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  • @PediongYu89 Me too.. I have skin problem for about 19months now.. My blisters started on my arm and spread to my upper back and then to my face.. 3 dermatologist were unable to help me.. But when I tried this acne solution program, it has done wonders. It heals my skin quickly and my face looks better than it has in the past 12months. Anyway, here's the acne solution site, StopAcneNow.co.cc

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  • When people say things like, I have lyme disease- it isn't a big deal- they are totally and completely ignorant of how the human body works. A disease does not act in the same way to everyone. Yes, many people get lyme disease and it isn't a big deal. For some, it ends their life. Start understanding that having a disease doesn't put everyone in the same category. There are different levels of every pathology because every body is different.

  • @truthmovement this is so true

  • Lyme has destroyed my ability to earn an income. destroyed my marriage and family. we are all still under the same roof but the anger and pain is felt by all.

    Getting a negative test return 3 years ago and agreeing with it is the worse thing i could do. now i have glasses, numb face, work hard to walk straight, mumble my words when im just a bit tired. Have Tonsilitis and got some meds. Im going to work for more meds tomorrow as it seems to have taken away some of my symptoms.

  • Hopefully, this documentary and others like it that show how our governing bodies are stacking the cards against us with special interest groups and quid pro quo with most if not all bureaucracies. We are conditioned to think that our government, physicians and academia all have our backs and it just is not true.There is hope, though. We still have a power as a people if we would just wake up and smell the propaganda, rhetoric and distractions. We can be the change we want to see in the world

  • I have lyme...it has destroyed my early adult years and from personal experience in late stage is outrageously painful and debilitating. watching this video is my story again and again. it is a double edge on this subject because A its nice to know im not alone in this story and B sad that I am not alone...If its anything Ive

  • learned with this disease is to continue to strive for awareness no matter how disheartening so that one day it wont happen again to anyone else. As I say to all those who dont have it "trust me, you do NOT want to be here."

  • @LS1toSVT It's not a big deal?...... My life is a living hell because of that damn illness! I can't do half the things I could have done before!! I had to give up so much! My sports, my academics, my social life, my family! All of it! I spend most of my days in bed either sleeping or crying my eyes out cause I just can't get up. When you say it's not a big deal... SPEAK FOR YOUR OWN DAMN SELF! Cause for me, it's everything. It controls everything.

  • @EasySilence64 You have to remember. lots of people troll these comments. But it doesn't matter. I feel your pain and life sucks sometimes for us but dont let trolls upset u. that is their goal.

  • @LS1toSVT It hasn't hit you hard, that's a good thing you're lucky. I've ended up being like that blonde girl with muscle twitching and rigidity. However after treatment and that hard journey I'm better. I don't know if I still have it as I need to retest but I feel great. I took Venus Fly Trap Extract, Cat's Clay and BurBur.

  • My doctor said I am not negative. Well, numb hands, feet, arms, legs, memory loss, severe jaw pain, emotional problems (cry for no reason) very low energy, kept having to sleep, felt like I could not research much longer. I kept talking to myself "What am I going to do?". I told myself, persist, keep lookingon internet, never give in, have faith, persist! I did, and eventually I found out about lyme disease. I remembered the 30+ ticks I had on leggings after my jog in wood, I'd just pick um off

  • @Catherine8raw I had never heard of this disease till tonight. Oh my god it sounds like a living hell. Please never stop searching for a cure. If it came from a tick then it's not man made like AIDS might be. I hope you stay strong. I'll always be thinking of the victims of this.

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  • If you have severe lyme, I have found that fats seem to help. Read a book on Chronic fatigue (50 cases) book, it has success stories, so many are stopping their low fat diet. In lyme the nerves and brain are under attack, the most fattiest parts. Fats have antimicrobial properties, help yourself, eat more fats, like butter/cream, lamb fats, beef fats, becareful you don't take harsh herbs if your vulnerable, lapacho will not hurt, herbs for liver fine. Vitamin C good, psysium husks for colon.

