Be a person, family or organization that has an interest in the objective of the Association of promoting and financing research, study and development of possible treatments and/or cures for Usher syndrome type 1B, especially for Retinitis Pigmentosa (RP), caused by the mutation of the MYO7A gene in Usher syndrome 1B.

Accept the Statutes and Internal Regulations of the Association as well as make the annual membership payments proposed by the Board and approved by the annual Ordinary General Assembly, that is, by vote of each of its members.