I don't know if this is crazy, but if im wrong don't fry my ass, but i'm the type of person that can't accept theres no cure for TMAU. don't roll ur eyes or anything or stop reading, bc this is not a rant, just a thought. Okay, so just think for a second. TMAU is basically a kind of disorder where your body has a problem producing enzyme FMO3, right? And that is why our bodies can't process trimethaline which is why we release it through our sweat, ect. and that makes the stink. Ok, check. Now why can't there be a way to externally take enzyme FMO3 injections, tablets, something! since we can't produce it ourselves. Like what i'm imagining, is a diabetic who can't produce enough insulin (only with a dash of stink, and outcast) so they go and take insulin shots everyday? Why can't ppl with tmau do that? or isn't there a tablet you could take, or even a certain food or herb that contains plenty of enzyme FMO3. I know some of ppl on this site have experienced tmau 4 years and r like, 'i've had it 4 years and i would have thought of that' but still, there shuld be a thread, and i think this is very important, where we try and put our minds together and think of possible solutions. Even if not all of them are possible or available we can at least put our heads together and maybe some ideas will come we'll end up searching it out of curiousity and it can lead to more help for us or at least be a small stepping stone to a real cure or treatment. If anyone has any ideas that have come across ur mind u shud put it here because you don't really know if it could actually be a good idea. Ive never been 2 like the research lab u go 2 where they test 4 tmau but if we culd b emailing ideas to a specialist at a center where they study tmau who knows it culd b helpful. Maybe the answer could b simple to a huge but not so complicated problem...