We're exploring adding Glutathione to our protocol to fight oxidative stress.
Curious what method works best based on your experience? And where did you order it from?
Thanks!
We're exploring adding Glutathione to our protocol to fight oxidative stress.
Curious what method works best based on your experience? And where did you order it from?
Thanks!
I tried inhaled glutathione using a nebulizer. It did not seem to make any difference.
Having done the intranasal..I don't think the nebulizer is comparable. I think it would create a mist that you breathe and it would go to the lungs. In Mischley's study the application was done with a syringe shaped, ultra-fine mister that you put up your nostril and then push the... plunger (? I don't know what it's called!) When we described the process to a psychiatrist friend he said, "Every addict knows the quickest way to the brain is through the nose!" So, at 58 y/o I learned how to "snort" my drugs!! ;-D
Do you take NAC or Melatonin? They supposedly boost cellular glutathione production and are very effective antioxidants on their own.
Haven't tried NAC. Adding Melatonin this week before bed.
I participated in Laurie Mischley's 2015 intranasal study. I had been taking NAC and had to stop 90 days (I think it was 90) prior to starting the research. Stopping oral NAC I noticed a significant increase in stiffness. I was in the high dose arm, (I learned later) but had an immediate pronounced improvement! (Unlike some other subjects). After the 3 month study we had 30 days with no glutathione or NAC and the stiffness gradually returned. With the study complete I resumed NAC and again received benefit.
Were the benefits equal? Maybe... close enough that when factoring in the cost/benefit ratio of the two, I've chosen to continue the oral only. Laurie insists that NAC is NOT good, but I've never noticed any ill effects. But I respect her opinion so for the last 5 years have used glutathione 500 mg orally. I use NOW brand although Laurie says any brand will do, even the cheap ones.
FYI If I miss a day or two of it, my mobility is negatively impacted. Hope this helps.
Thank you so much!
So now you're not on NAC but on Glutathione 500mg orally (assuming pills / tablets).
Does it slow down progression by tackling oxidative stress?
NAC is a precursor to glutathione that crosses the bbb (blood brain barrier.) Glutathione doesn't cross the bbb. Mischley just shakes her head and says people she's surveyed that are doing well, take glutathione. She hypothesizes that it provides glutathione elsewhere in the body allowing more "building blocks" (my term) to be allocated for brain needs of glutathione.
How would I know if it's helping oxidative stress? I'm a bit of an odd duck. I was diagnosed 11 years ago but have virtually no tremor. I think it's progressing slowly although I have many symptoms. So is it slow because of glutathione, or an active lifestyle, or good sleep, or 40 years vegan diet or low stress or the Lord's blessing? Probably all of them.
I do know that when I miss the glutathione I'm stiffer and slower.
Yes 500 mg glutathione capsules.
Just one capsule? What time of day? With or without food and supplements?
I was told that it is most effective to take Glutathione in the am on an empty stomach at least 30 min before food or coffee. I take liposomal glutathione
I'm using Glutathione for about 6 months now and noticed a difference within 30 days. I use a spray developed by a pharmacist that has been developing IV glutathione for years used by doctors for patients. But, he says the body can not use Glutathione orally or IV as it breaks down too quickly. Thus he developed a spray that goes through the skin. I don't have tremors, well, I have resting tremors, but I'm predominantly rigid PD. It's helped me tremendously in terms of energy and stiffness and I'm sure to help detox. Glutathione is the 2nd most abundant molecule in the body, next to water, so I've read. This is the product I use:
I have a hereditary Parkinson that responds extremely well to lithium so I can’t say whether it helped Parkinson’s disease or not. I did take it for three months as a rectal suppository high dose. That’s supposed to be well absorbed. I took it for a demyelinating neurologic condition., chronic issues associated with that. Two things improved one was pain., and some weakness that I’ve had for a decade. The pain came back almost immediately after stopping, but the weakness in my left leg has not come back and I’ve been off many months . I took it for three months, but I got the vast majority of benefit within the first 10 days. In fact, after about two weeks, I don’t think I got any additional benefit for the 2 1/2 months after that. Regular use of course my body would stop making it and I’m not ready for a lifelong commitment to it. plus not completely convinced about the safety of high dose. Plus, of course cost issues. I just decided next time to use it for for two weeks and cycle off of it. Giving my body a chance to fully recover and start making its own again. I’ll definitely use it in the future, but I’m not at a point where I would want to take it regularly.
I also had new onset diabetes. It didn’t improve that at all.
I use a lot of thiamine. But I never pushed dose to toxicity.
I looked at the research, but when it was used as a N I think it was Vietnam. There was a lot of renal failure associated with it. I made it illegal after that I think it may have just been contamination because these IVs were being done in areas that really were not sterile. However, there is a hypothesis that extreme up and downs problems.