Posted 6/10/2016 7:04 PM (GMT 0)
It can get pretty complicated. I did some pretty extensive looking into gene mutations, after having the 23 and Me testing done, running my results through the 3rd party analysis groups, and learning that I'm victim to a few of them.
There's a lot to it. People typically look to just the MTHFR or CBS genes, but there's a ton of them that play a part in the methylation cycle, and just focusing on one or two could prove a waste of time and/or even be damaging.
But, my mind, memory, all that, it isn't so hot, so I wouldn't be able to do it much justice.
Just take a look at this site:
http://www.heartfixer.com/AMRI-Nutrigenomics.htm
You don't even have to read any of the information (I would not blame you), just take in how thick of a topic methylation is. I feel that methylation is a huge issue for me, but I have given up on it for the moment. I've got a basic plan of action for my particular defects, supplements involved, etc. That's it. I can't handle anymore.
But, really, in your situation, I wouldn't do much, apart from make sure you're on a good multivitamin, supplementing for any possible vitamin and mineral deficiencies, etc. A good form of B12 and L-MTHF (might want to do a bit of reading on these to make sure you're getting the right type of B12 and proper dosages).
See, that's the thing, to really have an idea as to what's going on and what/how you can treat IN DEPTH, you're gonna need some testing, otherwise, again, it could just be a waste of time or you could aggravate certain portions of the cycle by supplementing with things that aren't needed. These gene defects don't always mean a lack of something, could be an overabundance.
So, yeah, for now, just go with the basics I mentioned, and detox your butt off, as Trav indicated.
I only care about methylation, because I feel it plays a big part in my multiple chemical sensitivity issues.
If not for that, I wouldn't even think about it, just detox.