What makes you…
In 2004 I had been living in Colorado for two years, I’d moved there after I’d fallen in love with a woman I believed was going to be my “life” partner, we’d got married and everything appeared on the face of it to be good. We both had great jobs, she a Graphic Designer and me heading a newly formed Fire Systems Group with ADT.. We were making great money, had a beautiful big house, great cars and as far as I was concerned we were living the dream.
After one or two difficult times at my thrice weekly visits to the gym, I went to my local doctor only to be sent to hospital for tests, I still had no idea of the urgency the doctor showed but after three days of testing the neurologist gave me the horrible news that I had what he perceived to be an incurable disease, multiple sclerosis.
The reactions from him after I refused medication really shocked me as I’ve written numerous times before…. okay, leap forward 15 years and in my view, my actions have been completely justified… still no drugs, not in a wheelchair and definitely in a better stae of mind than I was back then.
The past 17 and a half months sticking strictly to the ABP haven’t been easy, well I should clarify that, the first seven or eight months weren’t easy but it has since then. The first three were bloody hard as the bad days outnumbered the good but after that that ratio was reversed and now having a bad day is very rare… there are occasional difficult hours, but that’s it.
In my opinion the Ann Boroch Protocol is the main reason for my improvements, they have been helped, no doubt by having a positive attitude and truly believing…
January saw me starting the mega dosing with Lipospheric Vit C and that is accentuating the positive improvements coming from my life regimen… the ABP…
Knowing what I know now is very different to what I hoped in September 2017.. then the thought of slight improvements were just a dream, now the many small improvements are my everyday life, now I know without a shadow of doubt that living a healthy disease free life is going to be a reality… still a couple of years away, but when looking at the big picture, that’s nothing…
Having the right attitude, believing, following the protocol will, in time restore your health, can everyone do it? Probably not, can you do it?….yes!!! And that my friend is what makes you….
Special.
Keep asking…..
I think in life we all face problems, and when they appear to be insurmountable then most people will just accept it… what’s the point in beating yourself up when there’s simply no answer, no alternative solution on the face of it. Those problems are not your average everyday issues because those are dealt with, they are problems but we spend a little time and find an acceptable answer, they may have taken an hour or two or even a couple of days but when left to our infinitely more powerful subconscious mind the answer just appears out of the blue.
In my humble opinion, and I know enough to know I don’t know everything, I think about the issue, it might be a physical, financial, emotional or health problem, I ask questions of myself… how can I fix this or that?..how is it possible to correct something that’s wrong, my thoughts, my health… whatever… then I just leave it to it…. “It” being my subconscious mind that will continue to search for an answer while I’m reading a book, watching tv, meditating or sleeping.
In my opinion nothing is insurmountable, the solution is there, I’m just not aware of it now… there’s never a case of “I’ve tried everything”… it’s only a case of “I just don’t know… yet”… As I said, in my opinion, important issues are just that…. too important to just accept defeat and lay down, giving in is not an option……
People… friends…. family… doctors… scientists, don’t know everything…. never give up….
Keep asking questions…
I will find….
When I was diagnosed with MS, I had been living in Colorado in the U.S. for almost two years, I’d gone there to marry a woman I’d only known a short time… weeks actually, but believed it was the right thing to do. So I was around 5,000 miles away from my family and close friends in England when I was given the devastating news, the neurologist told me in a straight forward, no punches pulled way that my life was about to change forever, I would be on side effect laden drugs forever and my forever wasn’t going to be that long… when I categorically refused to take the drugs, he said he was offended that I was ignoring his advice and called me an idiot….
Well fifteen years later, I must tried about a hundred different therapies, pills, supplements and operations, in reality, some have done diddly when it comes to easing the symptoms, on saying that, I’m happy about everything I’ve done.
I don’t and never have taken any medication for multiple sclerosis, I don’t take drugs at all apart from Betmiga that helps my bladder control and Levothyroxin for my underactive thyroid.
Personally I am proud of myself for not simply giving up, I’ve said this a thousand times and I’m sure I’ll say it a thousand more… Drugs treat symptoms….. the majority have so many side effects, some even as bad or worse than the original problem……
I honestly believe that given the right nutrition the body will heal itself… I’ve studied a great deal about this, I’ve worked closely with an amazing man, Dr Hal Huggins, I’ve met equally incredible people such as Dr Thomas E Levy who not only is an oncologist but a lawyer as well. I’ve read numerous books by leaders in the world of natural healing, that’s true healing, not the pharmaceutical drugs way that temporarily helps.
