LOL! We don't always have to match. :excited:

 

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At least he looks better in those platts and that bathing suit than I do...:lol:

I love this design....

 

I like that design. I am really liking the wheels.

 

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I posted this in another section, so if you didn't see it . . .

 

Have MS, been in a WC before

not at the moment, but I am familiar with it. My first MS attack turned me into human luggage for a while.

 

disabled

I've been a paraplegic since I was 16. im 26 now.

 

I was presented with progressive MS 12 years ago. My wife at that time took the diagnosis more radical than I, thus becoming an ex a year later. Being confined to a wheelchair for the past 7 years. Now only having use of my left arm only. I was forced to sell my remodeling company 6 years ago.

Since that date, several years ago. I now look at every day as a challenge, such as I did being a Contractor. The challenge now being more in depth and relating quite often to diversity. There is very few things I can't do or places I can't go, or things I won't attempt. This is all contributed to my frame of mind and a never ending positive attitude. I must as well mention the many friends I have accumulated over the years. Most friends treating me the same as years past, not in notice of any disability. If perhaps I am in need of some type of assistance and request a little help from one or two individuals. I then get my ass chewed by the other 50 + as to "why I didn't call them?" Life is good!

Being a Vietnam veteran, the VA supplies me with all that is necessary as per medical issues. The VA purchased me a wheelchair of wich I use as a back up. I did quite a bit of reasearch and discoverd the IBOT. Fortunately enough I was financially capable of purchasing an IBOT http://www.youtubeibot This machine was discontinued production 4 years ago due to non endorsement by medicare. The reason being of the 30K cost. The many many $$ that are fucked away by medicare, 30K is dog shit. If an IBOT brought 10% of the wheelchair victims back into a productive part of society, wouldn't it be a no brainer? How about we eliminate the Obama welfare cell phones? I would think there would be ample $$ for everyone in need of an IBOT & a few bucks left over for a martini or two. Bottom line being,,I wish every individual confined to a wheelchair could have access to acquiring this chair.

What a fantastic outlook you have Captain. I thought I was the only one that captured and mastered this. I would love to indulge in a few,, or several cocktails with you & shoot the shit..

Happy Holidays & Cheers!! to you all,,,

 

Were you exposed to Agent Orange by any chance?

 

Sorry for the late response stumbler.

I can see why you may think that from the outside there is no way why we would not have any pain but every injury is different for each person. In my case I don't have any pain or Central Pain like JackassTales experiences.

I don't know if Central Pain with paraplegics is very common or that I am just lucky. Of the friends I have who are paraplegic I don't know if they experience Central Pain because I have never asked them. From me just being around them for long periods of time I can tell you that it doesn't look like they do. If my doctor asks me if I have any pain I just say "no" and that is where that conversation ends.

I am sure there will be a time when I do meet someone who may have the same level of injury as I do and that person may be experiencing Central Pain or maybe even some other kind of pain.

A lot of the times it may not even be physical pain that they are having problems with it could possibly be psychological pain. It could also be both and having both could make it all that much worse for them.

 

Are you a paraplegic Jackass? What level and for how long?

I am sure that you have had many discussions with you doctor about MS. MS can take many years to progress to where you may be in a wheelchair or it could even just take a few years. Take care of yourself and look into every possibility to prolong the progression.

Welcome nameless_1.

 

Good morning Capt! :rose:

 

No agent orange lioness, I was on a ship USS Jonas Ingram DD938. Cheers!

 

im in a wheelchair i have spina bifida i have a few pics here they are

 

sorry here they are

 

I have MS, paralysis comes and goes., I have been in a wheel chair. I am not at the moment but one hand is stiff and numb. Some days it is like a disappearing hand. Fastening a seatbelt is like trying to use a rubber chicken to do it. Sensitivity south of the border varies. It is difficult to climax, but I still adore giving head. If I can make someone lose the power of speech and swallow them all the way down I am good. Tho I might not cum myself with out extra help, I love penetration and being hammered. Love having hair grabbed and all that fun aggressive play stuff. I might get leg cramps now and then, not often but not fun and can scare a partner. They hurt like a mother and just have to be waited out if a neurological firestorm starts. I sometimes have to work around a weak bladder. So I kneel on a pad when deepthroating. I want to be able to focus on what I am doing instead of worrying about the rug. Things can be worked around. It took a while to get there though. My initial reaction was I didn't even want to go there anymore. I had to deal with being depressed about it till I adjusted to the new body image and figured out work arounds. I am experimenting with my TENS unit and toys. Do I expect anyone to want to take on someone with MS long term? Not really, but it is still fun to play. I may end up in a wheelchair again one day. So I take it one day at a time and make some nice memories.

 

Good outlook...do what you can when you can ...one day at a time...

very positive....I could only hope to be like that if I was in the same situation...

 

?

so where is everyone from? I'm in MO.

 

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