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Never ask if we can read lips. To me, it implies that you (the person who asks me) are not willing to meet half way and/or do not want to accommodate. You want me to do all of the work communicating with you.if you are curious on what it is like to read lips, please watch this link:2) If you see a Deaf ASL user, it is safe to call us Deaf, not hearing impaired. I resent to be called hearing impaired. To me, it means that I cannot function in this world because I don’t hear… this is wrong image of me. I CAN function just fine as Deaf person. If a person who lived all of their lives with the ability to hear, lost their hearing all of sudden. Then this person is hearing impaired because they do not know how to function in the world without hearing a sound.3) “Can you drive?” is one of my least favorite questions. Of course we can drive! If our visions passed the test, then we can drive. Looking back to getting our learner’s permit or update our driver’s license, do you notice that DMV always checks our visions (I do not know if all of the states do this as several states that I lived in test my visions), but they never tested our ability to hear??? If you ask me, how do I drive without hearing sirens, blaring horns etc. 1) I check my mirrors frequently, if I see sirens, I pull over. Also if I notice traffic pattern is off, then I assume that the emergency vehicles are coming. Blaring horns (in my perspective) is often associated with road rage, so it’s the other driver’s problem. 😉😉That’s it for now. This list shows my top three pet peeves questions.

That is usually a question asked on drivers license applications. You could contact your local DMV or wait till you need to renew your license to change it then.

Asking disabled people bathroom and sex questions is usually considered offensive. But since this is Quora, and not the tabs line at Secretary of State (it's like the DMV; also long story), I'll answer.You're in luck! I myself actually use a straight cath for intermittent catheter use. But I don't use it because of lack of mobility, or my fibro at all. I use it because my urethra can't always becounted on to do its job, thanks to another issue. And I don't always need to cath; it's a frequent (daily) but not every time thing. You'll find a lot of diversity in weeing methods with disability. With both my fibro and ME/CFS, I personally am, even on my worst days, able to get to the bathroom. But on to the question.First off, it's been my experience that if you're physically capable of pushing the pee out, both patient and doctor are loathe to initiate cathing.To cath intermittently, you really need to be able to get yourself to the bathroom and be in there long enough to perform the job. And if regular cathing is needed for a bed-limited patient, an indwelling catheter is usually used. If you're in so much pain you can't leave bed, the self-cathing position is probably uncomfortable, and a homecare nurse generally has too much to do to do it every time. Plus, that's bacteria going in every time, which docs like to avoid, and patients too. So, intermittent cathing is unlikely.As for answering if some fibromyalgia warriors find themselves so immobilized by pain they need to use a catheter? There's a very wide spectrum of pain and disability with fibromyalgia. Some people are able to work full-time with treatment. Some are unable to work at all, and spend a lot of their time restingI don't know of anyone completely bed-limited because of fibro. I assume there must be some people who are, just that it's relatively rare. If you're limited to the bed, for any disability, the doctor may prefer you use a bed pan rather than a catheter. If the patient is resistant (and why not: it's not fun having people stand there while you pee), then, yes, an indwelling catheter may be used. Like I said, cathethers are first used for people who can't initiate urination, then for lack-of-ambulatory-prowess issues. So, their use for fibro is probably rare. But rare doesn't mean non-existent or inconsequential. What's likely more common is someone who needs to cath, or is bed-limited and uses an indwelling catheter, because they have fibromyalgia plus another serious disability that further limits mobility or whizzing abilities.Covering my bases, if someone is occasionally limited to bed because of fibromyalgia, due to flares, a bedpan would likely be the first recommendation and choice. Catheters include a much higher risk of UTIs that everyone wants to avoid.Hopefully, this answer is comprehensive enough. It's actually made me need to pee.