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I have zero issue using the chair and or others embarrassment to my advantage when I am being treated wrong or unfairly. |
I like asm
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Should of kept your mouth shut, I had forgot who it was that pissed me off. I revoke my offer to cuddle and instead offer up the option for you to participate in a video taped demonstration of how to perform a sterile catheterization that I can share with gfy. |
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On a side note in case you are one of the many who can not see tidbits of info hidden within what many people say or talk about. There is an adult sales lesson hidden within this thread. Something that is highly important yet so often overlooked that it literally is mind boggling.
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I didn't read this thread to tell you the truth, I saw you started it and I posted, unless you are talking about keeping my mouth shut about this thing thats about it.
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Great thread :thumbsup Very informative and nice to read answers to questions that many of us wonder about.
My question is, being paralyzed, are you able to have children? |
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My testicles are perfectly fine and it is not like they died or something. So I can easily have a doctor harvest semen if I wanted them to either via syringe or through electronic prostate stimulation (same as they do for bulls). From there it is just a matter of insemination into a willing female. |
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Tard out. :1orglaugh
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first thread i've read to the end in a long time.
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you know what i like about internet message boards? you don't have a clue how people look like, what race, what color, standing on two legs or sitting in a wheelchair. i don't fuckin' care whether you sit in a wheelchair or not - you are obviously one of the smarter persons here and that's what counts. |
Can you play golf?
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ASM
i think it's great that you are answering questions. do you remmber how big was your tumor, how long it took them to find it out it was the cause and after the surgery there was no connection at all in the spinal canal? thanks |
Great post ASM. I've been in a chair now for 28 years and one of the biggest obstacles I've come accross is people's ignorance. Obviously it's not there fault, as many able bodied people have never personally known a person in a chair so they're clueless and want to treat you as a 'cripple' which is annoying as hell. Knowledge empowers and I really dig this post!
The top questions always asked is Does your dick get hard Can you have sex How do you use the bathroom The funniest thing for me is going somewhere with my wife (who is a hottie) people always assume she is my sister, or my nurse. Now that I'm getting older looking and since she's 8 years younger than me and hasn't aged since we've been married I'm starting to get "is she your daughter". I think it's funny, cause everybody knows a guy in a wheelchair can't be taggin a hot piece of ass! |
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I lived with my g/f for a few years.. one before she had the accident and 3 after she became paralyzed. It was really hard watching her go through hell, but damn she was strong and really kicked ass at getting her life back together.
I was amazed at how easy it was for her to get sick and learned a whole lot on caring for a triapalegic. I will never forget when my then 2 year old would lay in the bed beside her and pretend he couldnt get up or move and said he was "amy"..she would laugh hard at his imitation. |
Do you ever feel inadequate with the constant help offerings or get angered that people wont leave you alone?
Or is it a non issue since you have been in a wheel chair for so long? |
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And I've gotten the sister thing a few times too. "Is she your sister?" Next time I think I'll reply "nah just some hooker I found downtown last night." |
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I was in the hospital for two months close to three. They were about ready to just send me home to adjust and live with the fact that I had gillian berea syndrome. It is sort of a complicated issue, since after about two weeks into my initial stay I was very curious and became a "problem" patient. I constantly fought with the physical therapists. I kept saying I was in too much pain to do anything, which I was. They insisted I was just making it up and being lazy. (lots more to this story by the way) I also started reading all the assorted medical literature in the hospital in regards to my illness. This is where the problems really started. I knew damn well that I did not have gillian berea syndrome and that it had to be something else. So the just made new resident doctor and I began to really butt heads. Did not help at all that I was only twelve of course. It was very hard because not only was the doctor against me but he had all my relatives on his side. He was a doctor after all and I was just a kid. This resulted in the doctor fighting with me for no other reason than ego and he cancelled assorted tests (opps!). Well back to sending me home. They were ready to just send me home and let me be. Well my parents felt that I at least needed to go to a rehab hospital to better learn how to be in a wheelchair and live a normal life. As luck would have it my grandfather is very high up in the Shriners organization and with a quick call he had me into Shriners hospital within a few days. After arriving at Shriners hospital and getting checked in and shown around a bit. Getting my lectures on how they did not want to butt heads with me or have me fight all the time and all that happy horseshit (got to love how medical charts follow you through life) they scheduled my therapy for each day. The following day I met with my physical therapist and they had me doing some stretching on a mat. Well it hurt like fucking hell and at one point the therapist told me to sit still and she began to feel my neck area. Told me that was it for the day and sent me back to my room. Latter that night they sent me off to UCSF for a test. I was scheduled for surgery the following day. Apparently the therapist was able to visibly see the lump on the back of my neck and I indeed had a tumor. Shriners brought in a top neurosurgeon and had my tumor removed. Followed that with some radiation treatments and walla it was all over. Therapy could finally begin and there was no more pain. To bad the damage had already been done though, and if the original doctor had not cancelled some of those other tests or even looked me over better everything would of been a lot different. |
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You would be surprised how little people actually do offer help in reality. One would think that it happens a lot but really it does not. People in general are a lot more apt to ignore or go out of their way not to pay attention to you than to offer up assistance. It is a wheelchair thing. I do however have my own theory on this of course. Yet a blind person, a person in a cast, and so forth will get a lot more offers of help than a person in a chair. One thing that does annoy me is the religious people. That alone is a different story all together. |
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Great thread ASM/Sly. My father is handicapped (although not in a wheelchair). He has had polio since he was 6 and can walk but only with braces on his legs. He continues to do things like golf. While I don't talk to him due to other issues anymore, he was always one to make fun of himself as well. I remember us out golfing with a group of 14 or so other guys and we asked him his score on the last hole and he fell down the hill and was like "4.....4" as he was falling. So we called him 44 for a long time and he always laughed. I learned at a young age the handicapped are no different than anyone else, but I did always get pissed when I saw some 16 year old come runing out of a store into a car in a handicapped spot. Always a pet peeve of mine.
