Rather Be Healthy

It’s a well known thing that if something seems too good to be true, then it probably isn’t… true…
There are so many things in life that other people have but you don’t, that just seems… unfair, I mean why is it that this person or that person just appear to be “soooo lucky”.. they could fall over on a cow pat and get up smelling of roses but others just try lots of things but just don’t succeed, their business isn’t successful or they could never finish that book they started writing years ago.
In life you find that everyone is good at something, but you can say but I’m not interested in “needlework” or making “scrapbooks” or “getting fit”… its horses for courses…
But what if you were told that by doing that strange hobby of routine was actually very good for you, that you’d make lots of money or find your whole life would be soooo much better, the only problem was that it wouldn’t be easy, you’d have to really work hard at it, you’d have to overcome personal desires and preferences but your world would change, wouldn’t you do it?…
Yes you would obviously…
Now relate that analogy to your personal health, in my case I was one of those people that was very much an adrenaline junkie… I loved fast motorbikes and fast cars, I was fit, I skydived and rock climbed, not hobby’s liked or participated in by many people..
Then in 2004 I was diagnosed with multiple sclerosis so I went from being a fit and healthy man to the complete opposite.
As I’ve said before I’ve researched and researched trying to find a way of beating this disease in a non pharmaceutical way, not that any pharmaceutical can genuinely beat the disease.
I started on the Ann Boroch Protocol in September 2017 and have painstakingly followed the protocol.
I’ve no glaringly obvious symptoms, my legs are weak but that primarily can be attributed to being confined to my bed where I’ve been for almost a year because of a fall.
But even though that in itself is depressing and frustrating it hasn’t stopped me from sticking to compliant foods, I haven’t binged on tasty mouth watering snacks or fish n chips and mushy peas or several others yearned for by my taste buds…
Why?
Because I have set myself a goal, I’ve committed myself to being healthy again..
Is it easy…no!!!

But is it achievable….Yes!!!!

When I look back to the problems I was experiencing after I’d just moved to live and work in Colorado in the USA back in 2002, I wasn’t just shocked but really, really frightened.
It was quite an emotionally stressful time as I’d met and married a Colorado native and was working in the computer software industry, stressful in itself but then to be told I had multiple sclerosis, a disease considered to be incurable definitely made me feel sad to say the least.
My attitude in everything I’ve done in life, be it work or play is to be optimistic, some people might chose to see “the glass half empty” but I really see no point in what I consider a negative defeatist attitude.
So upon diagnosis after refusing to take the neurologists advice to take what they call medicine… hah!!! just pure and simply pharmaceutical drugs that mask a symptom. I spent hours and hours, whenever I could searching for potential ways of beating this hideous disease.
Between 2004 and 2017 I must have tried more than 50 different things, including ccsvi, full dental revision, body chemistry rebalancing, bee venom therapy, numerous dietary changes, hydrochloric acid treatment, XanGo, Aloe Vera and lots and lots of so called miracle supplements.
So when I Read “Healing Multiple Sclerosis ” by Ann Boroch in August 2017 I tried to not get too excited but I couldn’t control my enthusiasm because the ABP seemed so much more real than anything I’ve tried or read about before.
I started September 1st and experienced what everyone else does during the first three months, as in a really difficult time feeling good and horrendously bad every few days, but rather than accepting the really depressing experience as a negative and giving up, I took the advice of a woman that was successfully following the protocol and persevered.
If looked at purely from a timescale perspective it would mean I have been following the protocol for three years and five months, but I had a nasty fall in March last year which has knocked me back somewhat, I’ve been bedridden for 11 months and not been able to furniture walk or exercise as I did.
Anyway I feel very positive and optimistic about being able to focus on my genuine healing.
So the question I ask myself now is can I do it? You can bet you your last dollar on it that the answer is..
Yes I can..

