Just a desire…
The group I’m with is a closed group of people that have two things in common, firstly they have multiple sclerosis, secondly that they genuinely want to rid their body of it… I’ve written numerous times that it’s not impossible, it can be extremely difficult of course, but if a person genuinely wants something, they’ll do whatever is necessary to achieve it…
Everyone in the group is encouraged to post their problems, difficulties and progress…. all three happen so sharing with others who’ve been there before who in turn respond and share their own personal experience will significantly help. We want to inspire and motivate others to achieve what we know is possible.
Sadly there are nay sayers and trolls hell bent on jeopardizing the opportunity given to others, why? Well maybe it’s because their own lives have been ruined by the disease modifying drugs they were encouraged to take… or maybe, just maybe that they themselves are not really sufferers of MS but a troll employed by big pharma to restrict others from healing while perpetuating the disgusting profits made by the Drug Pushers..
There are questions asked, checks made and research done prior to being asked to join our group, we dont let just anyone have access to the various sections, but when cleared and accepted then all member information is free to be seen and all current and previous members have the choice to communicate with others.
I want to clarify the joining fee and monthly membership costs… Hmmm, what was that again… Oh yes it’s Zilch, Nothing, Nada…the only requirement to join is…
Just a desire to have your life back
Some people…
Every month I’ve noticed new people joining the various MS groups that are primarily for ms sufferers that are grouped together to give moral support and very little else. Some of them seem to be living in a very negative world and have absolutely no thoughts or belief in healing. These people write negative comments to anything positive or optimistic about the future.
The group I’m in are actively following a very specific protocol that truly works, the Ann Boroch Protocol was created by Ann Boroch obviously who healed herself… yes HEALED her body of the damage caused by the various symptoms collectively called Multiple Sclerosis. The process was’nt done overnight, it isn’t a quick fix pill, it took 4 years. Those 4 years were to slowly eliminate the foods…..yes foods that had been exacerbating the problem, then to repair, to enable the body to heal itself.
I think the pharmaceutical industry have completely bamboozled the general public and the medical profession into believing that the disease is incurable..the fact is the disease is incurable, but that’s not what we are attempting to do… big pharma try to negate one of the many symptoms. Yes their drugs can ease a symptom but the cause… the real issue is ignored and just gets worse.
It’s no wonder that most people have the negative pessimistic view, I feel bad for them but as long as I’m part of this group and getting better everyday I’ll continue to write and feel privileged.
Some people have no confidence and are rife with pessimism, luckily…
I’m not some
Calm…
Following a specific program such as the Ann Boroch protocol which has healed thousands, is a very specific and detailed change of life, I know from my 29 months so far that I’m on target to be symptom free with a “healed” body in a couple of years. I cant expect or believe I’ll be healed exactly after 4 years, everyone is different, from age now, age when they were diagnosed, lifestyle, how strictly they adhere to the plan and thousands of other variables.
A phrase I use quite frequently is “In the main” meaning overall I’m very happy about what I’m doing and the progress I’m making…
However…. over the last week I’ve experienced certain “issues” I hadn’t expected which during a few minutes of confusion had been quite worrying…
I’ve said before that I have a “hummingbird bladder” water tends to want to come out minutes after it goes in, obviously that in itself has been problematic, I’ve needed to drink at least 4.5 litres a day, so visits to the loo have been frequent, 25 times wasn’t unusual although it’s now down to 15…woohoo!! (Sarcasm).. I think it was last Monday that I needed a #2 first thing instead of my usual daily visit at 10.30… afterwards I felt ridiculously weak throughout my whole body.. That’s happened everyday since then..
Confusion and frustration had
been dominating my thoughts until Friday…Yesterday.. Now my thinking has taken a completely different tack, one that is actually pleasing me, I might be wrong but I dont think I am.
