BOOM! NAC=flu-like symptoms

Hi everyone. I started taking NACi last week. I take 500 mg capsules, one with breakfast and one with lunch. I have been on abxi for 8 weeks doxyi/azith.

While I had very mild symptoms when starting abxi, the NAC is very marked for me. headache, slightly runny nose, mild nausea, and loss of apetite(I've not eaten much beyond juice water club soda or yesterday's notable exception; a slurpy, in 4 days)
achy muscles. My stomach feels "hot" inside. That slurpy was very appealing! Clearly, this is the marked kind of symptoms I have hoped for to let me know I am in fact responding to the regimen.

Since NAC harms EBi's and EB's are metabolically inactive non replicating cells, I do not expect any large increase in function after this as someone might after flagyl for example. Rather I expect that by reducing EB loads, there will be few newly infected cells, and those already infected are frozen by the doxy/azith just waiting for my future flagyl pulse to clean things up. I have a wonderful sense that I am on the right track and this is working wonderfully well

Just wanted to share...
BLessings
Marie

I had a similar experience when starting the NACi, Marie; a lot of perspiration, with soreness round the eyes. After a day or two, tingling all over, particularly nose, lips and ears. It was more marked in the evenings. After a fortnight these symptoms began to go. Unless I'm mistaken this must mean an EBi load being broken up.

D W - [Myalgia and hypertensioni (typically 155/95.) Began (2003) taking doxycycline and macrolide and later adding metronidazole. No medication now. Morning BP typically 110/75]
Hi Marie,I was taking NACi for about 6 months before I began the abxi. I was only taking 600 mg once a day. When I heard the news that David Wheldoni posted, I increased it to 600 mg twice a day. It was then that I began to have feverish reactions--usually in the middle of the day. I have also had the wierd tingly lips and sore eyes as well as runny nose that DW talks about. I always take it with food.If you are having problems with symptoms, up the antioxidantsi with carrot juice,raw broccoli, blue berries and black berries. I also added Sun Chlorella mixed in juice.If you have a juice machine, try juicing carrot, kiwi fruit and fresh ginger root together. This seems to help me a lot. I just began my 3rd round of Flagyli (two days now)--minimal symptoms so far. Got my fingers crossed.Hang in there. Pain-free days lie ahead.Raven

Feeling 98% well-going for 100. Very low test for Cpni. CAPi since 8-05 for Cpn/Mycoplasma P.,Lyme, Bartonella, Mold exposure,NACi,BHRT, MethyB12 FIRi Sauna. 1-18-11 begin new treatment plan with naturopath

Here's a research article on NACi:http://tinyurl.com/dhoyq"N-acetyl cysteine inhibits induction of no production by endotoxini or cytokinei stimulated rat peritoneal macrophages, C6 glial cells and astrocytes."Raven

Feeling 98% well-going for 100. Very low test for Cpni. CAPi since 8-05 for Cpn/Mycoplasma P.,Lyme, Bartonella, Mold exposure,NACi,BHRT, MethyB12 FIRi Sauna. 1-18-11 begin new treatment plan with naturopath

Hello everybody,

It's interesting that you 've mentioned sore eyes. I too have just increased NACi from 1 to 2 pills, which I didn't take regularly in the first place, and started to feel sore dry eyes.  Hopefully that's a good sign that smth is going on and working.

 Vlad

Thanks for the feedback everyone! Gosh it's great having this place to share. I am now at day 14 of NACi and still headachy. I feel flat lousy but misery loves company, and I'm in great company.
Blessings
Marie

On CAPi since Sept '05 for MSi, RAi, Asthmai, sciatica. EDSSi at start 5.5.(early cane) Now 6 (cane full time) Originally on: Doxyi 200, Azith 3x week, Tinii cont. over summer '07, Revamp of protocol in Summer '08 by Stratton due to functional loss; clarithromy
Well, you know, being a recent convert to NACi in terms of entire treatment time, and never having taken amoxicillini apart from two weeks two months ago, when I had already started NAC, I think I must still have a lot of EBs to clear out.  I feel permanently as though I am about to come down with a cold, and this week when I have been taking the tinidizole pulse of a booster dose, I have also felt "flat lousy" for much of the time.  Last day today, though!Sarah
 
Completed Stratton/Wheldon regime for aggressive secondary progressive MSi in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.

