Regarding Dr Cs protocol on high dose B1 are there any Anglo-Saxons out there that use B1 injections? If so how many ‘mg’ did Dr C instruct to inject???? I read on his website that he injected either 2x100mg (4000mg oral tablets) or 1x100mg (2000mg oral tablets) each week (depending on height, weight, and stage of PD) BUT noticed that this dose was often too high for Anglo-Saxons…Any advice from experienced PD people would be appreciated… thanks.
Dr Constantini: Regarding Dr Cs protocol on... - Cure Parkinson's
Dr Constantini
i think you find most of takes pill form. Injecting yourself is not easy.
I do intravenous treatments every two weeks. 100mg B1 and 1500mg Glutathione.
And, if you don't mind me asking, what is the benefit you get from it?
Tx does it help? How long have you had PD and how long have you been doing the injections?
I was 'diagnosed' in March 2022. I started doing intravenous treatments in the summer of 2022.
yes, RonB1, how is that regimen working for you? where do you get the treatments?
I use benfotiamine oral, 1.8g/day, and believe it helps. want to change to ttfd but am unsure of the equivalent dose for it compared to 1.8g benfotiamine; i believe it would be about 4 times less or ~600mg/day?
anyone out there know?
I take B1 in tablet form, 100mg. Was originally taking 3days a week but reduced to 1. I would like the injection but it is costly. I feel it gives me energy, & help with constipation. I started taking B1 the 1st year of diagnosis. Currently I am participating in a pd study & don’t know what I am taking. I’m 5 years in & feel my symptoms are mild. Slight hand tremor… increasing during stress. My leg seems to have developed a slight tremor off & on over the last few months. I exercise every day. Try to eat right… I still work.