Herpes :: Causing Pain On Lesion And At The End Of Nerve?
Jan 25, 2016
I've got a bump on my buttcheeck, that when touched produces small local pain but notable pain on my tailbone. the distance between both spots is about 2 inches. Is it common for herpes lesions, when touched, to cause pain not locally but rather at the end of the nerve?
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I went on vacation for 2 weeks, did not masterbate or anything of the sort for that whole time and also showers were few and far between. When I got home I masterbated vigorously, 4 - 5 times throughout one day, dry with no lube or lotion. On the last go around I noticed a small a very dull sting, immediately checking only what looked to be a very tiny skin graze (as if skin was rubbed off) or cut on the under shaft of the penis, no redness, only a bit tender when messed with but virtually painless when left alone.
Day 2: Naturally I take a look at it, it's a bit red now with more of a mild "irritation" pain only when touched or squeezed, but still painless when left alone. At this point I started applying Triple Antibiotic ointment twice daily and keeping a band-aid around it. Also looked a bit swollen / slightly raised at times, while still being so small that to fully inspect it required good lighting and the skin to be stretched.
Day 3: after still applying triple antibiotic ointment and keeping a band aid on it, peeling it back it looked as if any "swelling" or raising had subsided. It now looks like a tiny rug burn, again as if the skin had been rubbed off. Any tenderness and pain was so little that I had thought it had disappeared within the day. Hardly tender when touched.
*I have not been sexually active for about 8 months now, all sex was protected except for oral, and with my girlfriend at the time.*
Main Question: Could this be an STD? Or trauma from a lot of masterbation at one time? Doing a lot of online research has freaked me out to think I might have herpes, but a lot of my symptoms don't seem to fall under the common symptoms of a first outbreak. I have an appointment at planned parenthood but unfortunately it's booked out pretty far.
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Does anyone that has back problems have sharp nerve pain in their groin private area? I have had back problems for years and sometimes would get a sharp pain up my vagina. After a bad muscle strain in my back and using the elliptical machine I've had twitching and burning all over but also in my private area. Like around my **** it will twitch or vibrate, and then I will get the sharp shooting pain up my vagina and around my butt. I notice it more if I bend over that's why I thought it might be my back. I remember when the stabbing pain started I thought it was a female problem and my OBGYN said everything looked normal with my cervix and my paps have always been normal so she didn't know. She seems clueless.
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My 50 year old husband has been a Type 1 diabetic since he was 21. It was a late presenting of juvenile diabetes or so they said then. He has always done well managing his diabetes, wearing a pump for the past 15 or so years. In the past week or so, he has begun to have severe pain/tingling in his feet/ankles - mainly at night when he is trying to go to sleep. He usually has to get up and walk several times before he can finally sleep - he is only getting about four hours of sleep per night. He has an appointment with his dr - but not until the week after New Years.
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i can't cope anymore with the pain! All my nerves hurt neck scapula biceps pain all the way down arm forearm aching hand aching does anyone else have the forearm hand aching pain.
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I have had diabetes for several years now. I have nerve pain in my feet that is usually not too bad and comes and goes. Lately, my left ankle feels like there is a hair being dragged across causing a tickling feeling. Tonight, my right ankle has this sharp stabbing pain in it that has almost caused me to fall while walking. I have medicine for the nerve pain but don't like the side effects so I quit taking it. Could the stuff going on with my ankles be due to diabetes?
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i been having daily chest pain under my armpit left side and chest pain left side and the pain goes into my arm and i get arm tightness i have had tons of ekg tests done this year going to the hospital blood work x ray and so on and everything comes back normal i notice a lot of the time during the week acid comes up into my throat area so i'm thinking this can be acid reflux.
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I had DeNovo surgery on my ankle 4 months ago - lesion was 11 x 13. Surgery went well. I was NWB for 6 weeks, then in boot for 4-6 more weeks with PWB. Started PT at 10 weeks and was out of boot at 12 weeks. No problem with recovery or PT until that point. After I was fully weight bearing I had much more pain. On sides and bottom of foot as well as at surgery site. Still have lots of pain and sensitivity if I walk barefoot. PT was successful as far as ROM and strengthening but he doesn't want to push me any further because of pain.
