Age: all ages
Pagination: 128 pages
Size: 210 x 148 mm
Binding: perfect binding
Language: French
Publication: December 2024
Free
ISBN: 978-2-38427-234-1 (printed book)/ 978-2-38427-235-8 (ePub)
The amyotrophic lateral sclerosis (ALS), relentless and silent, imposes a trial of every moment on those it affects. Through this collection of short stories, ARSLA not only provides a platform for voices that dare to confront this reality but also pays tribute to the resilience and humanity that endure despite the pain.
By bringing these stories to light, ARSLA unveils the incredible inner richness of those who, in the shadow of hardship, continue to hope and dream.
ARSLA, the French Association for Research on Amyotrophic Lateral Sclerosis (ALS) and other motor neuron diseases, is a public-interest association founded in 1985. The association works alongside thousands of patients, caregivers, healthcare professionals, and researchers to overcome Charcot Disease, a debilitating and incurable neurological condition.
ARSLA funds research teams, supports patients through the provision of technical aids, psychological support, support groups, and more. Additionally, it raises awareness among the general public, policymakers, and government authorities, amplifying the voices of those living with the disease.
ARSLA — 111 rue de Reuilly, 75012 Paris
Website: www.arsla.org
