Organizations
A Japanese patient association founded in 1993, centred on families affected by CIPA, incorporated as an NPO in 2002.
Records are grouped by source attribution. This does not confirm service capacity, legal status or international access.
Search covers what this site wrote about each entry, in any of the three languages. It does not reach into the source documents.
Tomorrow patient association
A catalogue of information on the condition, daily-life support, professional guidance, picture stories and historical surveys. Some entries link to files; others are bibliographic listings only.
Tomorrow patient association
An index to disease background, symptoms, participation and everyday-life questions.
Tomorrow patient association
A lead to a handbook for families, teachers and support workers.
Tomorrow patient association
A historical survey covering life experiences, difficulties and support systems.
Tomorrow patient association
A historical account of how Japan’s disability welfare systems affected people with CIPA around 2011, with discussion of reforms, services and policy documents from that period.
Tomorrow patient association
A two-page illustrated resource on risks associated with impaired pain perception and sweating, covering activity, wheelchair use, burn prevention, temperature management and everyday observation.
Tomorrow patient association
School-based picture stories help children understand sweating and pain. Care points for adults are written into the school nurse character’s lines and run through the narration rather than forming a separate appendix.
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