OS says too early to say it did or didn't work, but I think it didn't and he won't do MRI until 6 months. He'll give me pain meds, but I don't like them and don't react well to them. The foot pain is bad! Could it be nerve pain?
I knew this was a long recovery, but I wasn't prepared for this! I ran for 30 years, which could have contributed to this problem, but now I'm wondering if I will ever walk pain-free again?!
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June 2015 I got a flat white painless lesion on the inside vaginal lip,smaller then a dime. Didn't look like herpes pics. I went to the doctor she looked and open textbooks and said it didn't look like herpes. She did a culture but the culture got messed up so wasn't able to be tested. Never went back to get retested because the sore went away. October 2015, Same situation same size painless only hurt when urine passed over it but it didn't hurt to pee. January 2016 same situation took about a week to heal. Recently just got another one the end of March 2016 and pretty much went away in 2 days. What can this be, I'm scared to have sex.
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A few months back my Dr was checking my thyroid - said it felt soft - sent me for blood tests (MANY hypothyroid symptoms!) (which were ok - TSH only 1.1) and an ultrasound which showed a small 8x7x7mm hypoechoic mass lesion on the lower left lobe of my thyroid. I had a FNA biopsy two weeks ago, today actually, and already found out last Friday that 2 of the 3 pathologists said they can't say what it isn't but to remove it asap and the 3rd said absolutely consistent with papillary carcinoma and to remove it asap as well... so now I am just waiting to have it removed. My Dr absolutely agrees and said get it out! He said depending how bad it is they will decide whether they just remove the mass but will possibly remove the whole thyroid... do they end up doing two surgeries or do they get in there and see its worse then they thought and make the decision right then and there? He explained it is THE cancer to have - although no one wants any cancer... that it is very treatable etc. I'm just stressed and wondering about the whole thing. Is it normal to have normal thyroid levels but have PC?
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On top of everything else, it would appear as though I'm having issues with my TMJ...I believe I'm a jaw clencher when I'm anxious (which is pretty much always), and I'm also a sloucher at my desk, and this has caused the muscles in my neck to become VERY tense....could this tension be causing my headaches as well? And what about the persistent off-balance feeling that I seem to have whenever the tension strikes? My head just feels so heavy...as though my poor neck can barely support it. I had a massage last night and the therapist was astonished at how tight my muscles were, especially on the sides of my neck, behind my ears, and in my shoulders....all related? Does anyone else experience this? The pain is pretty intense and over-the-counter pain relievers (like Advil) don't do a thing for it.
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I'm 37 years old .After having slight pain and tenderness in my lower abdomen I decided to go to the ER where I was diagnosed with a lesion on my left ovary that"could be a complex ovarian cyst;however,there is a small chance that it could be something more serious like a mass" is the way that it was writing my discharged papers. The doctor said its 1 inch in diameter. I've been experiencing this pain off and on for a few months. Now I'm freaking out. I am going to schedule a follow up with my gynecologist next week. Should I be worried that this is cancer?
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I have recently been diagnosed with EBV. I didn't present with the "normal" symptoms. I first experienced joint pain, then muscle pain, followed by extreme fatigue and muscle weakness. That lasted for about a month, then I developed sharp electric pains in my nerves and associated muscle weakness and numbness that comes and goes in my arms and legs. The nerve sensations have lasted for about 2 months. I seem to be healing
As I haven't experienced as many sharp electric pains, just numbness and tingling. I have been to a neurologist and have had an MRI of the head and neck which came back normal. Has anyone ever experienced anything of this sort of nature? I've been experiencing symptoms from EBV for 3 months now.
It's also important to note I was tested for Lyme and other blood work was done. Everything was normal except the ebv (which showed I had either contracted ebv in the last 6 months or it was.
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I've been having issue with my arm for 6 months now, tingling, numbness, burning in my forearm, hand and up to my shoulder. I also have a stiff neck. It all started with pain in my hand,thumb and wrist while using the mouse (I am a computer IT analyst) and slowly started to affect the whole arm, shoulder and neck.
I have had an ultrasound to check for tendonitis, Nerve studies to check for Carpal tunnel and cubital tunnel and they didn't find anything. I had an MRI of my neck and it's normal apart from some cysts adjacent the nerve roots.
