I am in my eighth month of abxⁱ treatment.  I have had several improvements, but I never expected the two listed below to happen.

I have been a Coeliac for 25 years, and eaten only gluten free food since.  About a month ago I ate a Jatz cracker and didn't have a reaction, so I ate several more.  No problems!  Since then I have tentatively eaten things like 1/2 wholemeal sandwich, chocolate cake, biscuits, crumbed  food etc.   Usually I would have gotten a stomach ache or thrown up, but I haven't had a hint of trouble.  I feel I have overcome my gluten intolerance.

Hi guys,

wanted to post, that I am having a really good day!

The best I've had in a long time - prob ithe best in the last 3-4 months.

Feeling quite hopeful,....weird how things can change so dramatically...even in a week.

last week, I was thinking, that I had gotten so bad, I might need to leave my apartment, my job and get home care.

i guess the NACⁱ and vitamin A and C are kicking in? Well, they were in the last while, making everything worse and then the last few days....glimmers of major hope!

crossing my fingers and toes I go from strength to strength!

lea

Friday 1/2/13

Started second pulse today, felt sick but not as bad as last time. Yesterday I went to the hospital for the Fampyra trial follow up, went to Coles, came home had lunch then went to physio.  So lots of energy. I am using the walker not sure for how long but it was before I went to the hospital so maybe for a week or so.  Makes it easier to walk properly without a limp.

Saturday 02/02/13

Took antibiotic again today, did not feel as bad as yesterday, bit fuzzy in head, aches in muscles, nauseous and pain in side of head bit dizzy.  Feel as if I have a cold, my chest feels a bit wheezy and I get heart palpitations on and off.

Monday 11/02/13

Clairthromycin is VILE!

 NACⁱ still makes me feel a little flu-ish, while LDNⁱ is a breeze and I find Planieul & Doxyⁱ pretty easy to take BUT Clairthromycin is VILE!

I am sorry – I have to vent!  Clairthromycin tastes awful and I can’t escape the taste.  I wake up tasting it.  It makes me feel nauseous most of the time.

HOWEVER, since I’ve been taking it I’ve noticed two positive changes.  First I am now having two bowel movements most days – hopefully transporting more toxins from my body.  Secondly I have gone from 4-5 bathroom trips a night to 2.  I am thrilled to be sleeping more and waking up less.

I am now waiting patiently to fully adjust to Clairthromycin so that I can start my first flagylⁱ pulse.

Hi there,

I was wondering if any of you have any data

on how much Doxycycline, Azitromycin and

metrodinazol reduce the   lymphocyte levels in blood.

It sure would be neat to know what labs are studying c.pn, what aspect they are researching, and the progress thay are making! 

Just a quick note as I feel great today--much work to do with the garage disaster....one day it will be a thing of my past!  lol     Just one of those projects that--due to many years of neglect with my illness--just seemed to grow and grow.  

So, I have been ill over the past few months.  Hard to explain--I still functioned but haven't felt great.  Wondered if I was depressed....you know, not happy, not miserable.   Kind of blah.

Looking back I had added quercetin and bromelain due  to my belief that I have developed Dupuytren's on my  right hand (small white lumps--easy to see on Google images).  I am convinced this is what it is since I have had symptoms of it for years and my doctor agreed.

Hi all.

School time is now far away so please  excuse my mistakes, mister Google will help me to write these few lines.

I am a 57 yrs  old man diagnosed with PPMSⁱ 2 years ago.

My current base treatment consist of  interferon injections (every 2 days).

Last year, i read  the different theories from  dr Zamboni (jugular vein stenosis) ,  dr.Wheldon about the role of Cpnⁱ in MS and  dr Thibault presenting their synthesis. For me it all made ​​sense. For myself, the medical examinations have shown:

This is maybe a message for the administrator of this webpage.

Wouldn't it be very useful to have an entry on the left side of this webpage

where people who has been on Dr Wheldon's or similar protocol and the protocol is indeed 

working could have a small summary stating e.g. diagnosis, protocol, length, benefits.

The thing is that there are loads of people starting the protocolsⁱ, it seems they take a long time to work (it seems). I know that you still have a section with patient stories but they seem outdated. 

It takes long and i feel lost trying to find people for which the protocol has worked, so much informaton!

Considering how miserable I've been feeling lately with the allergy issue, starting the next pulse might not have seemed like a great idea. But instead of feeling worse, I've been feeling better. Not great, but better. I've noticed this before during other pulses, just never commented on it before.

My daughter and I are looking into  Cpnⁱ and the antibiotic protocol for M.E and our doctor is willing to precribe doxycycline for her skin but has suggested she tries Lymecycline instead as she is going  abroad to a hot climate for 7 weeks. We are wondering whether to wait until she returns before starting the treatment with Doxycycline or to start on the Lymecycline now and change to Doxycycline when she returns to England. Any help would be greatly appreciated.

This is from my journal in January.  It covers my first pulse. 

We live in a bushfire area and around 2 weeks after the pulse I had to evacuate with our animals while my husband stayed to defend the house.  Luckily the fire did not come too close and all was ok.  I was extremly stressed.  a week later there was another fire while I was home alone, which I could see, as it was accross the road on a hill about 2 klm away.  I was very stressed through this time as it brought back memories of Black Saturday in February 2009. we were ok then as well but it was the stress of not knowing what would happen for weeks after.  each time I went out I worried.  That is when my MSⁱ really started to progress quickly.

G'day everyone,
today is my first day at starting the protocol, please correct me if I am wrong or missing any supplementsⁱ.
NACⁱ 600 mg.
Acetyl-Carnitine 500 mg.
CoQ10 60 mg.
Vitamin C 1000 mg.
Vitamin D3 1000iu.
Fish oil 1000 mg.
Multi-vitamin.

I take the above supplementsⁱ once per day after launch.

I'm into my eighth month of the Wheldon Protocol for rrmsⁱ and am pleased to say that I've just started doing some part-time work from home. My health is improving slowly but surely and my brainpower is such that I feel able to tackle some brain taxing work - I'm a heritage architect.

I'm also doing my third flagyll pulse this week - I delayed the pulses to be kind to my body - and so far, so good.

Thankyou again Dr Wheldon (and others) for being so tenacious about researching and publicising this treatment! It is working....

Still fighting yeast.  On antibioticsⁱ 22 yrs for chronic sinus.  Also have nasal fungal. Treating with ampho b nasal wash.  Want to try caproyl, bentonite, and psyllium instead of diflucan again, (taken for years, dont think it works, also tried nizoral and sporanox) but can't find dosage or how to mix these.  Can't afford whole approach package.  I think they have to be mixed with water to form a gel that coats my colon.  I'm sure I have leaky gut.  Does anyone have the info on how much to take a day, dosage, if I can take all together. Also read somewhere that has to be in liquid form in order to coat colona does anyone know how to take this? Thx