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MALS in the Press

Love What Matters

"With tears welling up in my eyes, I was only able to mutter one question: ‘But why does it hurt so much when I eat?" Nobody answered me.
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Washington Post

Pain kept this young woman from eating for five years, and doctors didn't know why

Life 2.0

Buckley teen enjoying 'life 2.0' after years of chronic pain
Holding Hands

Think Like a Doctor

Pain kept this young woman from eating for five years, and doctors didn't know why

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Robin's Story

Virginia Woman finds answers after years of symptoms.
City Street at Dusk

All the Way to Cleveland

Learning how to become your own advocate.

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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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