National Median Arcuate Ligament Syndrome Foundation Inc
Our mission is to bring awareness, education and understanding to the condition Median Arcuate Ligament Syndrome (MALS). Our mission is to spread awareness, educate the public and doctors about MALS. National Median Arcuate Ligament Syndrome (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, Educational, and Research within the clinical and mainstream communities. Our vision is to see a future in which MALS patients receive a timely diagnosis and comprehensive supportive medical care; medical training involves research and awareness to better understand this multifactorial disease; and a partnership of trust builds between the MALS patient and medical communities.
ICO
831764075
2653
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28
Address
Dedham
Home | National MALS Foundation | Non Profit Organization Donate Home About Us MALS Living With MALS Team Approach Patient Stories Resources Shop Get Involved Contact More. Want to join our volunteer team. Click here to Apply. Together We Are Strong.
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🌟 I'm so grateful for organizations like the National MALS Foundation that are dedicated to educating both the public and medical teams about MALS. It’s crucial that we advocate for better diagnosis and care for everyone affected by this condition! 💪 #StrongerTogether #MALSsupport
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How do you feel about your life now versus before your MALS symptoms came into your life. MALS patients often say they are in survival mode versus truly living their lives. Plain Text: With chronic illness, you normalize things most people won’t ever feel.
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How do you feel about your life now versus before your MALS symptoms came into your life. MALS patients often say they are in survival mode versus truly living their lives. Plain Text: With chronic illness, you normalize things most people won’t ever feel.
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