Last year I had a MS (multiple sclerosis) fundraiser in a complete uproar when I told her that all I could give this year was several copies of a documentary, which filmed various people curing themselves of MS. It was this documentary. The person raising the money for MS told me that showing cures for MS would, “give MS patients false hope“. I asked her to let the group of MS patients decide for themselves but she would not let any medical based information about curing MS near the MS group. As for the cure for MS, it involves myelin sheaths. (the protective coating around nerves) Myelin shelths are 85% fish oil so guess what these people are missing in their diets? So if you never address “diet“, you’ll always have MS and you’ll always have a job as a MS fundraiser.
Just had another guy today approach me on the western side of town asking me to support a CF drive (cystic fibrosis). I told him I was indeed aware of who the person was (that he was raising money for) and that this person needed to stop drinking booze and stop eating bad food as his starting point. (and that I could not give money for drugs and surgeries because there’s no proof they help and that all the proof shows that they make people more sick) The man then told me that he took my accusations “as a personal insult” and that he had personal knowledge that the CF patient in question only drank alcohol after his treatments were immediately over. (the look of bewilderment on my face could have been sold for millions)
As for the cure for CF, it has to do with excess fibrin. Excess fibrin build up is tied directly to insulin production. Insulin production is tied to an unhealthy diet, high in chemicals and high glycemic carbohydrates. CF patients are also short of pancreatic enzymes because the pancreas is tired from producing too much insulin. (it can’t make insulin and digestive enzymes effciently at the same time) Guess what CF patients are eating too much of? Answer………food stuffs that spike insulin. (including booze, which spikes insulin through the roof)
I quit………but I may be back. This conversation today really taught me just how far we have to go as a society in order to save ourselves. I can only hope the time we need matches up eventually with the distance we need to travel because time appears to be running out and the pursuit of modalities, which only injury the body, are growing exponentially. No matter how sick people get, they just aren’t understanding that treating the body properly is the answer.
Crazy how some of these people choose not to see the real truth. I think we have been so blinded by the media we have no idea what we are even supporting anymore.
this is another most excellent article.
articles that document what it is that makes humans ill and what they could do to correct it, is GREAT!!!!
Thank you, Paul
Don’t quit J (I know you’re not anyway); your information has gone a long way to saving so many of us. I understand your frustration, but keep in mind that most people are just uneducated when it comes to how to keep themselves healthy, and as you’ve said so many times in your seminars – we are all victims of popular culture, and unless these folks are exposed to something other than what is pushed down their throats by doctors, media, and family tradition, then they are merely victims of circumstance.
Let’s keep on working on educating and spreading the message. These “radical” ideas on health may be counter-culture, but isn’t that how all great movements begin?
Thank you for being you,
Reinhard
Hey Reinhard,
Just what I needed and at the perfect time. Much appreciated Reinhard.
I think you need to get your facts straight. yes diet can help someone who has cystic fibrosis. the right diet will help anyone regardless if they have an illness or not. There is no known cure for cystic fibrosis. However, research inspires real hope.
Comprehensive treatment programs have dramatically extended the lives of people with CF.
Cystic fibrosis (CF) is caused by a defective gene which causes the body to produce abnormally thick and sticky fluid, called mucus. This mucus builds up in the breathing passages of the lungs and in the pancreas, the organ that helps to break down and absorb food.
This collection of sticky mucus results in life-threatening lung infections and serious digestion problems. The disease may also affect the sweat glands and a man’s reproductive system.
An early diagnosis of CF and a comprehensive treatment plan can improve both survival and quality of life. Follow-up and monitoring are very important. If possible, patients should be cared for at cycstic fibrosis specialty clinics, which can be found in many communities. When children reach adulthood, they should transfer to a cystic fibrosis specialty center for adults.
Treatment for lung problems includes:
Antibiotics to prevent and treat lung and sinus infections. They may be taken by mouth, or given in the veins or by breathing treatments. People with cystic fibrosis may take antibiotics only when needed, or all the time. Doses are usually higher than normal.
