I'll post more, I have to get the other off my laptop also ;)
NOT good news, collarbone and shoulder blade still broken and have a huge gap in the breaks plus bone fragments.. I had 2 FRACTURED RIBS AND DID NOT KNOW IT!! My "rotator cuff" is so torn it will NOT hold another shoulder replacement. The replacement is okay that is there but just holding on by a thread. Plus it appears I "may" have a particular illness that Lupus or RA can cause effecting at least my right lung.. The didn't do the CT scans bt on the fractures so the CT Scan was large enough to find the ribs and the lung issue... and i know I don't know what to say either other than I will live with it I guess... I don't think it is fixable... and if it is that bad as I said just the messed up rotator cuff leaves out a new replacement... I am more than FED UP!
I KNEW from the age of about 35 I HAD "lupus" "Ra" or some other autoimmune disease. I had already began with multiple joint pain/surgeries,, I could not be in the sun light long, I never could get my body temp to be stable (I was either hot or cold), I ran a low grade fever for several years, I had HORRIBLE MIGRAINES but they seemed to be "different" than a regular Migraine (Lupus Migraines. I went to my PCP, I went to my PCP while in Seattle WA, I asked and was X-rayed, had CT scans, MRI's, I was tired a great deal. RA RUNS in my family. I had knee surgeries, elbow surgery, shoulder surgery before 40, had a heart attack at 40. It TOOK me at least 15 years to find the RIGHT doctor to help diagnose me. In 2007 , after BOTH KNEES BEING REPLACED. My then Orthopedic doctor told me he felt I hd RA or some type of chronic illness attacking my joints. By then the pain was horrible, changed with the weather etc. Our town got a new PCP in thank goodness! HE is a GENIUS! He gets to know the patient in all manners, not just a body that needs help, he works with mind soul, what is happening in your life, tells things in plain English. Is THERE anytime you need him. I began seeing him about 2 months after he opened his practice. After 2 years or so, he began asking me about "autoimmune" issues, had anyone did labs, did I have "arthritis" run in my family? He DID ALL THE LABS HE COULD FOR AUTOIMMUNE ILLNESSES. Immediately, he said I feel you have Lupus, and maybe another autoimmune problem. So, I FINALLY SAW MY 1ST RHEUMATOLOGIST, in 2009 or so. He ran his own Labs and di a very thorough exam, questions, and within a week, he told me, he felt I had, Lupus, Sjogrens, Raynauds, "hypermobility syndrome of the joints" & that although the Lab for "RA" was negative I may have "seronegative RA". I went through 5 Rheumy's before I finally found 1 who knew my issues, was patient, kind, took his time really LISTEN still is very much active with all of it and he works with the Lupus, My Rheumy is more a "RA" specialist, so he sees me more for that.
so there is just a piece of y "journey" that is still ongoing.