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Mixed Connective Tissue Disease (MCTD) diet. Is there a diet which improves the quality of life of people with Mixed Connective Tissue Disease (MCTD)?

Diet and Mixed Connective Tissue Disease (MCTD): foods that patients report help their quality of life, with a medically reviewed summary.

Mixed Connective Tissue Disease (MCTD) diet
5 answers
Autoimmune protocol diet

Posted Sep 17, 2017 by Tina Cavitt 3820
An alkaline diet helps some.

Posted Nov 19, 2018 by Kelly 5450
Look for an anti-inflammatory diet. Two great ones are "Paleo AIP" and "Paleo Wahls Protocol"

Posted Nov 23, 2018 by Miguel 300
I don’t really know I barely have an appetite

Posted Apr 18, 2019 by DelightfullyChaotic 1220
Im not sure about a specific diet because Auto-immune diseases is your immune system attacking itself. There are 2 foods I know to avoid and that's. Red meat and white potato's. I love Steaks and I try not to eat Red meat no more than twice a month. I love potatos of course. I make homemade french fries never store bought. Had to limit that as well. I started buying the gold/yellow potato.

Posted Jan 12, 2022 by Kendalla 1100

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MIXED CONNECTIVE TISSUE DISEASE (MCTD) STORIES
Mixed Connective Tissue Disease (MCTD) stories
I was 14 when the pain really started. My hands would get so cold they would turn white, and then purple and blue. My parents always told me I was dramatic and that I wasn't as sick as I wanted to be, so it took me a long time to finally tell them wh...
Mixed Connective Tissue Disease (MCTD) stories
After an abusive childhood I finally found the person to spend my life with.  It took 30 years.  I wanted children right away due to our ages (30 and 36).  It took a year but I finally became pregnant and had a healthy 8 lb 1 oz baby girl.  I did...
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My son is 17yrs old and started showing symptoms 3yrs ago. He was perfectly fine and then he started having some pain. As an avid hiker , he brushed it off. But things just got worse. Rashes , fever blisters, swollen joints  and muscles. He has also...
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Have suffered from symptoms since I was a teenager but wasn't officially diagnosed until 2011

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MIXED CONNECTIVE TISSUE DISEASE (MCTD) FORUM

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