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Your idiotic and damaged posts show everyone here how sub human you actually are. Oh, please, keep posting your garbage, it is so inspiring for the rest of us to know that at least we aren't as bad as you. Larsen pet smart ny dog loved uquestions: 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. new online dating
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