One doctor wants me to see an orthopedic surgeon to have them checked and another thinks they are asymptomatic and aren't the cause of my problem.
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I have been dealing with pain in my feet for several years which has gotten progressively worse. The past 6 months or so have been so bad that 3 months ago my doctor prescribed Gabapentin which helped significantly for a brief few weeks, but I am at the highest levels now and there is a new pain in my right ankle that will just not go away. I am weaning off of the Gabapentin so that I can try Lyrica. I am being scheduled for a nerve conduction test to try and determine what is wrong exactly. I am not diabetic. I believe it is from too many years of standing/walking on concrete (I'm a caterer/chef) without proper foot support. My doctor seems to support this opinion, she does not seem to have any answers. Just had blood work done, I am in excellent health otherwise! Am so worried that I'll be unable to continue working. Pain is relentless. Cannot live on pain pills, just do not want to go down that road! Anyone out there have experience with this sort of problem? How about Lyrica?
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I have been taking Fluoxetine (Prozac) for nearly 7 years and will shortly be taking Gabapentin capsules (opened cos i cannot swallow capsules) for 2 weeks at 300 mg (once a day), then 2 weeks at 600mg (twice a day) and then 900 mg (3 times a day). My nervous system is shot meaning that my body produces too many chemicals making the slightest nerve pain excruciating. Also have a trapped nerve in my foot which means exercise is limited. Is it best to start taking these in the morning? By week 5 i will be taking them 3 times a day. Is it advisable to take them at roughly the same time of day?
I don't work fortunately so if i get any bad reactions i can deal with them at home.
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Has anyone tried methadone for nerve pain? I've just started a low dose and wondered if you had any side effects and how long they lasted? Most important, any relief?
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I am interested in how you have recovered and how your nerve pain is.
i just had an alif L5=S1 on oct 22 and i think things are going ok. I only have slight discomfort around my spine, have slight nerve aches in my left leg but my feet ache like i have been standing all day. My surgeon told me to expect nerve pain for up to 4 months but i cant help worrying when i get pain where i never had it before I don't get pain walking or sitting, only the foot pain when standing and nerve pains when lying down.
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For a few years my problem has been creeping up on me. Recently, it has become hard to remain standing much less walking. So I finally broke down and went to my doctor. I've had an xray and a MRI, with nothing coming up. I've seen two doctors and my current one gave me a shot in my back that gave me a decent amount of relief for a few weeks. So he set me up for physical therapy. I did that for about three weeks. The basic pattern was that when I usually left for about a good hour or so, I'd feel great. Then the pain and tightness would return and cripple me. So now I'm scheduled for a Radio Frequency Ablation. Which my doctor said will give me significant pain relief for up to 18 months or longer. So now I'm just waiting for my insurance to approve the procedure.
About a month ago my doctor wrote a long letter to my employer allowing me to work from home. I do have medication. Tramadol but if I take two it halves the pain but I still can't walk in a few minutes and on top of that the medication slows me down. If I take three, It puts me to sleep. Then out of nowhere last week, I got a new job. Clearly I haven't told them about my back problems. My start date is three weeks from now and I fear that I might not get insurance approval before then. So I'm debating trying to hit the gym and lose some weight. My doctor said that may or may not help. I am a bit overweight now due to depression and other reasons.
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I've been just prescribed Nortriptyline for IC, generalized nerve pain & Insomnia. My GP says it's a more recent form of Amitriptyline & better for nerve pain. she's started me off on 10 mgs x1 week, 2 x 2 weeks, & 3 x one month if necessary.
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In pain after botched bunion surgeries by podiatrist, underwent reconstructive surgeries with OS. Still in pain, now was diagnosed by OS with RSD. 3 phase bone scan showed "increased blood flow and soft tissue uptake in the right ankle and foot. There is intense increased uptake in the right first metatarsophalangeal joint likely represent reactive postoperative change and consistent with postsurgical changes and reflex sympathetic dystrophy in the right lower extremely". Pain management said that as I DO NOT have swelling, change in color and temperature, it is not RSD and sent me back to OS, who already told me that there is nothing else he can do surgically. So I have terrible burning and stabbing pain and muscle spasms. I just want to understand if RSD is a nerve pain or is the result of some abnormal process in bones as was indicated in my test?
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