- Because they don’t…..
The worlds medical experts all say that multiple sclerosis is incurable…
They say that because the companies that manufacture drugs have a hidden agenda. What you are lead to believe is that they are working tirelessly to find a way to cure a disease… whatever disease, but even though they have spent billions trying, they just haven’t done it.
Poor people… all that effort for nothing, but during that time they have created drugs that help a little to address some symptoms on a temporary basis… and fortunately they’ve also found stronger versions that will do the same after their first ones stop working…
Weird really…
Nothing to cure, but plenty to keep you taking them for as long as possible…
So in reality all that has happened is they have just improved their own customer base….
As per usual, I’m digressing from my original topic and ranting about my “pet hate”…. big pharma….
So, …MS…. and the unfortunate people like you and I that have it…
It isn’t a disease per se… its a collection of symptoms caused by bad choices of diet… I know that sounds strange, almost unbelievable after diagnosis and consoling words from the specialists… but its true….
When many other diseases are diagnosed after blood tests, there are definitive markers of that specific disease…. but not with MS..
You’re told its an “autoimmune” disease, as in your own body is mistakenly fighting itself…. hmmmm.
The human body is more advanced, more capable than the worlds most advanced computers, actually hundreds of times more powerful, not just a bit better.
That being the case, why would your own immune system try to kill itself?
Its not….
What its trying to do is remove toxic materials that are preventing its own organs from doing their job. Sadly the toxins are distorting the functionality of the specialised sections of the body and changing the composition and effectiveness of the blood….
So in my case and thousands of others before me, we are following the Ann Boroch Protocol (ABP) which slowly but surely removes the bad foods and toxins, then rebuilds your body, what happens over a 4+ year period is that your body is “healed”…
This happens when a total life changing attitude becomes your natural way of living..
At the end of August I will have completed three years, I personally believe that the only significant symptom I have now is a muscle weakness that is passing, slowly but surely .
I didnt develope the many symptoms of MS overnight, they took many years to show, so eradicating the toxins and correcting the imbalance and disfunction of the organs in my body will take 4 or 5 years, but it is happening…Going back to the title of this post…
Yes big pharma and the medical professionals that have been fooled by them, all know about the symptoms of what they perceive as multiple sclerosis, but not what it really is, unlike those of us that know of the ABP and its healing properties…..and ….
Because they don’t know me…
-
Just different.
All of my life I think I’ve had a different perspective to most people, I think I’ve seen myself in a sort of special way, admittedly there’s been a part of me that has loved happy endings as do a lot of people. But its the hero that didn’t consider him or her self to be a hero but overcomes adversity and wins against all odds that I’ve related to more than anything else.
I’m not a brave man or special, I dont think of myself as John Mclain… the Bruce Willis character in the Die Hard films, but I’ve loved the character who just does what needs to be done when no one else has stepped up to the plate…
So when I was diagnosed with MS in February 2004, only two years after making the massive move to the USA , the natural thing, the normal thing that people do is to pay attention to the doctors and neurologists that are so called specialists in the medical arena.
Their advice to me and anyone diagnosed with this hideous disease is to accept what the medical specialists and pharmaceutical giants all believe.. that MS is incurable so dont kick up a fuss, be a good boy, take the medicine and resign yourself to taking their drugs and not actually living a life again…
But as I said at the start of this post, I see myself in a different way.
For more than 13 years I refused all MS medication and tried more than 50 things like therapies, operations, tonics and supplements, some helped a little but none in a long term way.
But….
In August 2018 I read “Healing multiple sclerosis” by Ann Boroch and with the help of Janet Orchard I started the ABP..the Ann Boroch Protocol on September first.
So in 2 months I’ll complete my 3rd year of a 4 year plus protocol.
I’m not healed….Yet…. but I honestly believe I will be. It might be 4 years or 5 years but I’m 100% certain it will happen, why? Not because I’m special, because I’m not… but even though the majority of people wouldn’t or couldn’t keep going in the face of adversity my John Mclain me comes to the surface and reminds me that I’m….
Just Different….
