I've just realised I may be intolerant towards sulphur (sulfur).
I've been using transdermal magnesium sulphate for the last couple of weeks, and have just realised that taking more magnesium sulphate correlates with a worsening of symptoms the following day. My mum also mentioned to me yesterday that when I farted it smelled like sulphur!
According to my 23andme, I am heterozygous for one of the CBS genes, but normal for the others.
Does this sound like potentially a sulphur intolerance?
Can anyone link me to some good information about it? I am getting too overwhelmed by the Internet at the moment as my energy levels is very poor.
I have also been taking NAC for a few months - this is said to be a bad idea for people with sulphur issues - but haven't noticed any issue from it. But maybe NAC contains less sulphur compared with magnesium sulphate? Or maybe the beneficial effects of the NAC are disguising the bad effects of the sulphur.
I've been using transdermal magnesium sulphate for the last couple of weeks, and have just realised that taking more magnesium sulphate correlates with a worsening of symptoms the following day. My mum also mentioned to me yesterday that when I farted it smelled like sulphur!
According to my 23andme, I am heterozygous for one of the CBS genes, but normal for the others.
Does this sound like potentially a sulphur intolerance?
Can anyone link me to some good information about it? I am getting too overwhelmed by the Internet at the moment as my energy levels is very poor.
I have also been taking NAC for a few months - this is said to be a bad idea for people with sulphur issues - but haven't noticed any issue from it. But maybe NAC contains less sulphur compared with magnesium sulphate? Or maybe the beneficial effects of the NAC are disguising the bad effects of the sulphur.
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