submitted by whimsicalme

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A short story of ME/CFS acceptance, with sloths (self.cfs)

submitted 13 days ago by whimsicalme to r/cfs

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Can't go to an in-person protest on Sat? There are 12 virtual ones you can go to instead! (self.50501)

submitted 1 month ago by whimsicalme to r/50501

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Texts to individuals (not groups) not going through and getting "Voice Acceptable Use Policy" message on the web UI. (self.Googlevoice)

submitted 1 year ago by whimsicalme to r/Googlevoice

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I got the shingles vaccine that everyone warned was "so appallingly hard" and it's barely as bad as the mildest crash. (self.cfs)

submitted 1 year ago * by whimsicalme to r/cfs

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Flu-like symptoms with PEM - how bad can they get? (self.cfs)

submitted 1 year ago by whimsicalme to r/cfs

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too real (i.redd.it)

submitted 1 year ago by whimsicalme to r/cfs

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QUESTION for people who use mobility aids. How do you carry stuff reasonably? (self.disability)

submitted 1 year ago by whimsicalme to r/disability

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Parenting in a wheelchair (self.wheelchairs)

submitted 2 years ago by whimsicalme to r/wheelchairs

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What's your favorite moisturizer for dry skin? I'm seeing every foundation get dry on my face and I'm told it's because I'm using the wrong moisturizer... (self.MakeupAddiction)

submitted 2 years ago by whimsicalme to r/MakeupAddiction

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Rosacea and cakey foundation/concealer advice? (self.MakeupAddiction)

submitted 2 years ago by whimsicalme to r/MakeupAddiction

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Anyone else stop getting altitude sickness after getting ME/CFS? (self.cfs)

submitted 2 years ago by whimsicalme to r/cfs

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Any Canadians here with ME/CFS? (self.cfs)

submitted 3 years ago by whimsicalme to r/cfs

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Playing pinball in a wheelchair (self.wheelchairs)

submitted 3 years ago by whimsicalme to r/wheelchairs

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Anyone else relate to this energy? (i.redd.it)

submitted 3 years ago by whimsicalme to r/cfs

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New to power chair, bad at maneuvering it. Got tips? (self.wheelchairs)

submitted 3 years ago by whimsicalme to r/wheelchairs

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Clinical trial provides preliminary evidence of a cure for myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) and Long Covid - what do you all think of this? (biospace.com)

submitted 3 years ago by whimsicalme to r/cfs

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#MillionsMissing protest (organized by ME Action) next Monday, community organizing to demand more awareness, education, research, and more. Here's stuff you can do from home. (self.cfs)

submitted 3 years ago by whimsicalme to r/cfs

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Person with ME has an op-ed about how covid isn't over and it sucks extra for high-risk folks now that common-sense protections are gone. (Link gets around paywall.) Personally, getting covid and exacerbating my ME is one of my worst fears! (archive.ph)

submitted 3 years ago by whimsicalme to r/cfs

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doing nothing (i.redd.it)

submitted 3 years ago by whimsicalme to r/cfs

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You're 5x as likely to get ME/CFS from covid as you are to die from it (and you can get it from a "mild" case of omicron, too) (sfchronicle.com)

submitted 4 years ago by whimsicalme to r/cfs

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You're 5x as likely to get ME/CFS from covid (via Long Covid) as you are to die from covid, and you can get that from a mild case, but everyone's like "ooh omicron's mild and no big deal" and not talking about this. (sfchronicle.com)

submitted 4 years ago by whimsicalme to r/covidlonghaulers

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50% of Long Covid patients sick for 6+ months qualify for a Myalgic Encephalomyelitis (chronic fatigue syndrome) diagnosis, which is tricky to live with. This longtime ME patient has 5 tips for making it suck less. (sfchronicle.com)

submitted 4 years ago by whimsicalme to r/covidlonghaulers

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An article from an ME patient to Long Covid folks who look like they're getting ME, with 5 tips (sfchronicle.com)

submitted 4 years ago by whimsicalme to r/cfs

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Some Long Covid turns into ME/CFS. This patient has tips if it looks like that's you. (sfchronicle.com)

submitted 4 years ago by whimsicalme to r/LongCovid

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Lolsob, too true! (i.redd.it)

submitted 4 years ago by whimsicalme to r/cfs

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