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I was just diagnosed with MALS. My specialist says it's the worst case he's seen in 30 years and that it's getting worse very fast. Next week I will get another CT to discuss surgery options. Since seeing my doctor the spot where my compression is has become so swollen it's visible. The right side of my chest is much larger than my left. For a few days before the swelling I was able to feel the spot through my skin. I am unable to call my specialist because he is out with COVID right now. Has anyone had this? is this normal with MALS or do I need to seek help?
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Abdomen & Pelvis Pain
Celiac artery compression syndrome
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☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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