Hi all - could I pick your brains for a minute? Ever since my ME/CFS crossed over into the severe end of the spectrum, my sweat has been smelling very strongly of ammonia (bleach). Its been this way for a few years now and I'm sure it's been constant the last few months. After a week away holiday with my family last year, constantly pointing it out I figured I should probably get it looked into - so I went to my GP and saw two different Drs, both just dismissed it straight away and one even suggested some personal hygiene tips :| There's been a definite change to my normal 'aroma' though, and it really smells strongly of ammonia. Google says its either late stage liver/kidney disease which I'm sure Idon't have, or its because of protein breakdown, occuring because the body has used up its carb stores (similar to how people supposedly smell of bleach after marathons or heavy gym sessions). I'm not exercising at all though as I'm almost entirely housebound. I do find this interesting ive always said from the beginning my issues have felt completely food/metabolism related. Is this normal for PWME? Any ideas on what I can do - it is kind of worrying! Thank you!