Amyotrophic Lateral Sclerosis (ALS)

You can read the full paper on ALS in the link below:
http://www.keshefoundation.org/latest-papers/pdf/5.html

To join the ALS program or any other inquiries please contact, the

[e-mail]

With the release of this paper Stichting the Keshe Foundation for the first time in its history opens the doors of its research to the public for a glimpse into one of its most closely guarded research programs. This is the application of its spaceship program plasma technology in the domain of health in order to overcome and/or reverse some of the ailments, which the present world of science and medicine has no solutions for.

We have developed the health section of our spaceship program because we believe the spacecraft of the future will not be able to carry all the medicines and doctors of every discipline required to cover all aspects of the health needs of people in long-haul deep space travel. In order to meet every eventual medical need there would be more medicine than food and more doctors than passengers on board these craft.

In our health program we have set out to understand the fundamental basis and cause of each illness in the magnetical and gravitational structure of the human cell. From this we are striving to build one unifying health system that works in the same way as the human body and that can be used in space for all ailments by simply adjusting the operation of the body's system so as to help it overcome any problem.

In view of our development of plasma technology and its applications, amyotrophic lateral sclerosis (ALS) should no longer be a death sentence handed out by doctors, who tell their patients in the same breath that there is nothing that can be done to save their lives as the present world of science has no cure for this killing disease. The present medical world cannot explain the origin of amyotrophic lateral sclerosis or what triggers this process in the human body.

From our research we can with confidence state that amyotrophic lateral sclerosis (ALS) is a reversible condition in most cases, if it is discovered at the right time and handled in the right way by a competent team of physicians.

You can read the full paper on ALS in the link below:
http://www.keshefoundation.org/latest-papers/pdf/5.html

.

Amyotrophic Lateral Sclerosis - Death wish that comes true

ALS

M.T.Keshe (2000-2013) - All rights reserved

www.keshefoundation.org

Contact: [e-mail]

www.keshefoundation.org

My name is Mehran Tavakoli Keshe, I´m a director of the Keshe Foundation.

Keshe Foundation is a spaceship program

which is involved in plasma technology,

and it has proven through different aspects of its development

that energy and motion can be made

from plasma in a very simple way.

For years we've been asked how we have developed

and taken our technology in plasma technology,

which has to do with gravitational magnetic field of a system,

into the Health section of the technology,

and how we achieved so many different positive moves,

and changing diseases, using the new plasma technology.

For the first time, with this video

we open our doors to the world population,

to look and see how a simple technology

has changed the life of a man.

At the same time, with this video

we are releasing a paper for the first time,

from the Health aspects of the technology of the Foundation

and for the first time we allow the world's scientific,

and the world population, to have a glimpse

into one of the most secret and guarded

technologies of the Keshe Foundation.

We are opening our doors in response to the peace talks

which is taking place, and at the same time

ensuring that there is new development,

in Health, in Energy and in Space.

So, with this video we would like to show

how a life of a man who has been sentenced to death,

literally, by being told

that he has a disease called ALS,

and how he has changed his life

using the system, from March to September of 2013.

Most of the videos you will see

is being made by him, and at the same time

made during the processes we had with him,

during the system development.

We see how a man who barely could walk

now he goes to work in Rome and in Milan (city)

and at the same time he has been given a second chance

he is getting part of his movement back.

ALS is a death sentence when it is given to you by a doctor.

The only thing is

we do not know the time when it will be carried out.

You end up being paralysed, then you can not speak,

and usually followed by suffocation and death.

For the first time we have developed the technology

to be able to monitor and reverse this process.

This gentlemen is very tied up with this disease.

He can not do much,

but now he's getting control of his arm back.

He's getting control of his feet back.

He's getting control of his work, in a way,

being able to go to his office back.

He's joining the society in a slow but sure way.

This video is to show (that) now there is a solution for ALS.

This is one of the final cases

after we developed different systems

for this disease and M.S.

And we can say with certainty:

"There is a way out of this disease".

We welcome anyone who would like

to talk to us about this disease,

be it themselves being affected by it,

or you are a member of organization or association

which is working with ALS.

Or you are a pharmaceutical,

and you want to develop this technology

further for the world population.

Our doors are open and we welcome you for cooperation.

The same as what we did for our Energy,

and for our Space, with governments.

