Young Man with Severe ME can barely function
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Ben,
You are not alone! I am pulling for you, and others who also have cfs. Your video will surely help the powers that be to fund research to find a cure. Have strength, young man, you are an inspiration to others!!!!!
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ben, you ROCK!! this is an amazing piece! -- rivka
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6:23
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This was by far the best American local news piece I've ever seen on ME/CFIDS (I've seen dozens). Thank you so much WHAM and Ben for telling it like it is. CDC changed the name from ME to CFS as part of their war on ME patients and science.
justinreilly1 9 months ago 3
Good for you to do this video dont give up. thank you for sharing your story, helps to dispel the horrid ignorance . I hope you regain some health, if you have energy /desire to do so, you might want to consider doing some drawings for art4xmrv [all proceeds from sales go to whittemore peterson research,you keep the original work but the image[s] are made into cards/prints. I know yo barely have strength to eat,brush hair etc [can tell from video] but its a thought for better days. bless you
jessical1969 6 months ago