Medic Alert Bracelets - Do you wear one?

[Elaine H]

Hi Skillefer

I can't believe that in this day and age someone would literally want to be "labelled" EPILEPTIC, it might not be as taboo in the States as it is in the UK, but don't you think it's a bit of a label, and one that a lot of us are trying to escape from, I was in an ambulance last week, and the paramedic said to me, are you a well known "EPILEPTIC" I was like AAARRRGGGHHH!!! No actually, I'm a Taurus! it is an awful word, and one that conjures up such awful medieval visions of witches and six headed possessed gorgons!! Maybe it's just me, but I would love to hear what others think. It would be more respectful to have The wearer of this badge has epilepsy. Let me know what you think eh?

Cheers Mate

Elaine x

[Hadley]

I actually bought one for my son from stickyj.com. It is a small tag, with a watch type band so it can be replaced if torn up. He likes it and it doesn't look quite as conspicuous as the one on the chain. He actually had the dog tag looking one previously, but since it has his old medication on it, I opted to get him a new one.

[stilldancing_98]

I don't have one now, I would have to have diamonds in it.lol

[Elaine H]

I actually bought one for my son from stickyj.com. It is a small tag, with a watch type band so it can be replaced if torn up. He likes it and it doesn't look quite as conspicuous as the one on the chain. He actually had the dog tag looking one previously, but since it has his old medication on it, I opted to get him a new one.

Hi Hadley

I hope everyone could see the funny side of my reply about the stigma and ignorance attatched to epilepsy, worldwide I think, not just here in the UK. Of course, I really do think, especially with kids, that they need to have something on them that would let people know what the problem was, I just absolutely loathe and despise the word epileptic! It's like Heretic, lunatic, I think people put us all in the same category. Maybe it's just me, but you would not believe the ignorance and prejudice I've endured in the workplace over the last twenty odd years, I think anything to do with the brain and people think a. you're gonna be off sick every other day, and b. you won't be quick to learn the job, and c. you'll be on the floor every five minutes with your legs in the air, foaming at the mouth and peeing yourself!! (only on Friday nights!!! ha ha!!!) but seriously, we have to explode this myth, we have to educate "The Great Unwashed" epilepsy is nothing to be scared of.

I hope I haven't been on my high horse, and have a wicked weekend mate!

Cheers

Elaine xx

[BuckeyeFan]

I DESPISE that term epileptic!

I have noted that in several of my older threads and in my profile. My Mom and Sister are both fighting cancer. No one calls them cancerics.

The worst IMO is when they link it to mental illness!!!




I do not wear an alert tag, but it is not because of the stigma. I am just not into wearing accessories. I rarely wear a watch.

I guess if I found a gold colored chain I might wear that more often.

[Elaine H]

I DESPISE that term epileptic!

I have noted that in several of my older threads and in my profile. My Mom and Sister are both fighting cancer. No one calls them cancerics.

The worst IMO is when they link it to mental illness!!!




I do not wear an alert tag, but it is not because of the stigma. I am just not into wearing accessories. I rarely wear a watch.



I guess if I found a gold colored chain I might wear that more often.

Hi Buckeyefan

I'm so glad you agree with me about that awful label "EPILEPTIC" I think that because it sometimes accompanies Downs Syndrome, Cerebral Palsy, and other more severe disabilities, people actually don't realise that it can affect an individual on it's own, that's why I've lost eight jobs in my life, that's why I had a guy tell me... "You don't look like you have epilepsy!!!!" For Christ Sakes I said to him, well what am I meant to look like??!! I don't wear any id, I carry a card, but I, always the joker just wrote get me to a pub!! on mine, I remember in my childhood, way back in the sixties, one of the lads in our street had a sister, she had many illness's one of them was epilepsy, her mum and dad kept her on a mattress in the garage, we used to get taken in to file past her and have a look, it was bizzarre, she wore a padded helmet and had seizure after seizure, can you imagine the stigma attatched to epilepsy back then, she died very young, but I've never forgotten her, and my ideas of epilepsy were of course horrific! We have all got to talk to people and keep talking, I never ever make a secret of my condition, I'm quite proud to be me actually, and any opportunity I get to talk publicly I'm there like a shot!

It's your birthday soon isn't it you old fart? You'll never catch me up eh? Take care and have a great weekend mate!