And same as what we did with our World Peace Treaty.

If you want to talk, contact us. Please go to:

[e-mail]

which we especially opened this line for this disease.

Fill in the form and we will respond. It is very easy.

There should not be a death sentence

once you are told you have ALS,

for the majority of the ALS cases.

We have not found the solution for all of the aspects of different types of ALS,

but at least we have opened the doorway.

WE WELCOME ANY HEALTH AUTHORITY OR ANY GOVERNMENT

WHO WOULD LIKE TO LOOK INTO THIS DEVELOPMENT.

OUR DOORS ARE OPEN TO YOU! We are not hiding anything,

The same as we did not with our World Peace Treaty,

and with our Energy, and the Space technology,

We have shared them with the world population,

now we're sharing our Health,

directly with the world population.

Watch the video, I hope you enjoy

and take pleasure as much as we did,

seeing how the life of a man has changed

without even taking any medicine. Thank you.

Today is 8th of September, 2013. We are in Rome

and the purpose of this recording is to show

that the disease known as ALS or known as "DESMA"

can be stopped and reversed.

And today we have a gentleman with us is Mr. Max Vassan,

who has been through this process since March of this year (2013),

and this gives us a springboard to bring

this technology from the health aspects in respect to ALS

into the mainstream medical applications for the Foundation.

And I would like to ask, if you want to introduce yourself,

about who you are, and how long you have ALS.

My name is Maximiliano Vassan

and I had the diagnosis

for ALS. I received 6 years ago, it was 2007,

and I'm 44 years old now, I was 38

when I received this bad news and... that's it.

How has been your position before you started

this process with the Foundation?

The position was: I was closing. I was stopping

my life, more or less, not willing to go out.

Not willing to meet people so it was a... a total closure.

So, not only from the physical point of view

but from the psychological point of view.

So it was a kind of hopeless life,

more or less, without any big expectation for the future.

What was your condition when you started

this position, physically and mentally?

Physically... let me say the biggest changes were not

from physical side..umm, (rather) the psychological side.

I was afraid... I was afraid to go out,

to live a normal life.

So I believed that staying at home

I could... something could have happened,

and maybe to heal to recover...

but now I guess this was bad thinking,

because at the end the message was not of life,

it was a message of death, closed at home,

not going out with family, son and so on.

And in the past my physical condition was,

better before in the years, I mean,

but from the Psychological point of view I was really, really closed.

This is completely changed now.

So this is the biggest change

from the psychological point of view.

The physicality, the physicality , the first signal I got recently.

The big signal one week ago,

so part of the walking

it is improved since we met five months ago.

The rest is coming now,

so it's first psychological point of view,

these are most important, and then the physical now.

When was the last time you came to Rome,

where you worked, where you are going today?

I was here nearly one year ago, and it was for a job,

so I had to come for some professional situation.

And then I say: "I am not meant to come here in the future".

So wish was, "OK, maybe one day", but without really believing.

So, now I'm here because... I'm here for no reasons,

So, I'm here for a kind of holidays, let's put it.

Because, I'm here because I want.

So, before I had yet to come for a reason,

now I'm here because I want.

This life is slightly different, but internally is a big thing.

When you were here last time, could you walk on your own? Or?

No. Oh, maybe I could... but I didn't!

So, I was walking hanging onto the shoulder of my wife.

because I was completely insecure.

I was afraid at that time one year ago to go out... towards a pain.

it was pain... not being like physical pain, but it was really difficult.

I was afraid to go outside for my condition.

So part of it was related to the risk to fall down to hurt myself,

but also the rest was to meet the people in this condition.

So I felt really uncomfortable to go out.

You started the process in March? Yes.

When we saw you in the first meeting you could only walk

with the help of your wife holding your shoulder? Yes, yes.

At that time for me it was unthinkable to walk alone outside.

I was doing that at home, but at home was easy.

Outside, I completely needed the support of my wife

to be sure, so it was a kind of "safe" for me.

But now? Now? Now, every time she

offers me the, not the shoulder but the arm, I say:

"I don't want". So, I walk alone as much as I can.

If I see any obstacles on the steps and so on,

and I'm not gonna say, it's stupid, I don't want to fall down,

so i ask for help, but only in the situation where I need it.

You work at home upstairs? Yes.