All these things have helped me be stronger and be determined to succeed, but the overriding strength that will see me to be disease free is that I’m my mum’s son and whatever problem or disease befall me… whatever it is, I will never give up, I will fight to the end, and trust me……
I will find a way..
When so little…
I think for most of us that have what the medical fraternity of the world consider to be an incurable disease, multiple sclerosis is a depressing and daunting thing to live with. Doctors of all shapes and sizes will do what they can to mentally prepare you and in all honesty try to do their best…. it’s not as if they’re evil people and are getting pleasure out of seeing you’re life ebb away, no not at all, they have what they think are you’re best interests at heart…. Sadly, very sadly, they and the majority of people are mistaken, this disease isn’t incurable, it just needs to be addressed in a different way and when they and more importantly.. you…. understand that and truly believe it…. you can and will make an impact on the debilitating symptoms…
In September 2017 after I’d read a book detailing how a young woman had been on a four year quest, not just a diet but a complete lifestyle change that transformed her from a confused and frustrated young woman in pain and with what “they” said was “no hope” of truly living again, into a healthy happy, disease free woman. My life changed after reading that book and being given help and guidance by another beautiful person…. Janet Orchard because I started on what is proving to be an incredible Journey.
In today’s world, where having a pain just means that we should “take a pill”…. a world where we are constantly being brainwashed by advertising about having a health issues is normal, putting on weight, having bad skin, spots, greasy hair or whatever is to be expected and the answer is to simply to ignore the cause, just take, this.. or that to make it go away… all well and good if you believe it’s okay to keep paying to correct what shouldn’t be happening.
Putting life as we know it into perspective, in my opinion isn’t a difficult thing to do, I’ve accepted I can’t participate in the active life I had, I’ve accepted that so many things that are considered normal, just don’t happen anymore. I’ve accepted that pain, frustration, awkward limited mobility are my everyday’s….
When I say I’ve accepted them, I mean I understand that they are happening now, but since embarking on the Ann Boroch Protocol I’m in a transitional state….. all those things are still part of my life, but they aren’t as bad. It’s an incredible feeling really to know it’s happening little by little, the changes are small and subtle and it will take years, there’s no “instant gratification” that’s become normal.
Things in my life are very different, now it’s a case of true acceptance…. when so little means so much…
Not too much….
Some people are not specifically interested in the “why’s and how’s”… they just want to know that “it does”… that seems to be the case for most people, I know when I first started working for Dr Hal Huggins back in 07 in Colorado Springs, I was so “blown away” by his incredible work and results that I wanted to be a sponge and soak up as much information as possible. Having gained so much of what appeared to be extremely useful knowledge, I wanted to share what I knew with as many people that would benefit from it as possible, which resulted in me talking with almost 18,000 people in just under four years.
I’ve been on a daily mega dose of Lipospheric Vit C since the start of the year and quite frankly….. “I’m dead chuffed” by the results I’m having, so much so that I honestly believe it’s really boosting the already positive effect of the Ann Boroch Protocol which is changing my life. I’m sure the Lipospheric Vit C would be making a difference on its own, it isn’t reliant upon anything else, it just positively changes things. However….could it heal an MS sufferer on its own?… I doubt it…
The ABP is the life changer when it comes to multiple sclerosis but in all honesty Lipospheric Vit C is helping and to a certain extent, boosting things along.
How?… I could go into very detailed specifics but I know that’s not what most people want to hear, so I will give some detail but hopefully not too much.
All Vit c is water soluble so taking it orally means roughly only 20% will be actually absorbed, whereas taking it intravenously means it’s moved directly by the blood through the body getting it to the various organs. That’s got to be best… right!!! Years ago that would have been right, but not now, because now there’s Lipospheric Vit C. Now the vitamin is encapsulated in liposomes… nano sized phospolipids which is the same thing human cells are made of this means the vitamin c becomes an integral part of your own human cells and being utilised immediately.
The difference is almost 10 times greater and more effective than IV C….
I really hope more of you take advantage and the information wasn’t too much…
As good and better….
