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Herpes Cure And Treatment

I Have Shingles Why Do My Joints Hurt So Bad I Cry From Pain My Dr Says Its All In My Head

It got to the point I was crying from the pain. All I can describe it as if someone beat the st out of me and left me there, or a car ran over my side. I have been to my pain management doc and she ordered MRI and I am patiently waiting for results, This pain was very odd and came on suddenly while I was sitting watching tv, no bending or stretching, just sitting and its a pain like I never felt before. I was told I had the shingles 20 months ago in my head. Under my bra strap their is a spot that hurts so bad I cant even touch it! My dr did blood work and it all came back good. Like any other joint, the rib joints can get inflamed and painful. So if you’re having pain, don’t assume. 3 days later the nerve pain was so bad on my right side that I had a hard time sleeping. So why is this happening now? I did get the flu badly right after the alleged shingles diagnosis and am breastfeeding so it’s likely that my immune system is down. Does anyone have any ideas of what type of doctor I should see? Now I have constant, painful red rashes on my hands, joints, fingers, toes, lips, arms and worst of all, every centimeter of my testicles and becoming my penis as well.

The pain is on my left side only in a band near my waist line. I have had to do my own research. 2 times both times diagnosed shingles but no real rash, dr. sent me to muscle, bone, joint center they gave me every test there is, or so they say, on 2206 the doctor threw his hands up and said theres nothing more could be done, since then i have been in deep depression, mainly in bed, cry alot, its like no one believes me, they say i have some neve damage on the left side where the pain is but not enough to be this severe, they now rule out shingles because they say it has to have a rash, I have has the fever, chills. Sent me to muscle, bone, joint center they gave me every test there is, or so they say, on 2206 the doctor threw his hands up and said theres nothing more could be done, since then i have been in deep depression, mainly in bed, cry alot, its like no one believes me, they say i have some neve damage on the left side where the pain is but not enough to be this severe, they now rule out shingles because they say it has to have a rash, I have has the fever, chills. But. when he touched my skin it just burned and hurt so bad. I just wish that there was more that the doctors could do for me – for all of us really. I have had joint pain, swollen glands, tiredness (my mother said I was too young to be tired). Same old story, feeling terrible so you go to the doctor and are told it’s this and that or worse when you are told you probably need a psychiatrist because they can find nothing wrong with you. Finally, one astute MD noticed that I had a bad case of shingles on my leg and off to the rheumatologist I went. Sometimes the pain is so bad that you know you can’t think about anything but the pain and nobody can touch you, nobody can do anything to help you. Now if I wave my hand over this flame, it hurts and the pain warns me to stop. Patients are weaned off all their pain medication, an extraordinary challenge for most. I cried in pain! My Dr. said that I have munchimers (sp) and that there is no help.

Shingles Without A Rash

The weird thing is, when i do have these pains in my face (and they will strike in clusters over a few days) about 3 days later i often get a pimple on my cheekbone or temple around the area the neuralgia starts. If there is no pimple then it is just an incredibly sore area (hurt when touched) with the recent head pain i have found increased pimples on my head and sore sensitive areas. I have had only 2 attacks on the left top side of my scalp since 2003 which another doctor thought was Shingles. I’ve been told so many times: it is all in my head and I say: Yes! I have suffered severe headaches, light sensitivity, joint pain, back pain, and short term memory loss. I don’t feel like it’s my fault or that I can do anything about it, but it continues to be portrayed as myself simply not giving a crap or not paying attention. 15 pm wife rang hospital and they sent out medical team, and took me straight into A&E where i was admitted to ICU, it was there the 100s of questions were asked and i did not know what day it was even, they then had to ring to australia (i live in wales uk) for permission for me to have a scan, and they agreed and i was sent for scan, where it revealed excess fluid on brain, they checked me all over and found two small rashes, one in front under rib cage and one in rear at lower rib cage, they diagnosed this as shingles, so the DR turned around and said i have shingles on the bfrain as well, so they put me on a drip, 3 hours later i was getting worse, temperature sky high, diziness, eyes burning, DR examined again and said he was not happy with blood results, another 3 hours goes by, they sent my wife home and told her to ring hourly, 2 hours late they decided to do a lumber Tap, i have had a few of these before so knew what to expect, fluids sent of and about 4 hours later a different Dr came and told me i was being admitted as i had Viral meningitus and Encaphalitus, and shingles, i was put on acyclovir, but my vains kept collapsing, but they persisted and after about two weeks in hospital was given a feed direct to main artery as my arms were swollen and bruised through trying to get the needles in. So all those scary, crazy pics must be really bad cases. My pain began in my mouth, horrible sores that hurt so bad that I got headaches for days. I wake up and the side of my head is hurting, and I toss and turn a bit until I can get situated better. My doctor also said my shingles are drydoes that mean its not contagous? plz help!

