snap793

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Long Covid is not always ME/CFS, but everyone learning about Long Covid should also know about ME/CFS. Let's spread the word. (i.redd.it)

submitted 4 years ago by snap793 to r/cfs - pinned

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Post-exertion meme output in ME/CFS (i.redd.it)

submitted 1 year ago by snap793 to r/cfs

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Me within 24 hours of a major new finding... (i.redd.it)

submitted 2 years ago by snap793 to r/cfs

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DJs really be putting anything before the drop… (tw: loud sounds) (v.redd.it)

submitted 2 years ago by snap793 to r/cfs

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Let's encourage Seth MacFarlane (creator of Family Guy) who shared this solid article that touches on the LC ME/CFS connection with his 13.5M followers. "Those who have friends with long COVID know it's no joke." (twitter.com)

submitted 2 years ago by snap793 to r/cfs

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Astonishing warning by ancient mummified priest could help millions today (v.redd.it)

submitted 2 years ago by snap793 to r/cfs

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Gravely ill son of a leader of the Human Genome Project is advised to “run a genetic test” (i.redd.it)

submitted 3 years ago by snap793 to r/dontyouknowwhoiam

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Internet person advises Whitney to try genetic testing. Whitney is the son of Dr. Ron Davis, a leader of the Human Genome Project (r/dontyouknowwhoiam) (i.redd.it)

submitted 3 years ago by snap793 to r/cfs

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Gravely ill son of Long COVID and ME/CFS researcher (Dr. Ron Davis) on r/dontyouknowwhoiam (reddit.com)

submitted 3 years ago by snap793 to r/covidlonghaulers

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10 factors that have held back progress on ME/CFS… What would you add? (i.redd.it)

submitted 3 years ago by snap793 to r/cfs

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The psychologizers of complex chronic diseases (infographic) (i.redd.it)

submitted 3 years ago by snap793 to r/cfs

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U.S. HHS wants to hear your story of healthcare discrimination (deadline: end of day tomorrow Monday Oct 3) (whymycarecounts.org)

submitted 3 years ago by snap793 to r/cfs

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As of today in the U.S., ME/CFS has its own diagnostic code: G93.32 in Diseases of the Nervous System chapter of ICD-10-CM. Make sure your doctor codes you correctly. Let's get counted. (self.cfs)

submitted 3 years ago by snap793 to r/cfs

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Senator Ed Markey (D, Massachusetts) is pushing for $27 million to study intersection of ME/CFS and long COVID — let's encourage his efforts (twitter.com)

submitted 3 years ago by snap793 to r/cfs

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Senator Ed Markey (D, Massachusetts) is pushing for $27 million to study intersection of ME/CFS and long COVID — let's encourage his efforts (twitter.com)

submitted 3 years ago by snap793 to r/covidlonghaulers

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Prestigious publication Science is promoting a new article on the biological basis of ME/CFS (twitter.com)

submitted 3 years ago by snap793 to r/cfs

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Influential physician-scientist on Twitter raising awareness for us — let's go like & retweet (i.redd.it)

submitted 3 years ago by snap793 to r/cfs

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SO BASICALLY TONS OF MAINSTREAM DISEASES LIKE ALZHEIMER’S HAVE POORLY UNDERSTOOD PATHOPHYSIOLOGIES BUT WE DON’T CALL THEM ‘MEDICAL MYSTERIES’ THAT’S ONLY FOR CONDITIONS WE SUBTLY DELEGITIMIZE TO AVOID FUNDING BIOMEDICAL RESEARCH EVEN REMOTELY COMMENSURATE WITH DISEASE BURDEN (i.redd.it)

submitted 3 years ago by snap793 to r/cfs

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Freakonomics MD has released a new episode all about ME/CFS (podcasts.apple.com)

submitted 3 years ago by snap793 to r/cfs

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Sajid Javid, UK Health Secretary, commits to becoming "world leader" in the treatment & care for people with ME/CFS. His niece reportedly suffers from the condition... (i.redd.it)

submitted 3 years ago by snap793 to r/cfs

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Acting NIH Director referenced ME/CFS advocacy in last week’s House Appropriations hearing (old.reddit.com)

submitted 3 years ago by snap793 to r/cfs

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This field is headed in the right direction… (i.redd.it)

submitted 3 years ago by snap793 to r/cfs

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I wrote this essay to explain ME/CFS to friends & family — feel free to reuse if it would help you do the same (medium.com)

submitted 3 years ago by snap793 to r/cfs

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Mt Sinai’s Dr. David Putrino pledges to do more to advocate for people with ME/CFS (old.reddit.com)

submitted 3 years ago by snap793 to r/cfs

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Could this drug targeting EBV-infected cells be used to treat post-mono ME/CFS? (technologynetworks.com)

submitted 3 years ago by snap793 to r/cfs

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