Back in December last year when I decided that I’d start the one month experiment of taking much larger doses of Lipospheric Vit C than is usually taken on a daily basis, that being 1 gram and I would take 7 grams, I was basing this view on the many conversations I’d had many years ago with Dr Hal Huggins and the few with Dr Thomas E Levy. I also knew from experience how beneficial it was from my years of personal use, however, I didn’t know how, what I perceived as mega dosing would happen for myself an MS sufferer of 15 years. So in January of this year I started taking one gram every 2 hours and I did it that way for a month. I was very pleased by the what appeared to be an acceleration in the wonderful effects of my 17 months of following the ABP, I felt stronger, I noticed improvements in just about everything I felt from mental awareness, physical strength and my emotional state. That being said, I then tried taking the same amount but this time as two doses, 3 ounces in the morning and four in the afternoon. A week after doing this I can confirm that this is the how I intend to proceed at least until the end of March when I can evaluate this again.
My initial thoughts back in December were that I knew it would help, of that I had no doubt, I just didn’t know specifically for my condition, I didn’t have concerns as such, I just wasn’t sure if it could be as good as I hoped.
Five weeks in and I’m more than happy about what’s happening to my mind and body.
Now I have to make this clear….. I am not a doctor or qualified medical practitioner nor am I making specific recommendations to anyone. But I am telling you what I am doing and the effect it’s having on me, what you do is your choice…
I personally use Lipolife Gold that comes in a 250 ml bottle which I buy on Amazon…
5ml has the same effect as 1 gram of individual packets.
I take 15 ml in the morning on an empty stomach then another 20ml in the afternoon. I’ve personally tried before and after foods and not experienced any difference, but that’s me…
I suggest doing your own research, look at their website and you’ll understand why I chose to use them.
As far as I’m concerned, taking such large doses is having as good and better effect than I hoped.
As good, and better….
Back in December last year when I decided that I’d start the one month experiment of taking much larger doses of Lipospheric Vit C than is usually taken on a daily basis, that being 1 gram and I would take 7 grams, I was basing this view on the many conversations I’d had many years ago with Dr Hal Huggins and the few with Dr Thomas E Levy. I also knew from experience how beneficial it was from my years of personal use, however, I didn’t know how, what I perceived as mega dosing would happen for myself an MS sufferer of 15 years. So in January of this year I started taking one gram every 2 hours and I did it that way for a month. I was very pleased by the what appeared to be an acceleration in the wonderful effects of my 17 months of following the ABP, I felt stronger, I noticed improvements in just about everything I felt from mental awareness, physical strength and my emotional state. That being said, I then tried taking the same amount but this time as two doses, 3 ounces in the morning and four in the afternoon. A week after doing this I can confirm that this is the how I intend to proceed at least until the end of March when I can evaluate.
My initial thoughts back in December were that I knew it would help, of that I had no doubt, but how specifically for my condition I just didn’t know, I didn’t have concerns and I just wasn’t sure if it could be as good as I hoped.
Five weeks in and I’m more than happy about what’s happening to my mind and body.
Now I have to make this clear….. I am not a doctor or qualified medical practitioner nor am I making specific recommendations to anyone. But I am telling you what I am doing and the effects it’s having on me, what you do is your choice…
I personally use Lipolife Gold that comes in a 250ml bottle which I buy on Amazon…
5ml has the same effect as 1 gram of individual packets.
I take 15 ml in the morning on an empty stomach then another 20ml in the afternoon. I’ve personally tried before and after foods and not experienced any difference, but that’s me…
I suggest doing your own research, look at their website and you’ll understand why I chose to use them.
As far as I’m concerned, taking such large doses is having as good and better effect than I hoped.
Obviously not…
During the 63 years I’ve been alive I think lead an interesting and varied life, the early years in Liverpool were hard as I’m sure you can imagine, 9 of us living in a two up two down house with no bathroom just an outside loo with a chain pull cistern, no toilet seat and had to use torn up newspaper. As number three in the clan of seven kids it was no harder or easier for me, a difficult black and white life with very little in the way of home comforts taught me a great deal, I learned how to cook and look after myself and so many life skills not needed by the kids of today.
The Army as a boy soldier also put me on a four year learning curve that helped me so much in my adult life, I can’t say it was brilliant but I think I did reasonably well in computer sales and management leading up to a $500,000 house in the USA then becoming the client service director for Dr Hal Huggins who was the world leading authority in biological dentistry and body chemistry rebalancing.
