Resource Directory /

Springfield Resources

  • NeuroJourney

    NeuroJourney is an educational resource for parents, caregivers and clinicians navigating the ever-evolving needs of children with severe neurological impairment (SNI).

    You can find both practical and medical information and insights from parents and clinicians about the social and emotional experiences common to having a child with SNI. Resources include a Caregiver Worksheet as well as guidance to help build the care team, prompts for conversations with specialists and more.

  • Jack’s Basket

    Jack’s Basket supports new parents of a child with Down syndrome by providing information, a support system and a welcome basket to let them know they’re not alone. Baskets are available from the time of diagnosis (prenatal or at birth) up to the baby’s first birthday. Parents, friends, family members, healthcare providers or Down syndrome organizations can request baskets.

    The website also includes local and national resources to support people with Down syndrome and their families.

  • COVID-19 Test to Treat Site

    The Test to Treat site can help you be tested, treated and prescribed treatment for COVID-19 at little to no cost. The site provides information on accessing lifesaving treatments for COVID nationwide and contacting the Centers for Disease Control and Prevention (CDC) COVID-19 hotline and the Disability Information and Access Line (DIAL).

  • eHomeCare Online Course on Caring for Children With Trachs

    The eHomeCare program is a free online training program that aims to provide comprehensive information for those caring for children with a tracheostomy (trach) with/without a ventilator. The training is for:

    • Nurses working in home-based environments
    • Physicians
    • Respiratory therapists
    • Family members and caregivers of children with trachs with and without ventilators

    The course is available until Sept. 30, 2026. Learners can use this course for initial training, an annual review or as an ongoing resource.

  • National Alliance for Children’s Grief

    The National Alliance for Children’s Grief (NACG) is a nationwide, nonprofit organization that raises awareness about the needs of children and teens who are grieving a death. NACG provides education and resources for anyone supporting a child grieving the loss of a loved one.

    In addition to support toolkits on a range of topics, NACG also provides:

    • Information on how to talk about death to children
    • Online learning and webinars
    • A grief support resource library