I’ll start this post by saying that this is my opinion, one that has been formed through research, experience, fact and common sense…
The majority of people have views and opinions, and everyone has a right to have one, but in most cases, not everyone, but most, that opinion has been formed through doctors visits and advertising…. its not Fact… its been formulated by companies with a hidden agenda…
The Hippocratic Oath, is long and demands those trained as doctors do the right thing ethically and morally…but essentially the vow taken is: Do no harm….
So seeing a doctor because you have an ache or pain or “symptoms “… you’d expect that your treatment would essentially be to heal you.
Sadly the medical profession is now dominated by the pharmaceutical giants who in reality are interested in one thing, profit…
You arent “their patient”… indirectly and directly you are just a customer… a way of making more money.
About ten years ago when I was a director in Dr Hal Huggins organisation, I read an article that included text from a internal memo within one of the pharmaceutical giants that stated..yes stated that their intention was to have every American taking at least one pharmaceutical drug everyday within the next 20 years, so only ten more years before I have no doubt they will succeed..
They go about their business, a very lucrative business in a very clever way, well its clever from their point of view, but devious in all others. They use the media to promote themselves as knights in shing armour working tirelessly on behalf of mankind..(men, women and children of every race, creed and colour) , said in case some might take offence or misunderstand…
As i said earlier, its not done to make the world a healthier place, its simply to make billions in profit. They have no intension of eradicating disease, they simply want to solidify their financial future.
Whats happened is because of advertising, the media and sponsorship, the intermediate stages between them and us are financially encouraged and manipulated into promoting a drug… I had a telephone appointment with my local doctor a few days ago, during the conversation I was asked if I would take a prescription medication for my sciatica, I hate using that word, because it’s not medicine, its an addictive drug administered to address a symptom. Anyway I replied to the doctor these precise words “you and I both know that drugs treat symptoms”… his response was yes..
So why are the pharmaceutical giants not forced to conduct their business while conforming to the “Hippocratic Oath”.. simply because its not in their best interests…
Financially…
Special day…
I personally feel that having multiple sclerosis is an absolutely horrendous disease, one that can confuse and mislead others and to a certain extent, isolate you…
From first “knowing” in your head that the reason you feel so bad and think it might be MS causing your problems and then when the official diagnosis is delivered…. when the neurologist in my case said….
“There’s no way of breaking this to you gently, but you have multiple sclerosis ”
Its not something that other people can genuinely understand… you Will progressively get worse, especially if you take one of the D.M.D’s (disease modifying drugs) which in reality do nothing more than mislead you and others that you are getting better..
Maybe they should officially be renamed as Disease Misleading Drugs.
Anyway, I digress…when that diagnosis happens and the Neuro attempts to console you, then tells you that there are many support groups that will help you “accept and come to terms” with your news.
Regardless of this, you will have felt alone….
No one really understands the unique problems that you personally have…. they will all say they understand and feel your pain, but they don’t and their confusion will abound as on freshly taken drug days you will feel good, but that will soon change and you will feel and react differently which “misleads” others.
You’re probably thinking that this is a negative post…. hold on, bear with me!!!
All the above is true…but thats not where this ends, in fact its where the good part begins…
Why on earth would you want to be around lots of people with no hope for a life or a future…
A lot of us with ms have had it for a long time before finding the ABP…
in my case it was 13 years… in some ways I’m different, not better, but different because in my case I was living and working in Colorado when I was diagnosed… an arrogant English man offending an American neurologist didn’t go down too well.
That happened when I categorically refused to take the medication (drugs) he prescribed and told….Told me I’d be in a wheelchair in 6 months if I didn’t….hah…16 years later and still not..
So in September 2017 I started on the ABP.. and never looked back, now I am genuinely healing… not there yet but a lot better physically and mentally than I was..
Now I genuinely have a great “support group”, people who “understand”…
Now I’m part of a special group and know that We are all here for each other…
Now I’m proud to say that now I have real Connections….
Never, Never, Never…
I often write about the positive effects I’m having by strictly following the Ann Boroch Protocol, and its true. I dont write exaggerated effects as a way of misleading existing or new starters on this program, I tell it like it is…
My aim is to always inspire or motivate others while reminding myself of the changes I am personally experiencing.
