xks201
Senior Member
- Messages
- 740
ya prob the best time is night
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Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.
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I'm on replacement HC so I was curious if maybe I could use less HC with it.
Heaps, have you played with the timing of taking the PS? Meaning, how early do you take it to get to sleep at a good time and hopefully reduce morning effects?
I use a product called seriphos, which my dr claimed would reduce cortisol. I am so glad this is doing something positive for you.
This is great news Heaps. I'm hoping that this will continue over time. With ME and CFS sometimes we find things that seem to work or at least help and then a month or so later they stop working mysteriously. It's like the disease manages to work out a way around things sometimes. Then again there are breakthrough moments when a fix is found for a problem.
What's your fuctioning like during the day now on this combo?
Still going well madie, if i do get up in the early hours for a pitstop, i can go back to sleep where once before that would be me awake for the rest of the day until bedtime the next night. Even my wife has mentioned that im not waking up as much. Im still waiting for my withania and p5p from vitacost as well as more tryptophan, postage seems alot slower then iherb??How's your sleep holding up now that you're back at work?
cool, i hope it helps this time, maybe even start on 1/2 a capsule.Heaps, you've persuaded me once again! I've just ordered pure PS; should have it Thursday.