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Impart knowledge

KMSK Knowledge Books "Rare Diseases

An important contribution to the continuous knowledge transfer is made by our meanwhile five KMSK knowledge books "Rare Diseases". In each edition, 10,000 books are distributed free of charge to our dialogue groups (newly) affected families, gynecologists, midwives, pediatricians, family doctors, geneticists, physicians, therapists, psychologists, children's hospitals, health insurers, health policy makers, teachers, researchers at universities, pharmaceutical employees, IV employees, trainees and the media. In this way, we convey knowledge and understanding on the topic of "Rare Diseases in Children". The KMSK knowledge books are made possible thanks to long-term partners and the support of photographers and copywriters.
Knowledge book rare diseases 1/2018

Rare diseases - insights into the lives of affected families

With the first edition of the KMSK Knowledge Book "Rare Diseases - Insights into the Lives of Affected Families", we have raised awareness of affected families in Switzerland whose children are affected by a rare disease.


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Knowledge book rare diseases 2/2019

Rare Diseases - The Path - Genetics, Everyday Life, Family and Life Planning

The second KMSK knowledge book shows the life of the affected families. Different stages are illuminated: From the first signs of a disease, medical and genetic clarifications, everyday life to family and life planning.


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Knowledge book rare diseases 3/2020

Rare diseases - therapies for children and support for families

The third KMSK Knowledge Book Rare Diseases shows what concrete support options are available in everyday life, what forms of therapy have proven successful for affected families, and where they can go for help if they lose their way.


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Knowledge book rare diseases 4/2021

Rare Diseases - Psychosocial Challenges For Parents And Siblings

The fourth KMSK knowledge book "Rare Diseases - Psychosocial Challenges for Parents and Siblings" highlights the many problems that arise for affected families and shows what helps them to cope. Because, a rare disease whirls the life of affected families, destroys dreams and life plans, is a huge challenge for mothers, fathers, siblings but also for grandparents.


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Knowledge book rare diseases 5/2022

Rare Diseases - Digital Knowledge Platform for Parents and Professionals

What offers of help are there? What are they entitled to and who guides them through this unknown jungle? How have other families solved this enormous task? With our 5th KMSK knowledge book "Seltene Krankheiten - Digitale Wissensplattform für Eltern und Fachpersonen" (Rare Diseases - Digital Knowledge Platform for Parents and Professionals), which was created based on our new digital KMSK knowledge platform, we provide (newly) affected families and professionals with a sustainably effective aid tool.


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