Horses are not only “good for the inside of a man,” but uniquely suited for mental health therapy for veterans due to both instinct and behavior. When paired with a human, a horse will intuitively react to behavioral patterns or body language from the human.
This gives insight into how a person is being perceived. Because they are prey animals, horses are constantly on the lookout for danger and respond quickly with either confrontation or flight. This instinct allows for a deeper level of intervention with a therapist that surpasses any other mental health treatment.
StableStrides is a 501(c)(3) nonprofit whose primary focus is mental health therapy with horses. Situated in the large military community of Colorado Springs, CO, StableStrides is uniquely positioned to serve veterans, active duty servicemembers and military families. On a mission to significantly improve the lives of people through a connection with horses, StableStrides exists because of horses and their ability to touch the lives of people.
Horses and humans share a history that goes back to ancient times and has continued to today. Their role in medicine was first prescribed by Hippocrates (460 BC-375 BC) as a form of natural movement that strengthened the body. Hippocrates, the “Father of Medicine,” believed in health that united body and mind and studied treatment for trauma and mental healthcare. Since then, relationships between horse and human has been studied and incorporated into modern medical practices, both physical and mental.
The physical aspects of horseback riding are used to develop physical strength, muscle development and other physical benefits, while the relationship between horse and human is known to strengthen both mind and spirit. Today, the term Equine Assisted Activities and Therapies (EAAT) defines the use of the horse in recreational and medical intervention. A large portion of EAAT is focused on veterans and their healing journeys during and after service. When partnered with a horse, a veteran is asking the horse to enter into a relationship with them that requires mutual trust and some degree of vulnerability.
One veteran reflects on his mental health sessions at StableStrides by asking:
“How could they go from resting and relaxed to full alert, with a first instinct to run, then to relax again, in seconds? How they could let go of that tension and anxiety and just “be?” As a herd animal, they entrust leadership to the strongest. That leader makes the decisions for the herd for as long as it’s capable or trusted. How can a prey animal, the horse, come to trust an apex predator, a human, with their safety? What a concept. This huge, powerful animal, easily capable of killing me, that fears me because I am a predator, could come to trust and work for me because it wants to.”
As prey animals, centuries of domestication have done little to lessen the horse’s response to danger. They understand that their best chance in escaping danger is to flee. As a result, the horse’s “fight-or-flight” instinct is used for decision making. In addition, horses are extremely perceptive and communicate with body language to convey fear, anger, calm or anxiety.
In a herd, each member relies on the leaders in the hierarchy to make decisions for the safety of the herd, if that leader can be trusted. When in the absence of a herd, the horse will determine if the human is to be trusted as the leader. If not, the horse will decide on his own what is safest.
Therapists have selected horses to incorporate into therapy due to these characteristics, including what many call “mirroring of emotions”. While horses aren’t mirrors, they will often reflect their leader’s emotions. If their leader senses danger and responds with fear, so will the horse. If the horse senses calm in their leader, the horse will likewise be calm, trusting their leader’s instinct. In mental health therapy, the therapist incorporates the horse and the relationship between veteran and horse for a dynamic and therapeutic environment. Through the horse’s reactivity, a veteran and therapist are able to examine and process behavioral reactions or emotional incongruencies. This requires the veteran to be present and mindful as to what is unfolding, and to be transparent about reactions.
Many organizations such as StableStrides exist for the horse-human connection and improve lives through EAAT. Through a connection with horses, mental health therapy strengthens families and individuals. Because of the horse’s unique qualities and instincts, incorporating horses into mental health allows for a therapeutic intervention that surpasses any other form of mental health therapy.
As you wait for a vaccine, you can check out the CDC’s database to see how well your state is progressing.
The rollout of the COVID-19 vaccines has been frustratingly slow, so much so that some health professionals are now considering the potential benefits of delaying the second part of the two-dose vaccine in the interest giving more people the their first shot quicker.
Vaccines from Moderna and Pfizer-BioNTech were both approved for emergency use in December, but as of last week, the number of doses administered had barely reached a tenth of its original goal.
If you’re still one of the millions of people waiting (and you probably are at this point), you can at least check to see how well things are progressing in your state. The COVID Data Tracker from the Centers for Disease Control and Prevention includes an interactive map and state-by-state tallies. The tracker includes data on the total number of vaccine doses distributed and the total number of people who have taken the first dose. It also includes a separate data panel for distribution in long-term care facilities, which have been prioritized in the rollout process.
