The Ichthyosis Association in Norway is an organization that works to support people with ichthyosis, a group of genetic skin diseases characterized by dry and scaly skin. The association aims to raise awareness of the condition, as well as to promote research and development of treatments. Through information work and collaboration with healthcare personnel, the association seeks to improve the quality of life for those affected by ichthyosis.
The organization also offers a community for members, where they can share experiences and support each other. The ichthyosis association organizes activities and meetings to create networks among affected families and individuals. In addition, the association works to collect funds for research and development, as well as to inform about the latest advances in the treatment of ichthyosis.