Cheers
Elaine x

[paradise survivor]

Gee whiz, Elaine that must have been real jolt!! I am with you when it comes to dispelling myths. I got fired too, they said I looked like I was drunk or on drugs...I was, it was called Tegratol! Oh well I am now a stay at home wife and do what I want whenever I can. On bad days not so much, but on good days, look out....

[hawke86]

I have worn for a long time. Mine has saved my life several times. I'll keep wearing mine. My medic-alert bracelet stays on all the time. They are real good to have especially when can't speak.

[skillefer]

LOL....I agree with your earlier post....I try to laugh at epilepsy. When I get asked if I'm epileptic, I usually say, "No, I'm a Susan that happens to have epilepsy, as well as hypoglycemia, and hypothyroid issues...." The thing is, the label only has as much power as you give it. We call people with asthma asthmatics, so I understand why people call people with seizures epileptics. Because they figure if they can label it, it's easier to understand. And, I find that if I get angry about the label, it tends to confuse people and make them think I'm in denial. Whereas, if I laugh at the label, and crack a joke like, " What? You didn't feel like break dancing too??" It makes the people responding to the seizure more at ease. So the label of Epileptic doesn't really bother me....it's a word, and it only has as much power as I give it.....

As for my bracelet, I may have to add Hard of Hearing pretty soon.....who knows, maybe that'll buy me a couple of extra minutes when the EMT's are asking me those stupid questions "Where are you? Who are you? Do you know what just happened?" I've always wanted to answer them...."If you don't know where you are, we have problem. I know who I am, who are you? and If you don't know why you're here, then you might be in the wrong profession..." My hubby said I freaked him out once though...He kept asking me if I knew who he was. He asked it over and over. After a while I got a scared look on my face. In my mind, if he didn't know who he was, then how was he supposed to help me?? As I said...the ability to laugh is a good thing.

The thing is, how can we help educate people if we keep them in the dark? I proudly wear my Coping With Epilepsy t-shirt in public, and I definitely don't have issues wearing a bracelet.

[haird18]

LOL....I agree with your earlier post....I try to laugh at epilepsy. When I get asked if I'm epileptic, I usually say, "No, I'm a Susan that happens to have epilepsy, as well as hypoglycemia, and hypothyroid issues...." The thing is, the label only has as much power as you give it. We call people with asthma asthmatics, so I understand why people call people with seizures epileptics. Because they figure if they can label it, it's easier to understand. And, I find that if I get angry about the label, it tends to confuse people and make them think I'm in denial. Whereas, if I laugh at the label, and crack a joke like, " What? You didn't feel like break dancing too??" It makes the people responding to the seizure more at ease. So the label of Epileptic doesn't really bother me....it's a word, and it only has as much power as I give it.....

As for my bracelet, I may have to add Hard of Hearing pretty soon.....who knows, maybe that'll buy me a couple of extra minutes when the EMT's are asking me those stupid questions "Where are you? Who are you? Do you know what just happened?" I've always wanted to answer them...."If you don't know where you are, we have problem. I know who I am, who are you? and If you don't know why you're here, then you might be in the wrong profession..." My hubby said I freaked him out once though...He kept asking me if I knew who he was. He asked it over and over. After a while I got a scared look on my face. In my mind, if he didn't know who he was, then how was he supposed to help me?? As I said...the ability to laugh is a good thing.

The thing is, how can we help educate people if we keep them in the dark? I proudly wear my Coping With Epilepsy t-shirt in public, and I definitely don't have issues wearing a bracelet.

Hey your very smart we are ourselves created different and unique. We may not like what we have or are dealt but we are who we are not by choice!

[hawke86]

Having epilepsy is not that bad. I have faced death four times. You'll never know when it's your turn to go. I'm not trying to upset of offend anybody.

[RobinN]

You are not upsetting or offending.
Your story is as important as anyone elses. I am sorry about your near death experiences. I have never faced it. My oldest son has.. he fell off of a 40 ft cliff.

We all live with our struggles, some more than others. It is up to all of us to educate those that don't understand, encourage those that do, and continue to believe that tomorrow will offer us more special moments.

[hawke86]

Robin,
I agree with you. We need to educate all those that don't understand. Again I agree with you.

[stilldancing_98]

I will get one when I need one. My son should have one though. Maybe it is time to get one. Teresa