Hey Gang! So what is the latest with niacin? I only take Tru Niagen, but I’ve read multiple posts about niacin, nicotinamide, etc. Does anyone have an idea of which is best for slowing PD progression? I feel a bit overwhelmed with the surfeit of data! Any advice would be greatly appreciated 🙏
latest on niacin, nicotinamide, etc.…? - Cure Parkinson's
latest on niacin, nicotinamide, etc.…?


like you I take TruNiagen and have done for 3 years to fix my RLS. It worked wonders and still does. I also have PD for last 5 years so not sure if truN is helping Pd alongside c/l and other supplements. I also follow b1 protocol and that has produced great results for PD
interesting and good to know! I almost decided to try the B1 protocol but was a little intimidated because it seems like you have to go up and down with your dosage and monitor it and it seems a bit mysterious to be honest… How have you found that aspect of it?
I found it very easy over 2 years ago. Before starting you need to add 144 elemental magnesium daily and a good bcomplex with all low bs for 2/3 weeks before starting b1. I chose b1 sublingual from superior source Started as per the protocol of 50mg MWF each week. And achieved success in less than 4 weeks. Numerous symptoms were resolved and still are. I have a utube video called Parkinson’s b1 therapy Julie’s success story which show and tells of my improvements. Best wishes. Give it a try.
Could someone point me out to the correct protocol? I have the book but dont recall quite well specifics on how to progressively increase the dose
Be careful with high dose niacin (nicotinic acid). I did a protocol of increasing the dose gradually to a high dose and getting the flush for RA and I ended up in hospital for 2 weeks.. Severe hepatic toxocity. I was completely yellow and it took me over a year to get over the resulting side effects. I lost 5 kilos in a couple of weeks and could hardly eat and I was already slim. Doctors thought I had haemochromatosis as I have the gene. My iron levels and other vitamin levels were off the chart. After doing 3 blood lettings I then became anaemic which took another year to sort out with low b12 levels etc. Thank God I found a really good rheumatologist who is into nutrients and micro nutrition but as a result of this crisis my RA became worse. I don't take mexotrate or anything else. I'm doing the AIP elimination diet and intend to start Ivermectine. I didn't up until now to due to restrictions in purchasing.