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lilly2988
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My father suffered through a lung biopsy, for example. He yelled out, help! help! this elderly man, to stop the procedure! they put him upside down! The doctors told me to wait outside that I shouldn't be in the room. (They) forbid me to be with him. He had skin as copper and beautiful as a penny, but after the biopsy,when he came out, he was as pale as a sheet. There is much abuse in medicine to the public and is designed to make money for (themselves), becasue (they) keep hidden as much as possible about how they will damage us. Anyway, about your concern, I have knowledge about a place that does this procedure. It is the same situation. They don't care to let the patients go out of the office with more pain than when they came in. I am happy I found this website because there was question in my mind when one of my patients told me about this concern and she made me realise I am working in a place where (they) are hurting people! No one had ever told me what was going on behind closed doors. No one cared to say anything. but now I know. I would say no to any procedure. I just can't believe where this america has ended up. Its not happening in many other countries, mostly America that I know of. The nervous system has poor circulation except the brain becasue we need oxygen to think hence blood vessels, but the rest of our bodys nerves have poor circulation. at the place Im at, they do cortizone shots too. that makes the nerves, as slow as they heal, to heal even slower, so people are not even aware that they are making themselves hurt for the rest of thier lives basically. the way our bodies can heal is when we let NATURE heal it. when another thing and another procedure and another is advised by our decietful doctors, the body cannot heal. it is too busy trying to break down the cortizone shot and trying to heal the damage from the EMG, all at the same time. the body heals at a certain speed with the right nutrition and the appropriate sleep, stress reduction and alternative treatments like meditation and breathing relaxation. The things we were born with inside. When we trust these doctors who prescribe a certain dose to everyone across the board. there is no discrimination to individuals bodies. our bodies are all different, they digest differently, our livers are different etc. A lovely patient i was seeing at a nursing home died becasue she was the unlucky victim of some doctors medicinal experiment. she died and i cried! what is happening out there is really really bad! please send me a reply if you would like to. (c) |
lilly i have had a number of emg/ncs's and they really werent that bad for me with no lasting effects. It was the only pn related test that i have ever had that has come back positive and with which i have been able to track the progression in my legs, feet and hands/arms. People with PN react differently from each other with the same tests, meds, therapies. What is good or bad for one may well not be the same for another.
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painful post NCS
I too am suffering from a painful post NCS. I had been referred to a neurologist for my weirdo big toe (sharp, stabbing pain that didnt respond to either surgery, narcotics, lyrica, ssri's, lidoderm patchs..etc), so i was told "hey! lets figure out whats going on with you!" sure! im game! im 28, overweight, but other than that, in relative good health. i dont complain about aches or pains, just my stupid left toe. so, not knowing what i had in store for me PRIOR to the appointment, the dr came in, said we are doing this "NCS" thing, the nurse came back in, started hooking me up, and thats when all hell broke loose. figuring i'd be okay, and that i can deal with it (i have a fairly high pain tolerance), i was wrong. the nurse was apologizing left and right as i was crying. this was repeated on the other leg. then the dr. did what i call the "need thing" (ems, esm, i dont know the acronym). from that point on, my entire body has been on fire. i have been in constant, throbbing, aching full body pain that feels like its radiating from my lower back up through my arms, back, legs and feet. its almost like the NCS awoke something nasty within. unfortunately, 3 wks has passed, the neurologist doesnt believe me, and my pain gets worse every day. i just need help, and if someone, anyone feels so compelled to point me in the right direction, please feel free to do so.
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I had a very bad reaction after my EMG. I had been having parasthesias in my legs and some burning pain in my feet for a month, so Dr. ordered me an EMG. Night after the EMG I woke up with parasthesias all over my body. Dr. said it couldn't have spread due to the EMG, never seen it happen before. But within days it spread all over and then I started to have burning pain too, all over body. Dr.s insist EMG didn't spread it, but I'm not so sure.
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Question for Rose.......
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Your presentation and symptoms sound so like mine, I am just curious. Thanks. |
Burning Pain
I shattered my heel bone 11 weeks ago. Had surgury 10 weeks ago. Ever since the surgury i've had a burning sensation thats starts at my smaller toes and travels thru my ankle and up my leg. Along with the burning sensation i also have a tingle going along with it and involantary movement of my 4 small toes. Finally after a doctor visit 2 days ago he gave me a script for LYRICA. It seems to lessen the pain and is a med that works better the longer you take it' so relief is on the way. I'm scheduled for an EMG next week to find if my pain is form nerve damage. So for i've had numerous xrays and 2 Ct scans with no definate answers. So if an EMg caused her what to feel the pains i've been feeling for 10 weeks i don't know what to think.
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