Dr's here in Northern Ireland don't seem to understand, or care what Fibromyalgia is all about, what pain and suffering we have to go through. They think we're making it all up. I can't get anything stronger than Paracentamol for my pain, they're like taking smarties, I don't get any relief from the pains, and my Dr won't give me anything stronger. I think all Dr's should be more sympathetic towards all with Fibromyalgia, they are to people who have MS, and some of our symptoms are the same to what they have.
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