trying to get any actual diagnosis and support for my dysautonomia symptoms but i’m worried that they’re going to blame my diet. i know i don’t eat enough, and also i know that my diet has little to nothing to do with my symptoms.
Not eating enough can have major impacts on dysautonomia. I have fantastic medical interventions and if I go a few days not eating well enough, my symptoms roar back. Obviously it’s not all food but it’s a significant part
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Anonymous#14w
totally fair. and also i tracked all my symptoms and food intake for over a year and found no solid patterns. yes, diet and not eating enough can trigger flares or worsen symptoms. but i know that i have certain symptoms that will be there regardless.