The CDC’s map is color coded so you can see which states have received the most doses so far per capita. As of Monday, Maine, Vermont, Connecticut, West Virginia, Montana, and the Dakotas had the highest rates of people taking their first dose, while Arizona, Kansas, Michigan, and states in the deep south had the lowest. All told, more than 13 million doses have been distributed, the CDC says.
Armani Williams is a 20-year-old, Detroit-based professional NASCAR driver who is using his racing career as a platform to draw awareness to Autism, promote research-based solutions, and create better life outcomes for families impacted by the disorder.
Williams has competed coast to coast in the United States and throughout Canada. Williams is a two-time NASCAR Drive for Diversity Combine Participant. He currently races in the NASCAR ARCA Menards Series. He has raced as a professional in the ARCA Truck Pro Series, the former NASCAR Canadian Tire Series—now branded as the NASCAR Pinty’s Series, and the NASCAR K&N Pro Series East and West.
The sky is the limit as Williams climbs the ladder to the biggest races in ARCA, the NASCAR Gander Mountain Truck Series, Xfinity and Monster Energy Cup Series. Williams was diagnosed with autism spectrum disorder at the age of two, and he was considered nonverbal. He is the first openly diagnosed autistic NASCAR driver. Autism is a disorder that is characteristically marked by difficulty focusing on and processing different stimuli and tasks simultaneously, in addition to complications with communication. These are two key skills for any race car driver.
Initially, it seemed that Williams’s dream of becoming a professional NASCAR driver was impossible. However, Williams didn’t accept impossible. When he was eight-years-old, Williams began competing in go-kart racing, then bandolero styles vehicles, and quickly progressed to professional series. He raced in the ARCA Truck Pro Series in 2016, signing with SPEAR MotorSports. He broke records by becoming the highest finishing African American in a series race and the highest finishing African American in the series championship.
That same year, Williams was invited to compete in the NASCAR Drive for Diversity Combine and returned to the competition for a second year in a row. In 2017, Williams moved up to a higher level of competition to hone his skills as a race car driver and gain confidence in the former NASCAR Canadian Tires Series—now known as the NASCA Pinty’s Series of Canada. He was coached by team general manager and driver Joey Mc-Colm, along with NASCAR Monster Energy Cup driver D.J. Kennington. To date, Williams has 18 wins and two championships.
In 2018, Williams made his United States debut at the NASCAR K&N Pro Series in Memphis, Tennessee. On September 22nd of that year, Williams earned his first top 10 finish in his 8th start in a NASCAR Sanctioned race event, finishing 9th at New Hampshire Motor Speedway for Simone Autosport. His future plans are to compete in the Menards ARCA Series, NASCAR Gander Outdoor Truck Series, making his way to the highest level of the sport.
Williams’s future is both remarkable and bright. His personal diagnosis with autism and success on the track inspires his philanthropy off the track. In 2015, Williams and his family established the Armani Williams Race 4 Autism Foundation to raise awareness and promote research. He continues to speak to audiences and make appearances to local communities during race week to drive action and hope.
Williams believes that people on the autism spectrum can do anything, and he is proof of that. Team Williams Racing strives to inspire people living with autism to achieve their goals, and to empower friends and family to support best life outcomes.
The Armani Williams Race 4 Autism Foundation drives autism awareness, promotes research, and strives to provide life enrichment opportunities to people and families affected by autism spectrum disorder.
Armani Williams is rising in the NASCAR ranks and looking for sponsors and business partners that are passionate about Autism, and/or Diversity. If interested, please reach out to Team Armani Racing on LinkedIn-Armani Williams or at email@example.com.
New York brothers Bryan and Bradford Manning lost their vision due to a rare genetic eye disorder. Their new clothing brand, Two Blind Brothers, is funding research for a cure.
What would you do if the world around you started disappearing? When Bradford Manning began to lose his vision at about 5 years old, “panic and anxiety set in,” he tells PEOPLE. Two years later, a doctor diagnosed Manning with Stargardt disease — a rare genetic eye disorder that can cause blindness. Manning’s younger brother, Bryan, would soon be diagnosed with the same condition.
