Dillon, Wow what an awful ordeal, you are a survivor.  Are your symptoms 
totally gone now that you are taking the medication?  Dan T.

Dylan <[EMAIL PROTECTED]> wrote:  hey Quads,
Dylan here. I haven't written in in awhile. The last time I wrote in I was 
asking about some disreflexia/spasm spikes I was having. I wanted to know 
if other people had experienced them and/or knew what they were about and 
what I could do about them. I was getting concerned. I got some helpful 
responses. Here is the quote from that post -

>(06/20/06) like in the last month or two, I've started to have these 
super uncomfortable type of disreflexia/spasm. I assume that others of you 
must have experienced it as well.
>Its a different type than the normal disreflexia or spasm that might 
happen if, say, you are having a pressure spot or are cold or whatever. It 
seems to trigger in the morning
>after or during my stretching routine or just after I get in bed(they're 
usually weaker then). And the only thing I can do to stop them is to 
immediately sit up. If I don't, they
>(the spasm with its accompanying very painful disreflexia) will come 
through my body in a rhythmic pattern (like hiccups) but with each one 
getting stronger/worse until
>within a few minutes my heart is pounding in my chest, my whole body is 
clenched, and I get the worst headache imaginable. I can feel the blood 
pumping into my brain
>and it gets to where it feels like my brain could explode if I don't sit 
up. After I sit up it calms down pretty quickly, and if I've let the 
headache escalate by taking awhile to
>sit up, it takes about 45min for it to dissipate and go away.

The reason I'm writing in now is because they were serious and I am hoping 
that my experience can help prevent some other quads from having to go 
through what I did. Basically what ended up happening was that those 
episodes kept happening until one day, what I feared most - an occurrence 
happened where sitting up did not alleviate the symptoms. It became obvious 
that I need to go to the hospital. On the way there I could feel that I was 
not going to make it. My Dad was driving and I was telling him what my 
symptoms where and that I was about to leave. He helped me by just telling 
me to let go and to not be afraid. My eyes rolled back into my head as I 
reclined the wheelchair. Everything turned white. I woke up about 4 days 
later in the hospital. Apparently I had had a seizure. It actually, now 
looking back on it (it happened on Feb 19th) it has been an interesting 
experience. When I started becoming aware again I couldn't remember the 
things that had happened right after I lost consciousness. I also lost 
memory of many trivial things like the scenery around where I live, but 
that soon came back to me. The experience has changed my perception of 
things a bit. I can't say that being confined to this body in this 
wheelchair makes 'sense' to me now, but in a way I'm more able to observe 
everything more and see the layering behind what we see through our eyes. 
So that there are explanations for things as they are. Anyway I won't get 
too weird here :-)

What I really wanted to say, but got a bit side-tracked, was that the I 
found out the reason why it happened. At least this is what the ER docs 
told me, and what kind of upsets me is that I've been telling my docs about 
this for quite awhile and they never clued into or told me what was going 
on. Because I'm a quad and don't stand up, there is some chemical in my 
body that doesn't get produced and that eventually this caught up to me and 
caused me to have a seizure. Now the doctor has put me phenyton(phenytoin) 
sodium (dilantin). And apparently I should have been taking it earlier. I'm 
not sure whether using a standing wheelchair would've helped to prevent 
this sort of thing or whether it is a medication that all quads need to 
consider taking at some point. In any case, it can't hurt to share my 
experience and read up on this drug. If anyone has any questions that I 
might be able to answer about it I'll do my best to answer them.
Thanks, yours, Dylan


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