This disease is a hideous, devious, selfish, dont give a crap about anyone else but me thing and I believe it knows it’s on the losing team, it knows because I’m following the butt kicking ABP that its soon to be evicted from my body, so its kicking and screaming with a vengeance and desperately clinging on to whatever it can get its grubby claws into.
As I’ve said, I might be wrong, but I don’t think I am, I believe I’m on the verge of a major breakthrough, not complete healing of course but a big step in the right direction, I actually think this is the…
Calm before the storm
Needs…
As we progress along into this very detailed program that was designed, not to cure anything, but specifically to “heal he body”, it is very easy to make the mistake of choosing to substitute a food that is compliant for a food that tastes nice but is not compliant, Why? More often than not, its simply because of an overriding desire by our taste buds…I know during my first 6 months there were many times that the normal human side of me craved certain tastes or textures which led me to chew on a food that satisfies that overwhelming desire but created a problem…
I think it was probably a year or so that it became easier for me to stick to the required commitment, it was roughly at that time that there were far more good days than bad and a lot more choices even though they were not as tasty.
A major influence in doing it right was the fact that when I made the right choices they were more often rewarded by more good days which in all honesty inspired me no end.. Ann Boroch very clearly stated that during the first few months that good day(s) would be followed by bad, there would be no surprises, just fact, do it right and positive results would follow.
As I’ve progressed on and now into my 29th month I’m rarely surprised, I have minimized the distractions because now it’s not a case of “I think”… now its “I know”… that being the case it’s a rare mistake for me to succumb to the “I want, I want” taste buds and comply with the “Do it right” nag in my head…
I know it’s hard, I know desires try and try to negate all the successes and improvements, but I’m order to succeed, to restore health, to heal the body you Have to Believe.. you Have to differentiate between,
not what your body Wants but..
What the body NEEDS
This path leads to…
We all have a variety of anniversaries that are celebrated, birthdays, marriages etc are ones we tend to receive cards for and are celebrated, today however is a very different anniversary in my life, but not one I’ll receive something bought from Hallmark or one I want to celebrate.
So what is it? Today is the 16th anniversary of when I was originally diagnosed with multiple sclerosis, I’d been living just outside Denver, Colorado in the USA, it was a devastating shock, even more so than it would be normally as it was only two years after I’d made the life changing move from England to marry.
However, on reflection this could be an anniversary of me ignoring the advice of the doctors or the anniversary of me standing firm against the rushing waters or me deciding and proving how to win against the odds.
There is also the difference that I talked about yesterday, falling in love and how this deep seated emotion is relieving stress and filling my heart with joy and happiness and giving me so much optimism for a life of love, which as I previously said, I thought would never happen again, now I know it is and it is making it so much easier to walk the path less travelled.
The path I’ve chosen to follow isnt the smooth, paved and easy path, instead I chose the incredibly challenging one, full of awkward obstacles, the one 99% of people wouldn’t take. But it’s the one with the greatest rewards, the one that gives me a prize far greater than the Euromillions jackpot… this path leads to the best reward ever…
This path leads to Life.
Whatever…
29 months in to this truly life changing protocol and I’m reasonably confident of my dietary understanding, I occasionally make mistakes, but hey… I’m only human not the superman a part of my male ego thinks. Over the last year I’ve found foods that are not just nutritious and compliant, but tasty as well, so I’m happy with my progression… mainly..
Occasionally, as happens to us all, I experience “issues” that appear to have no rhymn or reason and although I’m not taking a step backwards, I feel like I’m standing still and a little confused.
As I’ve said before, the human body is an extremely complex thing, the 37 trillion cells all with an aim and memory are easily contaminated but are not easy to repair especially when influenced by foods, water and many other things including emotions, which in reality can have a far greater impact on healing than the majority of people think. In my particular case, my emotions have been extremely mixed, I have to remember I left America where I’d lived in the beautiful state of Colorado for 11 years then moved again only a year after starting on the protocol. My wife back in 07 had been unfaithful then divorced me only 5 years after I’d moved from England, so there was a lot of negative emotions crammed into my brain.
