ReportWire

Tag: down syndrome

  • Daytona high school staff member arrested for ‘kicking’ student with Down syndrome, police say

    [ad_1]

    A Seabreeze High School paraprofessional was arrested on Thursday for allegedly kicking a 17-year-old student with Down syndrome during a behavioral incident, according to the Daytona Beach Police Department.The incident was reported to the Seabreeze High School assistant principal, who notified the on-campus school resource officer. During the investigation, police recovered evidence revealing Dontel Wright, 50, intentionally kicked a student. The student then ran and attempted to hide from Wright behind the bleachers.According to the report, Wright then followed the student and forcibly pulled the student from under the bleachers.The student did not sustain any injuries.The student’s parents have been notified and have expressed their intent to press charges on behalf of their child.As a result of the investigation, police arrested Wright.This remains an active criminal case, and no further details are being released at this time.Volusia County Schools released a statement regarding the incident:”Volusia County Schools is aware of the recent arrest of a Seabreeze High School employee on a charge of child abuse. The employee has been immediately reassigned away from students pending the outcome of this investigation.Local law enforcement is leading the criminal investigation, and our Professional Standards team is conducting a parallel employment investigation. We are fully cooperating with law enforcement throughout this process.The safety and well-being of our students is our highest priority. We hold all employees to the strictest standards of professional conduct and do not tolerate any behavior that compromises the trust our families place in us.As this is an active investigation, we cannot share additional details at this time.”

    A Seabreeze High School paraprofessional was arrested on Thursday for allegedly kicking a 17-year-old student with Down syndrome during a behavioral incident, according to the Daytona Beach Police Department.

    The incident was reported to the Seabreeze High School assistant principal, who notified the on-campus school resource officer.

    During the investigation, police recovered evidence revealing Dontel Wright, 50, intentionally kicked a student. The student then ran and attempted to hide from Wright behind the bleachers.

    According to the report, Wright then followed the student and forcibly pulled the student from under the bleachers.

    The student did not sustain any injuries.

    The student’s parents have been notified and have expressed their intent to press charges on behalf of their child.

    As a result of the investigation, police arrested Wright.

    This remains an active criminal case, and no further details are being released at this time.

    Volusia County Schools released a statement regarding the incident:

    “Volusia County Schools is aware of the recent arrest of a Seabreeze High School employee on a charge of child abuse. The employee has been immediately reassigned away from students pending the outcome of this investigation.

    Local law enforcement is leading the criminal investigation, and our Professional Standards team is conducting a parallel employment investigation. We are fully cooperating with law enforcement throughout this process.

    The safety and well-being of our students is our highest priority. We hold all employees to the strictest standards of professional conduct and do not tolerate any behavior that compromises the trust our families place in us.

    As this is an active investigation, we cannot share additional details at this time.”

    [ad_2]

    Source link

  • Orlando half-marathon welcomes inspiring athletes with disabilities

    [ad_1]

    The 49th annual OUC Orlando Half Marathon is set to take place on Dec. 6 at Lake Eola, welcoming more than 5,000 participants to its inclusive event. Chris Nikic, a Special Olympics Florida athlete who made history in 2020 as the first person with Down syndrome to complete an Ironman triathlon, is preparing to run the hometown half-marathon for the first time.”To blow past everyone,” Nikic said. “I have been doing half-marathons, which is pretty cool, and the crowd.” He is also proud to be a leader in recruiting athletes to participate, saying, “I am the top leader in recruiting athletes to come out and participate.”Chris’s father, Nik Nikic, shared insights into his son’s training regimen, noting, “Noah and his friends are helping him train by running at a faster pace for him. And teaching him what it feels like to run at, say, an eight-minute pace versus a 10- or 12-minute pace.” Nik also praised the event, saying, “OUC is wonderful, especially with track shack being part of it,” and emphasized the importance of the marathon, stating, “I think this is a great opportunity. For us to be an example for the rest of the world, and Central Florida and Orlando is a hub for all these things anyway.”Another inspiring participant is Caleb Prewitt, who, along with his mother Karen, will be traveling from Jacksonville to run the OUC half-marathon and the 5K. Caleb has completed 127 races, and they enjoy running together while raising community awareness and promoting inclusion. Karen expressed their passion for the sport, saying, “Do we love running? Yes. We love running — we love racing — we do triathlons as well, so we are kind of crazy.”She highlighted the importance of inclusion, stating, “For him to be included – for people to see him out running – to see what people with Down syndrome and other disabilities can do.”Caleb shared his favorite aspect of running.”So, running with mom,” Caleb said. “We usually run together. I think it’s just the community — we are part of a number of running groups. We just have a lot of fun with it.”Chris and Caleb are among the many remarkable runners to cheer for during the OUC weekend in downtown Orlando.

    The 49th annual OUC Orlando Half Marathon is set to take place on Dec. 6 at Lake Eola, welcoming more than 5,000 participants to its inclusive event.

    Chris Nikic, a Special Olympics Florida athlete who made history in 2020 as the first person with Down syndrome to complete an Ironman triathlon, is preparing to run the hometown half-marathon for the first time.

    “To blow past everyone,” Nikic said. “I have been doing half-marathons, which is pretty cool, and the crowd.”

    He is also proud to be a leader in recruiting athletes to participate, saying, “I am the top leader in recruiting athletes to come out and participate.”

    Chris’s father, Nik Nikic, shared insights into his son’s training regimen, noting, “Noah and his friends are helping him train by running at a faster pace for him. And teaching him what it feels like to run at, say, an eight-minute pace versus a 10- or 12-minute pace.”

    Nik also praised the event, saying, “OUC is wonderful, especially with track shack being part of it,” and emphasized the importance of the marathon, stating, “I think this is a great opportunity. For us to be an example for the rest of the world, and Central Florida and Orlando is a hub for all these things anyway.”

    Another inspiring participant is Caleb Prewitt, who, along with his mother Karen, will be traveling from Jacksonville to run the OUC half-marathon and the 5K.

    Caleb has completed 127 races, and they enjoy running together while raising community awareness and promoting inclusion.

    Karen expressed their passion for the sport, saying, “Do we love running? Yes. We love running — we love racing — we do triathlons as well, so we are kind of crazy.”

    She highlighted the importance of inclusion, stating, “For him to be included – for people to see him out running – to see what people with Down syndrome and other disabilities can do.”

    Caleb shared his favorite aspect of running.

    “So, running with mom,” Caleb said. “We usually run together. I think it’s just the community — we are part of a number of running groups. We just have a lot of fun with it.”

    Chris and Caleb are among the many remarkable runners to cheer for during the OUC weekend in downtown Orlando.

    [ad_2]

    Source link

  • ‘I love dancing with my friends’: Purple Tutu in Alexandria gives special needs children ballet classes – WTOP News

    [ad_1]

    The program, which is now under the umbrella of ArtSpireVA, was originally started by its director Madison Harden with the goal of bringing ballet to dancers in the special needs community.

    This page contains a video which is being blocked by your ad blocker.
    In order to view the video you must disable your ad blocker.

    Purple Tutu in Alexandria teaches ballet to children with Down syndrome

    For the last nine years, children with Down syndrome in Alexandria, Virginia, have had the opportunity to be introduced to ballet thanks to The Purple Tutu.

    The program is now under the umbrella of ArtSpireVA, a group that works to make dance more accessible.

    Program Director Madison Harden brought The Purple Tutu to Alexandria with the goal of teaching ballet to dancers in the special needs community.

    Every Sunday, young dancers meet up at the Just Dance Studio and receive a free 30-minute ballet class, taught by members of the West Potomac High School Dance team.

    The high school’s connection to The Purple Tutu brings pride to Principal Jessica Statz.

    “We have so many great kids,” Statz said “This is one way we can showcase some amazing things that our kids are doing.”

    When you look around the studio, it’s hard to tell who is having more fun, the kids, the student teachers or the parents.

    “Seeing the girls smile is just amazing,” said Adelae Harden, a dance teacher and the program’s vice president. “I love being able to provide the opportunity for the girls to feel comfortable and dance and be themselves.”

    Adelae is the sister of the program director, Madison Harden.

    The program’s president, Rachel Jurta, is a senior at West Potomac High School, and she said seeing the girls grow each week through their relationships and their dancing abilities brings her joy.

    One of the young ladies bringing Jurta joy, is 13-year-old Elsie.

