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ASMD : Living with a rare disease - Testimony of Tristan and his mother

Tristan lives with a lysosomal storage disease called ASMD (Acid Sphingomyelinase Deficiency) or Niemann-Pick type B disease. On the occasion of the awareness month for this rare disease which is held every year in October, he shares his story with Marie-Christine, his mother. "I have an enzyme deficiency, this enzyme allows to burn fats that accumulate around different organs: liver, lungs and spleen. I couldn't make any effort, I was on oxygen 15 hours all day ... " Discover their harrowing stories and learn more about acid sphingomyelinase deficiency. To learn more, visit: https://www.sanofi.fr/fr/nos-domaines... 7000035510 B - 10/2021