Neuropathic Pain :: Head Hurts And Temple Tender - After Effects Of Shingles?
May 10, 2016
I was diagnosed with shingles in my forehead and eye 6 weeks ago,( the worst kind!!) and after weeks of discomfort with eye and forehead re-infecting, watering eye, headaches , itching etc, I now feel better in myself and my vision is ok, but unfortunately I have had complications ands am left with such painful neuralgia, my head hurts just to touch it and my temple is so tender, I have been told that this can go on for months or longer.
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I was diagnosed 10 weeks ago with shingles and unfortunately it was on my head, forehead and around my eye, which was very painful and uncomfortable, My vision is ok but I keep getting a very sore and pink eye, and have been told at the eye clinic that it is dry eye and I now have the same type of drops that I was given weeks ago. Has anyone else experienced sore itchy eyes so long after getting shingles and if so, any idea how long it lasts? my eye gets SO itchy and sometimes I have to rub it which I suppose is just making it worse!! There seems to be nothing i can put on my eyelid to stop the awful itching
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I suffer with pain on the left side of my face in the form of tingling feeling in the lip, gum, tongue, nostril and eye. Have been on amitriptlyne for a while and then on gabapentine and pregabalin but the last two gave me awful side effects so have come off them and just taking painkillers at the moment, but they don't do much at all. Has anyone tried a Tens Machine?
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I was diagnosed as having Shingles on Friday at the doctors. I started itching on my forehead Tues night and by the next day my forehead had all red marks on it? I didn't realise you can get shingles on your face?
I have had horrible pain on/off since, swelling on my eyebrow and jawline near my ears?
Anyone else had this? How long will it last? Also should I be off work with it?
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I was diagnosed with peripheral polyneuropathy 11 years ago. I take 300mg lyrica/day 60mg duloxetine/day and now they want me to take an opiate nucynta to manage my pain since I have trouble with pain. I live in California and recently got my MM license and obtained some Charlotte's web which is suppose to help with pain. Helps a little but pain killers work better. A friend of mine had me smoke some pot by way of vaporizing and it actually took my pain spike away for about 5 hours. Has anyone experienced this before? I'm afraid of what vaporizing cannabis could do to my health. However I feel like I actually have found a way to reduce my intake of meds and much more affordable.
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been taking this medication since September 2011 as i was having back surgery in the December.. looking back on it all now i have been severely depressed but haven't realised until now... i want to come off them without a visit to my doctor & was wondering if anyone knows the safest way to do this
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I had successful hip replacement last September.
Around mid November I began to have chills and tingling in random places all around torso above waist and below neck and only in upper arms
Several doctors, a physiotherapist, a chiropractor later I paid to see a neurosurgeon who said it was nothing serious - he is arranging an MRI scan.
Three days ago I started with a rash with swelling about 4 cm by 2 cm on upper left side of my head accompanied by uncomfortable sometimes feeling around my left eye and a strong headache between the two area.
I am controlling it with Gabapentin cocodamol and ibuprofen.
We have been in Tenerife for three weeks and go back to UK on 22nd March- I've booked to see GP on 24 tha want to ask for check for herpes zoster virus.
Can anyone out there say what is going on?
We're due to celebrate our daughter in laws birthday next Friday..... Should I stay away to avoid co tag ion?
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I have been on gabapentin for about 5 years. I have suffered from trigeminal neuropathic pain since a botched dental operation in 2003 and have tried a range of different medication that made me feel either spaced out, dizzy and sick or made no difference what so ever. Finally the pain clinic at Pontefract Hospital prescribed a combination of Gabapentin, citalopram and pain relief, zomorph. I can honestly say that it has saved my life. The pain had been so unbearable that I just couldn't see an end to it.
I take from 600g up to 2400g per day when the pain is at its worst. My memory has been affected but is nowhere near as bad as when on other similar medication. I do think it's like anything else in that people react to it in different ways and if it doesn't suit change it. During the summer, the pain recedes and I have gone on for days without any gabapentin and have suffered no withdrawal effects at all. Although I am not pain free, and I know that is never going to happen, the gabapentin makes it bearable.
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I was prescribed Gabapentin for fibromyalgia like pain - neuropathic pain. About 90 mins after taking one 300mg capsule I was experiencing some strong side effects. My spatial sense was distorted - I seemed bigger or smaller than I usually experience myself. I kept hearing indistinct voices - whole sentences in voices I did not recognise. I felt intense nausea. At one point I caught sight of my face in a mirror and had the feeling that the image was somehow independent of me, and that the face there was malevolent, and I was unable to break away for several minutes despite quite strong fear. I went to bed and as I lay there I felt like I was not quite in my body - lying beside myself somehow. My mind was caught up for a while in a series of incredibly violent and distressing daydream-like images over which I seemed to have little control. My body twitched and convulsed irregularly - although I've experienced this with intense anxiety and at this point I was really quite afraid! I woke early after a fitful sleep with an intense headache - behind the forehead, temples and also pain in my neck. Also some nausea. The headache lasted all day and into the night. It felt on a par with a moderately bad migraine (maybe 7 out of 10). I was unable to do much of anything except lie down and wait for it to pass (pain killers had no discernible effect on the level of pain).
That was one pill of 300mg. And needless to say I won't be taking another, let alone the prescribed 3 a day!