Growing up with the disease came with its many challenges and awkward moments, the brothers note:
(Image credit: Courtesy Two Blind Brothers)
meeting a new friend and immediately forgetting what they look like, constantly squinting to see what a teacher writes on the chalkboard, not being able to drive.
It can be super isolating,” Bryan, 30, says. “People can’t see your visibility, so you deal with people who make comments or do things that can really hurt if you aren’t willing to own up to who you are.”
The New York brothers have dedicated their lives — and work — to finding a cure for eye diseases like theirs. In 2016, they founded the clothing brand Two Blind Brothers, which simulates the experience of shopping while blind. All profits benefit organizations like the Foundation for Fighting Blindness that research prevention, treatments, and cures for degenerative eye conditions.
As the sun barely began to rise at 5:52am on Saturday morning, 7 November 2022, Special Olympics Florida athlete Chris Nikic and his Unified partner and coach Dan Grieb, entered the water in Panama City at the start of the IRONMAN Florida triathlon.
Sixteen hours and 46 minutes later, as the nighttime darkness settled in, Chris crossed the finish line and made history of as the first person with Down syndrome to finish a full IRONMAN race.
Chris conquered a 2.4 mile swim, 112 mile bike ride and 26.2 marathon run to complete the IRONMAN in a total time of 16:46:09. During the race, Chris suffered an attack by ants during a nutrition stop and fell off of his bike a couple of times. With blood dripping from his knee, he jumped right back on in a show of true sportsmanship and grit.
Chris’ achievement landed him on the Guinness World Records list. Craig Glenday, Editor-in-Chief, watched Chris persevere with great joy saying, “It’s an honour to welcome Chris into the Guinness World Records fraternity as the first athlete with Down syndrome to complete an IRONMAN, and I look forward to seeing what more is in store from this remarkable young man.”
To stay motivated during the long months of training, Chris and his father Nik developed the 1% better principle – get better, faster and stronger by 1% every day. According to Nik, IRONMAN is further proof that all things are possible with a plan and determination. “To Chris, this race was more than just a finish line and celebration of victory,” he said. “IRONMAN has served as his platform to become one step closer to his goal of living a life of inclusion and leadership.”
“I’m no longer surprised by what Chris can accomplish because I recognize who Chris is; a human being who has goals and dreams just like everyone else,” said Coach Dan. “He wants to make the path easier for those just like him and can follow his lead.”
“Now more than ever, during these uncertain times, we need to be more kind,” said Caroline Naif.
The Michigan mother of a determined 6-year-old living with cerebral palsy (CP) wants you to understand how kindness has made a difference in her daughter’s life.
“We are all facing challenges daily and life looks a little different for each of us, but we can and we will get through this if we work together, be patient and respect one another,” she said. Caroline’s daughter, Briella, was diagnosed with CP at 21 months old. This is the most common motor disability in children, caused by abnormal development or damage to the parts of the brain that control movement, balance and posture. CP looks different in each individual, and in Briella’s case, her speech and leg mobility are affected.
“Briella was born six weeks early, weighing only 3 pounds and 11 ounces, and spent the first 24 days of her life in the NICU. By her first birthday, Briella wasn’t hitting all of her mobility milestones, and right away, we admitted her into physical and occupational therapies. Later, an MRI scan revealed Briella had Spastic Diplegia Cerebral Palsy, caused by a lack of oxygen, either shortly before or after her birth,” said Naif.
Doctors told Caroline that her daughter may never walk or talk on her own.
At three-and-a-half, Briella had Selective Dorsal Rhizotomy, a life-changing lower spinal surgery to get rid of the spasticity and tightness in her legs to strengthen her mobility. This procedure also allows a more independent lifestyle. Briella took her first steps four months after her surgery.
“When you receive a diagnosis, you never know what to expect or how life will look down the road. Our family has gotten to where we are today by lots of research, faith, patience, inspiration and the friendships of other amazing warrior families through social media.”
Briella continues to become stronger and more independent with the physical and emotional support of Variety the Children’s Charity of Detroit – one of the international children’s charity’s 45 “tents.”
Briella, who has been a “Variety Kid” since age 2, received an adaptive bike, which she can pedal and steer by herself, rode Max the horse in the nonprofit’s equestrian riding program, and even modeled in the annual Variety SHINE Fashion show. Through Variety’s mission to simply serve Detroit-area kids, no matter the need, Briella’s never-give-up attitude has blossomed, and she took her first 100 independent steps without her walker earlier this year.