    For the past seven years, Elsie has been a part of the Purple Tutu program, and she said the teachers are her favorite part of the class. That answer was not a surprise after seeing Elsie run and jump into Jurta’s arms as she said goodbye after class ended.

    Elsie’s mom, Erica Kraft, said the ballet classes have replaced her daughter’s physical therapy.

    “Ballet gives her a lot of mental and physical strength,” Kraft said. “From the emotional part, it gives her such pride and confidence.”

    The only dad present at this class was Russ, the father of 16-year-old Sage, who has been attending ballet classes for eight years.

    “A lot of times they get kind of sidelined, and this is something just for them,” Russ said. “It’s great to see them all come together and have fun.”

    Just before Sage left the class for the day, she was asked what her favorite part of being part of The Purple Tutu was, and she answered, “I love to dance with my friends.”

    Get breaking news and daily headlines delivered to your email inbox by signing up here.

    © 2025 WTOP. All Rights Reserved. This website is not intended for users located within the European Economic Area.

    [ad_2]

    Jimmy Alexander

    Source link

  • Program provides mental health services to those who can’t express themselves well – WTOP News

    [ad_1]

    A program in Prince George’s County, Maryland, provides mental health services to those already facing big intellectual challenges.

    Anjolene Smack-Whaley’s son can struggle to control his anger and his emotions, which is understandable since the 24-year-old is on the autism spectrum.

    This page contains a video which is being blocked by your ad blocker.
    In order to view the video you must disable your ad blocker.

    Unique program provides mental health services to those who can’t express themselves well

    But it’s not any less difficult for her to have to deal with.

    “He would make a facial expression. He would talk really loud,” she said. “He would also threaten, ‘I’m going to do this. I’m going to do that.’ He’ll run outside… running down the street.”

    He also works, which means dealing with people who might have different personalities, which sometimes don’t always help situations.

    “When he has problems, especially with dealing with people, especially with the job, it was stressing me out,” said Smack-Whaley, who lives in Bowie.

    But about a year ago, she started getting her son mental health treatment as part of what’s known as Project LIVE (Living with Intention, Vision and Empowerment) through The ARC of Prince George’s County.

    “If I didn’t have it? Ooh, I don’t know. I don’t know,” she said. “I just can’t imagine. It’s just been such a blessing to me and my family with him in this program, because I see a difference in him.”

    Sometimes the mental health challenge might just be anger or frustration, but the loss of a parent or other traumatic experiences can cause the same sorts of mental health challenges that anyone else might deal with when things upend our lives.

    Project LIVE helps with extra challenges

    For most people, an unwillingness to express their feelings isn’t the same as being unable to. For those in Project LIVE, that inability is an extra challenge that needs to be addressed.

    “We found that three and five youth and young adults with intellectual and developmental disabilities have a co-occurring mental health condition,” said Dreu Lindsay, the project coordinator with The ARC of Prince George’s County. “Youth and young adults between this age group are not comfortable with going to a therapist or there’s barriers or stigma related to it.”

    The program aims to bridge all of those gaps, or plow through those barriers.

    “There’s this idea that when you have an intellectual and/or developmental disability, a lot of the behaviors that present are related to that disability and not that the behavior could be a presentation of something else going on, like depression or being suicidal or isolation,” said Lindsay.

    “Sometimes they’re not able to express it, which is part of what leads to the misunderstanding, because they’re not able to say, ‘I’m feeling this way,’” she added.

    But even when correctly diagnosed, the treatment that’s offered will often have to have a different approach. And finding someone willing to provide it can be a challenge too.

    “A lot of mental health therapists would not are not so comfortable or feel knowledgeable supporting people with intellectual and developmental disabilities, because they cannot approach it in the same way as someone who is neurotypical,” Lindsay said. “So the approach to treating them or even building rapport may take a lot longer for them to even get comfortable and open up.

    “When we first started out, we would do kind of more of an office setting. They (the patient) would come in and have therapy in an office setting, but our therapist quickly learned that they’re not comfortable coming to the office, so what she does is meet them in the community,” Lindsay said.

    “So therapy looks like walking around the track. It may be going to a local park and sitting at a bench like anywhere that’s comfortable for the student. It’s really more meeting them where they are, getting them comfortable in their element.”

    The training and approach is unique

    Most of the young adults they work with, who are between 16 and 25 years old, have autism, though sometimes it might be someone with Down syndrome or another disability.

    The grant that helps fund Project LIVE also helps provide training to other therapists willing to lighten the load carried by the therapist working with The Arc. Nationwide, there are very few programs similar to what Project LIVE does.

    “They can participate in talk therapy,” Lindsay said. “We are seeing differences made. We have families coming to us thanking us for our services.”

    That includes Smack-Whaley, who said her son looks forward to his therapy sessions, which are done virtually at her house.

    “He looks forward to when she schedules appointments. He makes sure he gets on for his appointments,” she said.

    “It makes me feel good. It really does,” she said, adding it’s now one less thing she has to worry about while parenting a special needs child. “Because now I don’t have to worry about him. He’s learning how to deal with people and and their personalities, because he has these coping skills.”

    Get breaking news and daily headlines delivered to your email inbox by signing up here.

    © 2025 WTOP. All Rights Reserved. This website is not intended for users located within the European Economic Area.

    [ad_2]

    John Domen

    Source link

  • News We Love: Unique achievement celebrated for boy with Down syndrome

    [ad_1]

    Harrison Dayton loves his food and toys, but his parents remember his time in the neonatal intensive care unit all too well.”We would shake him and be like, ‘Come on, take a breath’ — just hearing his crying and not being able to hold him the first day,” said Wendy Dayton, Harrison’s mom.The 2-and-a-half-year-old was born at 33 weeks and weighed just over three pounds at birth. He was diagnosed with trisomy 21, also known as Down syndrome, something that was uncharted territory for his family.”To be honest, I was devastated,” said Wendy, reflecting on the diagnosis. “I didn’t know what our lives were going to look like.”The Daytons are no strangers to hospital visits. On Mother’s Day of 2024, Harrison suffered a medical setback that left him intubated for 13 days.”I felt hopeless,” said Wendy. “The next morning, I had a conversation with his doctor and asked, ‘Am I going to lose my son?’”But things took a turn for the better this past fall, when Harrison took his first steps. In April, he could be seen practicing walking with a physical therapist.The Daytons are embracing new adventures as they prepare to travel to New York City next week for the National Down Syndrome Society Times Square Presentation, where Harrison’s photo will be displayed on a jumbotron.Wendy says it’s important that Harrison be featured on screen because “there isn’t a lot of representation of children with Down syndrome.””It’s such a hard journey for him, now he’s there,” said Wendy. “He’s happy, and he looks great and healthy, and it’s just truly amazing.”Despite their challenges, this family is navigating parenthood the best way they know how — by learning from their kids every day.”He’s a normal kid,” said Jake Dayton, Harrison’s dad. “We’re raising him the same way we raised any child.””He’s made us more empathetic and more patient,” Wendy added. “You look at life differently with him in your life.”

    Harrison Dayton loves his food and toys, but his parents remember his time in the neonatal intensive care unit all too well.

    “We would shake him and be like, ‘Come on, take a breath’ — just hearing his crying and not being able to hold him the first day,” said Wendy Dayton, Harrison’s mom.

    The 2-and-a-half-year-old was born at 33 weeks and weighed just over three pounds at birth. He was diagnosed with trisomy 21, also known as Down syndrome, something that was uncharted territory for his family.

    “To be honest, I was devastated,” said Wendy, reflecting on the diagnosis. “I didn’t know what our lives were going to look like.”

    The Daytons are no strangers to hospital visits. On Mother’s Day of 2024, Harrison suffered a medical setback that left him intubated for 13 days.

    “I felt hopeless,” said Wendy. “The next morning, I had a conversation with his doctor and asked, ‘Am I going to lose my son?’”

    But things took a turn for the better this past fall, when Harrison took his first steps. In April, he could be seen practicing walking with a physical therapist.

    The Daytons are embracing new adventures as they prepare to travel to New York City next week for the National Down Syndrome Society Times Square Presentation, where Harrison’s photo will be displayed on a jumbotron.

    Wendy says it’s important that Harrison be featured on screen because “there isn’t a lot of representation of children with Down syndrome.”

