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Salt/vitamin C protocol questions

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Lyme Disease
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Posted 9/29/2011 6:31 PM (GMT 0)
So my husband, deciding he would get more involved in learning more about my LD, searched online and found the Salt/C protocol and thinks I need to start this in place of my ABX. (which I had to stop because of issues with my current doctor).

I am no way going to begin something like this without doing some research on it and running it by you all and see if there's any info you can provide for me.

I found a LLMD in OH (I'm in MI) that I will have to wait until January to see, unfortunately due to finance reasons:(

Looking for something to try in the meantime, or do I just not do anything and wait until my appointment?

I feel I also may have babs and bart co-infections.

 

Posted 9/29/2011 9:16 PM (GMT 0)
That Salt/C "treatment" really bothers me. All of that salt can't be good for a person, especially if one has other medical conditions where a lot of salt could be an issue. As for the Vitamin C, well your body will only absorb what it can use at that time, the rest of it will be excreted through your urine, so I don't know how people can get a 'high dose' of Vitamin C to go along with all of that salt.

This is just my opinion though, as once I saw how much salt people were being told to take made me decide to find something else.

If you want to do something while you wait, I would suggest you look into some of the 'at home' protocols that you can do. Here is a link from out "New to Lyme?" thread:www.lymediseaseresource.com/Protocols.html

There is also Dr David Jernigans formulas that have helped many Lyme sufferers. Two links for you to check out:
www.jernigannutraceuticals.com/Downloads.html
and
www.jernigannutraceuticals.com/Lyme%20Disease.html

I neither benefit from nor am compensated for any thing from any of these sites, they are just suggestions for you to check out and decide on your own whether or not to use them!
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