“Briella is a shining example of why Variety is committed to serving kids through programs that enable and empower mobility, confidence and independence. The support and services that Variety provides are simply life-changing, and we are proud to be a small step on Briella’s journey to walk,” said David King, President of Variety the Children’s Charity of Detroit. Briella’s story and involvement in Variety programs were recently featured in a national webcast by the clothing brand Justice.
Over the last 12 months, Briella also started talking in full sentences and began to read. Caroline is encouraged to see Briella’s communication and physical strength grow. “We are finally starting to hear her sweet voice, and it is priceless. She works so hard at school, in therapy and at home as we work toward her goals. My husband and I have seen the growth, and Briella is more centered and aware of her body, giving her less fear to tackle different movement and mobility challenges in physical therapy and daily living.”
Despite meeting challenges many kids her age will never have to consider, she continues on with determination and greets each obstacle with a smile. Briella loves to play, swim, ride her bike, go horseback riding, read books, work with arts and crafts, and attend school and physical therapy. Briella loves to play veterinarian with her stuffed animals and talks about someday being a teacher or working with animals.
“Briella has many goals to keep working towards as she grows from child to teen to adult,” said Caroline. “Ultimately, it’s getting her comfortable with daily living skills and having her involved in the process as much as possible, whether that’s helping brushing her own teeth, getting dressed or assisting with meals. We want Briella to be as comfortable and independent as possible, but at the same time, want her to be able to express her feelings and ask for help when needed.”
“Our world is starting to become more adaptive and inclusive for kids like Briella, but unfortunately, we still have a long way to go by making buildings, stores, schools, playgrounds- you name it- more adaptable and accessible for kids and adults who have mobility issues.”
Briella is a shining example of someone who has, and will continue to surpass expectations with unmatched determination.
You can follow Briella and Caroline’s journey on Facebook and Instagram at Briella + Me.
It began in 2011. Selma Blair didn’t know where it all came from—the overwhelming fatigue, anxiety, depression, neck pain, and severe vertigo.
She didn’t understand why that after she’d drop her son, Arthur, off at school, she was so exhausted that she had to get back into bed. She was puzzled by the sudden loss of feeling in her leg.
Selma would go to doctors seeking answers, but they dismissed her symptoms, believing her exhaustion and fatigue were the result of her becoming a new mother. As the constant pain continued, Selma began to self-medicate to dull the pain.
“When I first suspected that something wasn’t right with my health, with my brain, was when I was pregnant with Arthur,” Selma shared with DIVERSEability Magazine. “I really knew something was wrong when I ran into a UPS truck…literally. I mean, I just skimmed it, but I realized my perception was really off. That’s when I went to the eye doctor thinking it was just my eyes, but it was a perception coordination thing. I’d felt exhausted for years, but it really reached a point that I couldn’t deny it when I was first pregnant with Arthur, and certainly right after his birth.”
It wasn’t until 2018, when she was filming the movie After, that Selma finally got answers.
“When I was in Atlanta the first time shooting the beginning of the film, I had extreme vertigo on steps; I was walking with Josephine Langford down some steps, and I was like, ‘whoa, something’s really happening.’ I couldn’t feel my left leg or my right side and was having difficulty writing and texting, so I sent my manager a video telling him that something very strange is going on.”
Selma heeded the advice from a new doctor who urged her to get an MRI, during which she was in tears, frightened of what was happening to her body.
The results were undeniable: 20 lesions on her brain—it was multiple sclerosis.
“I cried. I had tears. They weren’t tears of panic—they were tears of knowing I now had to give in to a body that had loss of control,” she said in an interview with Good Morning America’s Robin Roberts. “There was some relief in that, ’cause ever since my son was born, I was in an M.S. flare-up and didn’t know. I was giving it everything to seem normal.”
The Journey with M.S.
Multiple sclerosis, or M.S., is a potentially disabling disease. It impacts the brain and central nervous system. It gradually affects the entire body. It causes the immune system to eat away at the protective covering of the nerves.
Having M.S. is an emotional, painful, and unpredictable ride, sometimes leaving people who suffer from the disease wanting to give up.
