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Living With MALS

MALS can be a debilitating condition.

It can make you question your own body and even your mind at times.

We hope that this part of our website can help bring some peace when it comes to that. If you find you are still feeling lost please reach out to us. We are always around to help support our community.

Doctor

Finding a doctor can be an overwhelming process when you are seeking a diagnosis or are newly diagnosed. We have a list that is compiled purely from patient referrals to help with that search.

Trying to go through this fight alone is incredibly hard. We hope that we can help you find a community to support you through your journey!

Support Group Circle
Food Packaging

Eating Post-Op can be an intimidating task. We hope these Tips can help make it not so scary.

Blogging

Follow what we are doing in real-time! We will be posting the important updates to the site and what's going on with our foundation in our blog!

There is a lot of misinformation about what a Celiac Plexus Block is for within our community. We wanted to help dispel some of the myths that surround it.

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P.O. Box 1292

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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