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Videos

This is just a small collection of our videos if you would like to see the full catalog please check out our Youtube, Facebook, Instagram, and TikTok pages.

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Educational Video on MALS

We have been filling a critical role in providing clinicians and patients with clinically accurate information about the medical condition called Median Arcuate Ligament Syndrome (MALS). In creating and releasing this educational video in partnership with Osmosis and the National Organization for Rare Disorders (NORD), we will be helping more clinicians understand this rare condition and will be ensuring that patients move more rapidly toward diagnosis. 

Faces of MALS

For Awareness Day (February 17, 2023) we released a video called "Faces of MALS" We really wanted to showcase that MALS can come in all ages, genders, and races. There are times when physicians discount a diagnosis because a patient doesn't fit the MALS stereotype. We wanted to show that MALS doesn't care who you are. So why does a doctor?

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Copyright ©2023 National Median Arcuate Ligament Syndrome Foundation, Inc. All rights reserved. National MALS Foundation is a registered 501(c)(3) nonprofit organization. Please note that the National MALS Foundation provides the information on this website for the benefit of the MALS patient and clinician community. National MALS Foundation is not a medical provider or health care facility and thus can neither diagnose MALS nor endorse or recommend any specific medical treatments. Patients must rely on the personal and individualized medical advice of their qualified health care professionals before they seek any information related to MALS diagnosis and treatment.

© 2023 MALS Foundation

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