On the second floor? Yes.

How has that situation changed there?

I have these steps... it is quite tough because the steps are high.

This is kind of measurement for me.

It means I can measure my carefulness everyday doing these steps.

The situation I was used to when I started living in this house,

it was OK... I was able to go without problem,

but anything was worsening the situation, so more difficult.

In the last month, even after the treatment

I had kind of, let's say, changes in a situation, so not improving.

Last week, as you know, was kind of a bad week where I reached the limit.

It means immediately, I was not able to do these stairs.

It was a kind of shock. I was afraid that day.

But then I understood that it was only from the mental point of view, I was afraid!

The week after, I mean last week, I had experienced a completely new situation.

It means, everyday from Monday to Friday, I was stronger

and lifting the arms stronger, but much stronger.

And every day was better than the previous.

This happened from Monday to Friday.

This never happened in 6 years! Yes.

So you have some control of your arms and walking? Yes.

I started to have control on the right arm.

On the left I can not lift so I'm very weak,

but let's say I started very light control of shoulder.

It means it's not enough to move to rise,

but if I lie on the bed with arms, let's say on the high side,

the left is going falling down because gravity so I cannot control.

the right I can control a little bit.

So I brake it when is falling down.

This you couldn't do before? No.

This I discover by chance same week of August last,

because I was expecting during the movement this arm falling down

and that, unconsciously, I was controlling.

So, that's why I recognized there is something strange, it's not normal.

And then after that day, this control stays up to present.

Some days it is better, let's say, some days a little bit worse,

but this control is present up to date.

And you are walking? The walk you do?

The walking is a tricky point, because, I improved.

Because one year ago I was walking, only with my wife.

Now I walk as much as I can alone,

so I don't want a support.

Some days I walk much better than others.

I started to walk also on the ground and grass.

I mean difficult paths, and this has changed.

The problem of walking is that for me is it's so, let's say,

minimal changes day by day that it's difficult for me to recognize the changes.

So others told me: "Look, you are walking in a different way".

So it was difficult for me to believe that I was walking differently.

But looking at my first video, and remembering how I was walking one year ago.

I must say I walk in a different way.

So I compare to my previous situation when I was running and doing everything,

so if you compare to this you are deluded,

but compare to one year ago... now I'm walking!

I don't have any big slant or big autonomy really,

but walking is different for sure... and it's better.

Your son made a comment about your walking?

Yes, my son, my son, my own son...

it was a day when I was supposed to be tired, the weekend tired.

and I was feeling myself bad going after from the car,

normally when I sit for a long time, I'm tired.

I said OK, I need some time to sit up.

And my son who was behind me said, and the sentence was like:

"Dad, to be without muscles or to be a ill man, you walk fast!"

I said: "Why? Why you said that?".

So for me I was walking bad and slow,

but, for my son I was walking fast.

And my son see me every day. So my feeling was wrong.

That's why I said it's difficult.

For the walking the best effects

I see from the others. The people was looking at me in one, two, three weeks, one month.

For me it was the same, for people sometimes it is shock.

Then I can't believe everybody is lying to me or so.

That's why... the changes were so small,

and alot of them sometimes for me it is difficult to believe.

So I'm becoming used to the changes.

But, yes, one year ago I was walking totally differently than now.

Better? ... Better!! But then you started Interacting in society...

Can you tell us what was that like?

This was starting after a couple of months,

Yes, after the start of the treatment.

And this was the one of the most important changes and the first to come.

So, the psychological point of view, as I told you.

Before I was not simply willing to meet the people,

friends, parents or people that are part of our life...

simply taking children to school and so on and so on, and other families.

As I told you I preferred staying at home, alone,

and I feel safe. It was at home I feel safe.

And my family can go out and enjoy and so on,

but at the end this was not good. So I started it.

How long did you do this for? ... Years. About 3, 4 years?

Yes, go t on this. So I probably closed any intellectual activities

because I felt uncomfortable doing these.

So what happened? Then the first step...

The beginning was kind of a challenge, a big conflict inside.

So, I accepted to do something that I never did before.

So to meet the people directly.

For years I refused to meet in a specific situation:

parties, or a dinner, or social events.

The beginning was a big conflict, I do, I don't do, and so on.

