It is the true teacher who leaves the class knowing they have learned the most.

Tucson, AZ
Joined September 2006
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Replying to @spacedoutsmiles
Most environments disable me if I have no place to go hide. If I have a safety zone and it's close by I manage much better.
That common terms are required is not my complaint Jamie :) it focuses conversation, research, life choices! I'm just a pedantic semantic 馃槀.
Replying to @mholzschlag
i apply it as i'm autistic and Some badly designed environments disable me. :)
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Another "D" word makin' me craycray? "Deserve"recklessly slung about @nerdworldorder (great handle btw). Who's measuring who deserves what?
Are folks using "neurodiverse" as an individual adjective? Seems more appropriate to groups/organizations.
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My personal use? I'm beginning to avoid many words that start with "D" especially those with the prefix "dif" I am #TheSemanticResistance 馃槀
i think so, i assume for most people its just a slip of the tounge / word mix up. They dont know the other term
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Replying to @playwrightswife
ooh, #2 is a most precious and rare gift. Good onya m'dearest. And 1 is funny because: true ;-)
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I was pretty active in the 80s/90s in our #CFS #ME support networks. It's how I came to be online in 1988! Isolated at home 300 baud modem 馃榾
Finding a solution is my other full time job. Currently working with the @OHCforMECFS.
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If your #ME #CFS #CFIDS involves one of those or other "emerging" oncoviruses it's a significant risk unless treatable and found early #a11y
Finding a solution is my other full time job. Currently working with the @OHCforMECFS.
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Patients who are using physicians? I encourage you to demand thorough testing for oncoviruses (EBV, CMG, HCV, HPV etc). #cfs #me #cfids
Finding a solution is my other full time job. Currently working with the @OHCforMECFS.
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I want to talk about this as #CFS / #CFIDS / #ME was the diagnosis I was given in 1985. 32 years of that awfulness. And then #aplasticanemia
Replying to @mholzschlag
I've had it (in childhood). Know lots of others with it too, inc @katetowsey (who is investigating alt treatments)
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Lil chat about #CFS #CFIDS #ME a syndrome of "unknown etiology" - It spiked in the early 80s but persists. Poorly managed. #healthcare #a11y
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Replying to @sophiedennis
Wow, Sophie, since childhood? I'm so sorry. That's fairly rare in my experience. Hiya hiya to you too @katetowsey more coming.
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Agreed @Oh_ingrid implications in words like "disability and disorder" often are deflections from people not facing discomfort born of fear.
Totally agree with this. I prefer ASC to ASD as well. Disorder implies purely negative impact & ignores gifts.
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Replying to @Sidra__Perveen
Thank you my dear, you are lovely! Cheers to you and all success in your studies :)
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Here is a definitive case of #StupidSemantics "Leaking his tax return would be a good move for Trump" Leaking? Excuse me, I need to ROFL. 馃槀
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Any #CFS / #CFIDS / #ME Chronic Fatigue Syndrome/Myalgic Encephalomyelitis patients, parents, family or friends with it? Speak up! #helpcare
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Replying to @ShaneHudson
yes! That was the most advanced in my memory (fact check required however) of all. And it's not all that different now ;-) haha
TRIVIA: #webdev #webdesign - in 2005 we saw a huge rise in the advancement of "web #apps" but iPhone/Android? 2007/8. Name an app from 2005!
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Yes - absolutely in teaching - again, it's how we learn. I have that #2 thing too. It's not always a good quality with me though lol
So there it is. It's not hate. It's been a series of nightmarish events. I raged through it. There is no hate. There is love for I have you.
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Wrongdoers will adapt, or they will fail. They will be revealed. They do not need my disruption. Truth and wrong acts always out eventually.
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