Discomfort In The Urethra After Sex - A Lot Of Pee
Hello, I'm 15 years old(gay) I had sex about 3-5 days ago and 2 days after sex I felt discomfort in the urethra and the pain is bare able just comes and go like at least 10 times a day and I thought it was because of when I had sex I didn't ejaculate I precummed a lot so I masterbated and a lot of semen came out and I felt a like better but then It came back so I thought it was still like left over precum so I masterbated again and now it coming in waves everything works just fine just I feel like I have to pee a lot, please help!
View 1 RepliesBurning Sensation In My Urethra In My Perineal Area After Sex
A few weeks ago I had sex with my girlfriend of 3 1/2 years. About half an hour after, I started to experience a burning sensation in my urethra in my perineal area. I took some ibuprofen and a hot bath and the pain subsided after about an hour. We had sex again over the next few weeks with no more issues. However we had sex the other day and the same result. A mild burn in my urethra. I thought that it might be the fact that I drink a lot of soda (bad for you I know) so I have started drinking strictly water the past few days in hopes that it would go away. It hasn't. I went to the doctor and they said it was probably a UTI and so they prescribed me ciprofloxacin. I just started taking it today and the pain has been off and on for about five days. I have no other side effects other than a burning in my urethra. It doesn't hurt to urinate, no discharge, etc.
View 1 RepliesKidney Stones In Urethra - Urinary Incontinence
A CT scan showed my husband had a kidney stone in his urethra. He is not sure if he passed it yet or not. One day he had huge, huge pain and I took him to the hospital and they gave him pain pills but since then (a week ago) he's had no pain, so he thinks he might have passed it. Only one problem - he has urinary incontinence which is driving him crazy. Any thoughts?
View 2 RepliesWomen :: Painful Burning Sensation In Urethra - No UTI / STD
I am a 21 year old female in the UK, and I have been suffering with a painful burning sensation which I believe to be coming from my urethra since September 2014. The pain comes and goes throughout the day, and it will be at its most intense after having urinated, and after sex. At its worst I struggle to walk. The need to urinate has increased but there is no difficulty in going, though I do now most often have two streams when urinating which sometimes will stop and start. On multiple occasions there has also been thick blood in my urine too.
No UTIs have ever shown up on the paper dip test at my local GPs, though I have had UTIs in the past. I have tested negative to all STDs. I have had ultrasound scans which have shown nothing abnormal. I have had numerous internal examinations by doctors and one by a Gynaecologist, all have said everything looks normal and healthy.
My GP has had me try at least 6 different types of antibiotics but none have had any effect on me, except for Cephalexin which I took once a day for 28 days, the pain felt lifted and sex was possible again, but 3-4 days after having finished my course I was back to how I was before them.
I drink plenty of fluids (including cranberry juice) and eat healthy, I don't drink alcohol, smoke, or take drugs. All pain killers have very little effect on the pain, only a hot water bottle sat between my thighs brings any relief. Taking cranberry capsules, and/or cystitis relief sachets has had no effect.
I am about ready to give up on my local GP, its doctors and the NHS, no matter how many appointments I make and attend no progress is ever made, no tests are ever taken and my request to be referred to a Urologist has been repeatedly turned down, I am only ever told to drink more water and to try a new antibiotic, which I pay for each time, no one seems willing to search and to find out what is causing the pain. Affording to go private is a problem for me though, and so I just hope there is someone out there who can relate to me and give me guidance/knowledge on what to do.
This pain is now negatively affecting all aspects of my life.
Clitoris Situated In Wrong Place - Directly Under My Urethra
I'm pretty sure my clit is in the wrong place, I've never had any problems with it 'working' however it is situated directly under my urethra, like the top bit of it is sort of attached. Will this cause any health problems?
View 1 RepliesKidney Stones :: Stuck In The Lower Part Of Urethra
recently been in hospital with renal colic but have not passed the stone yet it appears that it's stuck in the lower part of the urethra. I'm back at home now with medication. Has anyone else had this problem if so what was the outcome. I'm hoping it's going to pass on its own but no signs as yet .