Inhaled medicines to help open the airways
DNAse enzyme replacement therapy to thin mucus and make it easier to cough up
Flu vaccine and pneumococcal polysaccharide vaccine (PPV) yearly (ask your health care provider)
Lung transplant is an option in some cases
Oxygen therapy may be needed as lung disease gets worse
Treatment for bowel and nutritional problems (see: Cystic fibrosis – nutritional considerations) may include:
A special diet high in protein and calories for older children and adults (see: Cystic fibrosis nutrional considerations)
Pancreatic enzymes to help absorb fats and protein
Vitamin supplements, especially vitamins A, D, E, and K
Your doctor can suggest other treatments if you have very hard stools
Care and monitoring at home should include:
Avoiding smoke, dust, dirt, fumes, household chemicals, fireplace smoke, and mold or mildew
Clearing or bringing up mucus or secretions from the airways. This must be done one to fours times each day. Patients, families, and caregivers must learn about doing chest percussion and postural drainage to help keep the airways clear
Drinking plenty of fluids. This is particularly true for infants, children, in hot weather, when there is diarrhea or loose stools, or during extra physical activity
Exercising two or three times each week. Swimming, jogging, and cycling are good options. Avoid contact sports, scuba diving, and endurance activities such as marathons
AFTER THE ANTIBIOTICS OR DRUGS STOP WORKING THEN THE PERSON WHO SUFFERS FROM CF WILL NEED A TRANSPLANT. DIET WILL NOT SAVE THIS PERSON A LUNG TRANSPLANT WILL AND I BELIEVE THAT IS THE REASON THEY ARE RAISING MONEY TO HELP WITH THE PROCEDURE. I’M SORRY MR. CHRISTOFF THIS PERSON YOU ARE SPEAKING OF MAY HAVE ENJOY HIS OR HER LIFE AND WAS NOT AFFRAID OF LIVING, THEY SHOULD NOT BE OUTCAST BECAUSE OF IT. I BELIEVE THIS PERSON IS AROUND 35 YEARS OF AGE WHICH IS ABOUT THE AVERAGE AGE OF LIFE EXPECTANCY FOR SOMEONE WITH CF. IF HE OR SHE WOULD HAVE ABUSED THEIR BODY LIKE YOU SAID WOULDN’T HE OR SHE HAVE PERISHED BY NOW???
As usual in these cases the only thing to offer is an extraordinary improvement of the CF on film. All I need is the person in question and their willingness to eat a different diet. Only real live organic foods would be used (at my own expense). The full journey would be filmed and updated weekly. All real food, no side effects and nothing but upside in regards to lifespan, energy and vitality regardless of the final results. Although this would place everything to rest rather quickly, not one person has ever taken me up on the offer because these diseases are never about what they seem.
Disease is about looking outwards and never inwards. It’s about blaming imagery forces instead of taking responsibility. Disease is about thinking the body is faulty as opposed to seeing that it’s working as designed. Chronic disease is about playing the victim in a victim based society. Disease is about disempowerment vs. empowerment. Disease is about body love and respect vs. body disrespect. Disease is about taking responsibility vs. finger pointing. The only reason a CF patient makes it to approximately 35 is because conventional medicine does nothing to save them and everything to increase damaging the body. Send a CF patient over to see me and you won’t see the CF patient anymore.
The above list (in the person’s e-mail) is straight off a website and I understand their concern. Antibiotics disable the immune system further as discussed here by Dr. Wilson http://www.drlwilson.com/articles/antibiotics.htm so they in fact make all CF patients much worse and if you trace back the history of many CF patients you see antibiotics use as much higher than average population. Dr. Sherri Tenpenny discusses how child vaccinations are designed to make innocent parents and their children patients for life. Where does the evidence lie? http://www.youtube.com/watch?v=0GtFlvNztV0
The gene theory of disease is also highly questionable as is discussed here by Dr. Dean Ornish. http://blog.ted.com/2008/06/24/dean_ornish/ Yes genes can be found to be turned “on” and others turned “off” but that doesn’t mean their “on” or “off” positions are permanent. All are controlled by diet and genes are controlled by the body given the environment. A CF patient is highly immune agitated via environmental pollutants so their genes that produce mucus appear turned “on” but you could shut them “off” if you tried reducing the attack on the immune system.
