Added: 5 years ago
From: fosforitooo
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  • We have many specialised CFS videos on our channel - please do feel free to take a look and thanks for this great video

  • Their is a cure for CFS. But since technology is causing it, it's interferring with our hormones n our biorythms The diesease is most probably a reality

    of EM sensitivity to the wireless technologys They have advanced the tech of wireless knowing all along it harms our DNA. Information War

    n Science in the (Un)Natural Interest

    comes first. My government has covered up the facts concerning the harm of the non thermal technologyies of MW, RF and EM of the extremely low freq of wireless

  • UK is years behind the US in scientific research and in biomedical research in particular. The level of education here (I spent a few years working at schools) is extremely low. NO wonder that UK hasnt' produced scientists of a world class for many decades. All we have to do is hope for America to lead us and to do the pioneer work for us, and then to follow. When US tells others what to do we don't like it but in many areas it has all right to do it. By the way, I'm not American.

  • Read Explaining colours to a blind man. Not only will it enlighten many as to what living with a mental illness and chronic fatigue syndrome is like, it also gives comfort to those sufferers who think there is no hope and that they are alone. It is very informative, sometimes shocking but also very funny in parts. All in all, a good read and highly recommended.

  • dont trust the they are thye cause for our illness, they pretent to help us but they are the cause for our ailements! chemical treails, immunization shots full of mercury, flouride in the water, which causes cancer, poisons in the food, poisons in the candy, poisons in the prescription drugs! shame on you cdc, fema , and all of the other eugenic mongers. you will go to hell, for the many lives that you have taken!

  • chemtrails causes this illness

  • Thank you sooo much for pointing this out!

    I've been doing a lot of research since I suddenly got extremely exhausted two months ago, and I think you are right.

    Keep mentioning the CTs wherever you can. We need to create awareness for the cause, not the symptoms.

  • @bloodhive Is that a scientific analysis based on years of biomedical research? While I'm not going to state outright that you are incorrect (since no one could do such a thing, speaking from a strictly scientific point of view in which all possibilities are "kept on the table") it seems highly unlikely since people have been getting this illness for far more years than "chemtrails" have been around.

  • Thank you for the compliation. Do you have the source video or can you direct me to it.

    Thanks again,

    Posting on my CFIDS group.

    Marti

  • i think i took it from the CDC website...

  • Finally after all the time that people have been dealing with this, and the hypothalamus its so much more to it than doctors could even comprehend, finally this is getting recognition. Its just not been soon enough for all the ones who have taken there life from the hopelessness they feel. I hope things start changing real soon, because its been too long weve been going through this with no help or answers

  • look at the Polio Virus/ CFS link.......google it...

  • This is an excellent video!

    To all those with CFS/ME: look into antiviral medications! I've been on them for two months and I think I'm seeing some improvement. Many others with CFS/ME are also seeing improvement.

    Google: Montoya, CFS, valcyte, Stanford to learn more.

  • have you improved since taking the antivirals?

  • The lack of recognition is everywhere in the World, regardless of what the CDC or WHO say. The country with more recognition is the UK and still patients suffer similar situations to all of us in other countries.

  • great video.Very important. In Spain NOBODY was aware the CDC declared CFS OFFICIALYY an aillness.Society and health professionals NEED to know that this is really a very disbling illness.

  • great video.Very important. In Spain NOBODY was aware the CDC declared CFS OFFICIALYY an aillness.Society and health professionals NEED to know that this is really a very disbling illness.

  • Well, I want to give a positive hope for everybody, because I was diagnosed with CFS after an EBV infection, and after 2 years, finally I am starting to have a "normal" life, I can work, and even do some sports without falling sick. My EBV is negative now, and my IgG became low after a treatmen with Zeitrex for 14 days, and now my main problem is my intestine,I have parasites that were just discovered and i will treat them with antibiotics...

  • Really good video. I'm glad the awareness is growing. It took me years to get diagnosed so, although I've had improvement, I don't really expect a cure.

  • Awesome, I really envy you in the US - one hear a lot about your country, with war and everything which clouds the good things, such as this. We don't have any of this in Sweden. A small group of doctors all over the country, but that's it. No one is guiding either patients nore doctors, nore government.

  • Now if we can only get the doctors to be willing to test for and diagnose this when a patient shows syptoms!

  • Why, if they can do this in the States, is it not happening in Britain? Why when this clearly says that the debate over ME/CFS being psychological should be over - do the NICE guidelines focus precisely on it as a psychological problem?

    Love to all,

    Joss

  • Excellent! Good to here that there is an awareness campaign going on in the US, and that the US oficials spent 4 million $ on this campaign, through TV, Press, Magazines... and another 4 million$ for research for treatment and causes... This is s very severe illness, but there is hope, and people should know, is not as severe for everybody, and is not true that is for the rest of your life, depends on each person...

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