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Erythromelalgia diet. Is there a diet which improves the quality of life of people with Erythromelalgia?

Are you aware of a diet that can improve the quality of life of people with Erythromelalgia? Is there a diet that is suggested to avoid when having Erythromelalgia? See if there is a diet that can improve the quality of life of people with Erythromelalgia, recommended and to avoid food when having Erythromelalgia

Erythromelalgia diet
6 answers
Avoiding alcohol, smoking, caffeine, sugar, spicy foods, and large meals is a good first step toward avoiding flare-ups.

Posted Sep 16, 2017 by Jeff 3050
problems have been reported with spicy, hot foods, alcohol, diet drinks, tomatoes and nightshade vegetables

Posted Dec 27, 2017 by mleaver 2500
Avoid spicy foods and caffeine

Posted Apr 4, 2018 by Alys 2500
Some people find it helpful to eat a diet that is low in histamines

Posted Jan 18, 2021 by Kathy Vanicek 2500
It depends what your EM is caused by. Mine is not improved by diet.

Posted Aug 14, 2021 by saguaros 3000
NO, stop beating yourself up

Posted Oct 8, 2021 by Carol 500

Erythromelalgia diet

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World map of Erythromelalgia

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Stories of Erythromelalgia

ERYTHROMELALGIA STORIES
Erythromelalgia stories
My symptoms first started in October of 2010.  I began to investigate my symptoms on the internet.  After searching I came upon Erythromelalgia and ALL my symptoms matched.  I then began my search for a doctor who could and would help me.  I fina...
Erythromelalgia stories
I started getting stange burning in my feet and calves about a year ago.  Went to many doctors and had all the test.  None could diagnose me.  Said probably samll fiber neuropathy even thought the skin biopsy was negagive.  Stumbled across the Li...
Erythromelalgia stories
A lot of medication since 5 years Nothing help  
Erythromelalgia stories
I can't remember a time when I didn't have hot feet. I haven't been diagnosed, but my sister has. I also have neuropathy. My feet look black most of the time and I just had an ultrasound and doplar done only to find my circulation is excellent. 
Erythromelalgia stories
I was diagnosed in 2015 bij the Academisch Ziekenhuis Maastricht (academical hospital in Maastricht, netherlands). After a 1,5 year journey of searching for answers. I love to be in Facebook support groups, they really get what I am going through.

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Erythromelalgia forum

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Erythromelalgia forum
Are there any eythromelgia 'experts' in the uk?

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