Surely, that should apply.

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Okay to start with I must say that I’m sure my opinion is very similar to the majority of most people in that my view of teachers and doctors and the NHS in general is one of respect.
However I don’t think either profession are doing themselves any favours whatsoever by striking.
Yes they do deserve better pay, but the way they are going about trying to get an increase is absolutely farcical, how nurses and doctors can go on strike putting the lives of innocent and sick people at risk in an attempt to justify why they deserve better pay, completely escapes me.

Teachers!!!!
So tell me how it’s considered perfectly acceptable to fine a parent £60 when their child misses school, but a teacher can stamp their foot down, like a spoilt child demanding more money, and forcing parents to either miss work themselves or pay someone to look after their child.
Surely the same should apply to them as well…

Stubborn.. hmm…

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Stubborn.. hmm…

Ever since I started on the Ann Boroch Protocol, I’ve tried a few additional things that I thought would help and speed up the process of healing.
Some have definitely helped, albeit a little like beetroot juice capsules, which has helped increase the red blood cell count, which in turn increases the oxyhaemoglobin to organs. One or two other additions haven’t necessarily helped or hindered, so they were only used for a few months, but I have to say that although I’d added certain things and made the occasional mistake, I’ve stayed at least 95% compliant with the Ann Boroch food recommendations.
On those occasions, I’ve had my wrist slapped, justifiably, and got back on track.
I’m sure everyone, to a certain degree, thinks that “they know best”….
I mean, think about it. Ann Boroch didn’t know everything?… but she did know a damn site more about healing the body naturally than anyone else that I’ve met or talked to or read about.
So, yes, have thoughts, but trust me, very few people are more inquisitive and willing to research and try alternatives than me, so learn from my mistakes and those more determined and focused and have a 100% not 99% belief, I’m referring to Janet now and her mentor Ann Boroch .
Getting back to the headline, am I stubborn, yes, but not too stubborn to admit my mistakes. The Ann Boroch Protocol works, it will take longer than you’d like it to, but healing a supposedly incurable disease takes time.

But … Because…

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But!!! …Because!!!…

Over the years since originally being diagnosed with this horrendous disease… multiple sclerosis, I’ve tried at least fifty different “things”that professed amazing results. Most, as I’m sure you know we’re nothing more than “snake oils ” that drained my rapidly diminishing bank balance.
The nutrional beverage called XanGo was different and certainly helped… I say and emphasized “Helped”, it didn’t cure or heal me, but it helped significantly.
However, it was the Ann Boroch Protocol that healed my body…
No one!!! No one… not Ann… R.I.P.
Not the wonderful Janet, not Martha and definitely not me benefit financially in any way, shape, or form by helping or encouraging others to follow the ABP.
Now, please understand that the protocol isn’t a “one size fits all” method of healing the body of the damage done by having MS for several years.
It would be misleading to say or infer that.
There are approximately 2.3 million sufferers currently, so, following the protocol is extremely important, although there has to be minor modifications, yes, minor modifications, not radical changes, the basis of the ABP has been successful 10,000 times, give or take.
Everyones individual circumstances are different, where we live, the foods we’ve eaten, our support network, and hundreds of other things.
I’m personally pushing myself physically, much more than I believe most others could do, I’m not unique or special, but I know I’m different.
I’m in a rise and recliner chair, not a bed, because it’s easier to do the exercise I need to do to rebuild muscle in my legs.
The ABP is not rocket science, and it’s not difficult to follow, it’s the individual things, specific to me and you, that are hard.
But they’re done, because we know they work…

You’ve got to…

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You’ve got to…

I honestly believe in the Ann Boroch Protocol as the basis of healing the body of multiple sclerosis even though the medical fraternity all say that the disease is incurable.
I’m looking at it a little more closely, and the classification given to it by big pharma, they say… that its incurable, but what they are really saying, is that from their point of view, it’s far more lucrative to say that they can’t find a way of beating it, but the have created drugs that simply ease one or two of the “multiple” symptoms which will make “MS” more bearable for the sufferer, while lining their own pockets with lots of cash.
I said at the start that I genuinely believe that the ABP is the basis of healing your body of multiple sclerosis.
So am I saying that you have to buy something else or try another protocol..NO.
But what I am saying is by just buying a new car or a first class ticket on a train or plane doesn’t get you from A to B..
What gets you there is You either driving the car or You getting to and from the station or airport.
The protocol, the car, the train or plan, are just methods, it’s your interaction with them that makes it happen.
You !!! Yes You have to make the commitment to make it happen.
You don’t just buy the car or the ticket and amazingly just arrive at your desired destination.
You’ve got to do your part, it will work as you want, but please understand that…
You’ve got to TRY…