It’s common for pain to continue for several weeks after the telltale rash and blisters of shingles have cleared. The nerve pain from shingles and PHN can be severe, and often the doctor will need to prescribe strong pain medications. It hurts all the way to the bone and clothes or light make it worse. I have nerve damage in my neck plus surgery and they say I need another surgery because my hold nerve cord is being pinched by the level above where the floating plate is. This may have a profound impact on your sleep patterns, so do your best to cope with the inability to fall asleep. I hurt so bad, my crying spells are out of control, I have to take a pain pills to sleep night, and make it through the day sometimes. My doctor said that gabapentin is as addictive as ibuprofen. Tapering has caused even more severe weakness, aches, and pain in all my muscles and joints. Taking turmeric supplements eased the pain of post-shingles nerve irritation. I later took turmeric capsules and completely cured all of the pain. A couple of hours later, on our way to our family doctor, my wife said that her arm felt hot, and the pain was not as severe. I have severe nerve pain and if I am not currently shoving pain pills down my throat then I will be in unrelenting pain. In some instances, doses of up to 3, 600 mg per day have been tolerated. Patients who experience the following side effects of gabapentin should check with their doctor immediately. Just prescribed this drug for shingles on top of my head pain was on the left side and unbearable. It is billed to insurance as all medical so should be covered by insurance. Klee’s production slowed noticeably as scleroderma began to take it’s frightening hold. I had to use a walking stick to get around because my back and legs were so bad. One doctor told me it was all in my head. He said that the marks on my back were nothing serious but he would do a biopsy if I wanted just to put my mind at ease. An extremely agonizing and painful experience! Helps me to sleep but am able to also do things around the house and walk.

Shingles Rash: Is Pain Afterwords Normal?