However…. six weeks ago or is it seven…. hmm, whatever… I had a nasty fall that quite frankly buggered my knees…I’ve been limited to my bed ever since, apart from bathroom visits of course.
My plan was to allow the damage done to my ligaments, tendons and cartilage’s to heal, not an easy thing to do knowing that blood doesn’t flow through any, so daily TEN’s machine use and rest has been the only treatment.
Being confined because of the “lock down” is bad enough but being in bed is a tad worse…
I’m not better than anyone else, but I know I’m different, I am a very positive and optimistic person and I constantly tell myself I’m winning regardless of how depressing my condition is.
Sadly, a couple of days ago it all seemed too much, I actually felt down, I wasn’t depressed exactly but the negativity of my weakened legs, the pain in my knees and the excruciating agony of the sciatica which feels like a knife in my left butt cheek then streaming down my leg and needles being pushed into my toes just seemed too much for me.
I felt like I was being knocked down hill and all my previous work has been wiped away, I actually felt like giving up…
On Saturday I thought about several things that could possibly be restricting my progress, certain supplements I’d not been taking came to mind, that was rectified when my afternoon carers came and I’m noticing the difference as I’m writing this at “O dark thirty”…. (after midnight).
Anyway just so everyone knows, even though I always appear to be super positive, that occasionally….no, not occasionally, more like once in a blue moon I experience negative thoughts. I admit I had that on Friday and for a day or so I went through my Darkest Hour…. yes just watched my hero Winston Churchill, so I had a very tough time emotionally but it’s gone now and I’m back to being me…..so as he said…
Never, never, never give up..
Take nothing….
As I’m approaching the end of my 32nd month on the Ann Boroch Protocol, I personally feel very confident of achieving my goal of removing the so called incurable disease from my body, yes it will take four years or more, but that’s a small price to pay when the result is good health again.
I know that I’ve spent the past 5 1/2 weeks in bed, but that hasn’t been because of the protocol, its nothing to do with potential failings or deviations or cheating with foods. It was the result of me overdoing things, thinking I was strong enough to push myself through obvious signs that my legs weren’t as strong as I thought, my bad….
Being over confident, sadly is part of me, I am always telling myself to just try a little harder, I tell myself to not just “try” but to “do”…..
I’ve forced myself into a position that I know what to do but my battered body is just not fit enough….If I had a swivel joint on my knee, I’d kick my own ass…
Anyway, as I’ve said before, apart from the daily weakness that spreads through me around midday everyday I really am not aware of the many MS symptoms that once ravaged my body.
So in my humble opinion, the ABP works, it’s important to ideally keep eating from the 90 day food list, and….
Take nothing for granted
But I’m….
Firstly I have to say….Covid19…
Horrendous..
How its affecting everyone in the world…
Horrendous…
Killing someone is terrible, but killing the thousands and thousands worldwide…
Horrendous…
……….
Just over two weeks ago I’d been feeling really good, primarily because of the really positive progress I’m making by following the Ann Boroch Protocol….
I’ve said before that the majority of MS symptoms have gone after 31 months, it’s obviously going to take another couple of years of strictly adhering to the ABP before I can jump up and down shouting that I’m healed, but I have every confidence that I will.
Going back to the Sunday 16 days ago, I was cleaning the loo as I’ve previously said, when both thighs gave up resulting in me being dumped on the floor with my legs bent at 90° to each other. I know I’ve written about this before, but bear with me, theres a point…
So after the paramedic visit and being put in bed, I’ve been hoping my knees would recover, but, having previously had 7 surgeries over 20 years ago they are not recovering as quickly as I’d hoped, but I believe they will.
Something I’ve said before and a life philosophy I live by, is..
“What you believe…you make true”
………..
Getting back to Covid19…
I moved into the house I live in now, a lovely 350 yr old converted barn owned by my beautiful sister in September 2018…
I’ve seen a doctor twice, primarily to register as a new resident, also to have a blood test. I’ve been out for a meal once but I’ve not actually been outside since for about 15 months….
