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
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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.
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
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
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
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
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.
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
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:
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.
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