For what it’s worth, childbirth and shingles still vie for 1, but I knew both of those were supposed to hurt a lot. Went to the dr and he said, yep, looks like a bad sprain, just stay off it for a couple weeks. Twisted my ankle once and it hurt so fucking bad that I can’t believe breaking it could have felt worse. I limped into the house crying my head off, and to make it worse, they all spoke French and couldn’t understand what was wrong! Lucky my English speaking grandmother came back from the neighbors down the road right away. For ANYONE to say that I have a predisposition to a lower tolerance of pain can imbibe my sclerosing figurative penis. I know that I hurt so bad sometimes that even sitting hurts, and sometimes I can’t open or close my hands. I want to see who all were involved in themthen I want to ask my doctor if she subscribes to these notions. The next day, as I was screaming in pain, my husband took me back to the ER, where I was treated as a drug addict and told I couldn’t get anything for my pain. I agree with u but I pray to find a doctor that cares enough to run all the tests n get to know everything possible to properly help me get my life back as I have a life filled with pain I wake up in pain n my day ends even worst Ive suffered for years n now have much more conditons in my older years I have migraines arthritis both types n chronic neck n spine n hip pain from two prior serious car crashes along with other conditions I may have fybromyalga IL find out soon but I hurt so bad that I vomit violently when my head hurts from my neck n the back of my head n I cry everyday I barely tap a bone n I fall to the ground crying in pain n I pray for God to send me a doctor who can help me whatever way that gives me a pain free life or atleast a livable life cuz I tired of suffering cuz of the dopeheads who just want a high n the money grubbing dealers loosers who feed that need! I have gotten headaches so severe that I vomit violently n not just migraines but headaches from the pain in the back of my head n neck n I cant get help anywhere since I moved to the city I used to be treated with hydrocodone years ago in my hometown by my doc who knew me all my life but when I moved its been hard to find a doc who really cares to really study my case so he can truelly help me n my only desire is to have my life back n this pain has taken my life so I know what pain does to a persons life n me n many others suffer because of loosers who misuse the medication that is intended for true pain when the pain is worst than the risk of medicating because anything u consume will forever effect ur body these medications r toxins so they should b avoided if at all possible but for us that have a real true need due to conditions that r so severe they disrupt our lives or in my case makes life so painful that I cant see reason to go on n if I wasnt a cristian whos more fearful of facing the Lord for taking my life then I would have long ago cuz this painfilled life is so horrible Im trusting the Lord that one day he will help me n send me a doc who can see the truth with the smarts God blessed him with n so he can help me n yes I do pray for healing n I do know God can heal me but for some reason I do have these conditions n that is a medical fact n because of dopeheads who wanna just get a high I suffer along with many othersN UNTIL A PERSON HAS LIVED A LIFE FILLED WITH DAY N NITE PAIN THEY WILL NEVER GET IT! PS Im sorry to judge but those r the facts n its not rite for innoscent to pay for others who do wrong! How do you know how drug addicts talk to Dr’s? Have you asked any drug addicts how they talk to Dr’s? Part of the problem is with you. I figure if I share my story, perhaps I can entice you folks to do the same and we can do some kind of unscientific study. The next day, my doc said I should go to emergency room just to get it checked out. Body aches (muscles and joints) so bad that I have to lie in bed all day Balding (so not cool). I have in common with our GF friends here but this one so painful and so unknown, like celiac there are ways to treat it, that are way better than the medical community has knowledge of, I hope your IC stays in check just being GF, mine takes a bit more management but it is doable. My head ache was so bad I could hear a pin drop, it would hurt. I slept for days. If you think you have a medical emergency, call your doctor or 911 immediately. I’m exhausted, my joints and muscles ache, I feel flu-ish, and have strep throat this time around. It’s basically chronic, severe nerve pain that is caused by the damage done to the nerves by the varicella zoster virus (imagine a wire without its plastic casing, with all those little wire endings exposed that’s what my T1 through T3 nerves are like now). Tear-inducing, gut-wrenching, gasping-for-air pain when I’m having a serious flare up, and on those days, all I can manage to do is curl up near an ice pack and cry softly until the pain subsides to a manageable level. My grandma had shingles, and we had a Dr of Chinese Medicine do shiatsu on her. Where do you have possibly contracted Morgellons? I have cut my nose to pieces trying to rid myself of these and just now coming to terms with fact that they are not real, except in my head (but in my heart I know they truly live! to torment me, bite me, cause my family to turn away from me. All that I wrote is me being lighthearted about this so don’t get defensive about the seeming cut ups. They ran for their life literally. i limp from joint pain. I limp from joint pain. hips are bad pain. Hips are bad pain. phones a! nd landl ines have a habit of not working or fouling up. Phones a! nd landl ines have a habit of not working or fouling up. I cry every day and night. Every bone in my body hurts, I need knee surgery, lower back surgery, neck and upper back surgery, but we have no family to help. But some doctors just do not want to touch severe pain patients. Im sorry to go on and on and on but im so frustrated that some SUIT up in DC, the DEA, FDA and whoever else thinks they know better than me what I am feeling and they have concluded my pain, your pain all of our pain its not worthy of relief using the same methods my doctor of many years was treating me with. My mom has been bedridden, crying everyday from the pain so I called another dr who ordered an mri and said she needs surgery and said she must be in alot of pain. I am not really sure its nerve pain, but it sure feels like it. I was ok all day, so I guess it wasn’t. Do you also find that when people touch you, you cry out in pain? Only a caricature image of my head with steam coming out my ears helped me cut through the discomfort. Do we want to know? My cancer was such that I left no stone unturned. I feel like I am one of the lucky ones who so far has not had bad side effects with this drug. 15 months and I am beginning to get some joint and bone pain but nothing I can’t deal with. Some thoughts about my grief were just too hard, too raw, too real. Not only does your heart break, but so does your body. Rachele Chrismer says:

