The Caffeine ME/CFS and FM Poll

With regards to caffeine, after you got ME/CFS/FM

  • I became much more sensitive to caffeine; just a little bit sends me flying

    Votes: 4 18.2%
  • I became a bit more sensitive to caffeine

    Votes: 6 27.3%
  • No change

    Votes: 3 13.6%
  • I need to more caffeine to get the same effect

    Votes: 0 0.0%
  • I can drink gallons of it without any effect

    Votes: 3 13.6%
  • Caffeine ultimately leaves me depleted

    Votes: 8 36.4%
  • Caffeine has no real effect

    Votes: 2 9.1%
  • Caffeine boosts me up without leaving me depleted

    Votes: 6 27.3%

  • Total voters
    22

Abrin

Well-Known Member
Caffeine is one of the most useful supplements I use...it blocks adenosine (the hibernation molecule) and perks me right up temporarily.

I definitely have to watch it though because it is a fine line between just enough and too much.

Supposedly green tea is better at smoothing out the highs and lows and I think that must be true because I can drink a lot of it and not notice the caffeine at all - either the positive or the negative on energy - independent of all the good EGCG.

Thanks for your response in this thread @Remy . I use caffeine in very small amounts to help give me more energy for when I have things that need to be completed on my to-do list but I have been worrying that I might be making things worse. It is good to know that as long as I am keeping it to small amounts that the temporary benefits I am getting from it wont' necessarily be setting me back.
 

Feral Boy

New Member
I love to drink coffee, but it makes me both jittery and tired. I probably drink too much: usually a triple-shot Americano, and sometimes a second round. I'd rather not calculate how much caffeine that would be.

Instead, I usually drink a pot of yerba maté in the a.m. I think I adjusted the dose to come in at around 200mg caffeine. That, plus 10mg amphetamine salts, (usually) gets me going.
 

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