Looking for a cure for als? It’s been there all along.

It’s repeated over and over. “This thing called als, or motor neuron disease, was first described over 140 years ago, and still no cause or cure has been found.”

Well repetition does not make something true and that no cause no cure for als thing is a case in point.

The cure for als has been around all along, and it’s not in the form of a pill, or stem cells, or anything else imposed from the outside. It’s a whole different thing. The cure for als is in the form of information, understanding, knowledge and common sense.

For instance, in case you are not aware of this, the incidence of als in people who have served in the military is generally somewhere between 1.5 to 2 times that of the general population. So common sense says that something that goes on with people in the military causes als to happen.

Here’s another clue. While many are aware that als is also called Lou Gehrig’s disease, far fewer are aware that Lou Gehrig was a stress case who did not take very good care of himself , had major emotional issues and was basically addicted to playing baseball. Could that be why his nervous system crashed? Common sense says that that sounds likely.

Meanwhile, unbeknownst to many, there are people all over the place who have healed themselves after being diagnosed with als. In fact I listed some of their accounts on this blog post.

Here’s the real deal. After over a decade of working with people to help them heal, I reached out to someone diagnosed with als. I had read that supposedly there is no cure for als, and yet I had seen this kind of story before and knew from the beginning that als would be solvable.

Since then I have talked with likely over a thousand people diagnosed with als, I lost count, and I have read about many more, and here’s what I have found.

There is a cause for als, and it’s obvious to anyone who knows where to look. It’s not just one thing exactly; it’s generally a combination of things like stress and certain things in people’s diets that freak out their neurons and emotional repression and things like that. This isn’t the kind of stuff you easily see looking through a microscope. It’s the kind of thing you find out by interviewing hundreds of people for hours.

Also, what I have more than confirmed is that there are available ways to solve or cure als or heal “naturally.” In fact one of the more bizarre things I uncovered was this als healing account by Evy McDonald. What made it so bizarre to me was that it was written in 1988. In other words, there I was thinking that my way of solving als by using a holistic approach was something original, and meanwhile over twenty years before I had that idea, someone had been saying pretty much the same thing. She had even presented her story to organizations involved in looking for ways to cure als, just as I have. So in addition to my figuring out how to solve als and helping people do that, there have been many many others who have followed similar paths and achieved similar results.

Could medical methods have some place in solving als? Probably. While it may not be possible to really “cure als” by doing things like using medication or injecting stem cells, probably medical techniques can help people somehow in their healing processes, maybe by temporarily stabilizing their health, or by helping them rebuild once they have stabilized themselves.

Anyway, the reality is that rather than really needing to look for a cure for als, what needs to happen now is for the word to get around that there are available today ways to solve als, and for people to learn how to apply the current body of knowledge. The faster we do that, the faster we can make als a memory and make progress at healing our world.

P.S. To see this in action, check out the fundraising page for Healing ALS, a film in production that will include interviews with people who are succeeding in solving als and information on how they are doing it. Very cool. They already have some film segments posted along with more information on people healing. http://www.healingals.org/

Diagnosed With So Called ALS? Just To Be Clear, There’s No Such Thing.

There’s a story out there, one that involves people being diagnosed, as they say, with this thing called ALS. “You have ALS,” they are told, a so called incurable disease with no known cause. The only thing is there’s a big problem with this story. There’s no such thing as ALS.

“Hey, but wait.” you might say. “People are getting weaker, and what about the genes that people say cause ALS to run in families? Surely there must be something going on.”

Yup, something is going on. People are getting weaker and genes are doing things. The thing is that ALS is not doing it. ALS cannot do anything.  There is no ALS attacking people or striking randomly. There is nothing called ALS that one can find using a microscope. People do not “have” ALS. ALS does not really exist.

Here’s what’s really going on.

People have nerve health problems and those nerve health problems look similar. The people’s nervous systems are deteriorating in a cascading fashion, often rather quickly. So someone came up with a name for those nerve problems that look similar, the name ALS. So that’s all ALS is, a name.

So this ALS, this name, is not causing anything. Rather, people’s nerves are deteriorating for many reasons and each story is a little different.

Some people’s nerves go partly because they never give themselves a break, instead choosing to keep going and going, using caffeine and whatever else to keep up the pace until their systems break down. Lou Gehrig’s case is a good example of this. Others have been exposed to substances or have been eating things that somehow figure into the destruction of their nerves. Maybe that’s why there seems to be a link between smoking and neurodegeneration. Certain types of ideas and mental patterns tend to figure in, people repress emotional stuff to the point where their systems no longer function and relationship issues and other forms of stress tend to be involved as well. Generally, there is some combination of things going on.

So there is not really a fast paced form or slower paced form of ALS. There is no ALS for there to be a form of. The reason some people’s nerves degenerate faster than do others’ is that the factors in and patterns of their lives are making their nerves degenerate faster.

Genes, proteins, mitochondria or other little biological things are not causing ALS. Sure biology is involved whenever something happens to a person’s body. That does not mean that these things are causing it. All that’s going on is that biological things are happening because of the stress and other factors and patterns which truly underlie the neurodegeneration.

While people may be struggling or feel that they are fighting various forces to stay well, they are not exactly fighting ALS. There is not really any such entity to fight. Similarly, while people may be surviving through all kinds of problems, there are not exactly ALS survivors. There is not exactly ALS to survive.

What is really going on is that people so called diagnosed with so called ALS just have nerve health problems that are created by the way they and those around them have been living, and that’s good news.

It’s very good news, because what people can create, they can change, and so people directly or interpersonally experiencing so called ALS can change things for the better. By changing what they do, how they think, what they eat, how they handle emotional issues and in general by changing how they live, they can change things so that they heal.