Myalgic Encephalomyelitis is caused by a virus, strongly thought to be an enterovirus as this is what history shows. M.E. has a sudden onset not gradual. There have been over 60 outbreaks of ME worldwide since 1934. So YES the public need to know as it's just as contagious and serious as polio. If you dont recover within a few weeks or a few months you have it for life. People have had it for 50yrs. It ruins your life and no one is immune. People also need to know that M.E. is not CFS.
This is a fantastic video!. If only those who dont believe in M.E could live with it for a month then all would believe in a day or even an hour!!. M.E is a living hell. Peace to all fellow sufferers.
I like how you portray both the pain and helplessness of ME, having dysautonomia myself, after a car accident my 3-year old and I were in 3 yrs ago. You are also a strong and talented person. Keep the info coming; especially, describing specific complaints and/or a list ~ one day, a patient is going to complain about something that places a 'click' in the researcher's ear....I believe that ME and dysautonomia have lots in common. God Bless You.
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spacedreams2111 6 months ago
Myalgic Encephalomyelitis is caused by a virus, strongly thought to be an enterovirus as this is what history shows. M.E. has a sudden onset not gradual. There have been over 60 outbreaks of ME worldwide since 1934. So YES the public need to know as it's just as contagious and serious as polio. If you dont recover within a few weeks or a few months you have it for life. People have had it for 50yrs. It ruins your life and no one is immune. People also need to know that M.E. is not CFS.
SeraphinaRaine 9 months ago
Kings College London.
Cured me........well they got my CFS to a place where my life is enjoyable again. 4 years it took to get back to 'normal'.....
Jaffa1311 1 year ago
Is it always an infection that starts it?
People should open their eyes, society needs to understand.
lifegiving09 2 years ago
This is a fantastic video!. If only those who dont believe in M.E could live with it for a month then all would believe in a day or even an hour!!. M.E is a living hell. Peace to all fellow sufferers.
LUCAX651 2 years ago
IT IS FRUSTRATION to the Max..!!
karmakomodia 2 years ago
Thank you to all involved in producing this excellent video!!
Every nation needs to adopt the Canadian Government's Definition- it is 100% accurate and dispells the illusion of random tiredness.
justinreilly1 2 years ago
I like how you portray both the pain and helplessness of ME, having dysautonomia myself, after a car accident my 3-year old and I were in 3 yrs ago. You are also a strong and talented person. Keep the info coming; especially, describing specific complaints and/or a list ~ one day, a patient is going to complain about something that places a 'click' in the researcher's ear....I believe that ME and dysautonomia have lots in common. God Bless You.
DysautonomiaMD 2 years ago 2