You’ve got to…

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You’ve got to…

I honestly believe in the Ann Boroch Protocol as the basis of healing the body of multiple sclerosis even though the medical fraternity all say that the disease is incurable.
I’m looking at it a little more closely, and the classification given to it by big pharma, they say… that its incurable, but what they are really saying, is that from their point of view, it’s far more lucrative to say that they can’t find a way of beating it, but the have created drugs that simply ease one or two of the “multiple” symptoms which will make “MS” more bearable for the sufferer, while lining their own pockets with lots of cash.
I said at the start that I genuinely believe that the ABP is the basis of healing your body of multiple sclerosis.
So am I saying that you have to buy something else or try another protocol..NO.
But what I am saying is by just buying a new car or a first class ticket on a train or plane doesn’t get you from A to B..
What gets you there is You either driving the car or You getting to and from the station or airport.
The protocol, the car, the train or plan, are just methods, it’s your interaction with them that makes it happen.
You !!! Yes You have to make the commitment to make it happen.
You don’t just buy the car or the ticket and amazingly just arrive at your desired destination.
You’ve got to do your part, it will work as you want, but please understand that…
You’ve got to TRY…

Stubborn … hmmm…

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Stubborn.. hmm…

Ever since I started on the Ann Boroch Protocol, I’ve tried a few additional things that I thought would help and speed up the process of healing.
Some have definitely helped, albeit a little like beetroot juice capsules, which has helped increase the red blood cell count, which in turn increases the oxyhaemoglobin to organs. One or two other additions haven’t necessarily helped or hindered, so they were only used for a few months, but I have to say that although I’d added certain things and made the occasional mistake, I’ve stayed at least 95% compliant with the Ann Boroch food recommendations.
On those occasions, I’ve had my wrist slapped, justifiably, and got back on track.
I’m sure everyone, to a certain degree, thinks that “they know best”….
I mean, think about it. Ann Boroch didn’t know everything?… but she did know a damn site more about healing the body naturally than anyone else that I’ve met or talked to or read about.
So, yes, have thoughts, but trust me, very few people are more inquisitive and willing to research and try alternatives than me, so learn from my mistakes and those more determined and focused and have a 100% not 99% belief, I’m referring to Janet now and her mentor Ann Boroch .
Getting back to the headline, am I stubborn, yes, but not too stubborn to admit my mistakes. The Ann Boroch Protocol works, it will take longer than you’d like it to, but healing a supposedly incurable disease takes time.

What does it say…

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What does it really say…

For most of the latter part of my life, to date, I’ve studied and researched about health, nutrition, and the benefits of eating healthy, uncontaminated and organic foods and being drug free, of course.
So, when I got the job of becoming the client service director for the world leading authority in biological dentistry and body chemistry rebalancing, I was over the moon happy
So I think you can understand my confused emotions when it comes to the attitude of the powers that be, from health officials in the government, all the way down to officials supposedly concerned for the general public health.
For instance, in my case, I’ve obviously got a very weakened and compromised immune system as I have MS,, so getting that horrid Covid19 you’d imagine I’d be one of the many serious sufferers fighting for life.
As it happens over the past 3 years, I’ve been diagnosed with it three times and amazingly beaten it in a few days every time. Now, was I lucky? was it just the “Jabs” that saved me no!!! because I’ve never had any…
What I did take was mega doses of Lipospheric Vitamin C which has repeatedly been scientific proven to kill all known virus, including coronavirus., but because it doesn’t make billions for big pharma, it’s not recommended.
Now let’s also look at my own situation,my carers are allowed to give me the painkillers and thyroid medication prescription by the doctors, but are NOT allowed to help me with the natural supplements I take? Now I’m not criticising them or their immediate bosses.
Weird….!!!!
If I was to take a month supply of the prescribed medication in one go, it would more than likely kill me, or at least do serious damage.
But if I was to take a years worth of any five supplements I take, together, the worse it would do is make me vomit or have diarrhoea.
So the carers who are paid to help, can give you a potential killer, but they would lose their job for helping me take the life saving supplement.
Does that make sense? It doesn’t to me.

Taking this into consideration, use your common sense, what does it really say about the incredibly profitable “sickcare industry” who are advising and influencing the Health Service..

Not try…

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Not try…

As we all know, multiple sclerosis is a debilitating disease, not only physically but emotionally as well. There are times when your brain tells you to do the most basic of actions, it might be a simple stretch of scratching an itch on your leg or arm, but this freaking hideous illness has commandeered the communication pathway from your brain to the appropriate limb. This results in the most frustrating time when you “want” but “can’t”… making you feel sooo frustrated and annoyed and mad and angry, not with loved ones or friends near to you, but yourself.
But… this is exactly when “YOU” have to be strong emotionally, just keep telling yourself that although everyone else around and in contact with you who have no idea why you don’t just take the prescribed medication instead of doing this ridiculous ” it’s never going to work diet” that you’ve been told about.

