The National MALS Foundation is a nonprofit organization dedicated to spreading awareness of MALS, a rare debilitating disease.
The National MALS Foundation is a nonprofit organization dedicated to the mission of providing hope and support (body, mind and spirit) to those suffering from the debilitating symptoms of Median Arcuate Ligament Syndrome (MALS) through Advocacy, Awareness, Education, and Research within the clinical and mainstream communities.
We started this foundation to:
Be the voice and bring awareness to such a debilitating disease; advocate for faster and more reliable diagnostic tests, pre- and post-surgical protocols. Including short and long term follow-up, and a smooth transition of care for comprehensive supportive services based on body, mind, and spirit--full-body care.