View 10 RepliesVaginal Health :: Lump Between My Urethra And Vulva Opening Is
I'm 17 years old and I am not sexual active and I am a virgin. I have an important question about my body, my hymen to be exact. At least I think so. Anyways for years I've always had this lump looking thing between my urethra and the top of my vaginal opening, it's soft, I think it only hurts a little when it's touched with dry skin which is hardly, It's never bothered me but lately I've been wondering if that's even suppose to be there, I urinate fine without pain or burning and I get my period normally too. Now to describe it better, there's my urethra and then connected is the lump that's fairly large, not BIG but if a doctor checked me; its impossible not to see, then it connects inside with my vaginal opening but just the top of it, then I have a normal vaginal opening below it, and I can see what looks like my hymen, looks normal to me there. I've used tampons with no problems and such but I'm thinking if I have sex in the future, it would be painful or impossible to just pass it without rubbing it which would hurt I'm thinking. So about 2 years back I went to the doctors because I was sure I had a yeast infection, they checked me out down there and did a pap smear, I didn't mention the lump because I was there for another reason but the doctor also didn't say anything about it so I had been relieved and thought it must be normal then but when she put the metal thing during the pap smear; I felt it hit the lump and it hurt but then after she pulled out; I felt no pain at all, but then I think about how it would be if I had sex in the future and how it might be a problem, I just can't figure out what it is. I'm thinking of just getting a pelvic exam in general and have my doctor just check that all out to make sure I'm fine but I honestly feel completely alright and just want to know what it is.
View 1 RepliesUnprotected Oral / Vaginal - Burning Urethra / Wrinkly Glans /Swollen Meatus
I have been experiencing numerous symptoms since a brief encounter consisting of unprotected oral and protected vaginal sex on February 20th.
Day after encounter:-
Itchy mons pubis
Day 2-3:
The tip of my penis felt numb. I'm pretty sure I felt tingling at the base of the scrotum, which may or may not be irrelevant.
Days 4-12:
The tingling in my urethra turned into continuous burning--not any worse when urinating--which the doctor at CityMD didn't have much to say about.
Small papules formed on my upper inner thighs. The doctor prescribed me hydrocortisone, which has been somewhat helpful. My thighs still feel chaffed sometimes, but this could be unrelated. My scrotum was bright red and scaly. A different doctor (at a different CityMD) prescribed econazole, which has been fairly helpful.
Days 13-17 (current day):
The burning in my urethra has turned into more of an "ache", and has become more intermittent.
My tailbone just recently started aching, and I have been constipated, but both of these things could be irrelevant.
Throughout all of this I have had an inflamed/swollen meatus, a wrinkly/shriveled glans, and particularly dribbly clear pee left over when I go to the bathroom. If the dribbly clear pee is considered discharge it is watery odorless discharge.
My fear has been that the symptoms not explainable by the fungal infection are due to an atypical presentation of HSV-1 or HSV-2, or perhaps some other virus. There have not been any lesions, but the tingling testicles early on and the current tailbone (proximal to the sacral ganglia?) pain seem like they could plausibly be nerve-related.
I have also read about other things, like Mycoplasma genitalium and Trichomonas. I don't know if these possibilities are worth exploring or not. I am pretty sure I want a type specific IGG test for herpes 1 & 2 in any case. Could this somehow be prostate related?
One more thing: While I have not gotten any results back from my full panel STD test at CityMD, I am pretty it'll come up clean. My partner from the 20th had clean results. Also, for what it's worth, my urinalysis didn't show anything obvious at CityMD. I have not taken any antibiotics.
Inner Ear Disorders :: Possible Perilymph Fistula?
My story is as follows: about a month ago, I began having ear pain that would alternate between ears. After a few days of this, the pain settled in my right ear, where I developed both pain and fullness that persisted for about two weeks. My ear constantly had the sensation that it needed to "pop," such as what one experiences when on an airplane. I went to my GP after a week of these sensations, who told me that it was likely Eustachian Tube Dysfunction and that it would resolve soon. She prescribed decongestants, antihistamines, and a steroid nasal spray. I took Sudafed and Allegra (but not the spray, as I am scared of steroids) but they did not seem to help.
Well, in the meantime, my blocked ear was annoying the crap out of me, so I decided to go online and look for some home remedies to try. One thing that I found was something called the Valsalva maneuver, in which you close your mouth, pinch your nose and blow out against closed airways to unblock the ear. I tried this several times over the course of a few days in attempts to get my ear to unblock. Most times it was difficult to get the right ear to "pop," and even when it did, it did not alleviate my symptoms.
