Absolutely gutted by this piece by - I was def guilty of thinking CFS wasn't so serious due to the name: wapo.st/1IfofmH
Collection Tweets
Journalists ME/CFS
By Bob Bob @bobbobme
This is a list of tweets by journalists re Brian Vastag's blog about ME/CFS. You can 'favorite' and 'retweet' them to show appreciation.
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RT : Please read my friend 's heartbreaking appeal to the NIH to fund ME research: lastwordonnothing.com/2015/07/14/dea
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Heartfelt plea from former WashPo writer to NIH director: time to fund research for disease that disables thousands lastwordonnothing.com/2015/07/14/dea
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A poignant skewering of for its handling of disabling, orphan illnesses. lastwordonnothing.com/2015/07/14/dea
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3yrs ago, a sudden fever struck a veteran science writer - still sick, he presents an opportunity to NIH ow.ly/PENxm
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A must-read: I’m disabled. Can NIH spare a few dimes? wpo.st/BFJR0
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I’m disabled. Can NIH spare a few dimes? wapo.st/1Js2db5
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"It received $5 million in 2014, less than hay fever, which cripples no one. That’s not enough money to equip a lab...for a year."
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"On the list of illnesses the NIH studies, ME (listed as “ME/CFS”) is near the bottom in funding, ranked 231 out of 244."
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Former WaPo sci journo , stricken with ME, writes open letter to NIH director: Can NIH spare a few dimes? wpo.st/j7NR0
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My friend writes open letter to NIH asking for $ for myalgic encephalomyelitis research washingtonpost.com/news/to-your-h
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Very moving open letter to from the brilliant : "I'm disabled. Can NIH spare a few dimes?" wapo.st/1CRV8DB
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important piece by on living w. chronic myalgic encephomyelitis and dearth of NIH funding for it. lastwordonnothing.com/2015/07/14/dea
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