But, for Selma, that is not the case. “There’s no tragedy for me,” she told Vanity Fair. “I’m happy, and if I can help anyone be more comfortable in their skin, it’s more than I’ve ever done before.”
The 48-year-old actress is resilient, using M.S. as a way to fight, giving hope to others suffering from the disease, and being an advocate for people with disabilities.
Through her journey with M.S., Selma decided that she would open about her disease and not hold anything back from the press or social media. “This is my journey…and all are welcome here,” she writes on her Instagram page.
“It just made sense to be candid. At the time, I was in a long flare and was very symptomatic. It was all new to me, and I just didn’t want to bother playing any type of game of peekaboo,” she said.
This candidness is evidenced through her interviews, such as her appearance on Good Morning America, in which she appeared with a cane and her statement of wanting to make canes chic, which touched many viewers who witnessed the interview, many of whom have their own canes.
Selma rocks her cane, viewing it as a great fashion accessory. When she first stepped out with a cane at the 2019 Vanity Fair Oscar Party in Beverly Hills, Selma turned heads, and prompted others to show the same courage. Twitter feeds were filled with praise for the star:
“The real winner of Oscar night is Selma Blair.”
“#SelmaBlair in tears as she attends the @VanityFair #Oscars party made me cry. I’ve often been walking on aid and exhaustion can just hit and you think, how am I going to do this? But you keep going. She is amazing.”
Selma was—an is—an icon.
Advocating and Raising Awareness
Selma aims to bear all and to help raise awareness for those suffering from this little understood disease and those who, like Selma years ago, have no idea they have M.S.
Selma shared her insights into the struggles that impact her not just as a woman but also as a single mother.
“One of the bigger things is honestly the fatigue. As a mom or anyone trying to do something primarily by themselves with a little tiny person witnessing everything you’re doing, it can feel unsustainable. Figuring out intricacies of neurological disorders is a constant reckoning of how to do better, when to sleep, what you can do, what is very emotionally triggering, you know. There are many layers of it that I now see, people with the disabilities are so busy in our minds.”
Through the sharing of her journey, Selma makes it her mission to help those struggling with M.S. and other disabilities. She credits others who have taken this path of openness and advocacy, such as Michael J. Fox, with inspiring her to do the same.
“I remember when I was younger and Michael J. Fox came out. I was
such a humongous fan of his, and seeing him be so candid about something that seemed so far away from me at the time. I’ve kind of held his example, and I’ve learned that there is an intrinsic value in opening up some of your experiences to people, because the conditions we deal with are often very isolating and when there’s someone that’s out there that could possibly really shed a light on it and bring more attention.”
Her grace and humility as well as her willingness to be a light shining into the unknown darkness for people with disabilities is heroic, though she shrugs off such a label.
“I’m not a hero. I make no bones about that in my life. But I am very honored if my experience, my mess ups and my triumphs help other people,” she said.
For those who are struggling with the disease or for those who have recently been diagnosed, Selma offers some insight and advice:
“Some people said you’ll be better right away. Some said no, healing is not linear. It can take two years. I kind of have fallen in between all that, and I think I would tell someone, ‘Your whole mind can change. Try not to be afraid. I’ve learned so many things, and I pray that you continue to search for what can make you happy and calm. But it takes time. I’m just starting to feel like I’m learning now.’”
To 9-year-old Arthur, his mom is a hero, and he does not view her experiences negatively. “He says, ‘Mommy’s not sick. Mommy’s brave,’” Selma shared with People.
Selma’s commitment to Arthur has remained steadfast and honest. He has seen her face these challenges but remains extremely proud of his resilient mother.
She stated, “He said, ‘I love when you come to school because you make the kids laugh and you answer all their questions.” She remains completely open about her struggles, even with Arthur’s classmates, explaining to them why she may walk differently.
“I explain what’s happening and that my voice doesn’t hurt, and we have really decent exchanges. I had no idea Arthur was proud of that. I thought ‘I’m probably an embarrassment,’ but to know I’m not was one of my proudest moments.”
Selma’s resilience started at a young age. She was born outside of Detroit, Michigan, in the suburb of Southfield. Her interest in acting took hold at an early age, and she credits a high school English teacher, Mr. Toner, with pushing her forward, telling her never to give up, which would serve her well in years to come.