But I did it. Then, continued treatment and passing the time,

the wish to meet the people, to go out, was stronger and stronger and stronger.

So, from one social activity became two, three and four.

And if before it was a pain, a fear about situation, about the reality,

at the end, it became not.

So, the fear was much weaker compared to the wish to go out.

And I reached the point this summer, in August,

that I met all these people without any,

without care about what they could think about me, and so on.

Can you tell us the situations?

The situation was, it was middle of August, in Italy,

and they invited some gentlemen of school company of my son,

invited us in the countryside, for a BBQ.

Countryside for me means immediately difficulties,

and also their house, to reach the house,

there are hundreds of steps and long houses' steps.

For me in that moment it was impossible.

But now in the rest of it, OK, let's walk at least,

and I will see the situation,

so, I said: "First, let's go there... and then let's see what happens".

At the end, it was wonderful day.

So, I was able to walk in spite of

the ground... it was not easy.

We spent the day between friends, eating, drinking, laughing.

So, it was normal, very normal, the children were playing...

So, I was very surprised.

People doesn't care about me completely.

So, after, let's say, a few minutes,

I felt like normal. completely normal, in spite of all my difficulties.

Would you have done this last year?

No. All these social situation I have made since I started the treatment.

I would have never done before.

So you meet these situations personally. Yes. Yes.

And, would you have done that? No.

I avoided in the past, all these situations.

An easy example:

Every Friday, my son in summer time goes to summer camp.

And they organise every Friday, at the end of the week,

a small spectacle for the parents... they are going there since 3 years minimum.

I never attended to any of this one.

Because of your illness? Yes.

But the funny thing is that in the past my physical situation was much better

than now 2, 3 years ago, but I didn't know.

Now I attended, I attended to all the spectacles,

and I'm still alive, I enjoy.

And the funny thing is that my son again, saying, told me:

"Why you didn't attend in the past?"

And I couldn't answer, because he said:

"If you can come now when you are not in a wonderful situation,

why you didn't come in the past, when you were much better?"

I had no answer!

When you see the first change?

One week, two weeks, three weeks after you started?

I think after some weeks let's say, between two.

In the first answer, I started to see some psychological changes,

yes, in one month more or less.

What do you think the future holds for you now?

First of all I started again to think of the future... which is a good point.

Looking at these changes it seems to me that I started a new road,

that I can not stop on, so, I tried to making the office,

going out with friends and so on.

And, I don't want to stop,

So, my thinking now is that it was stupid, my behavior before.

I am wondering why it was that way...

now it seams strange what I did in the past.

You've been back to your office in Milan, one month or four weeks ago?

Yes, one month ago exactly.

This office I opened, personally, 15 years ago.

Then we changed the building but I never visited this office..

When was last time you were in there?

In this building I've been never.

I was in the previous building, but last time was 2008 I guess.

I stopped to go to the office in Milan, also because I was working in Rome,

so I stopped to go there, so it was very long time.

This was a new office opened two years ago, and I've never been there.

In August, it was the beginning of August, I was back to Milan meeting these guys and looking at the new office.

It was very nice because, let's say, I left Milan many years ago.

Strange thing was that, when I was there, even new office,

I was feeling was like I was working there since forever.

I had no bad feeling, oh my God, it's many years,

that I'm not here, and people will look at me strange.

I felt completely normal.

Are you going back?

Yes, in the end of this month.

I already fixed it, and every month I'm going in the Milan office.

Do you see yourself going back to work normal, in the future?

This is without, doubt, absolutely.

So today you are going to see your colleagues more or less for the first time?

Yes, these colleagues in Rome that for nearly one year that I didn't meet,

and they don't know anything about this... this treatment I'm doing.

So, I kept reserved, only 2 or 3 people know,

and even they don't know anything about that I'm here in this moment.

So, we are going to the company, and it would be totally shocking to many people.

So, I don't know the reaction that they will have.

Are you coming back to work in Rome?

Yes this is my target.

One of the things which is important to understand

by the work of research of Foundation,

is we call ALS "the death wish that comes true",

which means that psychologically, through certain reasons,

the individual sets off a certain kind of process which terminates the life.

This termination of life means they can

escape from the problems of \what they are facing.

Some people chose hanging by suicide.

Some people choose different methods of ending life.

