When the moderators put a kibosh on discussing food and how it relates to fibromyalgia, I for one was disappointed.
I have not said anything yet because I wanted to think about the issue and try to see both sides of the issue.
Since it has come up again I thought I would chime in.
My story is very similar to many on here, pain, fibro fog, nausea, fatigue, low energy and insomnia. I tried all the usual things--low impact exercise, supplements, medication, pacing and diet. I kept a journal of everything I did and took and ate, I would be better and then have a flare--I just could not see a pattern to it all.
'Almost medfree' and 'fishchris' kept me motivated on the eating and I would read what they and others said on here and kept searching for the answer. I have discovered I have fructose malabsorption and started following a low FODMAP diet and feel so much better.
I still have pain, but I sleep better which gives me more energy, less fatigue and therefore less pain. And best of all the brain fog has gone way, way down.
Food is medication, in fact it was the earliest known medication, it needs to be talked about on this forum along with exercise, other medications, supplements, brain fog, humor and other issues new members maybe reading about for the first time.
I wish I had know about fructose malabsorption 5 years ago. It may be common sense to eat a healthy diet, but what is healthy for one is not always true for another.
Sharon