Moving to New York, she was torn between acting and photography.
“When I went to New York, the purpose was a toss-up,” Selma stated. “I didn’t know if I could be a photographer or an actress, but with acting, you can at least go to a class and do workshops, but it was hard to just be an assistant for someone without a lot of experience as a photographer and break-in, so they were both passions.”
Over the years, Selma has played many roles with more than four dozen short and feature films. Her most favorite role was her first major picture, the 1999 film Cruel Intentions with Selma starring opposite actors Ryan Phillippe, Sarah Michelle Gellar, and Reese Witherspoon.
“It was kind of the dream come true first job. After studying in New York, I went to LA, and my first major part was in a real studio film. And while I had done a few small roles before that, that was really my first substantial role with stars that I had loved and they were basically my contemporaries, but, of course, they are already established actors. I laughed and laughed and laughed, and that’s when I kind of realized I really loved what comedy could be and how it could feel.”
Shining Light, Bringing Hope
Selma’s journey is one of inclusion, a journey that many have been on and, sadly, many more are just beginning. Through her candidness, she is willing to share her triumphs and defeats with the world to help others learn, to be a pathfinder for those suffering from the debilitating symptoms of multiple sclerosis. She is a hero of advocacy.
And through it all—her slurred speech, aches and pains, exhaustion, and much more—Selma handles it all with a smile, even amid the COVID-19 pandemic. “…Take this opportunity to be the best you can be, to help your days along,” she said.
For Selma, there is no tragedy—only positivity. “I don’t know if I believed in myself or had the ambition before my diagnosis,” she said to Vanity Fair. “And oddly now I do, and I don’t know if it’s too late.”
More than 1.1 million children under age 6 in the United States receive services for a disability,1 while 2.5 percent of parents of young children have a disability that affects their workforce participation.2
All families, including those with disabilities, benefit from access to affordable child care that will support their children’s development in inclusive and enriching environments. These programs also provide parents with the support they need to thrive. But the dearth3 of inclusive, affordable child care options causes job disruptions for parents of disabled children at twice the rate of those whose children do not have disabilities.4 This fact sheet highlights how the Child Care for Working Families Act provides a comprehensive solution to meet the child care needs of all families.
Families of children with disabilities and the current child care system
The current child care system requires additional public resources to reach all the families who need high-quality services. This lack of public investment results in a mostly private-pay system that marginalizes historically underserved communities.
Although 1 in 8 children ages 3 to 5 who is enrolled in an early childhood program has a disability or significant social or emotional challenges,5 nearly 1 in 3 parents of disabled children report that finding available slots is a primary difficulty in accessing child care, compared with 1 in 4 families with nondisabled children. 6
Nearly one-third of children with disabilities live in poverty,7 making most licensed child care options nearly impossible to afford.8
Children of color are underrepresented in early intervention9 programs through infancy and toddlerhood for reasons pertaining to disproportionate lack of access to quality health care.10
New data suggest that in all but six states, no more than 2 percent of children who receive a child care subsidy have a disability.11*
Children ages 3 to 5 who have disabilities are 14.5 times more likely to face suspension or expulsion than children without disabilities,12 due in part to the fact that only 1 in 5 early childhood educators and providers report “receiving training on children’s social and emotional development.”13
Child care workers, primarily women and disproportionately women of color, earn on average less than $12 an hour,14 and only 1 in 5 early childhood educators receives training on children’s social and emotional development.15 Both of these realities contribute to the inadequate support for providers caring for children with disabilities, given that nearly 10 percent of the early childhood workforce works mostly with children who have disabilities.16
The Child Care for Working Families Act benefits children with disabilities
The Child Care for Working Families Act (CCWFA) creates a new standard for inclusive and accessible child care by investing in communities historically underserved by an underfunded child care system dependent on parental fees to cover the high cost of care.17 Just as importantly, the CCWFA ensures that providers are appropriately compensated for providing quality child care. More specifically, the bill has the following benefits:
The CCWFA prioritizes policies and funding that serve disabled children in high-quality, inclusive early learning environments by:
Affirming the importance of child care in supporting children with disabilities by setting benchmarks that ensure the system provides care for children with disabilities alongside children without disabilities.
Investing in expanding the supply of high-quality, inclusive child care for children with disabilities and infants and toddlers with disabilities.
