just got my first NAD+ IV yesterday and walked out with basically all side effects possible (e.g., nausea, headache, fever). Today I’m feeling better, but still weak with brain fog, which I didn’t have for a long time.
Have to say that I was diagnosed 2.5 years ago, have mild symptoms and am stable since the diagnosis (doing sports, taking supplements and not eating gluten, meat and dairy).
Any experience or recommendations on NAD+ IVs? Would you continue it or stick to the oral supplements?
Many thanks and all the best to all of you!
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MAJ88
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I just recently listened to an interview on Dr Hyman’s podcast about NAD. The doctor he interviewed said he saw a patient with Parkinson’s walk out with no tremors after NAD IV however it doesn’t last so must keep it up. The doctor recommended taking NMN supplement as it is a precursor to NAD and will get into cells better than oral NAD. The doctor/scientist name is Dr Salzman and he promotes Wonderfeel NMN. It has the most NMN (and othwe good ingredients) that i have fouund
This is really wonderfully coincidental, but my HWP and I went to a new IV practitioner yesterday for MAH (ozone) IV therapy and she recommended NAD for him as well! We are going to do it in about a month. Here is what she recommended - do 5 treatments in 10 days. They can be done in any order/combination, but I think we will take a day off esp after the first one. She said that most of the side effects last during the IV itself. Then after the initial series of 5, she said that most people do one or two a year, but she does a have a woman pt with severe Parkinsons that comes in more often because it definitely helps her symptoms. I'm will be very excited to hear of your progress! HWP has minimal if any tremors, but drools, walks slumped, freezes upon standing, has some cognitive changes, etc. We have been getting chelation therapy (39x since October for heavy metals) and he gets the MAH therapy and high dose glutathione (1800 mg at this point) with each tx. After the MAH, he absolutely feels much better, walks better, is more animated, bright and engaged. But it only lasts 24 to 48 hours, no one is sure why. So we will continue with the MAH as well and I'm considering doing ozone insufflation at home.
Thank you to Kscott8 about the NMN, I will ask our new provider to see what she thinks - she has been doing IV therapy for 30 years! Please keep me/us updated, as we can share our experiences and maybe help others as well. Thank you and blessings on you!
Thank you very much for your feedback! I have not heard of the MAH ozone IV therapy yet and will check it out.
My practitioner suggested we do a blood plasma purification treatment, called INUSpherese. This is supposed to be followed by a few IHHT (Interval-Hypoxic-Hyperoxic Training) sessions, in order to improve mitochondrial performance.
Have you heard about these? I’m willing to try them, although it sounds a bit like Keith Richard’s full-body blood transfusion. But he’s still alive and kicking, despite “everything he consumed”.
Please keep me posted on your experience and all the best to your husband. He’s lucky to have you!
Very interesting about INUSpherese. Need to do more research on it, but I di find one doc in Kentucky, USA, rather far from Colorado. PLEASE, do let me know how this works for you... this seems REALLY involved and through. Thanks for replying... Will let you know how the NAD works, can't do it for another month due to scheduling stuff. Thanks!
Real Quick MAJ88, my HwP will start the 5 NAD IV treatments (in a 10 day course) in 2 weeks, however, speaking to the nurse who does the infusions, she says that when a pt is feeling bad, she will slow down the infusion considerably til its tolerated. Hope that helps if you are continuing it. Will let you know how hubby's treatment go!
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