Not bad for a Liverpool lad that had nothing but plenty of love and guidance from my amazing mum who I love and talk with at least twice each week. During my time with Dr Huggins, I am confident in saying that I helped many of the thousands I talked with. It’s in my nature to help others and I think I’ve done that since my return 6 years ago.
What I don’t understand is that my son hasn’t seen me or even called me in 7 years, my daughter came to see me a couple of months after I came back but since then she got married and has had 2 kids, none of those things she told me about, that information came via others who heard about it on social media.
It’s very sad and I try not to think about but inevitably do and have a cry, not a tough cookie after all…. whatever!!!, I’d like to think I’m a good man and I’m sure there are many others that think that way, I’d hoped my daughter Lucy and son Joshua thought the same…. Obviously not..
Bad day…
In the last few posts I’ve written that I haven’t actually had a bad day in more than six months, at the time I wrote them it was true, but that statement doesn’t apply now because it’s now 4.45 am Monday and I started having a bad day when I woke on Sunday morning. The difference in having the previous bad days either when I first started the protocol or two and three years ago is that they lasted longer and were much harder to deal with.
My throat is sore, I’ve been coughing every few minutes and on Sunday I was so weak I couldn’t stand or move with the help of the wall or furniture. The difference in my mind was that I knew, I absolutely knew I’d be okay in only a day. Three years ago when the same problem happened I was stuck in bed for five days… five freaking days…and even then I was terribly weak, as I said, it’s still the butt crack of dawn and I know I’m feeling better. Yesterday I couldn’t even type a few letters to play Words With Friends…. that’s not a problem now obviously as I’ve just typed half a paragraph.
It’s now just after 6 a.m. and after I wrote the first part of this I meditated for an hour, and just to confirm what I thought, I am feeling much better. Two main reasons, obviously having the mega dose of Lipospheric Vit C has improved what I believe is the most significant reason, my body is so much more capable of dealing with physical problems because it’s healthier, so many of the debilitating toxins have been expelled and the delicate, intricate organs are able to do what they were designed to do. That’s happened because I’ve been following the ABP, now understand this, no one has or will say that that the protocol cures anything because that doesn’t happen, but what is happening is that by removing all those bad guys that had taken up residence, by getting rid of them we are enabling our body to heal itself. There are multiple organs, pints of blood, thousands of miles of nerves and trillions of cells. No one can expect to completely understand exactly how to fix what is wrong. But what each of us can do is give them what they need to do what’s natural, optimal word….. natural, not synthetic…. get rid of the synthetic, chemical additives, the pharmaceutical drugs that have more negative side effects than long term positives.
Anyway back to my point, there was a problem, it might have been a virus going around, a bug, the flu… whatever it was, my delicate MS riddled body struggled… but because of the Lipospheric Vit C and primarily the ABP, I had a bad day, not 5 or 6..
Because what you….
Disease with any name or classification especially the ones that are supposedly incurable and ruin your life are terrible things to live with, actually that’s the wrong word to use, it’s not living, it’s existing because the disease takes away all semblance of life…
Since starting the Ann Boroch Protocol in September 2017 I’ve experienced significant improvements, I’m not healed yet of course, I’m only 17 months into it, but I’m absolutely certain that by persisting in it I will regain my life.
In the early stages I was having as many bad days as good but the bias gradually changed, after 10 months or so, bad days became a rarity so much so that I’ve not actually had a “bad day” in at least 6 months.
The changes, the improvements don’t just happen, they are earned by following the protocol correctly. I’ve had the odd difficult time but in reality they’ve been limited to an hour or two and they were brought on by my mistake or error in judgment by succumbing to taste bud desires. But in the main I’ve been good, 99% of the time I eat the right foods even though it might appear to be a boring diet. I meticulously take my supplements, no forgetting, no I’ll just not bother today. There are many days that I feel tired but I still try to do something in the way of exercise, I just use my common sense and not do as much, but I don’t cheat, doing the exercise properly a couple of times is significantly better than doing it wrong lots of times.
In my opinion, the ABP is as much mental as it is physical and dietary, training your mind as much as replacing toxins with healthy, good nutrition is essential.
I’m just a little more than a third of the way into what in reality is a complete lifestyle change, I’m doing this properly, no short cuts, no excuses, the right foods, the necessary supplementation, exercise, meditation and rest. Why will I win this battle, why will I heal myself, why will I live again?….. Because what you believe you make true…. and I absolutely, 100% believe……