3. CSUN Center on Disabilities 2022 Conference
    March 13, 2022 - March 18, 2022