29
May
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Stop trying to cure MS…
Isn’t it strange, tomorrow is World MS Day… as has been noted there are almost 2.5 million people worldwide with multiple sclerosis and this supposedly benevolent organisation is promoting awareness…
Awareness of what I wonder? That the worlds medical experts and the pharmaceutical industry can’t find a way or removing the disease from the human body, even though 2.5 million are suffering.
This is what the NHS say:
There’s currently no cure for MS, but a number of treatments can help control the condition.
The treatment you need will depend on the specific symptoms and difficulties you have.
It may include:
Treating relapses with short courses of steroid medicine to speed up recovery…
Specific treatments for individual MS symptoms…
Treatment to reduce the number of relapses using medicines called disease-modifying therapies…
Disease-modifying therapies may also help to slow or reduce the overall worsening of disability in people with a type of MS called relapsing remitting MS, and in those with a type called secondary progressive MS who have relapses.
Unfortunately, there’s currently no treatment that can slow the progress of a type of MS called primary progressive MS, or secondary progressive MS in the absence of relapses.
So no cure… okay we know this hideous disease can’t be cured, but why spend time and money attempting to do something with debilitating side effect riddled drugs trying to cure MS.
Hah!!!!
We don’t care about curing MS.. its a shitty hideous disease, I’m personally not interested in curing it…
But what about my body, your body, anyone that’s unfortunate enough to have this pariah residing in it..
Let’s focus on it!!!
So let’s devote our time and effort onto Healing our damaged body…
Using natural unadulterated foods and supplements let’s kick its ass right out of here. Then Heal the body, the temple we live in 24/7…
Hmm does that sound like a better aim for World MS Day…
The way I see it is that big pharma and the medical world are simply looking at the wrong thing..
Stop trying to cure MS… instead…
……………Heal the body……………..
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28
May
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I’m freaking….
During my day especially since I buggered my knees over 15 months ago and being confined to bed I’ve forced myself to try and exercise, limited as it is, I’ve tried to do something several times each day.
Mostly it’s my core and upper body simply because I’m unable to work my legs as all sufferers of MS will know, they just don’t work…
Anyway…. I mentioned about ten days ago that I’d incorporated something new into my life and no its not the horrendously expensive Protandim Nrf1 and Nrf2 which I’m sure would help although any results wouldn’t be seen for several months after starting.
What I am doing doesn’t cost an arm or leg, no, what I’m doing is quite simple and inexpensive, as I said last week I’m going to reveal all in another week, but at this time I’m just going to give an update on my personal progress.
Again I’m going to emphasise that this is an addition to the Ann Boroch Protocol which in my opinion is saving my life…. emphasis on Life…. not existence which is all that’s happening if you have a so called incurable disease…
It’s frightening that “medical professionals” Hah!!! just attempt to push mind numbing drugs onto us with the ridiculous excuse of helping us cope with the inevitable…
Our minds are exactly as they were prior to MS, its the freaking drugs that has caused mental limitations.
It’s so easy to go off on a rant!!!, so back on track….
I’m definitely easier to do things physically than it was ten days ago, before if I’d lay to my left in order to take pressure off my butt by resting my head on the pillow to my side which helped a little. It would take 20 minutes and completely exhaust me to get back to a sitting position.
Now I can get up immediately with no fuss, I can get into a comfortable position without any help.
If I said I was pleased by the changes I’m experiencing it would be a lie… because I’m not pleased….
I’m freaking Amazed…
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24
May
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I am genuinely…
When I started on the ABP back in September 2017 I was very hopeful of the end result which I knew would be four plus years away. I think when considered by non MS sufferers that four years would be too long to stick with any protocol especially one as strict as this, but for those of us that have been suffering, and it is Suffering with this hideous disease especially knowing that the “experts” all say is incurable, then four plus years is no big deal…
Anyway as most people know I had an accident in March 2020 that buggered my knees and kept me in bed since apart from bathroom breaks of course.
I feel confident in saying that the only obvious MS symptoms I have now is weakness, but knowing I don’t move around as I did 15 months ago so my legs, arms and my body in general isn’t getting exercised as it would normally have done, but even so I’m positive that the ABP has been doing a great job.
Okay so now I’m going to describe other changes that are attributed to something else, something I can honestly say is amazing me. This “something else” I’m not going to say what it is yet, it’s only been one week today since it was incorporated into my daily regimen. I haven’t and won’t change or stop the protocol that’s changed my life but something has been added.
This isn’t something I’ve discovered, I didnt read about it or did some indepth research, I was told about it so wanted to see for myself.
I’ll carry on and reveal all in a week or so but trust me when I say that at this time….
I’m genuinely amazed…
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