Hey Auriel,
I'm sorry you're having a hard time today, and that your pain is still worse. I can relate so much to the adult toddler vibe - I think my fella would agree, that was me yesterday too!
I’m still curious why I’ve not been tested for m.e m.s, no mri’s now the forum’s is talking about a.l.s and other initial things,
Lovely, I'm worried you read this in my post last night where I was talking about the positive of fibromyalgia not being progressive like some other conditions - although, of course, it is very prone to variation, and goes through ups and downs. I didn't mean to make you worry by mentioning those health issues!
ME (myalgic encephalomyelitis) is just another name for CFS (chronic fatigue syndrome), which I think you've had diagnosed - if I remember? It's a condition that - just like fibromyalgia - is not progressive, and is diagnosed based on exclusion and symptoms, so there isn't a test for it. Its presentation is quite similar to fibromyalgia, but with much more emphasis on extreme fatigue, and not so much on pain (I know you know that - just explaining for other readers!)
Both MS (multiple sclerosis) and ALS (amyotrophic lateral sclerosis) have signs and symptoms that differ from fibromyalgia - such as slurred speech and loss of limb mobility. These are not conditions that a doctor would necessarily test for unless they saw the right indications. Of course, if you have any concerns, definitely discuss them with your doctor and push for further investigation! But I think that so many of us - particularly on bad days - can fall into the trap of medical catastrophizing, and that can be really triggering. I really hope you're OK, and if you're going through strange symptoms, I'm here for you