What about glutathione IV ?

[Ric7]

Does anyone have experience with glutathione IV for Parkinsons?

[Smittybear7]

In 2018 I received about 28IVS of glutathione. At that's time I was diagnosed with Parkinson ism. I do think it had a positive effect but became cost prohibitive.

[LindaP50]

Husband got Glutathione injections. Started with once a week then went down to once every two weeks for a few months (as my memory recalls). Benefit for him was energy and an overall good feeling. After a few months he felt the injection benefits wore off more quickly. We drove 2 hours roundtrip and paid $75.00 for one dose (?) and sometimes got two doses for $150.00. Stopped due to the gas, travel time, costs of injection and that it eventually didn't work as well.

[healthabc]

yes, did it about 6 times. costly and not beneficial

[Sydney75]

My HWP has done glutathione push (injection into vein) he is profounding faitigued after injections, does not think it really helps. It would be less expensive to use daily liposomal . MD says faitigue is bc body is detoxifying.

[LindaP50 in reply to Sydney75]

Yes! My hubby used liposomal for his Lyme disease (before and after trying the glut pushes). Once he got the diagnosis of PD he stopped using.