Vivere la Paraparesi Spastica Ereditaria ETS (ViPS) is an Italian nonprofit association dedicated to people affected by hereditary spastic paraplegia (HSP), their families, and others connected with the condition. HSP comprises neurodegenerative disorders that commonly involve weakness and spasticity in the legs. ViPS shares information about the disease, diagnosis, and specialist centers for diagnosis and care.

The association works to reduce isolation, promote the rights and inclusion of people with disabilities, and support research into hereditary spastic paraplegias. Its activities include awareness initiatives, scientific and national conferences, online meetings, projects, and opportunities for members to share experiences. ViPS also publicizes research programs, research and thesis awards, and collaborations, including links with Telethon. Its website provides news, practical resources, information about rare-disease services, and contact details.

People can join through annual membership, which includes an association card, event participation, and a dedicated newsletter. Higher contribution levels offer additional recognition or dedicated events. Donations are also welcomed to help sustain the association’s work.