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I'm running into trouble more and more frequently with private security and law enforcement when out and about with a cane or staff/
No you did not.Did I miss somewhere in this thread that the OP is in fact disabled and in need of a cane?
Can we get a picture with you and you cane or staff. It's the critical missing piece from this thread.
So the OP does not need the cane but is rather a cane self defense enthusiast. Well that's just great.No you did not.
So the OP does not need the cane but is rather a cane self defense enthusiast. Well that's just great.
OP, if you are not in serious need of a cane then stop using one. Just because you can doesn't mean you should. The reason you are getting hassled is because you are doing something very socially out of place. Also, you are putting unnecessary negative attention on people with canes that need them. Think about it. I can just hear a LEO say to his/her partner "remember that creepy guy we stopped the other day that was carrying a weaponized cane for no reason? Should we be looking more at all canes as weapons?"
You're like the guy who walks around with an AR because you "can" and because it's your "right". Do something out of the norm and expect attention.
Troll.
I was diagnosed with Plantar's fasciitis back in 2013. I have a long history of seeing my Dr. and a podiatrist about the matter. I was told by both of them as well as the ADA's hotline, that NONE of this is or should be an issue (I didn't want to mention this as to not offend any potential LE or LE supporters on here, but I have filed complaints with the ADA in the past over these incidents and wonder if this is the source of these incidents increasing). The videos that you selected to post in this thread are several years old and quite literally have NOTHING to do with the subject at hand (why you chose older videos of me when I was thinner and not as slow moving as opposed to more recent ones where my weight gain and limp is more apparent, I don't quite know). I came here simply to see if what I was going through was unique to my municipality, but I clearly got my answer in the form of being told that personal opinions on my age, attire, appearance, and old youtube videos of me just playing around are somehow more relevant than my ADA rights, which, with respect, was an answer I probably could have gotten by just asking locals about this, as opposed to an online community of people from all over.
To those who responded and have never had to deal with mobility impairment, when you end up having to use a cane to get around at a young age, something that is easy to overlook should be considered, and that's dignity. Being accused of merely pretending to have a limp, is not pleasant. Having to struggle with things like carrying something through a door because you got a cane in one hand and your other hand full, is not pleasant. Having to have someone drive you somewhere that you would normally drive to, or even walk to, because your foot on some days hurts too much to be driving or standing on, not pleasant. Leaving your house and not knowing if someone is going to target you for a crime because criminals tend to favor people they consider weak and defenseless, not pleasant. Weight gain due to not being able to exercise and having to take things a little slower than you're used to, not pleasant. I don't quite know how to explain it, but there was a gentleman here who by his own admission, chose to use to Blackthorn cane rather than some other cane that was not very aesthetically pleasing, and it made the transition a bit more bearable to him. Well that just about sums up why I would rather use Cold Steel's walking aids rather than something you would get at Walgreen's or CVS. They look nicer, handle better, feel more comfortable, and get alot of compliments and questions as to where I got them, and in the end, it takes just enough of the sting off to make living with PF a little more bearable to live with. I personally don't feel that's too much to ask, but as with many topics, opinions may vary...
Wtf? Seriously bro... ADA for plantar fakeitis? I am fully disabled and sometimes have to use a cane. You say you were diagnosed in 2013 and apparently its fully taken over your “not pleasant” life, yet this video you say is old was in 2017, four years after your diagnoses as you state. This is bs all the way around and to try and justify it as you are disabled is messed up man... apparently you are attention seeking, so you got it and now complain what type of attention it is. Damn, this is sad! Get some Dr. Scholl’s and stop living off the checks you get for your “disability”.I was diagnosed with Plantar's fasciitis back in 2013. I have a long history of seeing my Dr. and a podiatrist about the matter. I was told by both of them as well as the ADA's hotline, that NONE of this is or should be an issue (I didn't want to mention this as to not offend any potential LE or LE supporters on here, but I have filed complaints with the ADA in the past over these incidents and wonder if this is the source of these incidents increasing). The videos that you selected to post in this thread are several years old and quite literally have NOTHING to do with the subject at hand (why you chose older videos of me when I was thinner and not as slow moving as opposed to more recent ones where my weight gain and limp is more apparent, I don't quite know). I came here simply to see if what I was going through was unique to my municipality, but I clearly got my answer in the form of being told that personal opinions on my age, attire, appearance, and old youtube videos of me just playing around are somehow more relevant than my ADA rights, which, with respect, was an answer I probably could have gotten by just asking locals about this, as opposed to an online community of people from all over.
To those who responded and have never had to deal with mobility impairment, when you end up having to use a cane to get around at a young age, something that is easy to overlook should be considered, and that's dignity. Being accused of merely pretending to have a limp, is not pleasant. Having to struggle with things like carrying something through a door because you got a cane in one hand and your other hand full, is not pleasant. Having to have someone drive you somewhere that you would normally drive to, or even walk to, because your foot on some days hurts too much to be driving or standing on, not pleasant. Leaving your house and not knowing if someone is going to target you for a crime because criminals tend to favor people they consider weak and defenseless, not pleasant. Weight gain due to not being able to exercise and having to take things a little slower than you're used to, not pleasant. I don't quite know how to explain it, but there was a gentleman here who by his own admission, chose to use to Blackthorn cane rather than some other cane that was not very aesthetically pleasing, and it made the transition a bit more bearable to him. Well that just about sums up why I would rather use Cold Steel's walking aids rather than something you would get at Walgreen's or CVS. They look nicer, handle better, feel more comfortable, and get alot of compliments and questions as to where I got them, and in the end, it takes just enough of the sting off to make living with PF a little more bearable to live with. I personally don't feel that's too much to ask, but as with many topics, opinions may vary...
I require a cane and am always treated quite nicely by Law Enforcement and TSA, in fact they often go out of there way to try and help.. Happy Holidays!I don't want to say anything that might be considered offensive or politically incorrect, just going to say that I'm running into trouble more and more frequently with private security and law enforcement when out and about with a cane or staff. I was told when I first started using one that there should be no problems in terms of people denying me entry to a place for having one, or people demanding an explanation as to why I need one, or any kind of hassle for using one in general, yet it's becoming more and more frequent. Just trying to figure out if I was the only one, and if this has happened to others, how they handled it.
Giving actual disabled people a bad name isn't a good look, it's embarrassing.