But, ALS in fact is the same process,

but starts with a process of psychological double trigger,

of which we understand the process.

And this psychological change, which then afterwards becomes a physical change...

As we see the arm is coming back, and the walking has changed.

It is the process of development

of the psychological change in the understanding of that

there is no reason to take such a step.

They literally trigger the death code in the brain

and the process as we see in Mr. Vassan, has started literally ten years ago.

It is something which is not gradual.

The first trigger comes at any stages of life,

and the second trigger happens when the second crisis comes.

And now we start understanding the process much better

and we see, more or less, the start of the reversal limit and the physical disability changes.

We have recorded the whole case from the beginning,

so the steps... we see changes in walking,

the drop foot has gone, the walking has changed,

we see changes in the arms on small stages.

So we today, we record the whole event, the process, by standards.

We are not taking any steps, we've done the same thing in Milan.

So, this is just for archives, and at the same time,

to show to the ALS community that there is a solution,

there is a new way to look at this disease,

and nobody should die from this disease any more.

I thank you for your time, and I hope we'll see a nice day today!

Thank you. I hope, this is the target of today.

Thank you. Thank you.

Due to restriction by the Company of the volunteer, all videos taken within

the offices of the company has been blocked. The Foundation does not understand

the purpose of this move in the celebrating the return of one of their workers back to work after years.

But due to legal papers which we had to sign for the company three weeks after recordings

we have to withhold the footage of these meetings, which was so wonderful, away from public.

We hope one day commonsense will prevail and we all share

these wonderful moments with each other and with the rest of the world.

Today is 6th of October 2013,

After the two surprise visits to my company,

beginning of August in Milan office, and beginning of September in Rome office,

I did it again, second time.

And in both cases it was in general much easier, and much normal, the approach.

So I had no big fears or worries to go there... simply a pleasure to live and

to go out and meet people, the others, my colleagues.

So, this was very nice. And even coming back,

the thinking was to the next appointment, next meeting.

So I decided with pleasure that, for example, I will go

once a month in Milan office, if not more. OK?

And also periodically to the Rome office.

In this case, logistics is more difficult, so I have to organise better.

But in general I noted that I'm thinking again

in terms of the future, not past or present situation.

All together, this result, what I achieved in the last couple of months,

for me was really unthinkable only three months ago. So, I mean in June.

This is unbelievable, unbelievable at this stage.

In other nice discovery I made is that all this activity, what I did, what I'm doing,

has an impact also on the others, for example, my colleagues.

I learned that at the end they don't care about my physical situation.

They are, of course, ready to help me...

and they are sorry, but this is not the main point. They don't care about this.

What really important seems to be my presence there

for the fact that I move, I travel just to go there to meet them,

and this is the important part,

and it's different than what I thought, completely different!

So, this awareness helps me again,

because this reduce a lot the psychological part of this illness.

This illness is composed of two parts, main parts...

One is physical: the daily difficulty to do things, simply.

The other part is psychological: this is the driver of the illness.

And we can summarize in one word: it's "Fear"!

Fear of the situation, fear of going out, fear of the others, what they could think and so on.

Reducing the fear is the most powerful part

and is, I think, an important step.

Indeed the evidence of today is that despite my physical condition

was much worse in the past, some years ago,

I'm now doing things that I never did, I never wanted to do,

even if when my physical condition was much better than now.

This is really surprising me a lot, because it's nonsense, it's not logical...

Now that I'm worst I'm doing more than when I was much better.

Another achievement, nice thing, in the last month,

was, from the physical point of view

but it's linked to the psychological part,

normally at the end of the day, late evening or at night time

with very low energy, so really weak,

and I have home stairs in my house

that is quite tough to do... it's kind of challenge every time.

Couple of times, I was able to did all set at night

later with some efforts, but it's kind of very unusual thing to just go upstairs,

and to spend some time with my children when they go to bed.

So this was wonderful for me, wonderful for them, and a big achievement.

So simply the wish to go upstairs. And all these facts together are,

as I said before, quite surprising, about this evolution.

Let's say, I feel positive, so these are positive feedback that helps a lot,

and I hope this will continue also in the future.

This story to be continued

with future videos

from this volunteer.

A L S - " Death wish that comes true"

For the ALS technical document on a new approach,

access:

www.keshefoundation.org/latest-papers/download/5.html