Coping strategy cards
Short, concrete things to try during a wait or before a procedure. Plain language, no clinical vocabulary.
Resources
Printables for families and patients, a wish list for anyone running a collection, and a short directory of organizations that do this properly and at scale.
For families & patients
The same materials that go into a kit, free to print at home. Designed to be usable one-handed, in bed, in short bursts — the constraints that rule out most worksheets you'll find online.
Short, concrete things to try during a wait or before a procedure. Plain language, no clinical vocabulary.
Four techniques that need no equipment, no privacy, and no ability to stand up.
A set a child can keep on a tray table. Written to sound like a person, not a poster.
A short guide for siblings, who carry a specific and under-discussed load.
The Chapter Starter Handbook is the one document that collects all of it — the five-slot kit blueprint and three age tiers, the never list, the hospital outreach template, and the Approval Sheet a child-life specialist signs. 17 pages, free, no application required to read it.
For schools, clubs & workplaces
One rule makes or breaks a drive: collect only from the approved list. "Bring anything" produces used toys, food and scented items that no hospital can accept — which wastes your effort and ours.
The full list is Part Three of our chapter handbook, along with the restrictions behind it. If the hospital you're collecting for has its own prohibited-item list, theirs wins — ask us and we'll help you reconcile them.
Directory
These groups have decades of expertise, staff clinicians, and support lines. For anything urgent or diagnosis-specific, go to them before you come to us.
The professional body for child life specialists — the people who do this work full time, on every ward. Useful for understanding what a hospital's child-life team actually does.
Hospital gowns, play kits and virtual-reality programs aimed squarely at the experience of being in hospital, whatever the diagnosis.
Video and written guidance from parents and clinicians for families caring for a seriously ill child. Unusually honest about the hard parts.
Family-led organization on navigating care, insurance and school for children with any special health care need, with affiliates in every state.
Somewhere for a family to stay and eat when their child's treatment is far from home.
Grants wishes for children with critical illnesses. Referrals can come from a parent, a doctor, or the child themselves.
Free resource kits for newly diagnosed families, plus school re-entry and survivorship support.
Support and plain-language resources for families navigating any serious pediatric diagnosis, including transition-to-adult-care guidance.
Seizure first aid training, school resources, a 24/7 helpline, and local affiliates across the United States.
Information and state-level support networks for traumatic brain injury, including returning to school after injury.
Practical guides and short videos on daily life, school and equipment for children with cerebral palsy.
Care centers, equipment support and summer programs for neuromuscular conditions.
Shunt and surgery information, school support, and a community for families managing hydrocephalus.
A database of rare conditions plus assistance programs — the right starting point when a diagnosis is uncommon enough that little else exists.
If you're a family, a teacher or a clinician and there's a resource you keep wishing existed, tell us. It's a good candidate for the next thing we make.