M.E. on Australian Television
Loading...
Loading...
1,736
Loading...
7:48
A short CFS documentaryby DiamonDie29,303 views- 6:17
How does Myalgic Encephalomyelitis affect my life?by AHummingbirdsGuide26,412 views
- 6:41
How ME effects meby patrick3235784 views
- 2:02
How has Chronic Fatigue Syndrome affected your working life?by mecfsaustralia1,688 views
- 9:40
Flouride Aspartame, and Agenda21by srsilent00112,895 views
- 6:32
The Lightning Process on TV!by jerichopenguin13,679 views
- 2:16
A Big Fat NO from The Prime Minister ME/CFSby Elfins1,387 views
- 5:44
WHO's Right? ME is neurological not psychiatric - pt2by GBCTwo320 views
- 1:10
Lightning Process - former rugby international Austin Healeyby ukeft8,248 views
- 4:53
Lightning Process - Phil Parker - Jess's recovery from ME/CFS PVS using The Lightning Processby thephilparker1,350 views
- 3:25
Why 'CFS' is a wastebasket diagnosisby AHummingbirdsGuide6,970 views
- 5:55
CDC Coverup of 'CFS': *MUST WATCH VIDEO* (2 of 2)by thx1138mindlock2,894 views
- 9:07
I Remember Me - Chronic Fatigue Syndrome CFS 3 of 9by ncf12,569 views
- 5:52
WHAT ABOUT ME? New Documentary about the illness M.E. (Myalgic encephalomyelitisby doubledmedocs9,180 views
- 4:54
Toby Hall, CEO Mission Australia on a Human Rights Charterby IsaiahOneAustralia198 views
- 10:52
Symptoms of Chronic Fatigue / ME & Fibromyalgia Explainedby mtyrsi7772,242 views
- 2:36
Chronic Pain, PTSD and CFSby emofree25,526 views
- 1:45
Lee Mack - Sign Languageby ComedyDVDCentral27,700 views
- 3:23
If Onlyby cslangman38,150 views
- 0:25
ME patient blood ban protest - London 1st November 2010 (part 2)by GBCTwo673 views
Subscribed!
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 10 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