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Tag: pain management doctor

Shit Doctors Say

Doctors can say the most awful things to chronic pain patients. Continue reading “Shit Doctors Say” →

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October 7, 2014March 9, 2017

Vicki60 Comments

ABOUT ME

Hi! I'm Vicki. My blog is called "Miss Diagnoses" because I have too many diagnoses and because my Lyme disease was misdiagnosed for many years.
In addition to being a professional patient and spoonie, I'm a compulsive reader and doodler. Sadly, my writing and drawing are limited by repetitive-strain injury and hand neuropathy; I use assistive technology, but I can't post as often as I'd like. You can find me on Twitter, Instagram, Facebook, Pinterest, and I have two short cartoon videos on YouTube.
Twitter and Instagram: @miss_diagnoses
Facebook, Pinterest, and YouTube: @MissDiagnoses

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Categories

Allergic Contact Dermatitis
Awareness Month
brain fog
Brain Fog Posts
Chemical Sensitivities
Chronic Illness
Difficult Relatives of Spoonies
Disability Rights
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Food Allergies
Hashimoto's Thyroiditis
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Recent Posts

Difficult Relatives of Spoonies, Part Three December 22, 2019
Difficult Relatives of Spoonies, Part Two November 27, 2019
Interviews with The Mighty.com and RawlsMD.com September 26, 2019
Spoonie Artist Guest Post: Kat Woods (@hopehealcook on Instagram) May 21, 2019
Spoonie Artist Guest Post: Bethany@lymelifecomics May 20, 2019
Spoonie Guest Artist:Yulia Greyman (@FunWithCFS on YouTube) May 12, 2019
Lymie Movie Classics, Part One May 8, 2019
Spoonie Guest Artist: Jennifer Bialk Scott May 3, 2019
The Spoonie Awards (Because We All Deserve a Medal), Part Two April 27, 2019
The Spoonie Awards (Because We All Deserve a Medal): Part One March 30, 2019

I’m on Facebook! Come visit.💚

I’m on Facebook! Come visit.💚

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These are my #topnine2019. I didn’t get as many done as I wanted to in 2019 because of my tendinitis, back injuries, a horrific breakup, and a lot of family issues. It’s very frustrating to not be able to do cartoons about illness because you’re too ill! 🤣 I’m hoping 2020 will be better, although I had a dream that 2020 would be really bad for me but 2021 would be beautiful. Weird! Then again I took a lot of CBD oil before bed that night. Happy New Year everyone and I hope 2020 will be a great year for you. I’m slowly catching up so I will be getting back to doing my regular posts and putting out my artist guest posts. (To the three brilliant artists whose guest posts I haven’t finished, I haven’t forgotten—there’s just been a LOT of stuff going on!) Happy New Year from my sofa where I am peacefully avoiding drunken partiers, yay! #lymedisease #lyme #lymewarrior #lymediseaseawareness #lymedontkillmyvibe #spoonie #spoonielife #spoonieart #missdiagnoses #allergies #mcas

Sending strength and hugs to my food allergy peeps for the holidays—may you all survive your families, lol...”Difficult Relatives of Spoonies, Part Three—link in bio. #lyme #lymedisease #glutenfree #dairyfree #allergies #mecfs #lymehumor #spoonie #missdiagnoses #spoonieart #spoonieartist #lymesucks #lymewarrior #mastcellactivationsyndrome #mcas #foodallergies #foodallergy #foodallergylife #allergyfriendly #mecfswarrior #myalgicencephalomyelitis #lymediseaseawareness #lymedontkillmyvibe #spooniecartoon #lymelife #spoonielife #spoonieproblems #medicalhumor

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