    “It’s such a hard journey for him, [and] now he’s there,” said Wendy. “He’s happy, and he looks great and healthy, and it’s just truly amazing.”

    Despite their challenges, this family is navigating parenthood the best way they know how — by learning from their kids every day.

    “He’s a normal kid,” said Jake Dayton, Harrison’s dad. “We’re raising him the same way we raised any child.”

    “He’s made us more empathetic and more patient,” Wendy added. “You look at life differently with him in your life.”

    [ad_2]

    Source link

  • CVS, Walgreens now require prescriptions for COVID vaccines in Colorado

    [ad_1]

    People who want to get an updated COVID-19 vaccine at CVS or Walgreens pharmacies in Colorado this fall will need to present a prescription.

    State law allows pharmacists to administer vaccines recommended by the Advisory Committee on Immunization Practices, a group that counsels the director of the Centers for Disease Control and Prevention about who will benefit from which shots.

    In previous years, the committee recommended updated COVID-19 vaccines within days of the U.S. Food and Drug Administration approving them. This year, the committee doesn’t have any meetings scheduled until late September, and may not recommend the shot when it does meet, since Secretary of Health and Human Services Robert F. Kennedy Jr. appointed multiple members with anti-vaccine views after removing all prior appointees in June.

    The lack of a recommendation also means that insurance companies aren’t legally required to pay for the COVID-19 vaccine without out-of-pocket costs. Most private insurers will cover the updated shots this year, though that could change in 2026, according to Reuters.

    Initially, CVS said it couldn’t give the COVID-19 vaccine to anyone in Colorado or 15 other states, because of their ACIP-approval requirement. As of Friday morning, its pharmacies can offer the shots to eligible people who have a prescription, spokeswoman Amy Thibault said.

    As of about 10 a.m. Friday, CVS’s website wouldn’t allow visitors to schedule COVID-19 shots in Colorado.

    Walgreens didn’t respond to questions about its COVID-19 vaccine policy, but its website said patients need a prescription in Colorado. A New York Times reporter found the same in 15 other states.

    The FDA this week recommended the updated shots only for people who are over 65 or have a health condition that puts them at risk for severe disease.

    The listed conditions include:

    • Asthma and other lung diseases
    • Cancer
    • History of stroke or disease in the brain’s blood vessels
    • Chronic kidney disease
    • Liver disease
    • Cystic fibrosis
    • Diabetes (all types)
    • Developmental disabilities, such as Down syndrome
    • Heart problems
    • Mental health conditions, including depression and schizophrenia
    • Dementia
    • Parkinson’s disease
    • Obesity
    • Physical inactivity
    • Current or recent pregnancy
    • Diseases or medications that impair the immune system
    • Smoking

    [ad_2]

    Meg Wingerter

    Source link

  • 1-year-old daughter of NFL cornerback Charvarius Ward has died

    1-year-old daughter of NFL cornerback Charvarius Ward has died

    [ad_1]

    The family of a San Francisco 49ers player is mourning after the death of their 1-year-old daughter.Charvarius Ward posted on social media Tuesday saying his 1-year-old daughter, Amani Joy, died Monday morning.”She was the best blessing we could have asked for, and her joyous spirit made us smile from ear to ear,” Ward said in the statement. The 49ers issued a statement Tuesday saying, “The 49ers family is devastated by the sudden passing of Charvarius Ward’s beloved one-year-old daughter, Amani Joy. Amani truly embodied pure happiness and brought joy to all those around her with her sweet demeanor and contagious laugh.”We will continue to grieve with Charvarius and Monique, while sending them our love and support during this unimaginable time.”Ward’s Instagram account @itslilmooney shows two photos of Amani Joy, including one posted on March 21, World Down Syndrome Day. Amani Joy was born on Nov. 17, 2022 with Trisomy 21, Ward said in the post. Ward’s update on Tuesday said Amani Joy overcame adversity at a young age and was always happy, lighting up every room with her smile.”Having the privilege of being her parents and seeing the world through her eyes has changed us for the better,” Ward said. “She will forever be daddy’s best friend and mommy’s little girl. We’ll miss you and love you forever, Amani Joy.”

    The family of a San Francisco 49ers player is mourning after the death of their 1-year-old daughter.

    Charvarius Ward posted on social media Tuesday saying his 1-year-old daughter, Amani Joy, died Monday morning.

    “She was the best blessing we could have asked for, and her joyous spirit made us smile from ear to ear,” Ward said in the statement.

    The 49ers issued a statement Tuesday saying, “The 49ers family is devastated by the sudden passing of Charvarius Ward’s beloved one-year-old daughter, Amani Joy. Amani truly embodied pure happiness and brought joy to all those around her with her sweet demeanor and contagious laugh.

    “We will continue to grieve with Charvarius and Monique, while sending them our love and support during this unimaginable time.”

    Ward’s Instagram account @itslilmooney shows two photos of Amani Joy, including one posted on March 21, World Down Syndrome Day.

    Amani Joy was born on Nov. 17, 2022 with Trisomy 21, Ward said in the post.

    Ward’s update on Tuesday said Amani Joy overcame adversity at a young age and was always happy, lighting up every room with her smile.

    “Having the privilege of being her parents and seeing the world through her eyes has changed us for the better,” Ward said. “She will forever be daddy’s best friend and mommy’s little girl. We’ll miss you and love you forever, Amani Joy.”

    [ad_2]

    Source link

  • Student with special needs finds acceptance and brotherhood in Clemson fraternity

    Student with special needs finds acceptance and brotherhood in Clemson fraternity

    [ad_1]

    Clemson, South Carolina — At Clemson University in South Carolina, the ClemsonLIFE program gives students with intellectual disabilities a chance to learn life skills for independent living.

    But as much as the program offers, junior Charlie McGee wanted the whole college experience, from alpha to omega. McGee told CBS News he wanted to join a fraternity in order “to have a great time and experience the brotherhood and more joy.”

    Unfortunately, rushing a fraternity is a process. There are interviews and mixers, and even then, there’s no guarantee of acceptance. In fact, no Clemson fraternity had ever taken a student from the ClemsonLIFE program. This marked the first year that members of the program could rush fraternities.

    Last month, when McGee found out he had received a bid from Phi Kappa Alpha, he was so excited he ran out of his left shoe and into the loving arms of his new fraternity brothers.

    “That was one of the coolest moments at Clemson that we had, was seeing that right there,” one of the members of Phi Kappa Alpha told CBS News.

    Several fraternity brothers told CBS News that, at first, some members doubted a person with Down Syndrome could fit in with the group. But they were willing to help McGee, only to learn later that McGee was the one actually helping them.

    “The joy and light that we were missing in our chapter, that we didn’t know we were missing from the beginning, is unreal,” said one fraternity member.

    “He kind of broke all the preconceived notions that I thought of that a fraternity man should be like,” said another. 

    Other Greek life groups have come to the same conclusion. This year, a total of six fraternities and five sororities at Clemson welcomed students from ClemsonLIFE.

    According to McGee, this will be a game-changer. He believes something magical happens whenever you’re accepted this fully by others. And then he adds that when he’s with his fraternity brothers, “My disability, it doesn’t really exist.” 

    [ad_2]

    Source link

  • Viral ad campaign challenges perceptions for World Down Syndrome Day 2024

    Viral ad campaign challenges perceptions for World Down Syndrome Day 2024

    [ad_1]

    People with Down syndrome have a message for the world: “Assume that I can.” An international awareness campaign, launched ahead of World Down Syndrome Day on Thursday, challenges negative biases that people with Down syndrome can face. 

    A young woman, played by Canadian actress Madison Tevlin, discusses the low expectations others have for people like her — whether it be going out to bars, education or even dating with a disability.


    ASSUME THAT I CAN | World Down Syndrome Day 2024 (Official Clean Version) by
    CoorDown on
    YouTube

    “Your assumption becomes reality,” she says in the video. “But hey, if your assumptions become reality, then assume that I can.”

    The video then shows Tevlin’s character drinking at a bar, learning Shakespeare and living on her own. 

    “The message really says a lot,” Tevlin told CBS News. “It’s impactful and powerful to so many people out there in the world.”

    Italy’s CoorDown partnered with the National Down Syndrome Society in the U.S., the Canadian Down Syndrome Society and other organizations around the world. Since its launch on March 14, the campaign has a lot of people talking. 

