Anyone using glutathione suppositories?

[Manypony]

Dr Laurie Mischley recommends. Not sure if it’s this brand

[Smittybear7]

I never used the suppositories. I did have glutathione IVs in 2017. That was when I was first diagnosed with parkinsonism. I think they really helped. Just became cost prohibitive. Be interested to hear other people's response. Suppositories are probably cheaper than the IVs. Keep me posted and good luck to you.

[Manypony in reply to Smittybear7]

the suppositories aren’t cheap! I’m doing a little more research. I’m not great on computer but I’ll do my best to get back with results if I decide to use them. In other news, I’m going back on mucuna. I’ve used it before but I feel like returning to it now. I took one capsule tonight and got placebo relief 🥲 I’ll take it

[Bolt_Upright]

HU has an old post on this. They seemed to make some interesting points: healthunlocked.com/cure-par...

[Manypony in reply to Bolt_Upright]

yes, another source to compare with, thank you.