Part 1 of 3 - M.E. / CFS (Chronic Fatigue Syndrome) Living with M.E. / CFS
Andrea Martell and http://www.BlueRibbonCampaignForME.org are making people aware of CFS/ M.E. (Chronic Fatigue Syndrome). In this ‘Just Cause; video, Andrea explains what it is like living with ME / CFS.
Also find Andrea & Blue Ribbon Campaign via Twitter:
Andrea:
http://twitter.com/Killandra
Blue Ribbon Campaign:
http://twitter.com/blueribbons4ME
To see all three videos via our website, you may visit: http://www.thejayandjuggyshow.tv/just-causes-videos.html
Duration : 0:6:29
Overcome Chronic Fatigue Syndrome with The Best-Selling Natural Energy and Mood Support Supplement on the Market. For the latest health news and information Follow Us on Twitter.
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July 30th, 2009 at 6:26 am
Thx, fogggygyrl. I …
Thx, fogggygyrl. I appreciate your kind words. I just hope that the vids we produced will cause the awareness needed to get things rolling for you and all with CFS.
July 30th, 2009 at 6:26 am
Jason, your comment …
Jason, your comment that you want to help our movement brings tears to my eyes. Thank you so much!
I can relate to your first caller. I used to sleep through my classes in college when my ME was mild. Now I’m mostly bedridden. When I can get out briefly and I see my neighbors they’ve let me know that they understand my situation. I’m really lucky to have neighbors like that. I hope they don’t move.
July 30th, 2009 at 6:26 am
Yea. Thanks for …
Yea. Thanks for the advice.
July 30th, 2009 at 6:26 am
That really sux, …
That really sux, ryanmc353. You guys should sue the pharmicutical company that makes the tablet. I usually do not encourage that kind of thing but given all the poisons they promote I say go for it.
July 30th, 2009 at 6:26 am
Yea… too late now …
Yea… too late now tho … hes blind in 1 eye
July 30th, 2009 at 6:26 am
Well that sucks. If …
Well that sucks. If he is taking something that is affecting his eye sight, he should defintely stop taking it! I am not a doctor but I know that is a serous side effect.
July 30th, 2009 at 6:26 am
My dad has M.E. He …
My dad has M.E. He used to be dying with pain in his legs and its something to do with his nerve endings or something. But then he got a tablet and now he’s ok..but its affected his sight ;/
July 30th, 2009 at 6:26 am
Read Explaining …
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.
July 30th, 2009 at 6:26 am
no problem at all. …
no problem at all. I was totally in the dark about it until Andrea approached me. Now I understand that some need help with the movement. We are doing what we can to help :-). By all means, if you want to post your vids to ours please go right ahead!
July 30th, 2009 at 6:26 am
I am honored that …
I am honored that you posted this as a video response to my video and would like to thank you personally for helping to raise awareness! This is such an important thing for everyone affected. The only way for us to escape the stigma attached to having such a misunderstood disease is to educate people. Again, from the bottom of my heart, I thank you. Teri