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This website contains promotional content and is intended for Healthcare Professionals based in the United States only.

Image of a hand holding a compass pointing to ASMD, which leads a path through the forest.

JJ’s Story: Living with ASMD

Find out how JJ handles the physical and emotional challenges of living with ASMD

Jack’s Story: Living with ASMD

Jack shares how he balances life as a kid while managing his ASMD

Each patient story reflects the real-life experiences of individuals diagnosed with ASMD. Individual experiences may vary. Content from these videos should not be considered medical advice.

Patient support networks

Below are various professional medical organizations, national disease groups, education websites, and patient assistance programs that work to support ASMD patients and their families and caregivers.

This listing is provided as a resource only and does not constitute an endorsement by Sanofi of any particular organization or its programming. Additional resources on this topic may be available and should be investigated. Sanofi does not review or control the content of non-Sanofi websites.

National Niemann‑Pick Disease Foundation (NNPDF)

An organization dedicated to supporting and empowering patients and families affected by Niemann-Pick disease
 

National Organization for Rare Disorders (NORD)

A nonprofit patient advocacy organization fighting to improve the lives of patients with rare diseases for over three decades through providing services and support

Patient website

Sanofi is committed to assisting you in educating your patients about ASMD. The website below provides information on ASMD for patients and caregivers.

Visit Patient Website
Photo of two patients with ASMD.

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