LymeNet Flash: Salt and Vitamin C protocol

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Medical Questions » Salt and Vitamin C protocol

UBBFriend: Email this page to someone!

Author

Topic: Salt and Vitamin C protocol

dzeb
Member
Member # 4426

posted

I am seeing a lot of positive things about Salt and Vitamin C.
What is this protocol? Does it have to be prescribed by an MD? If not where do I get this?

Posts: 75 | Registered: Aug 2003 | IP: Logged |

pq
Frequent Contributor (1K+ posts)
Member # 6886

posted

search this topic on this board for pros and cons... much discussed... i'm impressed by some of the results.

in my half-a...'d approach, doing just table salt, w/o the vit. c, or just sea satl/gray-salt, and inconsistently, at that, i've had impressive relief from some very scary sensations, inclu., those that sent me to the e.r. in the past; and, had i taken this, i'd conjecture that i could have pre-empted the e.r. visit.

adrenal gland t hing, or part of endo. syst., at least involved here, or what?

paradoxical effect here is that i feel relief, and a little to moderately better, doing just the grey salt, and sea salts of any kind...even table salt. never did the straight, NaCl...

Posts: 2708 | Registered: Feb 2005 | IP: Logged |

sweet pea
LymeNet Contributor
Member # 6495

posted

Go to:

health.groups.yahoo.com/group/lymestrategies/

and

lymephotos.com

Even though the website names don't refer to Salt/C, they are both dedicated to the subject.

The protocol is literally just salt and Vitamin C, so you don't need prescriptions. But of course you might want to consider talking to your doctor first before trying it.

Posts: 449 | From Vermont | Registered: Nov 2004 | IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/