Students with disabilities are more likely to experience suspensions and other informal removals from school compared to their non-disabled peers. A new toolkit from the U.S. Department of Education is designed to help educators take a proactive and preventative approach to address behaviors that can interfere with learning and keep kids in school. https://bit.ly/4hUnSRR All students benefit when positive strategies are used to create a more inclusive learning environment!
The Arc of the United States
个人和家庭福利保障
Washington,District of Columbia 15,534 位关注者
For people with intellectual and developmental disabilities
关于我们
The Arc is the largest national community-based organization advocating for and serving people with intellectual and developmental disabilities and their families. With approximately 140,000 members affiliated through over 600 state and local chapters across the nation, we are on the front lines to ensure that people with intellectual and developmental disabilities and their families have the support and services they need to be fully engaged in their communities. The Arc promotes and protects the human rights of people with I/DD and actively supports their full inclusion and participation in the community throughout their lifetimes. If you are interested in a career with The Arc, visit our job board: https://www.thearc.org/what-we-do/resources/job-board.
- 网站
-
https://www.thearc.org
The Arc of the United States的外部链接
- 所属行业
- 个人和家庭福利保障
- 规模
- 11-50 人
- 总部
- Washington,District of Columbia
- 类型
- 非营利机构
- 创立
- 1950
- 领域
- Intellectual Disabilities、Autism、Developmental Disabilities和Down Syndrome
地点
-
主要
2000 Pennsylvania Ave NW
Suite 500
US,District of Columbia,Washington,20006
The Arc of the United States员工
动态
-
Barbara's son Jake is medically complex. He relies on Medicaid to provide skilled nursing and personal care services so he can be safe and supported at home. However, due to severe staffing shortages, only a small percentage of Jake’s authorized hours get filled each month. This means his family must fill in the gaps in care to provide that support. Barbara shared, "I am typically ‘on duty’ 24/7, providing clinical care without any qualification or expertise other than lived experience. The relentless task of providing full-time care results in chronic sleep deprivation, exhaustion, and isolation. There are no days off." Medicaid isn't just a program—it's a lifeline that makes living independently possible for millions of disabled Americans. Without more funding, this crisis will only get worse. Join us in telling Congress that lives depend on Medicaid funding. Take 2 minutes to send your message now! https://bit.ly/4hJrqGu #CareCantWait #WeActWednesday #NationalFamilyCaregiversMonth
-
Barbara is a caregiver to her 70-year-old sister, Patricia, who has intellectual and physical disabilities. “I have witnessed how public support for the intellectual and developmental disability (IDD) community has changed over the last 50 years from a focus on what people with IDD were not capable of to a focus on what they are capable of,” says Barbara. “On a personal level, I watched my sibling grow in confidence and happiness as she moved into a group home and was given opportunities to socialize, to pursue her interests, and to express her needs and desires. Inclusion, accessibility, and support services have made a huge positive difference in her life.” Barbara reminds us of the vital role family plays in the lives of people with disabilities. They aren't just support systems—they're champions of inclusion, accessibility, and human potential. Today, we honor their dedication and call for better understanding and support for all caregivers. #NationalFamilyCaregiversMonth Read Barbara and Patricia’s full story on our blog: https://lnkd.in/eeBjV4Hd
-
"I don't know any other way—this is our normal," says Anne Couldridge, Executive Director of The Arc of Cumberland & Perry Counties (CPARC), when people tell her "I don't know how you do it.” In a feature with First for Women, Anne, a full-time caregiver for her 24-year-old son Connor, who has autism, shares her joyful everyday moments with Connor, like dancing to his favorite live concert and laughing over chef Gordon Ramsay. But she opens up about the challenges her family faces, including navigating the "chronically underfunded and understaffed" disability support system. Anne adds: "Soon, we were faced with what so many families are faced with: one parent leaving the workforce to stay home and provide stable and consistent care." To support Connor, she and her husband have built a close-knit "tribe" that understands their family's unique needs. Anne also makes sure to carve out time for herself—whether it's gardening, genealogy, or a quiet morning with a cup of coffee. Anne's deep love and pride for Connor shine in everything she does, including her career. "What is most important is Connor's happiness and well-being and he deserves to have a well-lived life on his terms—not societal norms,” she says. In sharing her family's story, Anne offers a window into the daily realities and unwavering commitment of caregivers supporting loved ones with intellectual and developmental disabilities. As she says, "Caregiving is not my identity; it's just a part of my family's dynamic." Read Anne’s full story in First for Women: https://lnkd.in/eeTRRwJG #NationalFamilyCaregiverMonth