Anyhow on to my question. Do you ever feel like you are a burden? I guess I would think that if this was me, I would feel like I wouldn't want to put my family / friends through taking care of me and helping me do certain things. Your thoughts and again great info. -Andy |
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On the other side, if I know some people wish to do something or whatever that I know damn well I can not do, would not do, or generally would be useless attending I will just excuse myself from going. I may go to the lake with friends and just sit around while they swim (yes I can swim, I just usually do not) and that does not bother me. Though if they wish to maybe go up to some of the waterfalls and so forth I often will excuse myself from going. They would be more than happy to tug me along up the trails but alas I feel it would be more of a burden for them to do so and it rarely would interest me enough to go through with it typically. I know when and if I would actually enjoy doing something and that is the key. If I enjoy it and they know I do then nobody feels as if it is a burden at all. |
I don't have anything to add, I just want to thank you guys for such an informative thread :) ASM, I've enjoyed your siggie for a long time so it's nice to know a little bit more about the STFU guy, lol.
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You want to curb away from situations where people will feel like they "have" to do something for you instead of "wanting" to do something for you. |
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lol...i do miss using my husband as a shopping cart a bit when we were shopping. Or better yet when were coming back and he would hook the bags onto his chair so I could push him and not also have to be carrying stuff. |
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I am like a nazi on this even now. People parked in disabled spaces without a disabled badge (which you have to have in the UK to use those spaces) makes me so mad. |
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btw, this thread is awesome. The nuggests of wisdom hidden inbetween penis questions are golden. |
ASM and Sly - this was a great read - kudos for being so honest and answering all questions.
I really hope you take full advantage of your disability where possible :) A good mate of mine is deaf and going out anywhere with him is absolutely hilarious! He can lip read and talk BUT in public he sometimes switches off to get his own way ie when he's haggling price on anything - really opens up your eyes as to what people will do to get out of a situation they can't deal with. Whenever I want a really good price on something I send him in - it's almost worth paying him to haggle. |
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To me murderball was about type A jocks who are now in wheelchairs. It was inspirational in its own ways. It also showed how some may over compensate or even make the able bodied feel disabled around them. Does that even make sense? I have tried assorted sports but was never super into them. They are brutal and "we" seem to have zero sympathy for each other. My last sport attempt was water skiing and I will tell every one know that I will fucking never ever do that again. For those that are not to familiar with a handicapped water ski. It is a device the marque de sade would of been proud to call his own. It is effectively a snowboard type device with a rudder, on top of this is a metal chair or sorts that you loop your feet into to secure yourself to the ski. Sounds simple enough of course. Now you must somehow keep the tip of the board well above the water line when the boat takes off. Not an easy task to say the least since the whole board and your life jacket is buoyant. If you do not you will end up doing what happened to me. The boat takes off, my ski temporarily dipped into a wave about by two inches and well I was on a one way trip to the bottom of the damn lake at an incredible speed. Same principle that keeps you on top of the water makes you a great diving submarine. Assuming you ever do get to where you are on top of the water and doing what you are set out to do, ski. For the love of all things sacred do not and I repeat do not crash. It is one thing to crash when you are doing this able bodied style, now try to imagine you are in a near fetal position and very attached to a board when you crash. I think it would be the same feeling one would get if you were in a kayak sitting side ways on the side of a steep hill and someone pulled you down the face of it. |
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holy shit, if i was paralyzed like that with no hope for normal sex i'd off myself.
seriously, there would be no point in living. i'm sorry about your situation. |
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