Shortly after trying this maneuver, however, I read that the Valsalva maneuver can actually DAMAGE your inner ear and cause a perilymph fistula if done too forcefully. (I don't think I did it too forcefully, but I can't be sure.) Learning this sent me into a panic, and ever since, I have been experiencing a vague, constant dizziness that lasts all day. I have had trouble focusing my eyes and it feels, at times, like my brain is being sucked up and out of my skull (sorry). In the meantime, the sensation of fullness and pain in my right ear has improved greatly, but I am still being plagued by this constant dizziness. This dizziness has been present for a full week now. I have no sensitivity to loud noises, no hearing loss, and no episodes of vertigo. I do have a bit of wooziness when I am a passenger in a car, and I have felt extremely, unnaturally ill and fatigued throughout this ordeal. For those of you who have had PLF, does this sound like it could be a possible PLF? Is it even likely that I acquired a PLF after performing the Valsalva Maneuver?
Thank you so much for your help. I am hoping and praying that this dizziness is a fluke and not related to a PLF or inner ear damage, but the possibility scares the ****** out of me, regardless. I have had an extremely stressful year between losing my job, acquiring a crippling hip injury, and dealing with a host of other health issues, and the possibility of chronic dizziness is not something I feel capable of dealing with at this point.
Perilymph Fistula :: Is There Any Surgery?
Anyone out there had this surgery? I'm in week 3 and wondering what to expect going forward.
View 3 RepliesPerilymph Fistula - Surgery Or Not?
To cut a long story short - mid August 2014 I did a sinus rinse for chronically blocked sinuses. It went very wrong and I ended up with water trapped in my left middle ear. It didn't come out by itself and the pain and pressure was getting too much. I saw a GP and we agreed on using a nasal balloon to equalise the ears and try to get the water out. I also tried a few valsalva actions.
One day (first week of September), I was using the balloon when I felt a painful loud click in my right ear. This is where my real problems started.
I now deal with: constant tinnitus in right ear, dizziness, vertigo, some nausea, really bad head pressure, auras, vibrations and buzzy feelings throughout body, deep pain in ear - can almost feel blood or fluid in right ear.
Saw GP and it is a suspected Perilymph Fistula of the round window in the inner ear. I am seeing an ENT privately, hopefully in the next 2 weeks. Thing is, I am in England, UK and I am worried that they don't really deal with PLFs. Then I will be stuffed!
I am currently doing as much bed rest as I can as I read online this is best at this stage. I am however very very worried about what has happened. I am worried about leaking CSF fluid too. I certainly have enough head pressure.
Can this really heal with bed rest or do I need surgery? Also, I am scared about my tinnitus getting worse with surgery. Anyone who has had PLF repair surgery, what was the outcome? Did your tinnitus get worse or better in the end? Did the head pressure go? Has anyone recovered just with bed rest?
Share Your Perilymph Fistula Experience
I am going through a possible plf and trying to talk to people who know about these. Please if you are still around I'd love to talk. There are very few people out there and. Very little information.
View 14 RepliesENT :: Perilymph Fistula Or Middle Ear Fluid?
I was hoping for some advice on a problem that I've had for 3 years. My main problem has been on and off vertigo and imbalance, however I don't think I have rotational vertigo because most of the time I just feel like inside my head is spinning? It also feels as if the ground is sinking beneath me.
Dizziness started 3 years ago, about 2 months after a serious bout of the flu which took months to recover from. At the time my ears were extremely blocked and I would do the Valsalva maneuver to help unclog my ears. It wasn't until now that I discovered you aren't supposed to do that? Anyway my dizziness was consistent 24/7 for nearly 1 year, at which time my symptoms seemed to disappear. As of April this year my symptoms returned.
Over the years I have been to numerous GP's, ENT's, neurologist, and all of which were unsure of what was going on. Most of them have said they don't believe it's Meniere's disease. My main GP said I DIDN'T have fluid in my middle ears, however since then 2 GP's have both confirmed that I DO.
Current symptoms:
Brain fog
Dizziness/vertigo
My ears feel wet in the morning. Not enough to wet pillow
Tinnitus in both ears, slightly more prominent on the left side
Fatigue
Difficulty concentrating/problems with memory
Tingling/electric shock feeling on left side of scalp behind left ear
Anxiety
GERD and gastritis
A couple of things seem to exacerbate these symptoms, such as anxiety, hot and humid weather, having a hot shower (I now have to have cold showers, before I would have to sit down), menstrual cycle.