So yes theres probably 75% of the country in self isolation, theres often news coverage of people saying how horrible it is and how they are getting “stir crazy”…
I say think about all of the people with serious disease like me that have been confined to their house, or one room in bed, unable to get to the bathroom….
The country…the world will heal, in time if we all do what’s necessary..
Self isolation for a month or two or three in reality is no big deal…
……….
My knees are still sore, stopping me from strengthening my thighs, and I’ve been in bed for sixteen days…
But I’m okay
The body knows…
I’m sure that only 117 years ago when people heard about the Wright brothers making a flight in a “plane”.. that their initial thoughts were that it couldn’t possibly have happened. It must have been hearsay… gossip.. it wasnt possible…. then !!! but now, not only do millions fly everyday but “man” has flown all the way to the moon, and walked on it..
So… when people in general, medical professionals and sufferers
of multiple sclerosis hear or read that people with the disease have been healed, their disbelief is no greater than that of others back in 1903..
How has that been done?
Well as myself and thousands before me will testify, it’s by specifically following a dietary protocol, not just any one, but a very specific one called the Ann Boroch Protocol (ABP)..
Am I healed ?
Not completely yet… no..
But as I’ve said before, MS isnt a one size fits all disease… it’s a combination of many symptoms all of varying intensity that have been grouped together and called “Multiple sclerosis “…
Look at the 2.3 million sufferers worldwide who all have similarities but not exactly the same symptoms.
In my personal case, I never had some of the problems that others have, and vice versa..
But, of all the many significant problems I did have, 31 months into the 48 ish month protocol there is really only one major problem and one small one lingering on.
Weakness in general is the major one and having a “hummingbird bladder” is the small one.
As Janet can confirm, when leg muscle atrophy happens over decades, it’s very difficult to rebuild..
It does happen, but it’s a slow process.
The ABP clearly states what needs to be done, it’s not Rocket science, but it is specific.. Ann Boroch learnt of the primary cause which is Candida and how it wreaks havoc in the various organs which go on to create symptoms at various levels..
Eliminating sugar, dairy and gluten initially cause very negative responces in the body and repairing cells, tissue and organs takes time. But when done properly, they will create “Forever changes”…
During the 4 year ish protocol there will be phases of “die off” that appear bad but in reality are markers of saying bye bye to certain symptoms..
As I said, the ABP isnt rocket science, but it must be done correctly.. do it wrong and it wont work.. do it right and it will heal the body…
There are signs, markers along the journey, how do you know if it’s being done correctly? you will feel better in various parts of your body, it will tell you, and guess what?
The body knows best
Misleading, but…
The Ann Boroch Protocol is a 4 year program to follow to Heal the body….
There’s no curing involved, it simply enables the follower to eliminate the toxins and pathogens that have accumulated in the body over a number of years by eating certain foods… some of which had been laden with additives, MSG and E numbers which may have made the food taste better, to eat more and totally mess up the functionality and efficiency of human organs that were very specifically designed to keep you healthy.
Ann Boroch created the protocol to help herself as she had been diagnosed with MS..
As I said, the protocol “heals” the body….
Meaning it enables it to repair and rejuvenate cells that had previously been damaged, and encourage candida growth.
In Ann’s case the candida had run riot which resulted in symptoms that collectively are called multiple sclerosis..
However, variations of candida overgrowth and toxins will developed into other health problems and diseases.
I’m not saying that every illness and so called incurable disease is caused by candida, but many are which means the protocol will help with whatever serious health problem you have.
I’m sure many people have heard the phrase..
“You have to get worse before you’ll get better”…
Well with the ABP the body goes through various elimination phases that result in good and bad feelings, specifically die off…
This can happen and last for undefined periods that can give the impression the protocol isnt working..but trust me, it is..
For me personally, I’ve been experiencing just that for the past few days, weakness and loose bowel movement that would have been so much worse if I hadn’t been taking Activated Charcoal every 4 hours.
All in all I’m very pleased by the progress I’m making, my overall strength, balance and demeanor is massively better than it would have been after 16 years of this hideous disease.
I still have MS, I’m only 30 months into the 48+ month protocol, I’m experiencing die off right now, saying I’m happy, might seem a bit misleading… but I am healing…