What is Reddit's opinion of The Salt/C Plus Protocol for Lyme Infection?

From 3.5 billion Reddit comments

I never asked you to keep it to yourself. I think sharing treatments is very valuable. All I was asking was to share more information about the treatment, where to find others using it, what risks to watch out for, etc. I had assumed you would have much more research on this than myself, and thought it would be valuable to patients.

I did some quick research myself:

There seems to be a guy who wrote a book on it and people reported success: https://smile.amazon.com/Salt-Plus-Protocol-Lyme-Infection/dp/1463575483/

That same guy seems to have a website which links to a yahoo groups page with thousands of people in it.

I found this printout that has more details on a potential treatment and it makes an attempt to explain why it works, and what risks you have to watch out for:

https://www.connersclinic.com/wp-content/uploads/2015/09/Beating-Lyme-Section-4-PDF.pdf

But since I have never done it and only spent 5 minutes researching it, I have no idea which source is good, or if there are better places to learn more about it. I thought you may know more and that it would be valuable to share.

Lyme patients see so many different claims of cures it's hard to process. So in order for people to choose treatment plan over another it's very valuable to patients to show them information about a proposed treatment.