NAD+ Infusions?

[faridaro]

Has anyone here tried NAD+ IV? Here is intriguing video (mentions PD a few times) that makes me want to consider trying it.

youtube.com/watch?v=6NbcHcr...(Not working as expected?)

[Hidden]

healthunlocked.com/cure-par...

[faridaro in reply to Hidden]

Thank you!

[RBan]

I have been using sublingual NADH and def notice more energy (if I follow directions) this is good info. I’ll check whether IV is available in my area

nadh.com/pages/parkinsons

[faridaro in reply to RBan]

Couple of years ago I tried NADH (5 or 10mg/day) but then NR started gaining popularity and I switched to taking it 300 mg/day. Had not noticed any difference from neither one, so I gave up. Will have to take a closer look at both again.

[RBan in reply to faridaro]

it’s important to get the right brand as well. Needs to be patented to be effective. I find it gives me the energy to exercise in the morning but if I don’t exercise I don’t notice that much of a difference in how I feel daily. it seems like when I exercise, it activates the sublingual NADH. I’m only taking 20 mg in the morning I would love to take more but it’s just adds up moneywise

[natneuro]

youtu.be/jIB1vKz4jRg(Not working as expected?)

We just demonstrated lower NAD in muscle if PwP. The NADPARK study suggests oral NR raises NAD, making IV hard to justify, esp given the cost and inconvenience.

For those of you that are trying different therapies, PLEASE consider joining the MVP-Study.com. When we all share our data, we can see trends that are otherwise undetectable.

NAD supplementation is looking to be very promising and we need more people using NAD to enroll in the study before we can publish results. If you are using or (even better) considering using any sort of NAD fortification stuff, please enroll in the MVP-Study.com so we can tell you if/ how well it works, on a community level. 🙏🏼

mvp-study.com/

Laurie

[faridaro in reply to natneuro]

Thank you for sharing the NADPARK study, according to which findings daily 1000mg NR "nominate NR as a potential neuroprotective therapy for PD". Couple of years ago I used to take 300mg/day but didn't notice any results and had given up. Will try again with the higher dose in the near future.

[natneuro in reply to faridaro]

I don’t think you’ll be able to feel neuroprotection! It’s not a symptomatic therapy, but (potentially) a disease-modifying one.

[faridaro in reply to natneuro]

You are right, good point!

[RonB1]

I am currently receiving NAD+ IV's bi-weekly, here in Canada. In addition, I get B1, B12 and glutathione intravenously. I am newly diagnosed so my symptoms are relatively mild, however after each IV I feel a definite increase in energy and a slight reduction in tremor.

[faridaro in reply to RonB1]

Thank you for sharing your positive experience. Your periodic updates on this treatment would be greatly appreciated.