I am able to enternew situationswithout fear ofdebilitating anxiety,embarrassment,harassment, orviolence. I've used the term"crazy" or "insane" inconversationas a synonymfor busy, wild,extreme, confusing,evil.I've never hadanyonequestionwhether Ishould/can be aparent.I've assumeda disabilitymeanssomeonesuffers.I've askedsomeonechronically ill,"Have you tried . .. " (yoga,meditation, etc.)When I say that I amtired, overwhelmed, orin pain, people don'tconstantly tell me thatI'm lying, makingexcuses, faking,exaggerating, beingmanipulative, or beinglazy.My type of body orbrain is not used as ametaphor forbrokenness,awfulness,mediocrity, orignoranceMy and mycommunity’s access toand quality ofhealthcare isn’t rankedthe lowest in thecountry, despite higherrates of disability andthe existenceof a treaty.I've used the termblind, depressed,OCD, or barren asa joke or tonegativelyrepresentsomething.I see people with myphysical andcognitive disabilitiesand/or mentalillnesses in mediaand popular culturepresented accuratelyand positively.I haven't had mymedicationunavailable becauseits a potential COVIDtreatment(hydroxychloroquine).People speakto me ratherthan speakingabout me to theperson next tome.My sobriety isnot at riskbecause Ican't attendAA in-person.When I go out to eat,I don’t think aboutwhether I’ll be able touse the restroom. Orenter the building. Orcomfortably sit at atable. Or eat the foodwithout an allergicreaction.I've advocated againstshelter-in-place withoutconsideringthe message of"disposability" given themortality risks and medicalsupply shortages fordisabled, chronically ill, andelderly populations.I don't have to worrythat my natural bodymovements will resultin being beaten,tasered, or arrestedby the police,especially if I am alsowhite.I've held the doorfor someone in awheelchair withoutchecking in first.I can completely ignoretrigger warnings andcontent notes withoutanyimpact on me, soI don’t have to noticewhether they are thereor not.“The only disabilityin life is a badattitude.” Or other‘inspirational’memes."You have all thistime with shelter-in-placeto finallyclean/exercise/meditate/etc.!"I can access allonline videosshared byfriends onsocial media.There are notscientific effortsto eradicatepeople with myDNA.If I have COVID,I'm not excludedfrom a ventilator inTier 1 triage in theUS because I'mdisabled orchronically ill.I do not expectisolation rooms,restraints, andpsychotropic drugsforced upon meduring myeducational andmedical experiences.I am able to enternew situationswithout fear ofdebilitating anxiety,embarrassment,harassment, orviolence. I've used the term"crazy" or "insane" inconversationas a synonymfor busy, wild,extreme, confusing,evil.I've never hadanyonequestionwhether Ishould/can be aparent.I've assumeda disabilitymeanssomeonesuffers.I've askedsomeonechronically ill,"Have you tried . .. " (yoga,meditation, etc.)When I say that I amtired, overwhelmed, orin pain, people don'tconstantly tell me thatI'm lying, makingexcuses, faking,exaggerating, beingmanipulative, or beinglazy.My type of body orbrain is not used as ametaphor forbrokenness,awfulness,mediocrity, orignoranceMy and mycommunity’s access toand quality ofhealthcare isn’t rankedthe lowest in thecountry, despite higherrates of disability andthe existenceof a treaty.I've used the termblind, depressed,OCD, or barren asa joke or tonegativelyrepresentsomething.I see people with myphysical andcognitive disabilitiesand/or mentalillnesses in mediaand popular culturepresented accuratelyand positively.I haven't had mymedicationunavailable becauseits a potential COVIDtreatment(hydroxychloroquine).People speakto me ratherthan speakingabout me to theperson next tome.My sobriety isnot at riskbecause Ican't attendAA in-person.When I go out to eat,I don’t think aboutwhether I’ll be able touse the restroom. Orenter the building. Orcomfortably sit at atable. Or eat the foodwithout an allergicreaction.I've advocated againstshelter-in-place withoutconsideringthe message of"disposability" given themortality risks and medicalsupply shortages fordisabled, chronically ill, andelderly populations.I don't have to worrythat my natural bodymovements will resultin being beaten,tasered, or arrestedby the police,especially if I am alsowhite.I've held the doorfor someone in awheelchair withoutchecking in first.I can completely ignoretrigger warnings andcontent notes withoutanyimpact on me, soI don’t have to noticewhether they are thereor not.“The only disabilityin life is a badattitude.” Or other‘inspirational’memes."You have all thistime with shelter-in-placeto finallyclean/exercise/meditate/etc.!"I can access allonline videosshared byfriends onsocial media.There are notscientific effortsto eradicatepeople with myDNA.If I have COVID,I'm not excludedfrom a ventilator inTier 1 triage in theUS because I'mdisabled orchronically ill.I do not expectisolation rooms,restraints, andpsychotropic drugsforced upon meduring myeducational andmedical experiences.

Untitled Bingo - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. I am able to enter new situations without fear of debilitating anxiety, embarrassment, harassment, or violence.
  2. I've used the term "crazy" or "insane" in conversation as a synonym for busy, wild, extreme, confusing, evil.
  3. I've never had anyone question whether I should/can be a parent.
  4. I've assumed a disability means someone suffers.
  5. I've asked someone chronically ill, "Have you tried . . . " (yoga, meditation, etc.)
  6. When I say that I am tired, overwhelmed, or in pain, people don't constantly tell me that I'm lying, making excuses, faking, exaggerating, being manipulative, or being lazy.
  7. My type of body or brain is not used as a metaphor for brokenness, awfulness, mediocrity, or ignorance
  8. My and my community’s access to and quality of healthcare isn’t ranked the lowest in the country, despite higher rates of disability and the existence of a treaty.
  9. I've used the term blind, depressed, OCD, or barren as a joke or to negatively represent something.
  10. I see people with my physical and cognitive disabilities and/or mental illnesses in media and popular culture presented accurately and positively.
  11. I haven't had my medication unavailable because its a potential COVID treatment (hydroxychloroquine).
  12. People speak to me rather than speaking about me to the person next to me.
  13. My sobriety is not at risk because I can't attend AA in-person.
  14. When I go out to eat, I don’t think about whether I’ll be able to use the restroom. Or enter the building. Or comfortably sit at a table. Or eat the food without an allergic reaction.
  15. I've advocated against shelter-in-place without considering the message of "disposability" given the mortality risks and medical supply shortages for disabled, chronically ill, and elderly populations.
  16. I don't have to worry that my natural body movements will result in being beaten, tasered, or arrested by the police, especially if I am also white.
  17. I've held the door for someone in a wheelchair without checking in first.
  18. I can completely ignore trigger warnings and content notes without any impact on me, so I don’t have to notice whether they are there or not.
  19. “The only disability in life is a bad attitude.” Or other ‘inspirational’ memes.
  20. "You have all this time with shelter- in-place to finally clean/exercise/ meditate/etc.!"
  21. I can access all online videos shared by friends on social media.
  22. There are not scientific efforts to eradicate people with my DNA.
  23. If I have COVID, I'm not excluded from a ventilator in Tier 1 triage in the US because I'm disabled or chronically ill.
  24. I do not expect isolation rooms, restraints, and psychotropic drugs forced upon me during my educational and medical experiences.