I’ll tell you… why… and try to reassure you, that, the prescribed meds aren’t medicine per sè, they are pharmaceutical drugs that mask the cause and address a symptom, this isn’t just a diet that someone wanting to lose a few pounds on might follow occasionally. This is a “LIFESTYLE CHANGE ” this is a tried and tested and PROVEN method of changing your eating habits to remove the build-up of toxins that “HAS” restricted your life.
This is The Ann Boroch Protocol that in time WILL kick the bad guy’s ass out of the temple you call You !!!.
So my friend, when the frustration hits you, when those around you just lower their heads and shake it from side to side!!! Now you take a deep, resilient breath, and tell yourself, genuinely Tell yourself that you aren’t going to try, you are going to DO !!!

Sadly…

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Sadly…

At one point in time, maybe fifteen or twenty years ago, the UK was envied for having the best health service of any country. I think our facilities, such as hospitals and clinics, were very well equipped, but it was the quality and attitude of our doctors and nurses that put them above just about everyone else. The John Bull attitude of “we’ll find a way to fix it”. . and “you won’t beat me. “… put the NHS as the place to be if you had gotten sick.
I lived and worked in the USA for eleven years and obviously experienced the
“Who is your health insurance with?” Whenever I attended a doctors surgery or hospital, which I did on a few occasions. If you had good insurance, they couldn’t do enough for you, but the opposite would apply for those less fortunate. For the majority of my time there, my insurance was with one of the top three companies, when I was married ( a long time ago) our health insurance was $200 per month, and that was 2002-2008.
Anyway, back to the point of this post, on Thursday last week, I spoke with my local GP and explained my situation, a long story which I’ll not go into now, but trust me, there’s a logical reason that I’ve been confined to a Rest and Recliner chair for almost 3 1/2 years, so you’ll understand that my butt is sore, sitting in the same position 24/7 apart from 30 mins in the bathroom.
The doctor, a nice lady, arranged for a district nurse visit ASAP.
On Saturday, a district nurse came in, I realised, but said nothing that she was the same one that had been to see me in January. I was disappointed, to say the least, as this woman didn’t deserve to be classed as a nurse. Her first comments were that she didn’t know how to use the Rotunda I needed to stand and keep my balance. I’d explained last week to the nice doctor that my skin wasn’t broken, but the excruciating pain was like being sat on a drawing pin… permanently!! So when I saw the nurse..!!! unwrapping two hermetically sealed plasters, I asked what she was doing. She responded in that “I’m a nurse and know what’s best” attitude, and she made an “oh” exclamation as she saw the unbroken skin.
Again, I explained that, in my opinion, it was more likely a sciatic nerve issue, and I was hoping for a possible solution.
The look on her face was one of “there’s nothing I can do for you!! and started to walk out.
I had to really control my anger, and asked politely if she would move the Rotunda back against the wall, move the table she’d moved back so I could reach it and pass me the blanket I’d had over my legs that she’d thrown on the floor.
She did them like a bratty teenage girl being asked to stop texting on her iPhone.
Maybe she would rather have been on a picket line, but thats another post .
Because of my recent experiences and the news coverage, my opinion of some NHS staff.
Sadly, it isn’t good…

Make the right choice…

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Make the right choice…

I think what I should do is to put my thoughts into written words as I have them. What currently happens is that my overactive mind will be saying them, it might be something for the AB groups or for my blog, then the following day at the butt-crack of dawn I’ve forgotten the basic premise and rambled on into a hundred other topics. So what I vaguely remember from two nights ago is something like this:
Being diagnosed with a so-called autoimmune incurable disease is quite frankly… a devastating and heartbreaking thing to hear.
Coming to terms with the prognosis of there’s nothing that can be done to change what “they” believe to be the dark, damp, and frustrating stairway down to the end of your life.. is a very depressing place to be.
But…
Contrary to what the drug pushing nay sayers believe, there is a light at the end of the tunnel, okay its not easy, it’s not a “just take these pills for life” solution.
You have to make a choice to persevere with a lifestyle change. No more Dairy, Gluten or refined sugar… actually I personally will have some fruits with minimal amounts of fructose, but I have been AB compliant for 5 years.
The ABP, the Ann Boroch Protocol is that warming gut friendly, life giving light, my suggestion, for what it’s worth is to pay close attention to what people in the know who’ve been there, done that and healed their body by adapting to a lifestyle change say and recommended, rather than accepting the depressing naysayers words of “it’s all over now”.
Make the right choice…

We are here for you.

Janet, Martha and me(Stefan)