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I was collateral damage. He sure hated my brother, but even today, it wouldn't qualify as a hate. I was very, my brother was a lot older than I. I was in the hospital for a time, then when I got out, they were very careful of me. I couldn't go out to play at recess, I had to stay, alone, in the classroom unless someone was bad and lost play ground privileges. Made it very hard to settle in to a new school. I wasn't only the new kid, I was weird, and couldn't do what the other did. The only permanent damage is a difficulty remembering, I have to write them down, and words sometimes get lost on me. Simple words. I remember (as an adult) trying to tell someone the dog's ball was over by the couch. Only I couldn't remember the word couch. I could tell you it was, and beige, and you sat on it, and it pulled out into a bed, but couch, sofa, davenport, all gone. Once I hear the word, it's back like it was never gone. My old staff was awesome. They'd hear me talking to a patient, and if I froze, they'd toss in the word I needed, and we all went on without skipping a beat. If you didn't know about it, you wouldn't notice, everyone does it sometimes. How did you get hurt? injuries are really tough. lonely women McAllen
The Link: How do you feel about it? I feel like I am not a science experiement or a lab rat. I don't care if one side of my is bigger or not. Unless you can connect this to an increased medical risk or something like that, why are research dollars being wasted on finding "gayness." Find out what causes breast cancer or a vaccine for AIDs. I am a person. I am an individual. Who cares why I am. Is there another perspective that I am missing here? free sex tonight 19363questions: Yes, I had a spinal tap, several MRIs. The problem I found with the diagnosis machine that is western medicine: I had (the head of neurology at Kaiser) tell me I definitely had MS. Another Big on Hospital (not Kaiser, but a highly reputable medical center) told me I *might* have MS, but I also might not. Still another neurologist, highly recommended (my mom's an MD, BTW), said I definitely did NOT have it. The diagnostic tools they have these days are really *gray* *as in, not black and white); there are different levels of diagnosis: Possible MS, Probable MS, Definite MS. Their way of gauging? Well, say you've had 5 episodes of symptoms in 6 months and no spots (sleroses) on your or spinal cord? well, then they say you have Probable MS. But if you have spots on your scans and only symptoms in 10 years? Definitely MS. I have a problem with the term "psychosomatic". The mind and body cannot be separated. They are a whole thing. Just as "stress" can lead to heart disease, "stress" can lead to problems in the CNS. Also, if a doctor tells a patient s/he has weeks to live, the body is listening. Organs listen. Things in the body react to words. Stomach acid is released, that's something we've all experienced, yes? From words spoken? Well, organs do things to, as does, as does spinal cord, etc. Allopathy, or western medicine, has amazing things to offer, don't get me wrong. But my mother, whom I and adore and respect, taught me that if doctors simply don't know, they never say this. For whatever reason, they label, and thereby "diagnose" something as a syndrome, or they create a new disease. I don't buy it. I'm not saying MS doesn't exist, and I certainly don't know the OP's SO's story, but the diagnostic tools in my experience are bunk. Just my opinion. adult find friends
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