Hi. In short, ive had BC twice, both ER+, HER2-, and told in May its spread to liver, spleen, peritoenuem, all up spine, all ribs, both femurs, pelvis, lymph under arm, and skin mets. Prognosis 2-3 years. Im 50. Treatment is oophorectomy (cancer also found in ovaries & tubes), Lertrozole, Palbociclib trial drug, Zometa. Its hard enough coping with the DX but im suffering so much with the SE from the Letrozole. It's so bad im considering stopping it and trying another AI. Over the last 4 months the night sweats and hot flushes, and teeth chattering cold shivers have been debilitating and are getting worse. Changing nightwear 3 times a night, towels on the bed, nausea, embarrassing soaked clothes. I had a meltdown recently, screaming and crying "make it stop." GP tried me on Sertraline, didnt work after 28 days. Now 10 days in on Clonidine but no improvement at all. Please can anyone suggest alternative treatment for sweats? Should i switch AI? Should i be more patient? My meds are currently paracetmol, Amatriptylene (for pain relief), Letrozole, Palbociclib, Clonidine, and medicinal cannabis oil. Help!
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