Care Home Without Walls is an interdisciplinary law-and-psychology book about what happens when a disabled person’s ordinary home becomes the place where institutional levels of care, supervision, risk management and dependency are imposed without the staffing, safeguards, freedom or accountability expected in a formal institution. It asks how a person can receive sufficient support at home without family members being coerced into unpaid labour, without intimate care being exchanged for compliance, and without disability being used to erase autonomy.
| The book’s central aim To provide law students, lawyers, psychologists, clinicians, social-care professionals, advocates and disabled people with a rigorous method for separating lived harm from legal labels; identifying the evidence required for each claim; and designing support that protects safety, capacity, identity, belief, relationships, companion animals and freedom of movement. |
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Questions the book investigates
What the book does not claim
The book does not claim that every unmet need is slavery, every coercive choice is false imprisonment, every offensive remark is statutory harassment, or every distressing event produces a DSM disorder. Each legal cause of action and clinical diagnosis has separate elements. The book’s method is to preserve the seriousness of the lived account while refusing to collapse distinct tests into one another.
“Care Home Without Walls” is a proposed analytical and service-design concept, not a statutory entitlement or clinical diagnosis. Its practical purpose is to ask which functions an institution would provide, which of those functions are actually needed across the day and night, and how they can be delivered lawfully in an ordinary home with proper staffing, consent, contingency, review and accountability.