    “This video is driving the conversation,” Kandi Pickard, president and CEO of NDSS, told CBS News. “Bringing more awareness to Down syndrome, bringing more awareness of still these preconceived notions and stereotypes.”

    She says the NDSS has seen an increase in outreach from individuals that want to do more as a result of this campaign. The ongoing discussion will hopefully lead to a broader discussion about how these preconceived notions hold the disability community back.

    “We need to make sure as a society that we’re respecting that people with disabilities have a voice and that people with disabilities deserve to be heard and respected,” Pickard said. 

    What is World Down Syndrome Day?

    World Down Syndrome Day has been observed annually by the United Nations since 2012. The significance behind the date March 21st, or 3-21, is the fact that those with Down syndrome are born with three copies of Chromosome 21 instead of two. It is celebrated in 190 countries. 

    CoorDown’s social media accounts show people with Down syndrome who aren’t letting society define what it means to be living with an intellectual disability: They’re CEOs, chefs, Emmy-award actors, and more. 

    Mia Armstrong, a 13-year-old who’s already a highly accomplished actor, model and advocate, has added author to her credentials with her new children’s book, “I Am a Masterpiece!” In it, she shares her experiences living with Down syndrome and it is her superpower.

    In 2022, Sofía Jirau became the first woman with Down syndrome to model for Victoria’s Secret. 

    “I love the camera,” Jirau told CBS Mornings lead national correspondent David Begnaud. 

    Charlotte Woodward, is a graduate of George Mason University and an education program associate for the NDSS — and is advocating for a new law that prevents discrimination based on disability in the organ transplant process. 

    Charlotte Woodward

    NDSS


    End the stereotypes

    The message behind the now-viral campaign was inspired by the 2019 speech given by Italian Down syndrome advocate Marta Sodano at the United Nations. She noted that when teachers assume a student cannot understand, they will not teach, and the student doesn’t learn. 

    un755876.jpg
    Marta Sodano, self-advocate for CoorDown Onlus Italy, makes remarks during the annual observance of World Down Syndrome Day in 2019.

    UN Photo/Eskinder Debebe


    “If I think of all the things that were not explained and taught to me, well, I really get angry,” she said, according to a NDSS news release

    This is what’s described as a “self-fulfilling prophecy,” a phrase coined by U.S. sociologist Robert K. Merton in the 1940s. These stereotypes, biases, and low expectations can affect every aspect of people living with intellectual disabilities. 

    “These preconceived notions just don’t always presume competence within the disability community,” Pickard said. “Everybody’s journey is different, but we have to assume that people with disabilities can make decisions about what choices they have in their life.”

    Tevlin, who appeared alongside Woody Harrelson in the 2023 film “Champions,” is well aware of the so-called “notions” society placed on her. 

    “I have Down syndrome and it’s the least interesting thing about me,” she said. “It’s a part of who I am, but it’s not all of me.”

    In a 2023 op-ed for PORTER magazine, Tevlin said that a doctor told her parents that life would be hard for her.  

    “They were told that I may never talk or walk, and I may never be able to hold a job,” she wrote. “If only that doctor could see me now. I certainly talk and I definitely walk. In fact, I just walked a red carpet.”

    Tevlin also challenges society’s stereotypes by presenting her own story as a person who has passions and goals. She doesn’t want people to be judging those with Down syndrome and other disabilities. 

    “Take the time to listen to our stories and what we have to share with the world,” she said. “Just because we have Down syndrome, it doesn’t stop us or limit us.”

    [ad_2]

    Source link

  • Meet Victoria's Secret's First Model With Down Syndrome

    Meet Victoria's Secret's First Model With Down Syndrome

    [ad_1]

    Meet Victoria’s Secret’s First Model With Down Syndrome

    The world’s first down syndrome model, Victoria’s Secret’s Sofia Jiaru, creates history in the fashion world at the age of 25

    Unbelievable Facts

    [ad_2]

    Source link

  • Why So Many Accidental Pregnancies Happen in Your 40s

    Why So Many Accidental Pregnancies Happen in Your 40s

    [ad_1]

    After she turned 42, Teesha Karr thought she was done having kids. Six, in her mind, was perfect. And besides, she was pretty sure she had started menopause. For the past six months she’d had all the same signs as her friends: hot flashes, mood swings, tender breasts. She and her husband decided they could probably safely do away with contraception. But less than a month later, Karr felt a familiar twinge of pain in her ovary—the same twinge she’d felt every time she’d been pregnant before.

    Karr felt embarrassed. “Teenagers accidentally get pregnant. Forty-two-year-old women don’t usually accidentally get pregnant,” she told me. But, really, 42-year-old women accidentally getting pregnant is surprisingly common. Nearly 4 percent of all new babies are born to women 40 and older, according to the latest data from the National Center for Health Statistics. As many as 75 percent of pregnancies in this age range are unplanned. It’s a frequent enough occurrence that the plots of Downton Abbey, Sex Education, And Just Like That, Grey’s Anatomy, and Black-ish have depended on it.

    Many women still believe that by their 40s, unintended pregnancy just isn’t something they have to worry about. After all, many of us are told our whole lives that our biological clock is ticking, that our fertility plummets after 35, and that if we wait too long we’ll likely need some form of reproductive technology to get pregnant—if we can get pregnant at all. If conceiving at this age is so hard, surely you wouldn’t get pregnant by accident, right?

    To understand why pregnancy can, and does, happen at this age, it helps to consider the wacky in-between land that is perimenopause. This stage, which can last anywhere from a few months to about eight years, is typically assumed to be a smooth transition into menopause. In reality, it’s more like the hormonal chaos of puberty, when the ovaries first sputter to life, wreaking all sorts of bodily havoc as they try to figure out their new groove.

    In perimenopause, the ovaries are once again trying to adapt to a new normal. Only now they’re in overdrive, sending out scattered spurts of estrogen to recruit a much scarcer pool of eggs to release during ovulation. During this time, you might ovulate twice in one cycle, miss a cycle altogether, or experience unpredictable flash periods. “Those ovaries are kind of going nuts,” Robin Noble, a gynecologist and menopause specialist in Maine, told me. That can have all sorts of weird consequences. For one, extreme hormone spikes can stimulate the ovary to release extra eggs, which is one reason why fraternal twins are more common in older pregnancies.

    If your ovaries are still ovulating, however sporadically, then you can still get pregnant. The likelihood of getting pregnant does decline with age, particularly toward the tail end of your 30s. By 40, according to the American Society for Reproductive Medicine, the chance of getting pregnant during a single menstrual cycle is less than 5 percent. The problem starts when these low odds lead women to use less reliable contraception, such as the rhythm method or withdrawal. Thanks to hormone spikes and the menstrual cycle becoming less predictable, those methods become even riskier during perimenopause, and the odds can stack up.

    “I hear it every day,” Rachel Pope, an OB/GYN and the head of female sexual health at University Hospitals, in Ohio, told me. “Many women really think that their reproductive potential doesn’t exist anymore, which is not true.” In reality, you can’t be sure you’re in menopause—and therefore really done worrying about pregnancy—until you haven’t had a period for at least a year. For this reason, the Menopause Society recommends keeping a hormonal IUD in or continuing hormonal birth-control pills for a year after your last period, just in case.

    To add to the confusion, some symptoms of perimenopause—missed periods, fatigue, mood shifts—resemble early signs of pregnancy. Lisa Perriera, an OB/GYN and the chief medical director of the Women’s Centers, a group of abortion clinics across several states, sees women almost every month who are shocked to find that their body is still capable of getting pregnant. “I’ve definitely cared for my share of 47-year-olds that are like, ‘I just thought it was menopause,’” she told me.

    Because women in their 40s may be expecting aging-related changes in their body but not looking out for signs of pregnancy, many don’t realize they’re pregnant until 16 or even 20 weeks along, Perriera said. That’s what happened to Anne Ruiz. In 2017, the 43-year-old mom wasn’t experiencing any signs of perimenopause but figured her window for pregnancy was closing fast. Her period had always been irregular, so she wasn’t overly concerned when it didn’t come for a month or two. By the time she started getting morning sickness and took a pregnancy test, she was almost four months pregnant.

    Ruiz and her husband welcomed the news, but also felt overwhelmed. “It was probably maybe like 60 percent excited and 40 percent Oh my God, how are we going to start over?” she told me. She gave birth the next year and immediately got an IUD.

