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Do you know why you have hrmiplegic cerebral palsy? because i'm still confuse what's going on with me ,i went to see couple specialist here, they told me different thing. of them said i had stroke when i was in my mom's womb, the other said i had hemiplegic CP. yesterday i found out from my dad, when i was 1 year old. i had german measles and collapse for couple days, my doctor gave me the injection for it. when i wake up weakness on all my right body.
If you have cp down only on side then that is called hemiplegic cp. Go back and look at all your baby pictures. If your like me, you notice your cp more so than other people do, you should be able to tell when exactly when your cp came about. I know I can see it in all my baby pictures.
I did some research on Parkinsons a year or two ago, after seeing Michael J Fox's symptons on tv were similar to the way my body sometimes felt. It is pretty similar to CP (but I believe that it is closer to athetoid CP than spastic CP) as far as the symptons go, but it is considered a different condition. The reason why, is because with Parkinsons the cause of the symptoms continually worsens with time which causes the jerking motions to get worse and worse, but CP does not. Although the effects Cerebral Palsy places our bodies worsens, the cause of the symptons does not worsen. What I mean by that is that the brain signals that causes the spasms does not increase as we age. Our muscles do get more stiff and therefore causes more pain and longer recovery periods but the brain signals don't change.
As for the seizures, I get them fairly often, mostly with high fevers or tiredness. I'm not sure what the proper medical name for it is. For about 30 seconds up to 1 minute or so, I cannot move, I "blank out" or "zone out" as I like to call it, my mind wanders off almost like I'm hallucinating or dreaming, sometimes I have intense unstopable spasms and pain, I can usually see and hear (most of the time) but cannot respond. After wards I am completely exhausted and feel like I'm about to pass out or go to sleep. It's a pain in the rear-end. I've been dealing with it for as long as I can remember. It's terrible to go through but it is so mild even my family doesn't realize that I do it. Half the time I even don't realize that I've done it unless I realize that I missed a good part in a tv show or missed out on someone talking. Thankfully, it happens rarely.
I cannot tell you anything about doctors tests or medicines though. I haven't seen a doctor for any of my disabilities for almost 15 years and I don't take any med's for my conditions except for over the counter pain meds. I just don't trust doctors, too many bad memories from childhood.
Hi,
I just wonder if you can tell me what is telemetry?i never heard it before.i am on lamictal as well for my epilepsy but it doesn't worry me so much at the moment. i am more worry about my hemiplegic CP because my hand keep hurting and it's annoying bcause i can't do anything with it,also with my foot sometimes i have to drag my foot to walk.I am not sure if they can do something here in Australia. i heard about brain surgery but its to risky i guess