NACi is my friend, NAC is my friend....  I keep telling myself that, in hopes of convincing myself  (thanks, David!). Haven't quite doubled the dose, but I'm working up to it.   I don't feel 'lousy', but I don't feel as good as I did up 'til now.  Sarah, your description of 'permanently about to come down with something' is pretty accurate for me.  My sinuses keep clearing, yet I don't have the sick, sinus-infection feeling I've become so familiar with over the years.  This is weird, but I just keep telling myself it's all for the good and this too, shall pass.  (Two margaritas helped immensely last night.)  Hang in there, Marie!

The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi

Sinus problemsi seem to be an ongoing thing with me. I think the medications are affecting my sinuses. My doctor wants to point the finger at Allergic Fungal Sinusitus--certainly may be as it can appear in people who are on antibioticsi treatments. But as I have had sinus problems for years, I thought that the antibiotics would clear it up (if it was a bacterial infection.)  My nasal passages are filled with clear think mucus. I have tried saline nasal washes and sometimes they cause intense pain. I take NACi twice a day. I'm wondering if that is what is going on. I had been taking it for months before I went on the treatment but just recently went up to two 600 mg caps a day. When I increased the dosage, I noticed short periods of feeling feverish, usually in the early afternoon.Raven

Feeling 98% well-going for 100. Very low test for Cpni. CAPi since 8-05 for Cpn/Mycoplasma P.,Lyme, Bartonella, Mold exposure,NACi,BHRT, MethyB12 FIRi Sauna. 1-18-11 begin new treatment plan with naturopath

Sinus infectionsi are very common with cpni, often becoming chronic. As a youngster I had sinus problemsi for years until they gradually faded away. Now, since starting NACi, I am having a lot of nasal discharge. There may be two reasons for this; bursting the EBs and softening the mucus. Chlamydial EBs are very sturdy, geodesic spheres - they have an uncanny resemblance to WW1 sea-mines - whose coats contain proteins locked together by disulphide bonds. When they are burst outside host cells they die. One might expect their contents to be quite allergenic. This could give a flare-up of sinus symptoms. Actually, the symptoms I feel now are nothing like that dull, unremitting sinus pain, worse on bending forward, and while running, that I used to feel. This is completely different. The mucus-loosening properties of NAC may help, too.

Incidentally, a person with PCRi positive cpn infection, who has been on the Vanderbilt regimen (including anti EB medication) for some time, told me that he experienced no symptoms when he recently started taking NAC. Perhaps all his EBs were history.

On a further, speculative, note, I have wondered whether a proportion of the EBs were faulty, and lacked attachment mechanisms. This would lead, over the decades, to a large body of EBs which did nothing except take up space. These would be burst by NAC, too. As I say, this is speculation, but it might account for the extraordinary symptoms NAC produces. Since I started taking it the fining of the soft tissue in my face and neck has accelerated.

 

David

D W - [Myalgia and hypertensioni (typically 155/95.) Began (2003) taking doxycycline and macrolide and later adding metronidazole. No medication now. Morning BP typically 110/75]

Wow,  I wonder whether a low level cold which I've had for the last week or so is something to do with the NACi.  I only started taking it twice daily about 2 weeks ago.  Fascinating.  Thanks for all the inputs and for this website.

Started CAPi April 2005, right leg motor function now worse

Yes, it is I...KK2, in the NACi thread!  I know, I know, I am allergic to sulfa meds, and there is indeed a sulfur bond in NAC, but after researching this, and chatting with Dr. Stratton, I decided to try one 600 mg capsule--yesterday.  Apparently there is no more sulfur in a 600 mg cap of NAC than say in a 3 ounce  steak, so I reasoned it was worth trying as I can eat meat, no problem.

I was fine at first, but several hours later I felt my sinuses clog up, became sleepy, awoke later feeling flushed and ill as though I was coming down with something.  These all sound like typical NAC/ Cpni reactions.  The interesting thing is that I also have a mildly painful gland under my left ear[the side I usually get ear/ sinus infectionsi on].  Also a feeling of "fullness" in the left ear, gradually feeling more like an ear infection.  I decided to wait until today to try another pill.

Today, after one more single dose, things are about the same, with continued malaise,  but now add tenderness around the eyes, fatigue, nausea--maybe better described as an "anorexic" attitude toward food.  I am still on the fence about whether this is necessarily a mild allergic reaction.  I would expect things to settle down over time if it is simply the NAC "flu". 

I'll keep you guys posted.