    Facing a pregnancy at a time when you think it is no longer a possibility can be profoundly distressing. “I do see a lot of people shaken by it,” Pope said. “Having a pregnancy that’s not planned can be just so life-altering,” especially at a time when abortions are difficult or impossible to access in many states. A common first reaction is denial. After Christina Ficicchia started experiencing irregular periods, at 42, her gynecologist told her she was in perimenopause. So when she missed a period entirely, she assumed her menstrual cycle was on its way out. Then she started “feeling” pregnant—“after you’ve been pregnant a few times, you kind of know,” she told me. Yet even after a positive pregnancy test, she asked her doctor to take an in-office test to confirm the results. After planning her first two children, Ficicchia struggled to wrap her mind around the choice that she now faced: “It was one that I realistically never thought that I had to make.”

    Many women face extra distress because they know that being pregnant over the age of 40 comes with greater risks. The chance of miscarriage above that age rises to one in three, if not much higher, according to the Mayo Clinic. Pregnant people over 40 are also at a greater risk for preeclampsia, gestational diabetes, placenta previa, preterm delivery, hypertension, pelvic-floor injuries—“basically everything that could go wrong,” Pope said. Risks for Down syndrome and other chromosomal abnormalities also rise.

    After talking with her obstetrician, Ficicchia ultimately chose to continue her pregnancy. Despite her heightened anxiety, she delivered her fourth child, Emmerson, at age 43 with no complications. Karr wasn’t so lucky. After she and her husband adjusted to the news, Karr told her other children to expect a new sibling, and even told her colleagues. Then, at her eight-week ultrasound, the technician told her the fetus had no heartbeat.

    After finally having allowed herself to imagine another baby in her future, Karr was crushed. “I was pretty set with where I was in life and then this all happened and turned everything upside down,” she said. She is still trying to make sense of the loss, and dreads the weekly emails she still receives from pregnancy websites, telling her what to expect at each stage of pregnancy and advertising breastfeeding products. “If I’d known what was happening in my body, then this would have never happened,” she told me. “I was not informed.”

    Of course, bodies can be confusing even for the extremely well informed—for instance, doctors who spend their days explaining perimenopause to their patients. When Pope missed her period in July and started feeling tenderness in her breasts, she had a hunch that she knew what was going on: perimenopause. At 38, she was on the early side. Still, she thought, “this is probably it,” she said. A spontaneous pregnancy seemed unlikely, given that she and her husband had used IVF for their two children and were planning on using it again.

    “Then my husband, who’s a family doctor, was like, ‘Maybe you should check a pregnancy test,’” she said. In fact, Pope wasn’t perimenopausal. She was five weeks pregnant.

    [ad_2]

    Rachel E. Gross

    Source link

  • Child star Mia Armstrong is working on a picture book about her experiences with Down syndrome

    Child star Mia Armstrong is working on a picture book about her experiences with Down syndrome

    [ad_1]

    Child star and activist Mia Armstrong has a picture book coming out next year about her experiences with Down syndrome, what her publisher calls “all the joys and challenges.”

    NEW YORK — Child star and activist Mia Armstrong has a picture book coming out next year about her experiences with Down syndrome, what her publisher calls “all the joys and challenges.”

    Random House Children’s Books announced Monday that Armstrong’s “I Am a Masterpiece!” will be released next January. Illustrated by Alexandra Thompson and co-written by Armstrong and author Marissa Moss, the book is Armstrong’s way of helping kids see the world as she sees it.

    Armstrong has spoken often about Down syndrome, and has called it her “superpower.”

    “I wrote this story because I want to inspire other people to love their own stories and be proud of who they are,” the 12-year-old Armstrong said in a statement. “Down syndrome does not define me and is just one small part of who I am. I’m also an actress, a model, a voiceover artist, a rock climber, a thrill seeker, a daughter, a sister, and a friend. My dream is for ‘I Am a Masterpiece!” to help kids everywhere recognize that people with Down syndrome are capable, strong and unique and that all people deserve to be accepted and loved.”

    Armstrong is the first child with Down syndrome to provide the voice for a cartoon character, the superhero Eon on the Netflix show “Action Pack.” Her other credits include “Hello Jack! The Kindness Show” and “Carol of the Bells.”

    [ad_2]

    Source link

  • Our Son Was Born With Down Syndrome. This Is The Line I Wish We Weren’t Told Repeatedly.

    Our Son Was Born With Down Syndrome. This Is The Line I Wish We Weren’t Told Repeatedly.

    [ad_1]

    Our youngest son, John, was born in the middle of the night in a community hospital. Moments after his birth, I held our newborn in my arms as I had his two older brothers, bent over him and wept with tears of joy. He was so tiny, yet immense, as if he contained the whole universe. Forget exhaustion; my wife and I floated on the joy our son’s birth gifted us.

    A short while later, the covering OB-GYN came to speak with us.

    “I am so sorry. I have bad news. It appears that your son may have a slight case of Down syndrome,” she told us, and then left the room without saying anything else.

    We came crashing down. What did this mean? He was our boy, our son; how could anything be bad? Her tone and her words were devastating. We knew people with Down syndrome ― my wife had even worked in a group home one summer in college ― and we knew we would love him no matter what. But we were at a loss. What was happening?

    We held each other tight and whispered that we would be all right.

    John sleeping on his mother Carol’s chest the day he was born (1996).

    Courtesy of Mark X. Cronin

    As the sun came up on John’s first day of life, we began to get calls and visits from family and friends. Many grew quiet and somber when they learned that John had Down syndrome. Then we started to hear a line that many parents of a child with a disability hear: “God only gives a burden to those he knows who can handle it.”

    Though this sentiment was probably meant to be encouraging, it was not. I wanted to scream. Our son was not a burden. This was not bad news. And what a view of the cosmos! Like God is floating around in the clouds and when he sees a family doing well, he throws down a thunderbolt of misfortune as if to say, “Let’s see if you can handle this.”

    The nurses and staff also grew quiet when they entered the room and spoke in voices loaded with pity.

    Later that day, a close family member visited. She meant to be reassuring when she said, “Maybe he could grow up to get a job pushing a broom at Burger King.” I left the room so no one would see me cry.

    No one said anything like that about his brothers. When I held his brothers in my arms, I believed anything was possible for them: They could grow up to play center field for the New York Yankees; they could go to the moon; everything was laid before them. Now, I was being told that John’s life would be different, would be worse ― that his life would be small.

    Other medical professionals continued to layer on the gloom and doom. In a consultation with a cardiologist (John, like roughly half of the people born with Down syndrome, was born with a significant heart defect), we were told matter-of-factly, “You know, they try to save many of these babies nowadays.”

    John celebrates his second birthday in 1998.
    John celebrates his second birthday in 1998.

    Courtesy of Mark X. Cronin

    John is now 27 years old. He thrived in school, even earning recognition as Student of the Year at the tech school he attended as part of his high school education. He has participated in the Special Olympics since age 6 and has a wall full of the medals he has won.

    Unable to find meaningful work when he finished school, John came to me and said he wanted to go into business together. He suggested that we start John’s Crazy Socks, which we bootstrapped into the world’s largest sock store. More than half our employees are differently abled. The child who could not speak and needed to learn sign language to communicate is now an in-demand keynote speaker and has testified twice before Congress, spoken at the United Nations and been named EY Entrepreneur of the Year.

    John offers one example of how fulfilling life can be for a person with Down syndrome, though there are countless others. That first night in the hospital, we needed to hear it straight ― “John appears to have Down syndrome, which we will confirm with genetic testing” ― but more importantly, we needed to hear “Congratulations!” We needed to hear “What a joy!” We needed that doctor to say that you have just begun down a path that will bring you so much happiness.

    “We do not know the paths our children’s lives will take. We need to hear how wonderful and rich the journey will be. We should not hear the route is limited before our child takes a first step.”

    We are not asking doctors and medical professionals to shy away from providing necessary medical information. A child born with Down syndrome is likely to face a number of significant medical challenges. John required a bowel resection on day three of his life and open-heart surgery before he reached three months, but these medical interventions are available. And a child with Down syndrome may need physical, occupational and speech therapy that can begin as early as the first year.

    These demands can overwhelm parents, so receiving the right information and encouragement from health care professionals and connecting with a support network becomes even more important.

    John fishing from a friend’s boat in the Long Island Sound (2018).
    John fishing from a friend’s boat in the Long Island Sound (2018).