Youre right…
Having multiple sclerosis is a pig, its depressing, its debilitating its frustrating and contrary to what most others think….its so humiliating… From my own point of view I was a very active man both physically and in business, I wasn’t mega successful in either but definitely more so than most.
So having in this hideous disease has significantly changed my life, not being able to physically do the most fundamental of things has limited my very desire to live… that is how I believe the majority of sufferers think. But I see things very differently, I have a very different view on life, as far as I’m concerned I’m faced with two options, option one is to accept the depressing negative opinion that MS is incurable, once you have it you can either take drugs that mask the problem, they fool your mind and body by stopping the symptoms from being recognised. That method is great short term but stronger and stronger drugs will only work for a limited time before they have no effect and the symptoms become so bad the individual goes from seeming okay to suffering really badly.
Option two… is the choice I’ve made, to be optimistic and to believe in myself, to believe in the ABP..the Ann Boroch Protocol was designed to identify and eliminate the foods that have caused this hideous disease.
Yes, I’ve had a fall that seriously damaged my knees which completely stopped me from walking, being bed bound since March last year has resulted in severe muscle atrophy in my legs.
But, as far as I’m concerned, this is just a road block which I have to get around or over or under but I will do it.
The way I see it is to either be negative to give up and accept the bad..
Or to think positive and genuinely beat it… I….you…have two options..think about it..
If you think you you will lose or if you think you will win..
Youre right..

The world is full of successful people, people that have achieved so much, I’m not referring to the billionaires or multi millionaires who have more money than sense, so often they have just been very lucky or have inherited their fortunes from successful wealthy parents.
No, I’m referring to the ones that ignored the nay sayers and believed in themselves regardless of all the so called “realists” who are really just negative pessimists.
I personally believe in something I’ve written about many times, I’ve said:
“What you believe, you make true”
If you truly believe in yourself then it doesn’t matter how long it takes it doesn’t matter that another stumbling block or pitfall or obstacle has appeared in front of you, or me in my particular situation…. we just deal with it.
As far as I’m concerned, I started on the Ann Boroch Protocol in September 2017, at that time I’d had multiple sclerosis for more than thirteen years, a disease considered by all the worlds medical experts to be incurable. During the first two and a half years I feel I was progressing really well and on target to healing my body, removing MS completely within four to five years.
A fall I had left me trapped in a very painful position with my knees bent beneath me for almost two hours, the pain I was in was excruciating and then it was another four hours before the paramedics got me off the floor.
So my progress on the Ann Boroch Protocol (ABP) was halted temporarily.
It would be so easy to emotionally give up, but thats never going to happen because I truly believe in myself and the protocol.

So since the week before Lockdown last March I’ve been in bed, not just in bed, but in the same position partially sitting up for twenty three hours everyday, my bathroom breaks happen twice daily with help from my carers.
Seeing myself walking and going outside in the fresh air certainly seems like a distant almost unachievable goal, but its not to me…. it will happen, of that I have no doubt…
I watch positive YouTube videos everyday, several times each day actually, I read positive affirmations and books by people like Louise Hay and Eckhart Tolle and many others.
There is no future in accepting the negative advice from those who would rather see us fail and smile while saying…
“See, I told you it wouldn’t work”…
I constantly tell myself that I will succeed…I brainwash myself, I have to, I will get better, I will be healthy…
Why…Because of life and I believe in me..

So easy….
Having a disease like multiple sclerosis, which I’ve had officially since February 2004, is a demoralising thing.
That diagnosis and prognosis for my future, as I’m sure you all know was a tad depressing, especially as my life previously involved fitness and sports not participated in by normal people. I’ll not harp on about my physical past and achievements again, but accept it was quite…
“Radical” I suppose..
That being said, my attitude to life is one of me wanting to succeed and definitely not one of “giving up”..
So when the neurologis at The Rose hospital in Denver told me that I had MS and that it was incurable, I naturally felt deflated to say the least.
I’d only been in Colorado in the USA for 2 yrs, I’d moved there from England after I’d met a woman who….no, I’m not going to slag off but I will say wasn’t as nice a person as initially pretended to be.
During the 11 years I lived and worked there full time I never took any medication for MS and still haven’t taken any.
What I did do is constantly look for what is wrongly described as “Alternative or Complimentary treatments” and I’ve tried more than fifty things. It is only the Ann Boroch Protocol thats made a lasting difference.. obviously I’ve still a long way to go before I can say that my body has been healed, but it is happening and the multiple symptoms which when bunched together are classed as Multiple Sclerosis are becoming less and less obvious to me and my carers.
In my humble opinion, the only way to be when contracting this disease, is to remain positive and optimistic of possible improvements, a person, you or me has to constantly tell themselves that the disease is not going to win…we have to be strong mentally and emotionally, I’m not in the Special forces, I’m not a Marine commando, but I have to have that same mindset….I’m never giving up..
Getting back to the headline of this post, be strong, tell yourself that no matter how difficult it gets, no matter the pain and frustration, your focus and determination will see you all the way to the finish line…it can be hard, it will be difficult, but the rewards are worth it… regardless of the fact that …

Giving up and failure is so easy..