So I am pretty convinced that I either have a perilymph fistula or middle ear fluid. I have been using Nasonex for a couple of months which seemed to improve symptoms but now I am starting to feel worse again. My now current GP has suggested Ventilation tubes/grommets, however if I actually have a perilymph fistula will this improve symptoms or not have any benefit at all? I also have been prescribed SERC but I do not think it will help, as 2 years ago I took it and it made my symptoms WORSE.
I am wondering if I may have damaged my ears years ago when I had the flu by constantly trying to pop my ears. I have been allergy tested for Molds, grass, pet dander and dust mites, all negative. I have also been tested for MS which was negative, and all the routine blood tests etc. MRI showed I have a mid-septal deviation (my nose isn't straight) and previously enlarged adenoids, but apparently was of no clinical significance.
Perilymph Fistula Recurrence 24 Years Later
In the spring of 1990 after a chronic right middle ear infection, I began having bad vertigo, nausea, and disequilibrium problems. I saw the ENT recommended by my PCP and after testing that came back normal was scheduled for exploratory surgery. A perilymph fistula was visualized and patched. Recovery was normal with some slight dizziness continuing for a few months and then resolving. Postoperative testing revealed no loss of hearing from the surgery and I was released from care to resume normal life.
Fast forward to March 2014, severe disequilibrium, tinnitus, and noticeable hearing loss brought me back to the same ENT (A relief, as he remembers me as being his only visually confirmed PLF) Testing showed hearing in the right ear normal but not as good as the unaffected left ear, other testing showed a possible recurrence of a PLF in the the same ear (right). I am scheduled for surgery on April 30, 2014.
There was nothing during this time that would account for the fistula to recur, no heavy lifting, head trauma, air travel, upper respiratory illness, etc. He feels that I may have a predisposition to increased pressure in my inner ear that causes the fistula to recur. Has anyone heard of this? And, if so, why would it take 24 years to happen again?
Rectal Fistula Diagnosed Via Colonoscopy
I have had a rectal fistula diagnosed via colonoscopy. I have zero problems with it and would not have known I had it. From the operative report:
"midline anal fistula which was superficial with minimal amount of muscle involved within the fistula".
The surgeon said it should be fixed.
Why can't I just leave it alone? Do these ever go away on their own?
Prostatitis - Fistula Can Lead To Cancer?
Now 22 , at the age of 13 , i started to have urination difficulties , standing in front of the toilet for about an hour , feeling the urge to urinate even though i know at the same time that my bladder is almost empty and finally a drop or two come , it continued for about a year then it was gone , for the last three years i have been having the habit of excessive masturbation ( sometimes 4 times per day ) , most of the time i go directly into sleep after masturbation , and as result the usual need to urinate after masturbation is suppressed and the urine is retained till i woke whereas i feel its reflux in the ureter , during this period whenever i go to sleep with full bladder ( regardless after masturbation or not ) , the urge to empty my bladder never woke me up , but what came up recently that i started to drink half liter of beer before i go into sleep directly every night for the last 3 days , yesterday i felt my prostate hard as rock , this sensation is mild so far , it is expressed more when i sit on something hard or try to urinate , now today this morning when masturbated after 2 days of cutting masturbation off , this mild sensation became to increase , then afterward masturbation when i try empty my bladder i felt more pain and couldn't pass urine , when i tried about 2 hours later , i managed to do it hardly after i tried to strain my bladder , whereas during these 2 hours i felt urine retention but with much less of the natural urge which drive you to the bathroom but i still feel the pain of reflux at up the ureters , the one thing which is so clear , that my pain is expressed from the prostate as hardening or feeling it like a rock , with mild sensation of burning . Also i think it is important to mention that at the age of 15 i got " pilonidal sinus " and underwent surgery to remove it but , i stopped checking it for the last 5 years and i have been feeling it pain coming back for about a year or more , but i ignored it , whereas i am referring that i may have a case of prostatitis with infection originated from the fistula , i also doubt it may be prostate cancer , even i know the chances of having it at such age is almost nil , this is why i am thinking to take the test of " PSA "
View 5 RepliesPerilymph Fistula - Progressive Hearing Loss
Though I am actually considering that I have something called basilar migraines, which in many ways can mimic fistulas, I want to make sure that there is no chance of small bilateral fistulas in my ears.