    Courtesy of Mark X. Cronin

    John and I want to change the way the world thinks about people with Down syndrome. We learned firsthand the critical role that health care professionals play in setting the right tone and getting the right information to parents of a newborn with the condition. Making this possible requires two steps:

    • Health care professionals need to know of the full life that a person with Down syndrome can lead and how to speak to parents of a newborn child with Down syndrome.
    • Parents need to be connected to resources and networks where they can get information and support.

    Our medical schools and institutions (hospitals, health centers, etc.) should help health care professionals understand the reality of Down syndrome, not bad clichés from decades ago. John and I are regular speakers at the dental program at the University of Houston, and that’s one way for doctors and other medical professionals to better understand the life of a person with Down syndrome.

    The National Down Syndrome Society and their state and local affiliates offer extensive, easy-to-understand educational information for providers, parents and families and can connect people with local networks. A wonderful organization, Hope Story, which was founded by the parents of a child with Down syndrome, one of whom is a pediatrician, understands the urgency and importance of educating providers and offers resources and training for medical professionals, and it will connect parents with local networks.

    Many states are now passing legislation or establishing regulations to provide better information to parents as well. In New York State, Assembly Bill 4138 requires health care providers to distribute accurate, up-to-date and widely accepted information developed by national and local Down syndrome organizations. If passed, the bill would provide information on hotlines specific to Down syndrome, relevant resource centers and contact information for national and local Down syndrome organizations.

    The author and John give the keynote address at the ALCD Worker Recognition Luncheon (2017).
    The author and John give the keynote address at the ALCD Worker Recognition Luncheon (2017).

    Courtesy of Mark X. Cronin

    Our three boys are all adults now. On the days of their births, we never could have foreseen the paths they would take. Each had some heartache and disappointment, but each has enjoyed marvelous moments of self-discovery, and each has brought meaning and purpose into this world. As parents, we are so fortunate to watch them become the individuals they are.

    We do not know the paths our children’s lives will take. We need to hear how wonderful and rich the journey will be. We should not hear the route is limited before our child takes a first step. Their experience may be different, but not less.

    Here is the greatest truth about all three of our boys, but especially John: He has made me a better person. He made my wife and his brothers better people. That is what parents should hear: “You are fortunate because your new child will lift you and make your life better.” You should hear about the joy your child will bring to the world.

    On John’s first day of life, the people who knew best were his brothers, Patrick and Jamie. Only 6 and 3 years old, they responded with excitement and giddy laughter. They elbowed each other to see who would get to hold John first. They were curious about Down syndrome, but the only thing that mattered to them was they had a new baby brother.

    Here’s what I ask: Act like John’s brothers. When you see or speak to those parents with a newborn, celebrate as you would the birth of any child. Shout “Congratulations!” Bring flowers and balloons and an energy of excitement. Cherish the life and the opportunities. Never be blinded by potential limitations ― always be awed by the possibilities.

    Mark X. Cronin co-founded John’s Crazy Socks, a social enterprise with a mission to spread happiness, with his son John. The pair bootstrapped the business into the world’s largest sock store, earning them recognition as EY’s Entrepreneurs of the Year. Mark is a leader and entrepreneur who founded a software firm and led health care management and technology firms and several consulting firms. He has also organized political campaigns. Mark has spoken before Congress and the UN, given multiple TEDx talks, and is a sought-after keynote speaker. Along with his son and co-founder John Cronin, Mark is a fierce advocate for the rights of the differently abled.

    Do you have a compelling personal story you’d like to see published on HuffPost? Find out what we’re looking for here and send us a pitch.

    [ad_2]

    Source link

  • More women sue Texas, asking court to put emergency block on state’s abortion law

    More women sue Texas, asking court to put emergency block on state’s abortion law

    [ad_1]

    WASHINGTON — One woman had to carry her baby, missing much of her skull, for months knowing she’d bury her daughter soon after she was born. Another started mirroring the life-threatening symptoms that her baby was displaying while in the womb. An OB-GYN found herself secretly traveling out of state to abort her wanted pregnancy, marred by the diagnosis of a fatal fetal anomaly.

    All of the women were told they could not end their pregnancies in Texas, a state that has enacted some of the nation’s most restrictive abortion laws.

    Now, they’re asking a Texas court to put an emergency hold on some abortion restrictions, joining a lawsuit launched earlier this year by five other women who were denied abortions in the state, despite pregnancies they say endangered their health or lives.

    More than a dozen Texas women in total have joined the Center for Reproductive Rights’ lawsuit against the state’s law, which prohibits abortions unless a mother’s life is at risk — an exception that is not clearly defined. Texas doctors who perform abortions risk life in prison and fines of up to $100,000, leaving many women with providers who are unwilling to even discuss terminating a pregnancy.

    “Our hope is that it will allow physicians at least a little more comfort when it comes to patients in obstetrical emergencies who really need an abortion where it’s going to effect their health, fertility or life going forward,” Molly Duane, the lead attorney on the case, told The Associated Press. “Almost all of the plaintiffs in the lawsuit tell similar stories about their doctors saying, if not for this law, I’d give you an abortion right now.”

    The Texas attorney general’s office, which is defending the state in the lawsuit, did not immediately return an email seeking comment Monday.

    The lawsuit serves as a nationwide model for abortion rights advocates to challenge strict new abortion laws states that have rolled out since the Supreme Court overturned Roe v. Wade last year. Sixteen states, including Texas, do not allow abortions when a fatal fetal anomaly is detected while six do not allow exceptions for the mother’s health, according to an analysis by KFF, a health research organization.

    Duane said the Center for Reproductive Rights is looking at filing similar lawsuits in other states, noting that they’ve heard from women across the country. Roughly 25 Texas women have contacted the organization about their own experiences since the initial lawsuit was filed in March.

    The women who joined the lawsuit describe being elated about finding out they were pregnant before the experience turned catastrophic.

    Jessica Bernardo and her husband spent years trying to conceive, even consulting fertility doctors, before finally become pregnant with a daughter, Emma, last July.

    Almost immediately, Bernardo was coughing so hard and often she would sometimes throw up. Fourteen weeks into the pregnancy, test results revealed her baby likely had Down Syndrome, so she consulted a specialist who gave her devastating news: Emma’s heart was underdeveloped and she had a rare, deadly disorder called fetal anasarca, which causes fluid to build up in the body.

    “He handed me a tissue box,” recalled Bernardo, who lives in Frisco, Texas. “I thought maybe the worst thing he was going to tell us was that she’s going to have Down Syndrome. Instead, he said, ‘I can tell you right away…she wouldn’t make it.’”

    The doctor warned her to watch out for high blood pressure and coughing, symptoms of Mirror syndrome, another rare condition where a mother “mirrors” the same problems the fetus is experiencing.

    With Bernardo’s blood pressure numbers climbing, her OB-GYN conferred with the hospital’s ethics board to see if she could end the pregnancy but was advised Bernardo wasn’t sick enough. Bernardo spent $7,000 traveling to Seattle for an abortion a week later.

    Even if Emma made it through the pregnancy, doctors would have immediately needed to drain excess fluids from her body, only for her to survive a few hours or days, Bernardo said.

    “Reading about everything they would do sounded like complete torture to a newborn that would not survive,” she said. “Had I not received an abortion, my life would have very likely been on the line.”

    Other women facing similar situations have not had the financial resources to travel outside of the state.

    Samantha Casiano, a 29-year-old living in eastern Texas, found out halfway through her pregnancy last year that her daughter, Halo, had a rare diagnosis of anencephaly, where much of the skull and brain is missing. Her doctor told her she would have to continue with the pregnancy because of Texas law, even though her baby would not survive.

    With five children, including a goddaughter, at home she quickly realized she could not afford an out-of-state trip for an abortion. The next next few months of her pregnancy were spent trying to raise money for her daughter’s impending funeral, soliciting donations through online websites and launching fundraisers to sell Mexican soup. Halo was born in April, living for only four hours.

    “I was so full of heartbreak and sadness, all at the same time,” Casiano said.

    Women in the lawsuit say they could not openly discuss abortion or labor induction with their doctors, instead asking their doctors discreetly if they should travel outside of the state.

