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These sites are to help you find more information regarding MALS.

These are just a few of the charities we've found to be incredibly helpful. Many are of other conditions MALS patients suffer with.

We know MALS can be a strain on everyone's wallet. Although we are unable to help with that we wanted to help others find ways to save a buck.

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These are some files you can take with you to a doctors appointment to help others understand MALS better. 

We are showcasing some of the work our medical board has done regarding MALS. As well as other doctors who are making great strides in MALS research.

You can find videos showcasing MALS here. We have the educational video we did with Osmosis. Plus the Awareness videos we put out every year!

Some articles showcasing MALS. Most of these focus on a single patients story.

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Dedham, MA 02027

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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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