But I’ve been very lucky of late in that I firstly accepted that what had happened in the past, was just that… the past, not now and it wasnt all my fault, yes obviously I was equally responsible for all that had happened, but there’s absolutely no point, no benefit in holding on to any negative emotions, so I forgave myself..
I can honestly say that there has been another change, this time for the better in my life, yes I’ve publicly stated how another feeling, a very special emotion has now taken over my life…. I fell in love, not just a crush or really liking someone, no this is completely different, this is unconditional love and I know Gaby has the same feelings for me.
So when I started on the ABP in September 2017 my goal was to heal myself and to live again. Now however not only have I accepted my situation and forgiven myself but I also have the benefit of knowing I’m not just doing this for myself, now the beauty of succeeding is so much more, so now other people’s views and opinions are theirs and they are entitled to them, but acceptance and love are mine and knowing that means in order to heal, I’m happy and will do….
Whatever it takes
I can and…
Firstly I must apologise for my misunderstanding yesterday, I made a comment about something I should have understood, but obviously I didnt..
**********
Now… on to the main influence in our lives, that hideous disease that is sapping the life from millions of sufferers… multiple sclerosis.
Addressing it head on is far and away the best course of action, but sadly, very sadly the healthcare industry has morphed over the years into a Sickcare industry that manages symptoms instead of actually doing what they’re supposed to do, as in heal people. This travesty has come about simply because companies in the pharmaceutical industry have stumbled upon ways of making exorbitant profits by keeping people uninformed.
Think about it, do you know of any drug, masquerading as medicine that actually cures an illness or disease…. I can tell you now, there isnt, in fact it goes a whole lot further and gets much, much worse… Drugs treat symptoms and have dreadful side effects which perpetuate the problem……in fact they often add to it by convincing you there’s no hope. Go to the website of any over the counter or prescription drug and you’ll see a long list of all the possible side effects, these are real problems that happened to the initial testers..
I know the longer I think about these things the angrier I get, so I’ll move on…
I want you now to think about the books you’ve read or movies you’ve seen, in the main there’s a central character who has either been persecuted, dumped, tortured or subject to wrongful action. We feel for them and want them to get out of trouble or win their loved one back or kick the butt of the person or people that put them through terrible pain. We want them to win, to overcome and to succeed against all odds.
Well…. in order for me, for you, for everyone to succeed at the Ann Boroch Protocol we have to be like Ann, be like Janet, they aren’t stronger, it wasnt easier, they weren’t just lucky… but they were 100% focussed and committed and guess what…. that’s how I am…….Beating MS and being healthy is my goal, you have to believe, you have to have complete faith… I know…
I Can and I Will..
My reason…
When a doctor or neurologist issues that dreadful statement that you unfortunately have multiple sclerosis, he or she will be told that the disease is incurable, well in the neurologists view they are telling the truth and will attempt to make the inevitable downward spiral as easy to cope with as possible. They will also say that the current drugs available will ease your pain and make it less of a shock to your system, but the trillion dollar industry making billions and billions in profit simply dont have an answer. In reality the have never….. never actually looked for an answer because my friends that is just not a financially viable option….
So they go to great lengths financially to lobby, to persuade, to advertise and promote drugs that do no more than confuse the brain and mask the many symptoms that combined are called multiple sclerosis.
The results for 99% of the worlds MS sufferers is that muscles get weaker and waste away, the immune system becomes nigh on useless allowing other toxins and pathogens to take a greater hold leading to other disease, blindness, brittle bones and numerous other serious problems.
Not a nice prognosis and definitely very frightening…
However!!!!
There are some of us, thousands actually that see things very, very differently because we have ignored the nay sayers (doctors) and have done or doing the Ann Boroch Protocol which does’nt treat symptoms, it does’nt mask the problem, it addresses the CAUSE..head on…
It takes time, but in reality healing the body, the place you will live for life is by far a better option.
