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..
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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