Wheldon Protocol for rrmsi since Oct '05.  Added LDN 4.5mg qhs Oct '07.  All supp's.  Positive IGGi's for Lyme Disease,Babesia, & Erlichiosis Sept. 2008.  Currently:  Mepron 750mg bid and Azithromycin 250mg qdi for Babesia.

Possibly a reason that people experience problems with NACi (and I certainly can confirm this from personal experience) is that the majority of EBs are located inside of cells. And NAC does not kill those EBs instead it breaks down the disulphide bonds that cause it to start replicating. This happens in cells all of the time but NAC probably speeds this up greatly. At some point this is a necessary evil in order to erradicate Cpni but I think starting later and going slowly would be a good idea.

- Paul

While I just started the protocol on February1 with supplementsi including NACi, and I have already had one Flagyli pulse, that I completed a week ago, I also experienced some fullness around my head, ears, nose, throat, etc. But shortly after this "fullness" in my ears, my right ear bled briefly and then stopped. And I had a dry bloody nose before and after the bleeding in my ear. I've never had this happen before, in my life, that I can recall. All of these symptoms were exacerbated during my first Flagyl pulse and most of last week. It has stopped now, today, thank goodness. David Wheldoni and Dr. Powell both suggested that it made sense, since it is through the respiratory system that we get Cpni, if I understood them correctly. I, too, have had a history of sulfa allergy, but the NAC has been mostly okay. My constant is car/motion sickness, although I'm not moving. I was first diagnosed with Cpn over 10 years ago. I used zithi for almost one year, over three years ago and I'm just now on the right track thanks to Jim, David and Dr. Powell. altesa
CAPi 2/14/06 for Cpni-CFSi/FM/CD

 Paul- Maybe we should get a microbiologist to weigh in here like Chuck or David as my understanding is that the EBi's are mostly extracellular, and once they penetrate a host cell and form an inclusion they convert to RB's which are all intracellulari. The whole point of NACi is to get the EB's converting to RB's while they are still outside a host cell and thus are both vulnerable to your immunei system, and have not host-energy to draw on, according to Dr.'s Stratton and Wheldon.

The extracellular, infectious form (0.3 µm) is called elementary body (EB), and the intracellulari, replicating form (1.0 µm) is called reticulate body (RB). Infectious EBs start the cycle by attaching to a susceptible host cell membrane. They gain access into the host cell via either parasite-specified phagocytosis or receptor-mediated endocytosis. When inside the cell, the chlamydiae remain within an enlarging intracellular vacuole, a characteristic inclusion, avoiding lysosomal fusion and hence destruction. During the first few hours, EBs differentiate into metabolically active RBs.

From: http://herkules.oulu.fi/isbn9514269853/html/x467.html 

Dr. Stratton's slide presentation also calls them extracellular:

 

Slide from Stratton Slide from Dr. Stratton presentation

On Wheldon/Stratton protocol for Cpni in CFSi/FMSi since December 2004.

 

CAPi for Cpni 11/04. Dxi: 25+yrs CFSi & FMSi. Currently: 250 aithromycin mwf, doxycycline 100mg BIDi, restarted Tinii pulses; Vit D2000 units, T4 & T3, 6mg Iodoral

Thank you Paul and Altesa.  Your responses help me very much.  Slower is better- no doubt.  I cannot imagine taking more than one 600 mg capi of NACi per day at this point.  I may just do QoD[every other day] for a time.  The ear fullness is kind of warm and painful.  The feeling has conjured an eerie flashback of my 3-yr-old self being curled up on my folks' bed and holding an icebag over my left ear---same kind of pain. 

Altesa, I have had motion-sickness problems most of my life, and am uncomfortably sensitive to certain smells.  The smell inside a car on a rainy day can get me headachey and nauseous virtually immediately--something to do with the rain combined with car exhaust[UGH]  Also, it is interesting that your problems were worsened with Flagyli.  I just completed my 2nd five-day pulse last week and my ear/sinus was definitely affected more this time.

I plan to keep at it with the NAC as I am not seeing the rash that I used to get when I took Bactrim years ago.  I am becoming more confident each day that Cpni has been an unwelcome guest in my body for quite some time.