That’s called the science of epigenetics and it’s explained in this video. http://www.youtube.com/watch?v=a12fzb9ZJ9E&feature=related It means twins have the exact same genes but when you track their genetics when they’re older, all their gene activations are completely different based on what they experience everyday. In many cases one twin gets cancer and the other doesn’t because of what they have been exposed to in their lives. One eats bad food for example and the other doesn’t. http://www.youtube.com/watch?v=Xjq5eEslJhw
All it comes down to is that you believe someone can’t change and I believe they can. I believe any person can reverse disease at almost any stage and you believe this is not possible. What you think determines your fate. Henry Ford said, “weather you think you can or you can’t………you’re always right”. That is why I don’t give my hard earned cash to these people. They don’t want to help themselves or they would come over to my house right now, stay over and eat my food here for 2 weeks………….but they won’t. Who wants to help someone do more of what’s not working. Who wants to make sure their friend gets more of what never worked in the first place. CF patients don’t need more drugs…………they need less drugs……………they just need less of what hurts the body and more of what heals. It’s that simple. To argue the point is futile. You either get it and you’re healthy or you don’t and walk the planet playing genetic victim. It’s a choice.
To reverse CF you can’t hurt yourself with bad food, hurt yourself with marijuana, hurt yourself with booze, hurt yourself with surgeries, hurt yourself with toxic medications etc etc. Hurting oneself is the habit that needs to be kicked and it can be comparable to a full blown exorcism for people who have consistently abused themselves for decades.
An argument that can only be settled by doing an experiment either personally or for all the world to see. There is much fear when someone is faced with seeing that they’re not really sick and that genetics can be controlled by what we eat and how we think. Here’s another video clearly explaining that genes are measured to turn “on” or “off” by themselves depending on how the body is treated. http://www.youtube.com/watch?v=mJkCiYnuVw0 The body produces mucus naturally if it’s being attacked by pollution. Have you ever thought CF as being a description of the body doing exactly what it should?
This is someones life you are referring to.You have taken an individual’s illness and used it to make a blog..entertainment for you. What kind of person are you? You are a very sick individual to have done so.You are not God!!! Where did you get your medical degree? Right, you don’t have one! You really need to think of how hurtful this is to this individual and their family and friends. YOU have no right speaking of this! Unbelievable…I am speechless and hold no respect for you!
Watch the videos in the letter written and the life you’re referring can be extended with the information that was enclosed. To ignore the healing information enclosed acts as the ultimate disrespect for life. Yes, the bad guy is the person who tries to help someone live longer and the good guys are the ones doing the poisoning. Makes sense? Not really! To think that people get insulted when you forward information that could help them and even offer to take the person into their home for a form of organic rehab…WOW! It doesn’t make any sense but it never does. As for the people with the medical degrees………here’s the results of their knowledge for their patients. http://www.youtube.com/watch?v=FPI7zdGdqo4 This video was made by a medical doctor about how medical degrees are designed to make sure people keep their diseases instead of curing them. I have had this blog and this view long before your topic came around and hey……..you approached me………I never approached you for the CF charity drive. Not everyone in this town is going to give their last cent to the medical industry, when their efforts never produce health in their patients. If you don’t like the blog, don’t read it or start your own blog about what you believe in. You can’t make the body healthy by hurting it and that unfortunately is how GOD works and how GOD designed your body. Disease names are nothing but descriptions of how the body breaks (and what part is breaking) when you don’t treat it well. As for you judging me, you must be confusing me with someone who cares about what other people think. That’s one of the things you may be missing. My personal beliefs count more than fitting in or I would have just given money to the guy who approached me for the CF charity. You don’t get to my position in life following the crowd, taking medications, getting surgeries, getting drunk or high on a Friday night or supporting charities that only make disease worse etc. If you want to be healthy, learn from healthy people. If you want your worst life take drugs and then take more drugs for the side effects. That’s the best advice I can give. Here’s a math question for you. If no one can work because they’re all sick, how long do you think a society lasts? What charity drive do you run when no one can get out of the hospital bed because every other charity drive told people to take drugs, cut themselves open and ignore eating healthy food? We’re all in this together except the healthy people can see all this as clear as day. I would rather die a thousand deaths than follow a blind allegiance to the forces, which make sure we accept our worst existence. That’s what I stand for. The days of hurting the body in an effort to make it run better are coming to an end. Millions of people believe in the same and we’re all proud to spread the same message.
I think you people should see the positive in what Jason is trying to do. He’s trying to help not put people down. The MS comment about the fish oils was very useful. My boyfriends father has MS and they gave him needles to take every morning. Unfortunately, he’s not improving, he’s not getting worse, but he’s not getting better. I want to thank you Jason for voicing your opinion and although some people don’t understand and have negative things to say about it, you may have helped many people just from one simple article. Keep doing what your doing and dont let people like that tear you down.
Jessica,
Thank you for the kind words. The positive energy in them helps me grow to become a better person. Thank you again and I am glad the information helped a bit.