I tend to see nutritional deficiency theories of ME/CFS as a kindergarten medical science.
Nutrition involves just tiny a handful of vitamins, minerals, fatty acids, etc. But there are millions of pathways in the body which can become dysfunctional, and these dysfunctions are nothing to with nutritional levels. The area of nutrition is just a drop in the ocean compared to the full complexity of the body. Thus very unlikely that nutritional factors would be involved in ME/CFS, especially given how easy it is to correct these factors with supplements.
I'm not sure how you know where to draw the line between what is affected by nutrition and what is not? How do you know if a dysfunction has nothing to do with nutritional levels? I see the body as one fantastic system, all interconnected, with so much we have no notion of at all. What I do know is that the body doesn't materialise out of nothing and has to be continually renewed over time - where is it getting the materials from if not our food (and to some extent light/oxygen etc)? For me, nutrition is incredibly important. Just how I see it! I can see from the number of posts you have that you must have been enduring CFS/ME for a long time, and will have very different experiences and outlook to me, so that's OK. Here to learn and to see other perspectives!
Having said that, I found that taking high-dose selenium substantially improved my ME/CFS just on its own (see
this thread), so supplements can help in ME/CFS.
Greg would criticise your use of Selenomethionine. Doesn't think it's very useful, thinks it largely stays inactive in the blood (although it appears to be doing something in your case). He has always recommended Sodium Selenite (and I think he said the Selenate form would be OK too). He bases this on the fact that farmers use Selenite in animal feed, not Selenomethionine, and thinks that they would use whatever is the optimal form for healthy animals. So if I ever find myself inclined to moo and eat hay, I will know why!
I take 200 mcg Selenite daily (liquid form) along with Iodine (300 mcg) and Molybdenum (450 mcg), the latter also as a liquid. I have had 'start up' reactions (adrenaline type) to all three of these elements and had to build them up slowly, I think I'm on the right dose for me now (for the time being!). My digestion soon tells me if I am getting enough.
That's a great thread on Selenium, btw. *bookmarks*
Hi Jadzhia! Do you see anything wrong with a b complex that includes hydro, adeno and methylcbl? I found this one that gave me a lot of clean energy
https://rawrevelations.com/b-complex/ until I took too many days in a row and had a methyl trapping situation... but im thinking if i spread out dosing it might be good.
As yet I haven't found a B-complex I think would be right for me, so maybe I'm not the right person to ask for advice! Greg's group prefer those without B12 and folate added (he prefers us to get folate from leafy green veg) and of course to use transdermal B12.
i am slow COMT and homo MTHFR c677t. The only b vitamin that is showing to be low for me is folate, but I figured I should take all of the bs instead of just the folate. now with the methyl trap.. im assuming b12 might be appearing as normal on test but truly isnt functioning properly?
B12 can be deceptive on blood tests as you can have an inactive form in your blood yet these show as having high levels of B12, so your doctor thinks you are fine, but in fact you are 'paradoxically deficient'. Greg reckons the genes aren't a problem unless you have functional B2 deficiency - i.e. your riboflavin isn't getting activated to FMN/FAD. So much gets back to B2, I think it's very important to make sure you are getting enough, either via dairy products or supplements.