postpolio, fibromyalgia, bone mets who knows?

sas-schatzi

I have had muscle bone and joint pain my entire life b/c of post polio, then fibromyalgia b/c of AI's , and  now severe osteopenia b/c of AI's---If I get bone mets it will be so far advanced b/c I can't tell the difference --what then? I say it that way b/c most with mets, know that there is a change. Post polios, I don't think can.That's why I write this---are there any Postpolio's here that have mets that could tell the difference. Pain is a given.  I get my yearly Pets. I have had < half dozen days in memory of no pain my entire life and I'm 61(polio @2 pre vaccine). I don't expect much response here b/c most are to young to have knowledge of post polio--or polio. Put post polio together with Aromatase inhibitors---it's a firestorm of pain. I've asked multiple people what bone mets feels like---hmmm. What I hear is what I've felt my whole life long. Both suck. One just goes on and on and on, the other eventually kills. OR may be eventually both kill, but getting real tired of the pain.