Rather Be Healthy

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…

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.. 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 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…

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…

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…

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)

No!!! It just means…

Firstly I have to say that in life, we all have to have an open mind…
None of us know everything!!!
When the medical fraternity say that from their experience that a particular disease is incurable, does that mean it is incurable?
No!!!
It just means that they have been told by the pharmaceutical giants that its incurable.
Does That mean it’s incurable?
NO….
It just means that from their point of view it’s not financially viable to find a cure..
They probably could invent a “fix all pill” but in reality they can make much more profit by adding customers for however long their life will be.
Think about it?
When Ann Boroch was diagnosed with MS, there wasn’t a FIX ALL PILL, there still isn’t!!!
What she did was painstakingly research to find specifically what was causing the problems that cumatively are bunched together and called multiple sclerosis. She then set about creating what is now known as the Ann Boroch Protocol.
It doesn’t happen overnight.
But it does happen.
Buying the book, studying what she said.
Following the protocol correctly, and then after 4 or 5 years multiple sclerosis will not be a problem in your body.
There’s no “quick fix “, it just means that You will help your body to Heal itself…

I can and…

Every day is a challenge for most people, but even more so when you have one of the many “so-called incurable diseases” in my particular case, it’s multiple sclerosis.
Now I said “so called incurable diseases.” Because in my opinion most are not incurable, it’s just that the pariahs known a big pharma make billions in profit every year by glamourising their supposed efforts to find a cure and they use very clever advertising to make the uninformed public think they are, when in reality that’s never going to happen.
It’s a sad state of affairs when the genuine medical professionals are hampered by the giants that are happy to revel in extortionate profits at the expense of people who are dying.
You only have to look at one of the many true health pioneers, Ann Boroch who completely healed her body after she had been diagnosed with the same hideous disease I was told I had, multiple sclerosis.
Where’s Ann know? years after she healed herself, as have thousands of others that followed her protocol. Many of us know the truth, in that her life was taken by those that would rather gain lifelong customers.
I’ll not be specific, but I’m sure you can work it out yourself.
As far as I’m concerned from an MS standpoint, because of the ABP, that’s history, a fall because of my own overconfidence and the massive backlog in operations through the pandemic has kept me bedbound, but I’m 100% committed to repairing my leg damage and ĺiving again rather than existing.
Anyone who knows me will genuinely know that I can, and I will…

I was told, as 99% of other sufferers that I had multiple sclerosis which in the eyes of just about every conventional medical professional was an incurable disease.
In reality, an incurable disease is a disease that the medical professionals by way of the pharmaceutical industry say is incurable, or that they: big pharma haven’t found a drug that can fix it.
In reality, they aren’t and never have looked for a definitive way of genuinely healing any illness, let alone MS.
So, your choices are, according to them, to take the prescribed drugs that can ease one of the many symptoms.
What they don’t tell you is what the problem is or the scientifically proven side effects of the drugs that they, medical professionals that are supposedly looking out for your health.
Everyone knows what multiple means, so the sclerosis part?
According to Google;

Sclerosis: pathological hardening of tissue, especially from overgrowth of fibrous tissue or increase in interstitial tissue. also : a disease characterized by sclerosis. : an inability or reluctance to adapt or compromise.

My understanding of what was told to me by numerous neurologists is that an auto immune disease is basically a disease that the immune system is confused and in trying to protect you is attacking itself..

As I said, the NHS and every other conventional medical practice will only ever consider a form of treatment that is recommended by the pharmaceutical giants who in reality are not interested in anything but increasing their customer base and profits.

So after being diagnosed with MS, your genuine choices are to take the Dmd’s which as far as true health is concerned will do bugger all to help, or look for a genuine way of healing the body… Notice I said healing the body…  the Ann Boroch Protocol will do that,and not trying to cure MS, because the real problems have been caused by yeast, mould, gluten, dairy, and sugar.
These have exacerbated the rapid growth of Candida, which is the…
True problem…