BocowoA

[beauxreflets]

Half scared about the future prognosis; I took a little leap that may it seems.... - Well I will let you make up your own minds.

beauxreflets.blogspot.fr/

[JAYNIE]

fabulous.....U R a gr8 writer !!!! I am starting in 2 weeks with a personal trainer, and I hope I can feel like you do. I will give it my all, and will report here 2 weeks from the start.

keep us posted also.....

Jaynie

[beauxreflets in reply to JAYNIE]

Starting what in two weeks ?

Jaynie, please note - BocowoA is made from fresh GREEN HERBS and is not currently available in the stores.

[Jocee in reply to beauxreflets]

where do you get it?

[beauxreflets in reply to Jocee]

From the surrounding countryside

You will have to excuse me for not divulging more details as it should in my opinion be classed as a medicine; and given the hard journey I have been through, only taken under supervision.

I cannot supply it as I do not have license to dispense or the insurance doctors and pharmacy bodies must have.

[JAYNIE]

then why tell us about it???

[beauxreflets in reply to JAYNIE]

In the first place because it has provided such a quick good effect and therefore merits further research and development.

Secondly my Ma died from a form in Motor Neurons having assisted in my early research, so perhaps I felt I had a moral duty to share

Thirdly, even if it is not a Cure for all, the record and notes I have made may assist some looking at similar treatments.

Hopefully the right people will come forward so that it will eventually get it into the pharmacies.

[JAYNIE]

I did not mean to sound nasty, sorry if I over reacted

[beauxreflets in reply to JAYNIE]

No worries, I thought long and hard before going public, as the last thing I want to do is create any false hope.

Hopefully by describing aspects it will start the ball rolling, because the eventual Cure can only be found through team work.

[beauxreflets in reply to JAYNIE]

You did not sound nasty by the way - and I hope things go well

[Jocee]

Jaynie, you did NOT over react! Your first reaction was perfect..

[JAYNIE in reply to Jocee]

Thanks Jocee !!!!!!!

[ldq1997]

I am old and my eyes are bad. I have a problem reading grey print on a black background. I tried highlighting the print so that there was more contrast but this was a very tedious process. Then, I tried copying it into my word processor where it was reproduced in black print on a white background so that I can read it later. I am intensely interested in herbs so it is a great disappointment to me that this blog is in such a difficult format. Obviously you have some skill with computers to set this thing up in such an artistic format. But couldn't you put it together in another format which is easier to read?

[PatV in reply to ldq1997]

Yes, I had the same problem. Small white print on black background? TOo much for my eyes. I gather from comments improvements in PD were from having a personal trainer and herbs?

[beauxreflets in reply to PatV]

I have just posted the last blog entry in this thread.

The personal trainer as you put it, is a qualified Physiotherapist (specialising in muscle sports injury etc.) and they play a vital role in France within the Health system.

I know I am lucky to have this service and hope more emphasis is put into the benefits their skill, expertise and knowledge provide

[ldq1997 in reply to ldq1997]

For anyone with weak eyes like me, this blog can be found in black print on a white background on a UK bulletin board at parkinsons.org.uk/pdsforum/.... It is a lot easier to read there.

[beauxreflets]

Sit Ups and BocowoA

At the last session of French Physiotherapy with my Masseur Kinésithérapeute, the changes were plain to see. I could feel the complete changes in muscle tone in my abdomen, legs and arms. The ‘spark ups’ have given new life to the muscle fibres

When describing Parkinson’s to family, I would say; It was like growing old fast when you are far too young. Everything is as though one half of ‘being alive’ has been swept out from under your skin. Now I am pleased to be saying that that lost youthfulness (all be it very painful at times) is returning in leaps and bounds.

Walking the last few days has at times been very awkward to say the least, but the cowboy legs and hip sway have gone, while I am getting used to where the feet will be as I tread, adapting with the constantly adjusting gait, generally improving posture, and the occasional numb buttock (Sciatica due to a spine injury in my teens) and a fair wind.

Taking care of the spine plays an important part in daily thoughts, and when the back muscles are not in balance, I readily straighten and stretch my spine with some floor exercises, sites.google.com/site/beaux...