Wheldon Protocol for rrmsi since Oct '05.  Added LDN 4.5mg qhs Oct '07.  All supp's.  Positive IGGi's for Lyme Disease,Babesia, & Erlichiosis Sept. 2008.  Currently:  Mepron 750mg bid and Azithromycin 250mg qdi for Babesia.

kk2, I am taking 2 600mg caps of NACi per day. I wasn't really attributing my ear fullness to the NAC. However, like you, as a child I do remember seeking cool surfaces to ease the discomfort of my earaches. That sensitivity to certain smells that you mention is something that has bothered me for quite a long while now. I can taste toxicity, chemicals, fumes, etc. But what you're describing is something that seems to combine molds/moisture, with gasoline fumes. Since I've had an intense flying schedule for many, many years as part of my work, it got so that the smell of the fumes around airports was something I could not stand, especially when the engines are revving up and the air changes inside the cabin. It's smells like what you're describing. I've also learned that almost every environment where I have worked for so long has contributed to "re-infection" which just means, now that I've been reading this website, that it's more like reawakening the zombie bugs I thought were already dead. Inspite of all of the side effects, and even after mistakenly swallowing a blue Flagyli pill on the 6th day, thus making those side effects last longer than necessary, I can really say that my hands, arms, neck, shoulders (and body in general), feel better and more limber than they have in more than 10 years. I attribute it to the protocol, so I wouldn't know what to leave out. I guess that the feeling of hanging from my feet and swinging back and forth for days on end will subside eventually, as it has today. One day off and what a great day it's been. altesa
CAPi 2/14/06 for Cpni-CFSi/FM/CD

Paul- Maybe we should get a microbiologist to weigh in here like Chuck or David as my understanding is that the EBii'si are mostly extracellular, and once they penetrate a host cell and form an inclusion they convert to RB's which are all intracellulari.

Hey Jim,

One reason we should not have the microbiologists weigh in here is that they will suggest starting on NACi early;) All joking aside, this is really a very difficult dilemna and one in which reasonable people can disagree. I was just posting my opinion and I should have stated it as such or with information on both sides. So anyway I will try to answer this a little more thoroughly this time.

In the current protocol, one of the first "drugs" that is used is NAC. The reasoning behind this (which I find quite sound) is that if you are able to break open an EB outside of a cell that is a huge plus. You kill the "spore" before it ever gets into a cell and never have to deal with killing it in a cell where the killing process can cause damage or stress to the cell. And if your blood looks like the photo on the front page of this site, which has what are presumably huge numbers of EBs attached to red blood cells, this is obviously the only way to go. It is also highly probable that NAC opens EBs inside of cells either directly or by being converted to Gluthathione which allows the ABXi to kill them. Additionally NAC has some anti-oxidant and liver protecting properties.

However I do not think that photo is typical. I think most people have far fewer EBs floating around than this. And I believe the first priority of treatment is to get the replicating organisms under control as (1) they are making new Cpn and (2) they are causing most of the side effects which limits how quickly you can progress to adding more ABXi. I think the second most important part of the treatment is getting rid the persistent organisms as (1) they can at any time switch to a replicating state and (2) cause a lot of symptoms as well which limits the speed of treatment. This of course means that you are completely ignoring the EBs which do have to be dealt with. But while they are in this state they do not replicate or cause any symptoms. So my opinion is that they should be dealt with later rather than sooner.

I really cannot say which of these is the right course. I am basing my opinions on what seems right to me and personal experience only. So people should keep this in mind when considering this.

- Paul 

 Paul- I did my treatment in the "traditional" way which you cite- antireplicant abxi's, ramping up on flagyli and only 6-8 months in adding amoxi (thankfully switching to NACi). The only thing that differs in my experience is that I'm convinced that the EBi's are causing symptoms, as a lot of generalized inflammationi improved for me after I got over the NAC flu (about 2 weeks) and stayed on the NAC. I suspect (definitely  my opinion here as I don't have any references at this moment) that the envelope proteins of the EB's contain enough HSP60 to be locally inflammatory when they have built up in large quantities-- such as in a 25 year untreated infection! In fact, some of the antigeni based research I've read, most of which measures for EB antigens, also has measured for HSP60 as a confirmatory measure. So this bug gets us coming and going.

I love having your thoughts here for some good discussion and speculation. Helps me gain appreciation for the complexity of this beast and put together the anecdotal with some interesting speculative ideas. 

On Wheldon/Stratton protocol for Cpni in CFSi/FMSi since December 2004.

 

CAPi for Cpni 11/04. Dxi: 25+yrs CFSi & FMSi. Currently: 250 aithromycin mwf, doxycycline 100mg BIDi, restarted Tinii pulses; Vit D2000 units, T4 & T3, 6mg Iodoral

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