Requiring states to consider the additional cost of providing high-quality and inclusive care to children with disabilities when developing child care provider payment rates, as well as requiring that parents of disabled children are consulted in the process of developing these rates.
Requiring states to provide training opportunities for child care providers so that they can learn how to care for children with disabilities and conduct developmental screenings.
Prohibiting the use of suspensions, expulsions, and adverse behavioral interventions in all child care settings receiving public funds.
Establishing a new funding stream to provide early intervention services in child care settings.
Allowing states to prioritize funds to construct or renovate child care, including for providers who are caring for children with disabilities.
Breast cancer awareness month or National Breast Cancer Awareness Month begins on Thursday, October 1 and ends on Saturday, October 31 2020.
After skin cancer, breast cancer is the most common cancer in women, with an average lifetime risk of developing breast cancer at 12 percent. There are about 300,000 cases diagnosed each year, with about 15 percent of those (40,000 people) dying from the disease each year.
A clearer way of looking at it and why it’s so serious is that 1 in 8 women will have breast cancer, and 1 woman is diagnosed with breast cancer every two minutes. Additionally, and contrary to what most people believe, breast cancer doesn’t just end with the female folks, men can develop breast cancer as well (although its rare).
Always keep in mind that screening for breast cancer begins at 40 years old (for average risk women) with annual mammograms, and that catching breast cancer early can save your life.
Why Go Pink for October?
Every October, the color pink shows up in full force. From lapel pins to NFL uniforms, people integrate pink into their wardrobes to support breast cancer awareness month. As an awareness campaign, it’s incredibly successful. But awareness is just the first step. From awareness, public health education and advances in research are possible.
Lydia Komarnicky, MD, professor and chair of the Department of Radiation Oncology and a member of the board of the Susan G. Komen Foundation, says wearing pink “reminds people of the importance of the month of October and to get a mammogram if you have forgotten. More importantly, I think the pink shirt, ribbon, hat, or merchandise of your choice honors those who have successfully beaten the disease, those who are currently battling the disease, and also reminds us of those that have succumbed to the disease.”
History Behind the Pink Ribbon or Breast Cancer Awareness
Charlotte Hayey, who had battled breast cancer, introduced the concept of a peach-colored breast cancer awareness ribbon. In the early 1990s, 68-year-old Haley began making peach ribbons by hand in her home. Her daughter, sister and grandmother had breast cancer. She distributed thousands of ribbons at supermarkets with cards that read: “The National Cancer Institute annual budget is $1.8 billion, only 5 percent goes for cancer prevention. Help us wake up our legislators and America by wearing this ribbon.”
Statistics You Should Know
• About 1 in 8 U.S. women (about 12 percent) will develop invasive breast cancer over the course of her lifetime.
• In 2020, an estimated 276,480 new cases of invasive breast cancer are expected to be diagnosed in women in the US, along with 48,530 new cases of non-invasive (in situ) breast cancer.
• About 2,620 new cases of invasive breast cancer are expected to be diagnosed in men in 2020. A man’s lifetime risk of breast cancer is about 1 in 883.
• About 42,170 women in the US are expected to die in 2020 from breast cancer. Death rates have been steady in women under 50 since 2007 but have continued to drop in women over 50. The overall death rate from breast cancer decreased by 1.3 percent per year from 2013 to 2017. These decreases are thought to be the result of treatment advances and earlier detection through screening.
• For women in the US, breast cancer death rates are higher than those for any other cancer, besides lung cancer.
• As of January 2020, there are more than 3.5 million women with a history of breast cancer in the US. This includes women currently being treated and women who have finished treatment.
• Besides skin cancer, breast cancer is the most commonly diagnosed cancer among American women. In 2020, it’s estimated that about 30 percent of newly diagnosed cancers in women will be breast cancers.
• In women under 45, breast cancer is more common in Black women than white women. Overall, Black women are more likely to die of breast cancer. For Asian, Hispanic, and Native-American women, the risk of developing and dying from breast cancer is lower. Ashkenazi Jewish women have a higher risk of breast cancer because of a higher rate of BRCA mutations.
