ATIVESITE | Sanofi – Anna’s Story – Living with ASMD

Anna was diagnosed as having a lysosomal storage disease as an infant, but it wasn’t until she was twenty-three years old when she was identified as having Acid Sphingomyelinase Deficiency (ASMD) type B, historically known as Niemann-Pick Disease type B. Anna shares how growing up with this rare disease impacted her family and community. She also highlights how families and patients affected by ASMD play key roles in educating others, including physicians, on the disease itself, as well as the patient experience of living with this rare disease.

Notice:
• Each patient story reflects the real-life experiences of individuals diagnosed with ASMD. Individual experiences may vary.
• Sanofi does not provide medical advice, diagnosis, or treatment. The health information contained herein is provided for general educational purposes only. Your healthcare professional is the best source of information regarding your health. Please consult your healthcare professional if you have any questions about your health or treatment.

MAT-GLB-2001596-4.0 – 10/2024

Source Sanofi YouTube

Sanofi