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I Have Shingles Why Do My Joints Hurt So Bad I Cry From Pain My Dr Says Its All In My Head

It got to the point I was crying from the pain. All I can describe it as if someone beat the st out of me and left me there, or a car ran over my side. I have been to my pain management doc and she ordered MRI and I am patiently waiting for results, This pain was very odd and came on suddenly while I was sitting watching tv, no bending or stretching, just sitting and its a pain like I never felt before. I was told I had the shingles 20 months ago in my head. Under my bra strap their is a spot that hurts so bad I cant even touch it! My dr did blood work and it all came back good. Like any other joint, the rib joints can get inflamed and painful. So if you’re having pain, don’t assume. 3 days later the nerve pain was so bad on my right side that I had a hard time sleeping. So why is this happening now? I did get the flu badly right after the alleged shingles diagnosis and am breastfeeding so it’s likely that my immune system is down. Does anyone have any ideas of what type of doctor I should see? Now I have constant, painful red rashes on my hands, joints, fingers, toes, lips, arms and worst of all, every centimeter of my testicles and becoming my penis as well.

The pain is on my left side only in a band near my waist line. I have had to do my own research. 2 times both times diagnosed shingles but no real rash, dr. sent me to muscle, bone, joint center they gave me every test there is, or so they say, on 2206 the doctor threw his hands up and said theres nothing more could be done, since then i have been in deep depression, mainly in bed, cry alot, its like no one believes me, they say i have some neve damage on the left side where the pain is but not enough to be this severe, they now rule out shingles because they say it has to have a rash, I have has the fever, chills. Sent me to muscle, bone, joint center they gave me every test there is, or so they say, on 2206 the doctor threw his hands up and said theres nothing more could be done, since then i have been in deep depression, mainly in bed, cry alot, its like no one believes me, they say i have some neve damage on the left side where the pain is but not enough to be this severe, they now rule out shingles because they say it has to have a rash, I have has the fever, chills. But. when he touched my skin it just burned and hurt so bad. I just wish that there was more that the doctors could do for me – for all of us really. I have had joint pain, swollen glands, tiredness (my mother said I was too young to be tired). Same old story, feeling terrible so you go to the doctor and are told it’s this and that or worse when you are told you probably need a psychiatrist because they can find nothing wrong with you. Finally, one astute MD noticed that I had a bad case of shingles on my leg and off to the rheumatologist I went. Sometimes the pain is so bad that you know you can’t think about anything but the pain and nobody can touch you, nobody can do anything to help you. Now if I wave my hand over this flame, it hurts and the pain warns me to stop. Patients are weaned off all their pain medication, an extraordinary challenge for most. I cried in pain! My Dr. said that I have munchimers (sp) and that there is no help.

Shingles Without A Rash

The weird thing is, when i do have these pains in my face (and they will strike in clusters over a few days) about 3 days later i often get a pimple on my cheekbone or temple around the area the neuralgia starts. If there is no pimple then it is just an incredibly sore area (hurt when touched) with the recent head pain i have found increased pimples on my head and sore sensitive areas. I have had only 2 attacks on the left top side of my scalp since 2003 which another doctor thought was Shingles. I’ve been told so many times: it is all in my head and I say: Yes! I have suffered severe headaches, light sensitivity, joint pain, back pain, and short term memory loss. I don’t feel like it’s my fault or that I can do anything about it, but it continues to be portrayed as myself simply not giving a crap or not paying attention. 15 pm wife rang hospital and they sent out medical team, and took me straight into A&E where i was admitted to ICU, it was there the 100s of questions were asked and i did not know what day it was even, they then had to ring to australia (i live in wales uk) for permission for me to have a scan, and they agreed and i was sent for scan, where it revealed excess fluid on brain, they checked me all over and found two small rashes, one in front under rib cage and one in rear at lower rib cage, they diagnosed this as shingles, so the DR turned around and said i have shingles on the bfrain as well, so they put me on a drip, 3 hours later i was getting worse, temperature sky high, diziness, eyes burning, DR examined again and said he was not happy with blood results, another 3 hours goes by, they sent my wife home and told her to ring hourly, 2 hours late they decided to do a lumber Tap, i have had a few of these before so knew what to expect, fluids sent of and about 4 hours later a different Dr came and told me i was being admitted as i had Viral meningitus and Encaphalitus, and shingles, i was put on acyclovir, but my vains kept collapsing, but they persisted and after about two weeks in hospital was given a feed direct to main artery as my arms were swollen and bruised through trying to get the needles in. So all those scary, crazy pics must be really bad cases. My pain began in my mouth, horrible sores that hurt so bad that I got headaches for days. I wake up and the side of my head is hurting, and I toss and turn a bit until I can get situated better. My doctor also said my shingles are drydoes that mean its not contagous? plz help!