    Dr. Austin Dennard, an OB-GYN in Dallas, never talked about her own abortion with her doctors after they discovered anencephaly on the baby’s ultrasound during her third pregnancy last year. She worried her out-of-state trip to end the pregnancy could jeopardize her medical license or invite harassment against her and her husband, also an OB-GYN. Dennard was inspired to go public with her case when one of her own patients joined the original lawsuit filed in March after traveling to Colorado to abort a twin fetus diagnosed with a life-threatening genetic disorder.

    “There was an enormous amount of fear that I experienced afterward,” Dennard said. “It’s an additional way of feeling silenced. You feel you have to do it in secret and not tell anyone about it.”

    Dennard is expecting another child later this year.

    ___

    Associated Press writer Paul Weber in Austin, Texas, contributed to this report.

    [ad_2]

    Source link

  • Barbie doll with Down syndrome launched by Mattel:

    Barbie doll with Down syndrome launched by Mattel:

    [ad_1]

    The first-ever Barbie doll with Down syndrome has been introduced by toy manufacturer Mattel, who made the announcement on Tuesday. The company had worked closely with the National Down Syndrome Society to ensure the doll accurately represented a person with Down syndrome.   

    The doll’s dress features butterflies, as well as yellow and blue colors — associated with Down syndrome awareness. Accessories that include a pendant necklace with three chevrons represents the three copies of the 21st chromosome. The doll also comes with ankle foot orthotics, which many children with Down syndrome use for support.

    “This Barbie serves as a reminder that we should never underestimate the power of representation,” said Kandi Pickard, NDSS president and CEO, in a press release. “It is a huge step forward for inclusion and a moment that we are celebrating.”

    With its latest addition, “the most diverse doll on the market” hopes to continue to its journey of inclusivity. In 2020, the company’s Barbie Fashionistas line featured its first dolls with vitiligo, a doll with no hair, and a doll with a darker skin tone and a gold prosthetic limb. 

    Down syndrome is a condition in which a person has an extra chromosome, according to the CDC. Each year, about 6,000 babies born in the United States have Down syndrome and is the most common chromosomal condition diagnosed in the United States. 

    “Barbie has evolved significantly over the past several years as we’ve continued to increase our commitment to representation with a variety of diverse dolls,” Kim Culmone, senior vice president of Barbie and dolls design, said in a video announcement. 


    First Barbie Doll with Down syndrome by
    Barbie Life on
    YouTube

    This year, Mattel’s 2023 Fashionistas lineup includes new dolls in a variety of body types including a new Fashionista doll wearing braces and a Ken Fashionista doll with a prosthetic leg, according to the company.

    “Our goal is to enable all children to see themselves in Barbie, while also encouraging children to play with dolls who do not look like themselves,” Lisa McKnight, Executive Vice President and Global Head of Barbie and Dolls, said in a statement. “Doll play outside of a child’s own lived experience can teach understanding and build a greater sense of empathy, leading to a more accepting world.”

    “This is important not just for people with Down syndrome and their families, but also every individual out there who wants to play with dolls – whether they have a disability or not,” Michelle Sagan of the National Down Syndrome Society told CBS News.

    It all began a year ago, Sagan said, when they got a call from the company. The teams participated in countless meetings and strategy calls together.

    “Barbie was constantly asking for feedback and welcoming our ideas both big and small,” Sagan recalled. 

    Charlotte Woodward and Kayla McKeon — both women with Down syndrome — participated in meetings and strategy calls, offering their guidance on the design and style of the doll. 

    After numerous rounds of sketches and feedback, the doll’s physical features were reviewed by a medical professional. 

    The new doll’s face features a rounder shape, smaller ears, and a flat nasal bridge. Her body, meant to be more representative of women with Down syndrome, includes a shorter frame and a longer torso. Her palms even include a single line, a characteristic often associated with those with Down syndrome.

    “We hope that this will open conversations about Down syndrome and how wonderful this community is,” Sagan said. 

    [ad_2]

    Source link

  • Lifecast Body Simulation Global Releases World’s First Child With Down Syndrome Training Manikin

    Lifecast Body Simulation Global Releases World’s First Child With Down Syndrome Training Manikin

    [ad_1]

    Press Release


    Nov 8, 2022

    Lifecast Body Simulation Global, a leader in hyper-realistic training manikins, announced today the release of the world’s first Child with Down Syndrome training manikin. This realistic manikin was formed from a real-life 3D body scan of a seven (7) year old girl with Down syndrome named Gwen and will be available to healthcare education facilities around the world to facilitate specialty and inclusive training in managing Down syndrome.

    Down syndrome (also called Trisomy 21) is a genetic disorder caused when abnormal cell division results in extra genetic material from chromosome 21. While varied amongst patients, a few common physical traits of Down syndrome are low muscle tone, a difficult airway for intubation, smaller stature, gapping in the toes, almond-shaped eyes, a single deep crease across the center of the palm, smaller hands and feet – all of which are accurately represented in the child with Down syndrome training manikin.

    Gwen was created by Lifecast Body Simulation and the University of Greenwich in London who also received support from the Down Syndrome Association. Gwen and her family are truly supporting such a worthy cause in creating awareness of Down syndrome and giving healthcare providers an accurate means of training while continuing to support diversity and inclusion in simulation-based education and training.

    “Gwen is the world’s first truly inclusive manikin. Our goal is to make manikins that look like real people. We worked with the University of Greenwich in the UK to create this manikin lifecast and 3D scan of Gwen, a 7 year-old girl with Down Syndrome who lives in the UK with her dad, mum and brother,” says David Halliwell, Founding Director of Lifecast Body Simulation Ltd.

    The Gwen child with Down syndrome training manikin will make her official presence into the marketplace at the Association for Simulated Practice in Healthcare (ASPiH) on November 6 in Birmingham, UK and will be launching in the United States at the International Meeting on Simulation in Healthcare (IMSH) Jan. 21, 2023 in Orlando, Florida.

    Source: Echo Healthcare

    [ad_2]

    Source link

  • Bay Area Non-Profit Hope Services, Re-Opens and Welcomes Back Clients With Developmental Disabilities & Mental Health Needs to In-Person Programs

    Bay Area Non-Profit Hope Services, Re-Opens and Welcomes Back Clients With Developmental Disabilities & Mental Health Needs to In-Person Programs

    [ad_1]

    Press Release



    updated: Jun 18, 2021

    Hope Services, the leading provider of programs and services for the developmentally disabled and those with mental health needs in the Silicon Valley and the Central Coast, announced it will begin re-opening in-person programs this month to approximately 3,200 clients and 900 program staff & employees. The re-opening starts June 15 and will happen in three phases through September 2021 to ensure safety and proper protocols are in place.

    “These next steps will be difficult, and it will take a lot of work to continue to follow the guidance for keeping our community safe, but Hope Services is committed to the safety of our clients and staff. We appreciate the tremendous support and understanding as we venture forward to reinvent our programs to optimize learning for our clients.”

    “Chip” Huggins, President/CEO of Hope Services

    Hope Services has made tremendous adjustments since the onset of the pandemic, and re-opening will require continued resilience. Shortly after the shelter in place took effect Hope’s in-person therapy, programming, and services had to cease, Hope Services made the necessary pivot to create and implement From Hope to Home™; a virtual service delivery system developed completely in-house, and approved by the Regional Center. The continuity of services through the program helped clients maintain a needed structure and a daily connection to the Hope community in such a challenging time. The first phase of welcoming clients back begins with a hybrid model, blending in person services and distance learning.

    At one point the challenge of going from lockdown to full re-opening seemed almost unsurmountable. However, just as they did 15 months ago when the pandemic began, the Hope community got to work to identify challenges and solutions.

    Hope Services recognizes that although there is excitement to be together in-person, there may also be some anxiety around these changes. To help with this transition Hope continues to offer weekly staff sessions with the mental health team.

    The behind the scenes efforts of caring, creative, and dedicated staff, eager clients & client families, and community partners provides the opportunity to re-open, and once again welcome back Hope.

    Supporting link: http://www.hopeservices.org

    About Hope Services: Since 1952, Hope Services has provided programs and services to people with developmental disabilities and mental health needs. Hope serves more than 3,200 people and their families, and provides a broad spectrum of services for infants through children’s services (age 0-5); day services; employment and job training through local companies including The Home Depot, Costco, Target, Whole Foods, and Google; mental health services; senior services; and community living services. Hope Services is accredited by CARF International, the most prestigious accreditation agency in the disability sector. Hope also operates HopeTHRIFT, which supports the organization’s services and helps with job training skills.