I am becoming more convinced by the observation I recorded in the Coprinus fungi family, that a tiny tweak to the biochemistry changes everything. As a down rolling spitting mushroom evolves into a more dry umbrella ink cap that opens in the opposite direction; A tweak to the amino acids in the nerve cells will alter both capability and function.

Eating BocowoA just on the occasions when I need the boost (having already faded out the synthetic Levadopa completely) appears to be working exceedingly well, provided there is sufficient water on board. Through all the changes (from the initial revitalising gut sensation onwards) to each arrival at a new stage or plateau, it is clear that Natural Dopamine is being produced and retained. Added to which, I now appear to have a measure in control that allows me some choice to govern the speed in this apparent rapid recovery.

The bug bear of managing the medication times (while predicting what the day would bring in regard to achieving an acceptable balance) seems joyfully so far away, while each new day brings progress and the sense of recovering even more of my youth, as the spark up and waves ripple along old nerve ways, opening up the muscles with more vitality.

In the space of one month, the combination of BocowoA with the well-suited form in Physiotherapy, have provided the apparent gain of twenty plus years.

Well, how many folk even without Parkinson’s, can lay flat on their back, with their arms held straight (hands hovering over the thighs) and gently raise their head and torso upward into a sitting position? The last time I recall being this fit was in the 1980’s, when I knocked five out of six balls into the back of a five a side football net defended by Pat Jennings (International goal keeper for Ireland).

There are of course days in apparent contradiction to the claim of ‘active fitness,’ times when it outwardly appears things are just as bad or worse. This is when the brain is sapping all the energy necessary to reassign and reconstruct itself to the changes occurring in the body. The mind is willing but the body is weak, just as it feels like when recovering from a heavy bout of Flu. And I think it fair to say, that recovering from years of being ‘in decline’ will require some moments in meditative rest, as well as the usual nights sleep.

Knowing my personal history like the back of my hands, I have observed the reversal process so far, both physically and mentally; As the going truly reflects the way of manifestation, although not necessarily in the same chronological order, as the body heals to the building blocks of biological order, and one apparent major difference; in that the gain does not breathe the same sense in panic brought on by the shock factor of the earlier losses, when nerve ways effectively close parts of the body down, or indeed the aspect of hallucination (that occurs when areas of the brain normally associated to the role for the subconscious dreaming are commandeered to maintain different roles in conscious day time).

In all of this I know sufficient to say that, I still have a little further to travel before the full clean bill of health box can be ticked, but the level of partial control over the whole healing process is a huge personal assistance, provided those around you have a similar trust and faith, that the ill can and will be overcome with time.

As I write I am very conscious of the fact that I may not have found the total Cure; but a way that seems to suit, in arresting my current situation. I am equally aware that there are some people who are way beyond "the early onset stages" and more badly effected and in need of their current medical regimes; hence my reluctance to provide full details of the ingredients in BocowoA via this blog.

All I can do is openly invite a fresh approach to tackling the disease through sharing these thoughts, in the hope that something just as positive can arrive for others living in the hell of akin neurological disorders

[beauxreflets]

I hope this all helps

[PatV]

My neurologist who is a researcher visited 3 countries where when first diagnosed with PD pwp is given aggressive physical therapy. The rate of progression is remarkably less than in US !!! where we medicate, medicate, medicate, then operate

[beauxreflets in reply to PatV]

The physiotherapy is not and must not be aggresive. It is GENTLE MASSAGE; that helps the blood flow and nerves; TO STRENGTHEN AND BALANCE THE MUSCLES IN THE BACK , ARMS & LEGS, CONTERACTING AGAINST THE CONSTANT MUSCLE CONTRACTIONS THAT SQEEZE THE VERTEBRAE EVER CLOSER

THE LAST THING DAMAGED NERVES NEED IS ANY MORE DAMAGE!

GENTLY STRETCHING THE SPINE AND DRINKING WATER TO ASSIST THE SPINAL DISKS ABILITY TO CUSHION has kept me away from any need for surgery so far.

sites.google.com/site/beaux...

[PatV in reply to beauxreflets]

I quite agree. I don't think he means that the PT is aggressive toward the pwp, he means that the PT starts immediately and frequently and continues. Medicare pays for 6 (SIX! ) only treatments per year per condition which is RIDICULOUS! for a chronic condition! (sorry for the rant)