Hello folk - do any fellow aspergillus sufferers also have sweats every 20 minutes night & day? I've been sweating for 13 months now & Been on itraconazole and prednisone for 9 weeks & seem to be worse than ever. Should say I've got MDS (bone marrow failure/blood cancer) and am transfusion dependent. Oh yes, just been diagnosed with bronchiectasis which I've never heard of. Just need to know about these sweats as can cope (ish) with all the other stuff just about but sitting on underground soaked every day is getting me down. Be grateful for ANY response as docs don't seem to know or don't want me to know which is the feeling I get doh! Regards
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