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I've suffered with chronic pain in groin area for over 2years now after a few tests and Mri exam my specialist Dr Chawla told me there's no cure for Neuropathy besides help with medication and pain clinic. None of the painkillers have worked, bad time with side effects! I recently had Acupuncture with Gp only for the pain to spread all over body.
I have had no help and as single parent to 2 children this puts a strain on my depression. I don't want this to take over my life.
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I have been prescribed Amitriptyline for neuropathic pain, after Keppra did not suit me. The pain seems to be derived from a back injury, but a neurologist Thinks an antidepressant drug will help. The pain has been suppressed, but the side effects are a problem, like extreme tiredness and today dizziness when I was driving. Anyone had a similar problem and is it worth sticking with.
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I'm not sure Wat it is I have I have numbness in both feet and lower legs but my knees are in constant pain and buckle on random occasions or if I try and jog/run at the start of this I was detoxin of of alcohol addiction and that's when it started i've had and mri of my head and back bloods etc and all seems OK so it's leaving me and doctors scratching their heads?
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I had foot surgery 8 weeks ago - quite a major reconstruction that took a few hours.
when the plaster was removed at 6 weeks I was told that I had nerve damage causing partial foot drop and a lot of numbness and pain. I have just had nerve conduction studies and have started on Gabapentin and physio..
They said either the tourniquet or nerve block has caused it. I can't believe that this can happen, surely they know about these nerves and how to prevent problems.
Has anyone else experienced this and what has the recovery been like. I'm just wondering what my life is going to be like from now on.
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Six weeks on after first ever attack of shingles at the age of 75, I am Completely physically, mentally and emotionally drained, despite plenty of sleep and rest. Appetite is fine. Still suffering some ache in head owing to an effect called Cradle Cap which I have been prescribed ointment.
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It is now two months since I had an attack of facial shingles. Although I am almost totally recovered, I still have bright red spots on my face which are not blisters and are not crusting over. They show no sign of fading and still (rarely) itch. Is there anything I can use to get rid of them? I've tried calamine lotion and am currently rubbing an ointment containing aciclovir on them. I'm worried they may be permanent - I have sensitive skin and can't use make-up to conceal them.
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I am in pain, tired, no appetite, diarrhoea, vague. Are all these symptoms shingles related or are some of them due to Acyclovir, co-codamol or Ibuprofen.
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I am 27 years old and I had chicken pox when I was 2. When the shingles came out, it took me down like nothing else. It has been almost a month since I noticed the rib pain. It started with sharp rib pains that hurt really bad and thought it was my spleen. Then about 4 days later I noticed a round sore right under my breast where the rib pain was occuring. Then a couple of days later, it showed up on my back, directly across from the other ones. I had no idea what this was... I waited to go to the hospital because I thought it was poison ivy! I waited about 8 days to go to the hospital. Had I had known what it was, I definitely would have gone immediately. Oh, the pain was excruciating! Ibuprofen did not even touch it. I was prescribed Acyclovir, Prednisone, and a cream that did not help. I was also prescribed Dilauded for the pain and Promethazine for nausea. It has been a week since I finished all of the medication. The shingles are almost gone but there are about 4 really bad areas and they do not look like they are healing. Since last week, I have developed little pimple like things all over my shoulders, face, neck, back and buttocks. I have no idea why they are there. Did anyone have the same reaction? They will not go away! Please help!
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I'm seventeen and I had sex with my boyfriend almost a week ago (this isn't our first time) and after we..did it. I had tender breast I couldn't even touch them they hurt that bad and he didn't touch them during the intercourse I also have had insanely sore sides to the point I have to hold my sides when going to the washroom because the pain is so bad , what is wrong..
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So since 09 I have had incidents where I get pain in my upper abdomen. Usually it's shortly after a meal, but sometimes it does creep up on me a few hours post meal. It varies in severity and duration. In the beginning I only had it once/twice a year, but the pain was excruciating for 4-7 hours. Fast forward to 2011 I started having these incidents like every 4 months, but with less pain. In 2014 I had an incident every month, but pain again was less. Here in 2015, it seems to be going backwards. I have incidents every 2,5 months now and the pain is far from what it was in 09, but its still painful (its a dull squeezing kind of pain). Sometimes it will go away if I drink a smoothie containing ginger,lemon, beetroot and stuff like that. Other times I need to go for a walk. But then there are times when nothing but time helps. The only pattern I have been able to identify is, that if I am very hungry and eat some junk, then I MIGHT get it. Other than that, I have not been able to find any pattern to when I get them.
I fear it might be Chronic Pancreatitis. This worries me a great deal.
Stools have also been acting weird. Switching between brown/yellowish-brown in color and consistency is mainly normal, but also range between somewhat loose/normal/hard
My stomach is also somewhat tender to touch in the upper right side/middle. Feels sorta like how a black eye would. Nothing too painful at all, but still something I notice here and there, since I can sometimes feel it when I walk around.
Two months ago I had my stomach looked at by a doctor performing a gastroscopy. He didn't find anything there. No ulcers. He also did an ultrasound of my gallbladder and apparently also my pancreas (Only thing he said was it looked good and that I had no gallstones).
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What could it be?
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what would cause throat to spasm and feel like its being crushed(left Side) when swallowing. Ear hurts teeth hurts, eye blurry, cant talk or swallow left side of mouth feels tingly, numb ,mouth waters .last anywhere from 30min to 2hours
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