Until all the cell phone towers and all the WiFi is dismantled, we will keep on seeing an increase in this disease state. Google "Microwave Sickness" for a clue. Find out when the first commercial cell phone network spread across the U.S.A. for a clue. Was it the same year that people in the U.S.A started to get "CFS"? Is it any wonder that Simon Wessely, with connections to the Military-Electronics-Industrial Complex, has tried to label both CFS and ES (electrosensitivity) as psychosomatic?
Thank you.I'm Italian and I have severe M.E since 2008.In my country the situation for patients of M.E is tragic.We are around 500.000 people.We have around 15 doctors,no hospitals,no clinics,no supports,no human right! HELP!
I can't thank you enough, Mr. King. It is voices like yours and media attention that we sorely need to bring attention to our plight.
I have been ill for over 20 years. I do what I can for advocacy, but the price is steep. I can barely look at the screen and type this note today, and I am doing it lying down in a dark room.
Thank you, Mr. King. We need your advocacy, and the advocacy of so many more well people. I am 35 years old, developed ME/CFS at the age of 28 in 2004, and have been bedridden since 2007. I'm fortunate in that I can afford to see Dr. Paul Cheney, and that's given me some improvement - enough to be able to read online and to type this message - but there's so much more of life that I'm missing out on.
What a great idea. I have been ill with ME/CFS for 34 years, and at this point have no faith at all in government agencies or the medical industry. It's the patients themselves and advocates on our behalf who are giving this horrible disease the attention it so badly deserves. Thank you so much for your efforts on behalf of all 17 million of us.
Thank you so much Mr. King! Celebrities with ME/cfs have been cowed by the terribbly damaging *stigma* foisted upon all sufferers and therefore this very prevalent, 'diabolical' illness has had no well known figures actively advocating for us! I'm so very appreciative you have given voice and your renown to a group of people the world over who have been intentionally forgotten, belittled, abused and walked over for over three decades!!
Thanks to everyone involved in this project. It's a great idea, and as a patient -- one of the 1,000,000+ people in the U.S. whose lives have been upended by this disease-- I really appreciate what you're doing. I hope the doctors, researchers, and government agencies pay attention.
Thank you <3
MelRos29 1 month ago
Until all the cell phone towers and all the WiFi is dismantled, we will keep on seeing an increase in this disease state. Google "Microwave Sickness" for a clue. Find out when the first commercial cell phone network spread across the U.S.A. for a clue. Was it the same year that people in the U.S.A started to get "CFS"? Is it any wonder that Simon Wessely, with connections to the Military-Electronics-Industrial Complex, has tried to label both CFS and ES (electrosensitivity) as psychosomatic?
prd34 1 month ago
The "c" is soft in "encephalomyelitis" - You can click on the speaker for that word in the Merriam-Webster Dictionary online.
Thank you Dr.s King and Enlander and Deborah Waroff. This is much appreciated and good luck if you get in the Ampligen trial, Deborah.
fogggygyrl 6 months ago 2
Thank you.I'm Italian and I have severe M.E since 2008.In my country the situation for patients of M.E is tragic.We are around 500.000 people.We have around 15 doctors,no hospitals,no clinics,no supports,no human right! HELP!
47lavi 6 months ago
I think a doctor would know how to say Encephalomyelitis properly.
I like the idea of Ampligen from what I've read.
But then Prednisolone makes me completely well, but I'm not allowed it, except in absolute crisis.
BritishSnail 8 months ago
Thanks
God bless
BritishSnail 8 months ago
Thank you Mr King, please keep going, we need people like you.
mecfssux 8 months ago
On the next video, could you please make sure that the interviewers are microphoned. I had trouble hearing the questions the doctor was answering.
Thank you. Great start.
BecomingVisible4ME 8 months ago
thank you mr. king dr englander............We need your advocacy, and the advocacy of so many more well people.
you are a HUGE....Hope to educate the ' normal world ' about these terrible diseases.
I have been sick 25yrs +
Great Blessing's
angelonduty100 8 months ago
King is a stud!!
justinreilly1 8 months ago
Thank you, Mr. King and Dr. Englander!!!
frenchtuli 8 months ago
I can't thank you enough, Mr. King. It is voices like yours and media attention that we sorely need to bring attention to our plight.
I have been ill for over 20 years. I do what I can for advocacy, but the price is steep. I can barely look at the screen and type this note today, and I am doing it lying down in a dark room.
salchar 8 months ago
Thank you, Mr. King. We need your advocacy, and the advocacy of so many more well people. I am 35 years old, developed ME/CFS at the age of 28 in 2004, and have been bedridden since 2007. I'm fortunate in that I can afford to see Dr. Paul Cheney, and that's given me some improvement - enough to be able to read online and to type this message - but there's so much more of life that I'm missing out on.
jocelmeow 8 months ago
What a great idea. I have been ill with ME/CFS for 34 years, and at this point have no faith at all in government agencies or the medical industry. It's the patients themselves and advocates on our behalf who are giving this horrible disease the attention it so badly deserves. Thank you so much for your efforts on behalf of all 17 million of us.
all2trueable 8 months ago
Thank you so much Mr. King! Celebrities with ME/cfs have been cowed by the terribbly damaging *stigma* foisted upon all sufferers and therefore this very prevalent, 'diabolical' illness has had no well known figures actively advocating for us! I'm so very appreciative you have given voice and your renown to a group of people the world over who have been intentionally forgotten, belittled, abused and walked over for over three decades!!
4rstriper 8 months ago
Thanks to everyone involved in this project. It's a great idea, and as a patient -- one of the 1,000,000+ people in the U.S. whose lives have been upended by this disease-- I really appreciate what you're doing. I hope the doctors, researchers, and government agencies pay attention.
ixchelkali 8 months ago
Mr King, you are my hero. Thank you for listening and taking to heart all our stories you we have shared. You are making an enormous difference.
tracyannceecee 8 months ago
Thank you Mr King and thank you Dr Enlander; please keep looking and investigating, researching and demanding questions - we have a right to answers!
athomeinRwanda 8 months ago
thank you so much for doing this! -- rivka
CFSDemo 8 months ago
how very wonderful!!! thank you speaking on behalf of millions around the world. xo
asimmonssnapp1 8 months ago