• Breast cancer incidence rates in the US began decreasing in the year 2000, after increasing for the previous two decades. They dropped by 7 percent from 2002 to 2003 alone. One theory is that this decrease was partially due to the reduced use of hormone replacement therapy (HRT) by women after the results of a large study called the Women’s Health Initiative were published in 2002. These results suggested a connection between HRT and increased breast cancer risk. In recent years, incidence rates have increased slightly by 0.3 percent per year.
• A woman’s risk of breast cancer nearly doubles if she has a first-degree relative (mother, sister, daughter) who has been diagnosed with breast cancer. Less than 15 percent of women who get breast cancer have a family member diagnosed with it.
• About 5–10 percent of breast cancers can be linked to known gene mutations inherited from one’s mother or father. Mutations in the BRCA1 and BRCA2 genes are the most common. On average, women with a BRCA1 mutation have up to a 72 percent lifetime risk of developing breast cancer. For women with a BRCA2 mutation, the risk is 69 percent. Breast cancer that is positive for the BRCA1 or BRCA2 mutations tends to develop more often in younger women. An increased ovarian cancer risk is also associated with these genetic mutations. In men, BRCA2 mutations are associated with a lifetime breast cancer risk of about 6.8 percent; BRCA1 mutations are a less frequent cause of breast cancer in men.
• About 85 percent of breast cancers occur in women who have no family history of breast cancer. These occur due to genetic mutations that happen as a result of the aging process and life in general, rather than inherited mutations.
• The most significant risk factors for breast cancer are sex (being a woman) and age (growing older).
The outbreak of COVID-19 may be stressful—it can be difficult to cope with fear and anxiety, changing daily routines, and a general sense of uncertainty.
Although people respond to stressful situations in different ways, taking steps to care for yourself and your family can help you manage stress.
Stress during an infectious disease outbreak can include
Fear and worry about your own health and the health of your loved ones
Changes in sleep or eating patterns
Difficulty sleeping or concentrating
Worsening of chronic health problems
Increased use of alcohol, tobacco, or other drugs
Things You Can Do to Support Yourself
Take breaks from the news. Set aside periods of time each day during which you close your news and social media feeds and turn off the TV. Give yourself some time and space to think about and focus on other things.
Take care of your body. Take deep breaths, stretch, or meditate. Try to eat regular, well-balanced meals; get some physical activity every day; give yourself time to get a full night’s sleep; and avoid alcohol and drugs.
Make time to unwind. Try to engage in activities and hobbies you enjoy. Engaging in these activities offers an important outlet for pleasure, fun, and creativity.
Connect with others. Talk with people you trust about your concerns and how you are feeling. Digital tools can help keep you stay connected with friends, family, and neighbors when you aren’t able to see them in person.
Set goals and priorities. Decide what must get done today and what can wait. Priorities may shift to reflect changes in schedules and routines, and that is okay. Recognize what you have accomplished at the end of the day.
Focus on the facts. Sharing the facts about COVID-19 and understanding the actual risk to yourself and people you care about can make an outbreak less stressful.
Call your healthcare provider if stress gets in the way of your daily activities for several days in a row. Source: nimh.nih.gov
It doesn’t matter if you’re looking for a great date or a long-term relationship—check out the below dating sites to find someone for you:
Match.com This site has more singles than any other dating site — and that includes singles with disabilities. Match.com allows you to easily search and filter profiles for those with disabilities, as well as list your own disability on your profile if you so choose. http://www.match.com/free
Elite Singles 82 percent of its users have earned a bachelor’s, master’s, or doctorate degree, and 90 percent are over 30 years old. https://www.elitesingles.com/free
Zoosk Zoosk is quickly gaining in popularity with disabled singles due to its search-and-filtering capabilities similar to those at Match.com. Its demographic tends to attract younger than that of Match.com (18 to 28 typically). http://www.zoosk.com/browse-free
MySpecialMatch MySpecialMatch is a special social networking site for anyone living with different mental, physical, or emotional ability levels. From finding someone special to share your life with or sharing stories with a someone who fully understands you, Special Bridge really is “bridging the gap for love, friendship, and support.”http://myspecialmatch.com/
Whispers 4 U Since 2002, the team at Whispers 4 U has been helping thousands of disabled singles find love and companionship. They cater to those seeking everything from simple chats to finding solid dating potential, or even landing that one you keep. Video tutorials are in place for helping set up a killer profile and how to best utilize a webcam safely. Free and paid memberships options are available.http://www.whispers4u.com/