Welcome to
EURO-HSP

EURO-HSP is a Federation of national  associations related with a Rare Disease called Hereditary Spastic Paraplegia or Strümpell-Lorrain disease. The federation was made up during the project Rare! Together from EURORDIS. 

NEWS from EURO-HSP

Adolf-Struempell-Prize Winner 2026: Dr. Giulia Guarato

Euro-HSP is pleased to announce that the Adolf-Struempell-Prize-2026 is awarded to Dr. Giulia Guarato (IRCCS E. Medea , Italy).

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Adolf-Strümpell-Prize 2026

Best Paper Award Adolf-Strümpell-Prize 2026 for HSP-Therapy

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Project euroSPG11/15 started

By March 2025 Euro-HSP started supporting a new project for development of cure which focuses on SPG11 and related subtypes. This extends our…

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Adolf Struempell Prize Winner 2025: Mrs. Alzhraa A. Ibrahim, PhD

Euro-HSP is pleased to announce that the Adolf Struempell Prize 2025 will be awarded to Mrs. Alzhraa A. Ibrahim, PhD

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HSP Patient Journey developed by Adam Lawrence and Lori Renna Linton

Patient Journeys  are info-graphical overviews that visualize patients’ needs in the care of their rare disease. Because Patient Journeys are designed…

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EVENTS & MEETINGS

Euro-HSP will be at the Tom-Wahlig-Symposium 2026  (Recklinghausen, Germany, March 12 & 13, 2026)
 

On October 17, 2026 we will celebrate the annual HSP / PLS World Day!!! 

This year the celbration will be combined with the annual Euro-HSP convention. The organization is performed by Life4HSP. All patients worldwide will get the opportunity to joiny online (details to be fixed).

 

 


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„Vital to quality of life is the ability to work together, learn from each other, and help each other grow”

Support our current
euroSPG4 project

We would be pleased and grateful for a donation for our ongoing euroSPG4 project. 

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