-
Schools today face increasingly hostile threats, and all students (and their parents!) deserve to know that they will be safe if an emergency occurs. Unfortunately, students with disabilities are far too often left out of emergency preparedness, which could be life-threatening. In this The Washington Post piece, our CEO Katy Neas and parent advocates Nancy Baker Curtis and Lori Scott share why this matters and what parents and educators need to know. https://wapo.st/3UKP63x
-
Today is World Kindness Day. Let’s remember that kindness means creating a world where everyone feels valued—including people with disabilities. Saying hi, making sure conversations are inclusive, or learning about accessibility are all ways to show kindness. It’s not just about grand gestures—small, everyday actions can break down barriers and create a sense of belonging. People with disabilities often face isolation, exclusion, or misunderstandings. By taking a moment to listen, offer support, or simply make room, you can help build a more inclusive community. #WorldKindnessDay
-
Debbi Harris is a devoted mother to Josh, who is 31 years old and has complex medical needs and disabilities. Debbi shared with us the challenges and joys of being a family caregiver. "Josh's medical needs fluctuate daily, hourly, sometimes even more frequently. And those acute needs must be addressed so that he's stable and safe and comfortable, before any other plans can be carried out. "I have terrible chronic migraines and other stress-related health conditions. I'm anxious and terrified that something might happen to my son or to my husband. I try to write, play the flute, or read, but I cannot focus long, and I am needed all of the time. “Many people don't take the time to know Josh as a unique person. They limit his humanity and do not invest the time it takes to get to know him as the unique human that he is. We find ourselves feeling a bit isolated and left out much of the time. It has turned my shyness into boldness, as there is no room for silence when my son's health or well-being or access to something he needs to live is at risk. “It's captivating to watch how Joshua navigates the complex world around him with what we consider to be so many limitations. He has been through more medically than most people will ever experience, yet he comes back undiminished. He is happy to be back in his world again, and to see that is gratifying as a parent.” Learn more about Debbi and Josh on our blog: https://lnkd.in/erVqadZr #NationalFamilyCaregiverMonth
-
Do you get Medicaid home and community-based services (HCBS) or have a family member who does? Whether you get help with bathing, getting dressed, making meals, getting around the community, or in other ways, tell us why HCBS are important to you. We want to know your story! Take 5 minutes to share it with us here: ?? https://bit.ly/4fluffi #CareCantWait #SaveMedicaid
-
Mariela is a caregiver to her son, Samir, who has intellectual disability, hydrocephalus, and apraxia. We asked Mariela what she wants people to know about caregivers who support a family member with a disability, and this was her response: “It is important to fight for them, advocate for them, speak for them, include them, and don’t let people give up on them or label them. People with disabilities are perfect the way they are, so don’t outcast them, and don’t allow anyone to do it. They matter too.” Learn more about Mariela and her life as a caregiver on our blog: https://lnkd.in/equP-H5A #NationalFamilyCaregiversMonth
-
Last weekend, over 500 of us gathered for an unforgettable National Convention in Columbus, Ohio. We covered important disability rights issues—from education, employment, and criminal justice reform to advocacy strategies, navigating change, and leadership development. Lifelong relationships are made at our annual gathering, and in between all the learning and networking, we still found time for plenty of fun. The connections and community we’re building together are invaluable. Thank you to The Arc of Ohio and everyone who made it an unforgettable weekend! #TheArcConvention
-
+8