Option one: Take drugs, get weaker by the day, lose control of your body, be in pain, oh yes… And die early..
Option two: Start the Ann Boroch Protocol, have a difficult first three months but slowly improve and be pharmaceutical drug free, oh yes, be symptom free in four or five years..
I’m 2 years and 4 months in and massively better than I would have been, why is that, simple…. I chose option two because…
Living is my reason
Mind…
After two years and four months on the protocol I think I’ve become reasonably well versed in the foods I should and shouldn’t eat because of the positive and negative effects they have on the body. A confusing aspect of them is that the bad effects are almost instant but the good can take a while to materialise. In some ways that can be very informative and helpful, in others, as in the good parts we have to be more open minded and objective. In my early months I was almost desperately searching for pleasing, nice tasting alternatives to what had been daily snacks, sadly, most of them although tasting very acceptable, actually created problems sometimes within minutes, so they were never to pass my lips again. Sticking to the protocol however might well have been boring from a tastebud aspect but had great results.
As I was saying, I believe I’m probably halfway to healing and my diet consists of the same foods on a weekly basis with a few alternatives, but I’m not bored with it at all, I actually have some fairly basic but tasty dishes…
I have lamb mince seasoned with Mrs Dash chipotle and bone broth with steamed veggies at least twice weekly, the same applies to chicken chunks with none dairy cheese and white sauce using almond milk or coconut milk.
I’ve found seaweed thins to be tasty and beneficial.
I’m just getting over a “bug” that’s been made worse by a bout of D.O. which I’m nearly over, but all in all I’m feeling great, definitely a damn site better than I would have been if I hadn’t started on the ABP.
Yes the protocol is strict, yes the foods we can and cant eat are restrictive but the biggest yes is that the long term effects are so good, your choices are to eat lots of things that taste good but make your life a misery, or accept the food limitations and get your life back… it might seem difficult but it’s not, it’s just a …
state of mind
Storm…
About a year or so ago, I had flu like symptoms which as I’m sure you can appreciate can be even harder to cope with if, like me you have a serious disease, hence a majorly compromised immune system. I stand by my actions of refusing conventional western medicine , a.k.a. drugs that treat symptoms and do more long term harm than good. Several days ago, the bug hit me again and has been causing terrible problems, but the stubborn “I will not be beaten, regardless of what you hit me with” me, has remained strong. It’s been really hard, I’ve hardly slept, I’ve been completely exhausted and in a greater level of pain and discomfort than usual. Thankfully I’m reasonably confident I’ve broken it’s back and am feeling so much better, thankfully. Sunday afternoon was a “pig”…. about 4.30 I had a serious bout of spasms that resulted in me sliding off my bed, it probably looked like a “Mr Bean” comedy scene as I had my head wedged between the bedside table (nightstand) and my bed. My legs were twisted in a weird position and my naked ass pointing at the ceiling, but trust me there was nothing humorous about the pain I was in or the frustration of simply not having the strength to move.
After about 30 minutes of totally exhausting my head, untwisted my legs and moved into a better position, fortunately that was when my carer Kay arrived, I reassured her that it looked worse than it was so absolutely no need to call an ambulance.. another carer Sara was on hand and with a little assistance I was able to get back in bed.
It’s now about 20 hours later although I’m not back to my normal self but I am definitely a lot better, as you can see from being able to write about it.
For anyone on the life changing, life saving system I’m doing, The Ann Boroch Protocol, staying away from drugs that are simply treating symptoms is so important. We have a disease “dis-ease” that is trying every trick in the book to make you believe that nothing will help, nothing will restore your health..
But… we know that’s not true… we know the ABP will do it… in order for that to happen… You my friend have to help it to help you..
Believe in the Ann Boroch Protocol, believe in yourself!!!
I constantly remind myself that I’m strong enough to win this war, I constantly watch positive YouTube videos and affirm, then re-affirm my commitment.
In this scenario, multiple sclerosis is the devil
One of my favourite T shirts confirms this..