Been there…

My life so far has been interesting to say the least, I don’t consider myself better than anyone else, but I am different and have a lot of experience, experience that has helped a great deal over the past 65 years and as I’ve got lots of plans for the future they will help guide me through the next thirty years or so because I plan to be around and do so much more.
I was born in Liverpool in 1955 when it was very tough for every family to survive and more so for us as my mum had 7 kids and we lived in a two bedroom house with no bathroom.
School was hard and even more so than normal as the knuckle dragging morons would beat up those that had raised their hands and answered teachers questions or didn’t participate in the monthly fights between my school, Litherland High and Warwick Bolum…
I left school at 15 yrs old to go to the Army Apprentice College in Chepstow, South Wales.
I qualified with a City and Guilds in Carpentry and Joinery, I also got my degree in Building construction and building science which qualified me as a clerk of works.
Being in the Royal Engineers I also became a Combat Engineer, so bridging, demolition and minefield clearance was another skill.
After leaving the army I ran my own little business doing small building work but I also took my HGV class 1, 2 and 3, thats Heavy goods vehicle licence, so I can drive every vehicle from cars, small vans right up to the juggernauts you see with 40 foot trailers thundering down the motorways. From a recreation point of view I also have my motorbike licence.
Because it sounded like good fun, I took a parachute course then went on to free fall, skydiving was a major part of my life and I did 834 skydives and was #2 on the 60 man formation in 1989 which was in the Guiness book of records until 1997 when it was beaten.
I’m also a SCUBA diver, hang glider and I have my PPL, private pilots licence.
I know I’ve said most of this before, don’t worry, I’m not going doolally.
I worked in the I.T. industry for 25 years and as I’ve previously mentioned I’ve driven more that 1.5 million miles for work, going to and from appointments around the country.
I lived and worked in Colorado in the USA for nearly 11 years, 10 yrs and 10 months to be precise.
I was the Client Service Director for the world leading authority in biological dentistry and body chemistry rebalancing, Dr Hal Huggins. I sat in on many, many of his consultations, I studied all his work and learned so much from him. I wanted to take my doctorate but he told me I’d learn so much more genuinely useful information from him.
I’ve been back in England since November 2012, and sadly am not able to physically work..yet
Since being a part of the special group whos intention is to heal from multiple sclerosis, I’ve also written and published two books with a third on the way so I have been busy.
I’m closely following the Ann Boroch Protocol, I truly believe that I will once again be running the streets, not as quickly as I once did, but it will happen.
Everything I do during the 20 hours I’m awake is a challenge, since my fall last March, I’ve been in bed, I am in the same sitting or slightly leaning back position for 23 plus hours everyday, the other 45 mins I’m on the commode or having a shower.
So when chatting or talking with people far less experienced in life, (not you honey) but people that ….tut and roll their eyes, please have some patience and emember that..
I’ve been there, done that and have the T shirt and video.

A future worth…

2020 will be remembered for all the wrong reasons, the world experienced a pandemic creating more deaths than most countries had ever experienced outside of the two world wars.
It was a frightening time for everyone, just reading or hearing about the thousands being diagnosed everyweek, the emergency hospitals being built then being filled by patients, some on ventilators for weeks and weeks.
From my own personal level it was terrible, a week before Lockdown in March I had a fall in my bathroom which resulted in me being in bed for the remainder of the year…
In September I experienced all coronavirus symptoms including the worst sticky glue like flegm, I was extremely weak, even more so than just having multiple sclerosis. I quickly adopted my self preservation mode and started taking masses of Lipospheric vitamin C. I went through three bottles of 250ml in 9 days, a bottle is normally a months supply.
I know the majority of people will not believe it was covid19 or that the lipospheric vit c could help so much, but trust me, I’m telling the truth, lipospheric vit C will kill all known virus, and that has been scientifically proven.
If only the governments of the world would stop believing in the pariah’s. a.k.a. Big pharma.
Here in England we all owe a massive debt of gratitude to all the amazing staff of the NHS.. they have put their own lives at risk and worked tirelessly to keep us safe…. Thank you…
The strain on the prime minister who also was struck down with that hideous virus, the pressure to keep the country afloat must have been terrible. I know some will disagree and have a completely different opinion, but thats how I see it..
As far as the negative filled year is concerned, it created problems, thats true and sadly lots of people lost their lives, there’s nothing we can do about that now other than remember them fondly and move on.
2021 has just begun, let’s learn from the past and make the necessary adjustments to our lives and safeguard our future.
My 2020 was crap in so many ways…
I spent 10 months in bed, my lockdown was limited to my bedroom, my knees were badly damaged in the fall I had which has seriously restricted all movement, my thighs are so weak so 99% of exercise and movement is so limited, on top of that I’m not over it….yet..
On top of those issues I’ve had to drink about a gallon of water everyday or I have serious problems. Drinking so much creates other problems in that every 45 minutes I’m given roughly a one minute warning that I Will pee regardless of where I am or what I’m doing.
Nothing any doctor or…. has helped me combat this issue, until something I’d read last week then bought another supplement has made a difference.
It seems that for ten plus years, Ten years!!!! I’ve had a urinary tract infection. I say had, because I think its been addressed…. Yay!!!!
But…!!!!
I’m still 100% on the Ann Boroch Protocol and I am confident that my 100% healing will happen its just been delayed, it might appear to other people be a pipedream, a fantasy but I’m not other people, I’m me and I intend to live and have a future worth living…

