Rather Be Healthy

Consider yourself to be…

What I take everyday is not typical of those attempting to beat the so called incurable disease called multiple sclerosis, I say “so called” because as thousands already know its only incurable if all you do is take disease modifying drugs to ease the symptoms.
Whereas the select group of individuals that have a strong will and determination to genuinely remove the hideous life sucking pathogen then good health is on the horizon,
yes it can be hard at times and yes you will experience pain and frustration, but becoming healthy and actually “Living” again is genuinely possible.
As I said, the multitude of supplements I take daily isn’t specifically required, so don’t be put off by what I take, what is required is to make the commitment necessary to only eat the compliant foods.
I want to put things into perspective, my condition and situation is tough on me living alone, but there are many others worse off than me so I’m not complaining.
I’ve had MS for 18.5 years, I’m alone apart from 1.5 hrs per day.
The fall I had 27 months ago has kept me in bed 23.5 hrs per day.
I can’t lay on my side or front as I can’t roll over meaning I’m in the same position permanently, sleeping in a sitting position trying to keep warm in winter or cool in summer isn’t a comfortable thing to do.
I have to use a catheter 6 or 7 times a day, my carers get me onto a commode at lunchtime everyday which can be a little frustrating and inconvenient as my bowels don’t always want to comply with my forced regimen.
But as I said I know some others have a much tougher time, so I am always grateful to those carers helping me and count my blessings daily.
Now I know some people gripe about taking supplements or simply forget on some days. Again, what I take isn’t typical, this is the number of tablets or capsules I take daily…
6.30 a.m….. 41
11.30 a.m. … 36
6.00p.m… 36
8.30 p.m. 5
So that’s 113 each day, that’s broken down into 33 different groups, so don’t use the excuse of taking ten or so caps that Will help save your life.
Following this protocol WILL change your life…. rest assured if you do what’s required it will happen, as I said at the start by doing this properly, you can consider yourself to be in..
A very special group of people…

How much…

Looking at life when you have a severely incapacitating disease can result in a depressing and a no point in trying attitude, I mean the longer you have the freaking, hideous life draining disease the worse and harder it gets to not just “try” but also think it’s worth putting yourself through more pain, frustration and demoralising heartache.

On top of being one of the 2.3 million MS sufferers out of a population of around 7.5 billion….. hmm… if MS was a good thing it would make me a very lucky and special person, but sadly its not, it’s a life sucking problem, so ontop of that I had a fall 27 months ago that buggered my knees which has kept me in bed 23.5 hrs per day, which also means my once powerful thighs have wasted away and I have a butt that feels like I’m permanently sat on a drawing pin because of bed sores, so even moving a little trying to get a tiny bit more comfortable is horrible and knowing my seated position is how I am all day and night, yes I have to try and sleep sat up… not easy and a tad frustrating.
So… when I see these poor people suffering because hey haven’t been on holiday …”for two years” !!!! Ahh…poor people…
I think to myself, stop bloody complaining, my Lockdown has meant being sat in the same position in my bed for 27 months, I’ve only been out of my house once in 44 months, my own situation is bad but in reality there are millions and millions that have it so much worse.

Sorry, I’m digressing, getting back to us as in MS sufferers and me specifically.
I’ve always been the type of person that doesn’t just accept the bad things that happen in life, I try to make things better, not cover them up or ignore or sweep them under the carpet, but look for a way to genuinely fix it.
It’s not because I’m a scouser with a German (by birth) mother, I also survived Liverpool in the 50’s 60’s and 70’s and had a tough, “don’t look at me that way”dad who’s hand and my ass knew each other really well.
I don’t think any of that makes an ounce of difference in my attitude to this disease. Even before learning about the lifestyle and life changing Ann Boroch Protocol I was constantly looking for and trying whatever I could to beat and remove MS from my body..
I try then get knocked down, so I try again then get knocked down again but get back up and keep trying, I’m feeling stronger everyday and after 18 yrs and 4 months genuinely believe I’m sooo close..
Multiple Sclerosis isn’t incurable, well it is if you give up and stop trying.
The way I see it is, I can…. you can stop being a victim, make the decision to be a winner, it all comes down to…
How much to you want to live again…