Hi...and welcome!
I was dx'd with fibro about 15 years ago, but I also had signs of it long before that. I think am am not the typical fibromite, as I have had long periods of time when the pain was simply 'white noise' and I actually functioned like a normal, healthy human being. Which has often made me wonder about my dx also. I cannot, however, recall a day in all those year when I didn't take some kind of OTC pain killer. My symptoms did not even begin with pain. I had numbness and tingling sensations in my legs, and extreme skin sensativity. I went through every test known to man, including heavy metal poisoning. Everything was normal. Then one day the pain started...tested again for Lupus and other autoimmune diseases. Nothing. Went through another period of feeling somewhat normal. I finally went to a Rheumologist after some heavy duty burning pains and weakness in my arms and legs. Tested again...all normal. Then she did some trigger point testing and dx'd me with fibro/myofascial pain.
Unfortunatley, those days are over and I experience pain somewhere almost every day. The fog has increased and sleep has once again become an issue...or lack there of.
Yes...it it hard for friends and relatives to understand this disease because of the way it attacks us. Good days...bad days. Sometimes it hits us mid sentence. For me, stress or over doing on a day when I feel okay triggers a flare. I raked leaves last week and am still paying for it. I took a five mile hike up a mountain this summer...today I could hardly walk to the maibox. It's a very insidious disorder.
Others will chime in here and give you their opinions. I have never noticed certain foods triggering a flare...some have.
You are right...it can be a lonely disease, especially when family and friends see you having a good day and the next day you are gimping to the bathroom!
Donna