In February of 2004 I’d been living just outside Denver in the Rocky mountains for two years after moving there from England.
I had a great job in the computer software industry, I loved my work dealing with companies on the East Coast, my main customers were New York City Parks and Recreation and NYC Transport, I also dealt with similar departments in Boston and Pennsylvania, they were two hours ahead in Eastern standard time so I had to be in my office by 6.a.m. to deal with them at 8.a.m. their time, but I loved what I did.
A month after being diagnosed with MS I was to attend a trade show for NYC Parks and Recreation in Queen’s..NY.
At that time my symptoms weren’t obvious to anyone but me, a little weaker and slightly unstable but as I said not obvious to onlookers.
Sadly over the next year I became more aware of my limitations so started searching for a less stressful job.
I read about an amazing man called Dr Hal Huggins who was the world leading authority in biological dentistry and body chemistry rebalancing. His work with MS patients and mercury amalgam fillings and had made a significant improvement in their health which lead me to meeting Dr Huggins, being interviewed then accepting the offer of work as his client service director.
That was in 2007 and over the next 4 yrs was able to learn so much and to help literally thousands of people which made me a very proud and happy man.
By the end of 2011 my symptoms, primarily weakness and instability became too obvious which made me a liability to the company because of the work we did.
I left the company, mutual agreement, sort of, and found desk jobs elsewhere until it just wasn’t physically possible to work anymore.
I returned to England to be near family and hopefully get some sort of disability benefits as I’d none in the States and used all my savings.
Four yrs later I came across the Ann Boroch Protocol and started meticulously following the protocol in September 2017.
As far as I’m personally concerned, the only really obvious symptoms to me is stress which affects me more than at anytime in my previously physical and working life, in that it exacerbates my leg weakness, my weak bladder, co-ordination and grip strength.
But the fact I had a fall that seriously damaged my knees which has resulted in being bedridden since last March has definitely restricted my progress.
I was walking with the aid of handrails and furniture. Because of the pandemic I’ve not been able to have any physio or surgery so I’m sure you can imagine the muscle atrophy in my thighs.
But as far as I’m concerned this is just a blip, a speedbump on the road to recovery.
It’s literally 3 yrs 5 months since starting on the ABP but in all fairness I can take a year off the total time, being in bed unable to move around has been a significant hindrance to my four year plus plan.
So getting to the title of this post, I’m not healed yet but in comparison to where I was and would be if I’d not found the ABP…
……..I’m significantly better…