In May of 2021, Part 1 of this webinar series introduced attendees to the Division for Early Childhood’s (DEC) Recommended Practices (RPs), which offer guidance to parents and professionals who work with young children who have or are at risk for developmental delays or disabilities. Part 2 of the series built upon the information shared in the first webinar. In Part 2, presenters discussed a variety of practice ways to SHARE the RPs as part of the ongoing work of a Parent Center. Presenters then identified ways in which Parent Centers can use the RPs in their daily work with families.
Part 1 in this 15-minute webinar series introduces participants to the Division for Early Childhood’s (DEC) Recommended Practices (RPs), which offer guidance to parents and professionals who work with young children who have or are at risk for developmental delays or disabilities. The webinar is designed to familiarize participants with many of the resources and materials developed in partnership with the ECTA Center to support family use of the RPs in order to promote positive outcomes for young children (0-8) with or at risk of developmental delays and disabilities.
In this webinar for parents, Parent Centers, and community members, key representatives from the U.S. Department of Education and the Centers for Disease Control and Prevention (CDC) discuss safely reopening schools in the fall for in-person learning. Speakers share the process needed to get our children with and without disabilities back in the classroom, including testing and vaccine safety. The webinar is designed to give families an opportunity to express concerns, ask questions, and discuss how to sustain safe operations in schools. CDC spotlights the amazing array of resources it makes available in multiple languages about COVID-19 and vaccinations (including for adolescents), as well materials and toolkits tailored for specific audiences, such as families, community-based organizations, schools, and camp programs.
(2021, June) | Useful to Parent Centers and individuals and families with disabilities seeking information about vaccination for COVID-19, including where to get vaccinated. Have a disability and looking for where to get a COVID-19 vaccination? The U.S. Department of Health and Human Services has launched what it’s calling a first-of-its-kind national hotline offering information […]
In this 37-minute webinar, you’ll learn about the Centers for Disease Control & Prevention’s “Learn the Signs. Act Early.” initiative, the work of the Act Early Ambassadors, and strategies and ideas for how Parent Centers can collaborate with the Ambassadors in their states.
This webinar focused on OSEP’s new requirements for Stakeholder Engagement in State Performance Plan/Annual Performance Report (SPP/APR) package for 2020-2025. The webinar’s subtitle is: What Parent Centers Need to Know. The new SPP/APR package requires states to engage stakeholders throughout the entire SPP/APR process and describe its mechanisms for ensuring such engagement, including a description of the activities conducted to increase the participation of diverse groups of parents and build their capacity to take part in the state’s activities to improve outcomes for children with disabilities. Parent Centers have a key role to play in bringing the parent voice to the state’s SPP/APR activities.
In this webinar, the data team staff from OSEP’s Research to Practice division provide an overview of the types of data that OSEP collects from states and publicly reports under Section 618 of IDEA such as child count and exiting data. Participants are shown how to access the 618 data to answer some commonly asked questions about infants, toddlers, and children with disabilities receiving services under IDEA.
September 2020 A publication of the Center for Parent Information and Resources Written by Rosie Rowe, Executive Director, the PTI of Hawaiʻi English version | Word version (3 pages) and | PDF version (2 pages) Spanish version | Online in HTML | in Word and PDF Return to the Native American Resource Collection Native Hawaiians […]
Most parents in the United States depend on child care to maintain an often-fragile balance between work and family life. Although a shortage of affordable, high-quality care is an issue for all families, it disproportionately affects families of children with disabilities. This 26-page report from the Center for American Progress examines families’ child care experiences when they have children ages 0 to 5 with disabilities.
The study identified many significant obstacles that parents of young children with disabilities face when trying to find child care. Key findings are reported, including how parents managed their individual challenges, patching together help as well as making significant changes to their jobs to provide care. Following these analyses, the report discusses three specific policy solutions. Read more about the contents of the report and access it here.
Meetings to write, review, or revise a child’s IEP typically bring together a team of people who meet in person at least once a year. Now, because of coronavirus, school closures, and social distancing, IEP teams are meeting virtually, either in conference calls or via the Internet. This collection of tip sheets on planning for and participating in virtual meetings was developed collaboratively by six OSEP-funded technical assistance centers, and includes an infographic about virtual IEP meetings (available in English and Spanish); a sample agenda (also available in English and Spanish); technology tips for all participants; suggestions for hosting a virtual meeting; and tips for those participating in a virtual meeting. Read more about (and download) the tip sheets here.