Want more information on ASMD? Sign up or call to learn more at 1-800-745-4447, Option 3 for Patient Services, then press 1 ‘for more information on ASMD’
Monday – Friday, 8 am – 8 pm ET
Check out this video series to learn more about ASMD
Each chapter in the series breaks down a different ASMD-related topic from signs & symptoms to diagnosis to inheritance.
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.
Below are various professional medical organizations, national disease groups, and education websites 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.
An organization dedicated to supporting and empowering patients and families affected by Niemann-Pick disease
A nonprofit patient advocacy organization fighting to improve the lives of patients with rare diseases for over three decades through providing services and support
