I just took my first dose of LDNi last night (at one-third of the already tiny 4.5mg, so a 1.5mg dose).

Man, does it pack a punch! Within ten minutes I could feel a sort of raciness similar to the double espresso shot Arttile reports, though not quite that strong, and felt tingling and slight pain in my toes (peripheral neuropathy being one of my sxi).  

I did sort of get to sleep okay, but had very wild dreams, not especially good ones, either, and a dry mouth.  And now, 12 hours later, I just had a slight atrial fibrillation.  I'll try it again tonight, and if these sx don't improve probably won't continue.  I'm also monitoring my eye very closely to see if it helps or hinders it, as I have no room right now for any further redness or aggravation to it.

Hello everyone. I went to see a doctor I used to consult about my MCS issues, who seems to be interested in new treatments, to see if he would be agreeable to prescribing the protocol for me. I had printed out a lot of info from this website for him, which he perused while I was there and had a number of comments.

Firstly, he seemed okay with prescribing Azithroymcin and Doxyi or Minoi, as he has a lot of experiences with those, but didn’t like the idea of Flagyli, as he has had bad experiences with that (from the die-off reaction, no doubt). He said if he hated someone and wanted to cause them untold suffering, he’d prescribe Flagyl!

I am hoping he will be okay with Tinii as an alternative to Flagyl.

Hello wise and experienced people on the CAPi.

I heard about this recently from a naturopath, and have had a look at their website.  They claim it is very effective for ALL auto-immunei conditions.

I'm just wondering if anybody here has tried it, as I heard that possibly Dr. Powell prescribes it, or at least knows something about it.  Is it something you could do in conjunction with the CAPi? 

I wonder if it will help the immune system to eradicate Cpni-type infectionsi? It supposedly stops it from attacking itself (thereby relieving inflammationi) -- wouldn't that then give those embedded bacteria a clean slate to just proliferate without hindrance?

Just curious if anyone here knows anything about this.  Thanks. 

Hi everybody. I am beginning to take NACi at 600/day. I have taken it three times now, with breakfast. I notice a strong sulphur-like smell from the capsules, and also notice my urine smelled like that about 6 hours later. Sulfa drugs are contra-indicated with porphyriai -- I wonder if it's somehow connected?

Anyhow, I do notice some porphyric symptoms after taking it -- noticeable pressure at the back of my head, which is my main porphyria symptom, as well as a spacey, needing-to-eat feeling sooner than usual before lunch. So I guess this is the NAC doing its work on the EBs?

I would like to introduce myself, as I have been reading on this site for awhile now, and am considering doing the CAPi.

I have been on the Marshall Protocol (MPi) for about two years, in a sort of half-baked fashion, in that I have been on Benicar only for about half that time, and only did the low dose abxi for 13 months (minoi + clindamycin, no Zithi).  I am VERY CONFUSED about the Vitamin Di issue, as anyone familiar with the MP will know that we are conditioned to think of D as BAD.  My Vitamin D3 level is <4, and has been for almost two years.  I am slowly attempting to bring Vit D back into my life, via slightly more sun exposure, however this tends to aggravate sxi for me, so it is very limited.