As Ellie Goulding said……

Thinking back to February 2004 when I was originally diagnosed with multiple sclerosis and the thoughts whizzing through my head, I was understandably perplexed and confused and frustrated.
Only two years earlier I had moved to Denver, Colorado from England because I’d met a woman who I thought was an honourable and truthful person, we got on really well, I don’t think either of us were in love, but we both thought we would be good for each other.
I know, I know !! it was the wrong reason to get married … but we did…
After four years there and working in the I.T industry, I’d read about an incredible man called Dr Hal Huggins who was the world leading authority in biological dentistry and body chemistry rebalancing and was looking for a director to work in his organisation. He had been treating patients with MS as he’d found a connection between Mercury, used in amalgam fillings and MS. Over many, many years, lots of research and experiments he had a success rate of 86% in removing the disease.
So after a couple of 3 hour intensive interviews I was offered the position of Client Service Director.
I worked for him for four years and learnt a great deal that helped me cope with my own disease, sadly I was in the 14% of unsuccessful patients.
Anyway during my time there, my not so honorable and truthful wife was having at least one affair so we divorced in May 2008.
Getting on to the point of this post, eventually…..
Between 2004 and 2017 I must have tried at least 50 treatments, therapies, operations including a full dental revision, body chemistry rebalancing, CCSVI, Bee sting therapy and so many supplements that were touted as game changers for MS, but the best any did was to provide a temporary relief from the many symptoms of this hideous disease.
So when I read “Healing Multiple Sclerosis ” by Ann Boroch and her success, I was a little sceptical to say the least, but I decided I’d give it a try and commented about it on Facebook. That’s when I heard from Janet Orchard who explained about her personal journey and amazing success on the protocol so I had no hesitation in making a commitment to doing it.
There’s no doubt that the first two months were damn hard but three years and four months later I can honestly say its the best decision I ever made.
The fall I had back in March definitely slowed my progression down, but I’m still on track and I am 100% certain that I will be healed, yes it will take more than four years, but, no big deal…. I will be one of the thousands that beat this so called incurable disease.
If you’re on the protocol, be strong, determined, focused and believe… if you’re thinking about starting…. as Ellie Goulding said…
“What are you waiting for”….

Everything in the body is made of Proteins…dont misunderstand that, I said Proteins not protein..there are various classifications of foods we all know about, protein, carbohydrates and lipids (fats) but being healthy is not simply a case of just eating protein. Yes there are fewer calories in protein than carbs or lipids, but they also provide much needed nutrition for the body.
I said everything, meaning the organs glands, bones, muscle and connective tissue such as ligaments etc which are constructed by the body when possible from the necessary proteins. I said that the proteins required aren’t simply portions of the protein rich foods we’ve eaten, or not..these proteins are very specific and as everything else is, are made internally from amino acids..
I’m trying my best here to describe an extremely complex function in an easily understandable way, so please just bear with me.
There are 22 amino acids but only 14 can be provided by the foods eaten, the other 8 are extremely special and identified as Essential…. they are differentiated when written by having an L before its specific name. It won’t help by naming them, just know that an amino acid with an L.before it is essential

Anyway, if we could provide the essential amino acids, surely the body would have what it needed to rebuild and repair any particular component in needs. Sadly the answer to that question is no, not exactly because those 8 essential amino acids or EAA’s, need to be in specific proportion to each other.
Let me try to explain in another way….
What have matchsticks, chairs, tables, log cabins and some ocean going yachts have in common? Yes they are all made out of wood, but you wouldn’t try to make a log cabin out of matchsticks would you… although they are all made from wood, its different quality and quantity. The same basic rule applies to EAA’s and what they form as Proteins on route to the reqired need of the body.