It’s common for pain to continue for several weeks after the telltale rash and blisters of shingles have cleared. The nerve pain from shingles and PHN can be severe, and often the doctor will need to prescribe strong pain medications. It hurts all the way to the bone and clothes or light make it worse. I have nerve damage in my neck plus surgery and they say I need another surgery because my hold nerve cord is being pinched by the level above where the floating plate is. This may have a profound impact on your sleep patterns, so do your best to cope with the inability to fall asleep. I hurt so bad, my crying spells are out of control, I have to take a pain pills to sleep night, and make it through the day sometimes. My doctor said that gabapentin is as addictive as ibuprofen. Tapering has caused even more severe weakness, aches, and pain in all my muscles and joints. Taking turmeric supplements eased the pain of post-shingles nerve irritation. I later took turmeric capsules and completely cured all of the pain. A couple of hours later, on our way to our family doctor, my wife said that her arm felt hot, and the pain was not as severe. I have severe nerve pain and if I am not currently shoving pain pills down my throat then I will be in unrelenting pain. In some instances, doses of up to 3, 600 mg per day have been tolerated. Patients who experience the following side effects of gabapentin should check with their doctor immediately. Just prescribed this drug for shingles on top of my head pain was on the left side and unbearable. It is billed to insurance as all medical so should be covered by insurance. Klee’s production slowed noticeably as scleroderma began to take it’s frightening hold. I had to use a walking stick to get around because my back and legs were so bad. One doctor told me it was all in my head. He said that the marks on my back were nothing serious but he would do a biopsy if I wanted just to put my mind at ease. An extremely agonizing and painful experience! Helps me to sleep but am able to also do things around the house and walk.

Shingles Rash: Is Pain Afterwords Normal?