Essentially, I have had progressive hearing loss for 11 months now, along with a number of other symptoms that began to flare up in August. I have a history of 3 separate acoustic traumas that occurred earlier last year, and I have heard that under extraordinary circumstances acoustic traumas can cause fistulas at the oval window.
My triggers have included loudish noise above 80 decibels, middle ear pressure changes from flying on an airplane or wearing earplugs, strenuous exercise, lifting heavy objects, and clenching my teeth too hard at one point (I was angry).
Most times when I have an extended exposure to any of these factors, I am usually left with a small degree of permanent bilateral hearing loss. I am also often left with dizziness/imbalance symptoms, rocking boat vertigo, roaring or very high pitched tinnitus, parathesia in my hands and feet, pressure headaches that start at the temples and migrate to the sinuses, pressure behind my eyes and occasional aura, hyperacusis, middle ear myoclonus (muscle fluttering), feelings of cold liquid deep in my ears, and on a few occasions, a fuzzy lightheaded feeling that makes me feel I am going to pass out.
Many of these symptoms resolve, but some, like the vertigo and ear fullness, often stay around long term and present in daily episodes.
Do these sound like familiar symptoms to anyone who has (or has had) a PLF? Please do let me know of any similar experiences! Am on the verge of needing hearing aids, so I am trying to get to the root of the problem as soon as possible.
Bowel Disorder :: Anal Fistula Recurrence
So I have had an issue with fissures in the past, due to being on pain meds for pancreatitis for months and cooccurrent constipation. I have already had one surgery to heal the fissure, and it seemed to work. So when I started have that same burning pain when I had a BM I assumed that was what it was. I became really used to it, and it went on for a LONG time. Flash forward to now. I noticed a couple weeks back what looked like pus on my toilet paper when I wiped after urinating, and was freaked out. I pushed on the area near my anus and more pus came out. I assumed my fissure got infected somehow and left it alone. It happened again, this time I was home so I grabbed a hand mirror and looked down there. I saw a bloody spot that was leaking blood slowly about 1 inch from my anus, and I freaked out. I had NO idea what it was, so I googled it and looks like it may be a fistula. It seems to "close up" and go away for a while, then I can smell something and when I go the bathroom I am leaking a little bit of blood/pus from the hole. Seems to happen randomly, its opening doesn't seem to have any correlation with when I have a BM and BM's aren't bloody typically. I have been using anti bacterial soap down there frequently now and I can feel what feels like a ridge under the skin running from the hole to my anus if that makes any sense?
I am completely embarrassed. I am 28 years old and a female, someone who doesn't even leave the house without makeup and this situation is so bad. It smells, I feel like I smell 24/7 (nobody has mentioned it but I feel like I do) and I am almost too embarrassed to go to the doctor. Doesn't help that I am overweight, and though I am meticulously clean (I even use a bidet) I feel like somehow the doctor will judge me as a gross fat girl.
Crohn's Disease :: Fistula With Cutting Seton
I had a high transsphincteric fistula (multiple abscesses). CRS placed a cutting seton with fistulotomy in July. CRS told me that the seton would be in prob 4-6 weeks. It is now 8 weeks later, new CRS (first one moved), told me that he doesn't use these much as they are not tolerated well and that he thinks he will have to go back in and tighten it as it is not advancing. He says this is/can be a long process. Now I am to go back in several weeks to finalize new plan. Problem is, after surgery, I had Augmentin. The fistula track was not draining like it was supposed to and I got another abscess... after the fistulotomy and seton placement. CRS gave me Augmentin which I'm not sure really helped. So, I got a total body rash from the augmentin. I lasted 5 weeks before I was so miserable that I finally took oral steroids from Dermatologist with CRS approval. After I did two weeks of steroids, which helped tremendously, the rash came right back. Derm subsequently gave me a new prescription for prednisone (for one month taper!) and told me that it is a rebound rash after I stopped steroids. CRS says he won't do next surgery until I am off of prednisone for several weeks. Do I take the prednisone? or try to power thru the rash and not tear off my skin? How long will this next seton take to cut thru? wonder if it will get "stuck" midway too? More tightening procedures? Oh.. what to do?
View 1 Replies