This post is basically in regard to the accident I had at the beginning of March. I had been doing really well on the Ann Boroch Protocol and feeling great in my quest to heal my body of multiple sclerosis. To a certain extent I was getting a bit over confident and did more physically than I should have.. consequently the following fall has put my progress back by 9 months. But I honestly believe what I’m now doing is changing that.
I came across some very detailed information regarding not just amino acids or branched chain amino acids (BCAA’s) or EAA’s but Perfect Amino Acids..
Perfect because a 70 year old doctor who compete’s in Iron-man triathlons created them and have a 99% amino acid utilisation, that is quite amazing knowing that eggs have only 47% and that’s more than any other foodstuff.
So my thoughts are that taking them will naturally rebuild my damaged cartilage and help the thigh muscle in both legs.

The posts I write are for two main reasons, I want to document what I’m doing with the ABP and the progress I’m making and to hopefully motivate and inspire others on this journey.
So have my 3 years and 4 months on the protocol healed me of multiple sclerosis …
No not yet, but I’m very optimistic…

Now the following post is my opinion, but its an educated opinion of a scientifically proven fact….
That fact is that lipospheric vit C will kill all known virus…. I’ll say that again…all known virus including corona virus, Covid 19…

On Sunday last week I noticed a slight problem, more of an irritating problem than something to worry about, a bit of a cough and runny nose which I thought was no more than the basis of a cold so I upped my daily dose of “Lipolife”, the liposomal vit c from 1 x 5ml to 4 x 5ml…
On Monday morning I was feeling a little worse and I now had a strange chesty cough and I felt much weaker, the chesty cough was generating horrible flegm that was really hampering my breathing. definitely prompted me to double the dose over the next 24 hours.
I didnt panic but my thoughts started to wonder if I could have somehow caught that freaking corona virus, the only people I come into contact with are my carers, did I mention that I have multiple sclerosis? Well I have had it for almost seventeen years but have never taken any pharmaceutical medication for it, but thats another story.

Thinking about covid 19 thats killed hundreds of thousands of people in the past 8 or 9 months and my particular situation, I am a prime candidate…male over 65 yr old, and overweight.

I wasn’t scared or overly worried because I absolutely believe the information provided by Dr Thomas E Levy M.D J.D who helped develop the liposomal vit c..
A liposome is a nano sized particle almost exactly like a human cell, hundreds of thousands of them completely encapsulate the vitamin. So it passes safely through saliva, the esophagus, the stomach, the intestines until it is broken down in the small intestine and absorbed by the body.
Liposomal vit c is 8.25 times more effective than orally taken or intravenous vit c.

So between Monday 2nd November and Sunday 8th I’ve taken more than 100 x 5ml doses of liposomal vit C..
I personally use “Lipolife Gold” which is made in the UK and does not have any connections with China.

Going back to Thursday and Friday evening which was the worst time for me, my head was terribly stuffy, nose running, the back of my neck was aching like hell. The chesty cough was unlike anything I’ve ever felt before, my whole body spasmed, it felt like the cough was echoing inside of a cavernous chamber inside me. I was terribly weak, much more so than the problems created through MS, the worst part was the flegm that for no apparent reason, no warning it would suddenly block my airways which resulted in ten or fifteen seconds of no breathing, just a completely blocked throat, I can honestly say that during that short time which felt like eternity, I honestly felt I was over, done, bye bye life..
Anyway I did the NHS test on Saturday and the results show that I didn’t have corona virus at the time of testing, the wording in the results didn’t say that I “don’t” have coronavirus….it says I “didn’t” have it when the test was done. Again I’m stating the the lipospheric vitamin c kills all known virus and I took copious amounts after my symptoms started.
I’m 95% back to normal, obviously my normal isn’t the same as normal for an able bodied person.
Having multiple sclerosis means I have a severely compromised immune system, but I’m good, I’m not concerned, or suffering anymore.
I just wish that the governments of the world would wake up and start administering lipospheric vit C instead of wasting time, money and most importantly human life looking for a vaccine.

I honestly believe that I had coronavirus and as the results clearly state, I didn’t have it at the time of testing which was 5 days after I started taking megadoses of lipospheric vit C..

So going back to the title of this post…

“What does it take?….

Three bottles of Lipospheric vitamin C…