For what it’s worth, childbirth and shingles still vie for 1, but I knew both of those were supposed to hurt a lot. Went to the dr and he said, yep, looks like a bad sprain, just stay off it for a couple weeks. Twisted my ankle once and it hurt so fucking bad that I can’t believe breaking it could have felt worse. I limped into the house crying my head off, and to make it worse, they all spoke French and couldn’t understand what was wrong! Lucky my English speaking grandmother came back from the neighbors down the road right away. For ANYONE to say that I have a predisposition to a lower tolerance of pain can imbibe my sclerosing figurative penis. I know that I hurt so bad sometimes that even sitting hurts, and sometimes I can’t open or close my hands. I want to see who all were involved in themthen I want to ask my doctor if she subscribes to these notions. The next day, as I was screaming in pain, my husband took me back to the ER, where I was treated as a drug addict and told I couldn’t get anything for my pain. I agree with u but I pray to find a doctor that cares enough to run all the tests n get to know everything possible to properly help me get my life back as I have a life filled with pain I wake up in pain n my day ends even worst Ive suffered for years n now have much more conditons in my older years I have migraines arthritis both types n chronic neck n spine n hip pain from two prior serious car crashes along with other conditions I may have fybromyalga IL find out soon but I hurt so bad that I vomit violently when my head hurts from my neck n the back of my head n I cry everyday I barely tap a bone n I fall to the ground crying in pain n I pray for God to send me a doctor who can help me whatever way that gives me a pain free life or atleast a livable life cuz I tired of suffering cuz of the dopeheads who just want a high n the money grubbing dealers loosers who feed that need! I have gotten headaches so severe that I vomit violently n not just migraines but headaches from the pain in the back of my head n neck n I cant get help anywhere since I moved to the city I used to be treated with hydrocodone years ago in my hometown by my doc who knew me all my life but when I moved its been hard to find a doc who really cares to really study my case so he can truelly help me n my only desire is to have my life back n this pain has taken my life so I know what pain does to a persons life n me n many others suffer because of loosers who misuse the medication that is intended for true pain when the pain is worst than the risk of medicating because anything u consume will forever effect ur body these medications r toxins so they should b avoided if at all possible but for us that have a real true need due to conditions that r so severe they disrupt our lives or in my case makes life so painful that I cant see reason to go on n if I wasnt a cristian whos more fearful of facing the Lord for taking my life then I would have long ago cuz this painfilled life is so horrible Im trusting the Lord that one day he will help me n send me a doc who can see the truth with the smarts God blessed him with n so he can help me n yes I do pray for healing n I do know God can heal me but for some reason I do have these conditions n that is a medical fact n because of dopeheads who wanna just get a high I suffer along with many othersN UNTIL A PERSON HAS LIVED A LIFE FILLED WITH DAY N NITE PAIN THEY WILL NEVER GET IT! PS Im sorry to judge but those r the facts n its not rite for innoscent to pay for others who do wrong! How do you know how drug addicts talk to Dr’s? Have you asked any drug addicts how they talk to Dr’s? Part of the problem is with you. I figure if I share my story, perhaps I can entice you folks to do the same and we can do some kind of unscientific study. The next day, my doc said I should go to emergency room just to get it checked out. Body aches (muscles and joints) so bad that I have to lie in bed all day Balding (so not cool). I have in common with our GF friends here but this one so painful and so unknown, like celiac there are ways to treat it, that are way better than the medical community has knowledge of, I hope your IC stays in check just being GF, mine takes a bit more management but it is doable. My head ache was so bad I could hear a pin drop, it would hurt. I slept for days. If you think you have a medical emergency, call your doctor or 911 immediately. I’m exhausted, my joints and muscles ache, I feel flu-ish, and have strep throat this time around. It’s basically chronic, severe nerve pain that is caused by the damage done to the nerves by the varicella zoster virus (imagine a wire without its plastic casing, with all those little wire endings exposed that’s what my T1 through T3 nerves are like now). Tear-inducing, gut-wrenching, gasping-for-air pain when I’m having a serious flare up, and on those days, all I can manage to do is curl up near an ice pack and cry softly until the pain subsides to a manageable level. My grandma had shingles, and we had a Dr of Chinese Medicine do shiatsu on her. Where do you have possibly contracted Morgellons? I have cut my nose to pieces trying to rid myself of these and just now coming to terms with fact that they are not real, except in my head (but in my heart I know they truly live! to torment me, bite me, cause my family to turn away from me. All that I wrote is me being lighthearted about this so don’t get defensive about the seeming cut ups. They ran for their life literally. i limp from joint pain. I limp from joint pain. hips are bad pain. Hips are bad pain. phones a! nd landl ines have a habit of not working or fouling up. Phones a! nd landl ines have a habit of not working or fouling up. I cry every day and night. Every bone in my body hurts, I need knee surgery, lower back surgery, neck and upper back surgery, but we have no family to help. But some doctors just do not want to touch severe pain patients. Im sorry to go on and on and on but im so frustrated that some SUIT up in DC, the DEA, FDA and whoever else thinks they know better than me what I am feeling and they have concluded my pain, your pain all of our pain its not worthy of relief using the same methods my doctor of many years was treating me with. My mom has been bedridden, crying everyday from the pain so I called another dr who ordered an mri and said she needs surgery and said she must be in alot of pain. I am not really sure its nerve pain, but it sure feels like it. I was ok all day, so I guess it wasn’t. Do you also find that when people touch you, you cry out in pain? Only a caricature image of my head with steam coming out my ears helped me cut through the discomfort. Do we want to know? My cancer was such that I left no stone unturned. I feel like I am one of the lucky ones who so far has not had bad side effects with this drug. 15 months and I am beginning to get some joint and bone pain but nothing I can’t deal with. Some thoughts about my grief were just too hard, too raw, too real. Not only does your heart break, but so does your body. Rachele Chrismer says:

Resources

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Herpes Cure
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