    Contact: Stacy Houston – Marketing Manager, shouston@hopeservices.org

    Source: Hope Services

    [ad_2]

    Source link

  • New Film Exposes Nationwide Abuses of Seniors and People With Disabilities, Calls for Reforms in Guardianships

    New Film Exposes Nationwide Abuses of Seniors and People With Disabilities, Calls for Reforms in Guardianships

    [ad_1]

    Spectrum Institute Says the Enforcement of the ADA by U.S. Dept. of Justice Will Require State Courts to Provide True Access to Justice

    Press Release



    updated: Mar 1, 2018

    “Pursuit of Justice” is a film (36 minutes) by Greg Byers which tracks the advocacy of civil rights attorney Thomas F. Coleman, clinical psychologist Nora J. Baladerian, and a growing network of activists as they travel the country promoting reforms in adult guardianship proceedings involving seniors and adults with various disabilities. The documentary is sponsored by Spectrum Institute.

    Like the recent Oscar-nominated film “Edith+Eddie”, “Pursuit of Justice” shows how guardianships can be manipulated to abuse the rights of vulnerable adults. While “Edith+Eddie” involves an interracial couple in their nineties, “Pursuit of Justice” focuses on adults of various ages who have different types of disabilities.

    In addition to giving examples of injustices perpetrated on adults all along the age spectrum, ‘Pursuit of Justice’ offers hope that sustained and creative advocacy will eventually cause systemic reforms to the judicial systems in all 50 states.

    Thomas F. Coleman, Spectrum Institute

    Stephen and Greg are autistic men in their twenties. Mickey, in his thirties, had an intellectual disability. Kay, in her forties, has Down syndrome. Michael, an articulate young adult in his late teens, has cerebral palsy. David, a former NPR news editor was 59 when the onset of an illness devastated his mobility and impaired his ability to communicate.

    There are currently more than 1.5 million adults in the United States who are in court-ordered guardianships or conservatorships. Tens of thousands of new cases are filed each year. In these proceedings, judges take away the rights of adults to make basic life decisions – where to live or work, control over finances, medical choices, whether to marry or have sex, who to socialize with, etc.

    Each state uses its own rules in guardianship cases – rules which often deny meaningful access to justice to the adults whose fundamental rights are placed at risk in these proceedings.

    “Pursuit of Justice” offers a path for significant reform by promoting federal oversight of these state-operated judicial proceedings. Without voluntary changes by the states, it will require effective enforcement of the Americans with Disabilities Act by the U.S. Dept. of Justice to transform the status quo of unjust assembly-line practices into ADA-compliant proceedings that provide true access to justice.

    “Pursuit of Justice” was released on March 1, 2018 – just days before the film “Edith+Eddie” was considered for an Oscar at the Academy Awards. “Edith+Eddie” tells the story of an elderly couple who fell in love in their final years – only to be torn apart through an abusive guardianship proceeding initiated by an intruding relative.

    “Edith+Eddie” touches the hearts of viewers, leaving them wondering how such an injustice could occur. Although this masterfully produced and artfully directed film forcefully introduces viewers to a specific instance of oppression, the film’s audiences are left unaware that similar injustices are occurring every day in America and are ruining the lives of scores of adults of all ages, incomes, and political affiliations.

    In addition to giving examples of injustices perpetrated on adults all along the age spectrum, “Pursuit of Justice” offers hope that sustained and creative advocacy will eventually cause systemic reforms to the judicial systems in all 50 states.

    The combined impact of the films “Edith+Eddie” and “Pursuit of Justice” could make 2018 a watershed year for guardianship reform. These documentaries have just the right ingredients to become the impetus for significant and lasting political and legal reforms.

    Watch the film online at: http://www.pursuitofjusticefilm.com

    Spectrum Institute is a nonprofit organization promoting equal rights and justice for people with disabilities – especially for people with intellectual and developmental disabilities. In addition to its Disability and Guardianship Project, the organization also operates a Disability and Abuse Project.

    Contact:
    Thomas F. Coleman
    (818) 230-5156
    tomcoleman@spectruminstitute.org

    Source: Spectrum Institute

    [ad_2]

    Source link

  • Ron Suskind, Pulitzer-Winning Author, to Speak About His Family’s Journey in Connecting With Autistic Son

    Ron Suskind, Pulitzer-Winning Author, to Speak About His Family’s Journey in Connecting With Autistic Son

    [ad_1]

    A family’s story chronicled in the 2017 Academy Award-nominated documentary, “Life Animated”

    Press Release



    updated: Apr 24, 2017

    On April 27, Marbridge will host the fifth annual CoAct Project™, a national executive symposium to discuss best care practices, industry challenges, and building relationships to better care for individuals with intellectual disabilities.  

    Best-selling author Ron Suskind and his autistic son, Owen, will serve as keynote speakers; they are the subject of this year’s Academy Award-nominated documentary Life, Animated. Together, they will share their astonishing story of how Owen, following a diagnosis of regressive autism at 3 years old, slowly learned language and emotional dynamics by studying animated Disney movies. And how, through a series of startling breakthroughs, the family began to communicate with their lost son in movie dialogue.

    April is Autism Awareness Month. We now know that Autism affects one in every 68 children in the United States. We are eager to learn more from Mr. Suskind, and to explore the unknown capacities of the human mind. It is an honor to have Ron speaking at the CoAct Project this year, and to consider the impact this knowledge could have on so many individuals, their families and caregivers.

    Scott McAvoy, Vice President of Operations

    “Autism now affects one in every 68 children in the United States[i].  Currently at Marbridge, the autism diagnosis represents 25% of our resident population. We are eager to learn more from Mr. Suskind, and to explore the unknown capacities of the human mind,” states Scott McAvoy, Vice President of Operations at Marbridge. “It is an honor to have Ron speaking at the CoAct Project this year, and to consider the impact this knowledge could have on so many individuals, their families and caregivers.”

    • Autism Spectrum Disorder (ASD) refers to a range of conditions characterized by challenges with social skills, repetitive behaviors, speech and nonverbal communication, as well as by unique strengths and differences. There is not one autism but many types, caused by different combinations of genetic and environmental influences.
    • Autism occurs in all racial, ethnic, and socioeconomic groups, but is almost five times more common among boys than among girls.[ii]
    • April is Autism Awareness Month

    This year will serve as the 5th annual symposium of its kind at Marbridge, bringing together leadership, organizations and professionals in the field of intellectual disability, including Autism, Down Syndrome, Williams Syndrome, Cerebral Palsy, seizure disorder and traumatic brain injury. “In our conversations with industry partners, it is apparent that there are a host of topics and concerns we share,” said James Stacey, President of Marbridge. “In 2013, we decided it was time to establish a forum where we could discuss our commonalities and share best practices.  We are committed to this collaboration moving forward, and to enhancing the lives of individuals with special needs.”

    ABOUT MARBRIDGE

    Founded in 1953, Marbridge is a non-profit residential community for adults with intellectual disabilities (www.marbridge.org). Located on 170 acres in south Austin, Texas, the campus consists of three interconnected communities providing varying levels of care—from semi-independent care, to assisted living, to skilled nursing and physical rehabilitation services. With over 250 residents, the population represents a diversity of diagnoses, including Autism, Down Syndrome, Williams Syndrome, Cerebral Palsy, seizure disorder and traumatic brain injury.  With the unique Life Options Program, Marbridge provides a distinctly different lifestyle that ensures that each individual has the opportunity to learn, experience and achieve a whole new life at Marbridge.

    Contact: Scott McAvoy, Vice President of Operations, Marbridge Foundation

    512-282-1144, 512-845-4237 (mobile), smcavoy@marbridge.org

    #   #   #

    [i]  In 2016, the Centers for Disease Control’s Autism and Developmental Disabilities Monitoring (ADDM) reported that approximately 1 in 68 children in the United States has been identified with an Autism Spectrum Disorder (ASD). This rate remains the same as in 2014, which is the first time it has not risen.

    [ii] On March 27, 2014, the Centers for Disease Control and Prevention (CDC) released new data on the prevalence of autism in the United States. This surveillance study identified 1 in 68 children (1 in 42 boys and 1 in 189 girls) as having Autism Spectrum Disorder (ASD).

    Source: Marbridge Foundation

    [ad_2]

    Source link