Has anyone been tested for Glutathione deficiency since getting PFS? I’ve had a couple of tests for it and the labs are coming back with nothing, as if it’s undetectable, when it should really be found in large quantities. Yes, I will have more tests taken.
Glutathione has been discussed in the forum before, but not in any major way. There is a rare genetic condition that causes a glutathione deficiency, and I’m wondering if maybe we have that and it predisposes us to PFS.
Regardless, some of the symptoms of low Glutathione include many we all suffer with, including:
• Always tired
• Lack of energy
• Aches and pains - joints or muscles hurting
• Foggy brain
• Low Immunity
• Poor sleep
If anyone with PFS has been tested for glutathione before or after PFS, please consider sharing your results.