The video aims to help the friends and family of ME/CFS (including Myalgic Encephalomyelitis (M.E.), Chronic Fatigue Syndrome (CFS), and Post Viral Fatigue Syndrome) sufferers understand the illnes...
The video aims to help the friends and family of ME/CFS (including Myalgic Encephalomyelitis (M.E.), Chronic Fatigue Syndrome (CFS), and Post Viral Fatigue Syndrome) sufferers understand the illness and what their loved ones are going through. To view a clearer, larger version of the video, visit: http://www.sleepydust.net/me-cfs-chro...
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When I first got the disease I was not able to walk for 5 minutes. I almost slept all day and only came out for food. I had headaches, and oh so many muscle aches. You know what muscles are when you feel this. I've had cognitive behavioral therapy with physical training. Currently using extra vitamine b12 (intramusculair injections) , multivitamines and folic acid. I highly recommend it.
God bless all of you. Do your medical tests show nothing? Liver, thyroid, anything? I hope that one day you'll all be freed to live healthy lives. And may those around you give you the love and understanding we all need.
I don't, nor any of the people I know have this kind of illness, but I can immagine how it must be to be exchaused all the time.... I know how horrible borring / unsocial you feel when your not out with friends because your tired.. beeing like that each day would be a nightmare..
I'll add this to my favorites, might not be much, but maybe someone by a chance comes across the video and "opens" their eyes. 1 here, 1 there, it's all that matters.
I used to be an extremely optimistic and energetic 7 year old. Then i caught some really strange virus. I was hospitalized for 3 months with mono-like symptoms. I was never the same. I show ALL of the said symptoms. I almost certain it's post-viral fatigue. Thanks for the vid. At least i'm not alone.
i cannot thank you enough! The tears i have shed during this video have enlightened me to get as many friends and family to watch this! I am lacking so badly in support, i feel i can't go on like this, but with your help and this fantastic video, my hope has been reignited. Many many many kind thanks to you for taking the time to create this! For all other sufferers, you have my love and respect. For all those who know someone who suffers and supports them, thank you from the bottom of my heart!
My family wouldn't even spend 10 minutes of their healthy lives to watch this!!! Don't wait for your family to accept or change, just concentrate on getting well again!! I am far from healthy but MUCH less disabled than I was 6 years ago, and I'm not giving up!
Autoshare makes certain YouTube activities public on the services you choose. Select only the services you are comfortable with - like Facebook, Twitter, or Google Reader - to let your friends know what you like on YouTube. You can turn Autoshare off at any time.
I've had cognitive behavioral therapy with physical training. Currently using extra vitamine b12 (intramusculair injections) , multivitamines and folic acid. I highly recommend it.
I hope that one day you'll all be freed to live healthy lives. And may those around you give you the love and understanding we all need.
I don't, nor any of the people I know have this kind of illness, but I can immagine how it must be to be exchaused all the time.... I know how horrible borring / unsocial you feel when your not out with friends because your tired.. beeing like that each day would be a nightmare..
I'll add this to my favorites, might not be much, but maybe someone by a chance comes across the video and "opens" their eyes. 1 here, 1 there, it's all that matters.
Thanks for remind us others...
I am far from healthy but MUCH less disabled than I was 6 years ago, and I'm not giving up!