  • We have to help ourselves now. Communicate with lyme patients, buy every book on the subject, lyme solutions, lyme diet, and Connie S. books. Listen to patients. I am still walking, 16 months later on no antibiotics. I am less scared. I have saturated myself with the reality of lyme. It is a stradegy, but we have to fight it like people fight AIDS, like people fight cancer. We rely to much on doctors, we need to take responsibilty, our family/freinds need to research, if we can't.Don't give in

  • I think the patients can be as silly as the doctors... I have seen patients still eating sugar, potato, starchy foods which feeds the bacteria! Most patients I have leard that get anywhere are telling me they are eating lean meat and vegetables. I only got success on a low carb diet, low starchy vegetables, olive oil, or fatiest meat and low starchy vegetables, but fruit, starchy food messed me up! I find teasel root (herb) and Lapacho, milk thistle - burdock root very helpful.

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  • Well, do your "doctors" just buy their titles in the US? In other countries you diagnose and treat this relatively common disease rather quickly. But if you mix incompetent doctors with people with no knowledge about the disease, of course you will have a serious problem.

  • This video made me realise how serious it is, I had no idea...

  • where can we watch the whole documentary?

  • All these Doctors should get their licenses revoked for closing their eyes.

  • I'm sharing this because people close to me have the disease and Nobody talks about the severity of it. I guess it's just to controversial for some. But people need to be informed of the truth.

  • A good eye opener....

  • PLEASE PLEASE PLEASE do internet research on using SEA SALT for curing Lyme. I had it for seven months before I was diagnosed, and doxycycline only made me sicker. I took a shot of about 1/2 teaspoon of RAW SEA SALT in a small amount of water, and in only hours I felt better than I had in months! I continued this maybe three times a day for several days and it ended my Lyme. I take this "shot" every now and then just to be sure it stays gone. IT WORKS. DO RESEARCH. TELL THE PEOPLE!!

  • I have chronic late stage lyme disease I suffered from the end of 2001 till 2008 with being told its in my head im not sick had it not been for diagnoisis unknown with Dr , Raxlen and Jacklyn spars story I would have never put the puzzle together i have been on IV antibotics for a little over a year and i struggle day to day on the simple things but im not bed bound as I was over a year ago Judy Weeg is my angel she found me help in 08 and when that doctor refused more treatment she fought for

  • great documentary....undeniably makes the case....A+.....may the truth prevail

  • As a Chronic Lyme patient who suffered 15 yrs at the hands of Drs., I highly recommend the ILADS guidelines for testing. They have unbiased research to back up their info, and they saved my life.

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  • What a great documentary!! It's so importent that this film should be shown over the whole world.. It's importent for everyone!!!! Because Lyme diseases is a living HELL!!!

  • What we really need to do is team up, research, collect information from patients who have successfully treated themselves, i.e. many via herbs like Teasel root, meat & vegetable diets, alkaline diet, NAET, high fat, low carb diet (High fat diet = cure 4 TB when antibiotics were not available in the 1930-1940s). Thank you to those who write books, those who speak up, write websites/blogs and educate us when we have NO DOCTOR! Most doctors have limited toxic medicines anyway! Seek & you'll find.

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  • This film should be shown in every educational institution, by all MD's and health care practitioners, by colleges and universities, and in all libraries. More people need to write Oprah and tell her about this film.

  • The Doctors that tell you it's all in your head are not mistaken, THEY ARE LIARS! They know exactly what they're saying. THEY JUST DON'T CARE! They are ELITIST BASTARDS. Excuse my French.

  • Amen to that.

  • Yeah fuck these rich cunts! The government created aids and lyme disease (and many others) they don't give a fuck about you or your family. Eugenicists will rot in hell for the suffering they have caused of the innocents.

  • I don't agree. My doctor is completely blind to the whole thing. Most doctors when they go home, do not read long and hard in journals or keep upto date with disease and diagnosis, they should have better checks with their knowledge!!! The thing is with lyme patients most look fine, the Doctor doesn't feel or see the numbness, ataxia, memory loss. Lyme is a gr8 immitator and the burning pains could be other things. Alot of doctors are ignorant and have little medicine that is effective!

  • The best documentary of the year!

  • Isn't is awesome! I've already watched it 6 or 7 times! The documentary really shows just how hostile and crooked the IDSA Lyme Panel members are. I don't think they ever admit to the truth because it's all tied in to biological warfare and they don't want us to get well.

  • Awesome - a must see for everyone!

  • Great Film! I wish I could show it to everyone.

  • best documentary of the year!!!

  • FUI CURADA(((OBRIGADA SENHOR!!!)))

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