Recurrent UTI With Pain Near Ischial Tuberosity
Jun 4, 2015
I cannot find any doctor to help me. It started in November .. I thought I was having some back pain and went to the DR and found out I had a UTI. I was optimistic I would take the antibiotic and all would be fine. Well after I completed the Cipro the UTI was still there. They switched me to Macrobid and it cleared up. I continued having the pain in my back, hip and near my ischial tuberosity (sit bone). The sit bone felt very tender upon palpation and when i would press on it, it would also then initiate an anal reflex. (I think a sphincter is somewhere around there). I have gone to orthopedic doctors, and I have an appointment today with a Urologist as the UTI has come back twice since then. It all seems interconnected. I also have these shooting pain up and down my labia ... to my hip as well. It is all on my right side as well.
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I've been having pain sitting, standing, & walking very far (at all) for over a year now. I had a spinal fusion done at the L -5/S -1 level back in 2002, & my docs keep close tabs on my back. I've had a tiny tear in the L-4 for many years, but most the docs feel my current problem has absolutely nothing to do with my spine - I agree. I have been diagnosed with a hip labral tear in my right hip socket about 4 months ago, but not bothered enough to do the drastic surgery. Doc injected left hip socket due to pain, but again, not my main problem.
I've had physical therapy (which aggravated the left socket), steroid injections into the ischial tuberosity bursa (both sides) - due to the doc thinking probable ischial tuberosity bursitis, which it is not, & am scheduled for an EMG down both sides of my lumbar spine (I hate those tests - they really hurt!). Meanwhile, I've been working with my chiropractor who does adjustments, percussion massage, iontophoresis, & cold laser treatment on me twice a week.
NO ONE knows what this is, WHERE to send me, or how to FIX it!
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I have been suffering from pain on the gluteal region (it worsens when sitting), sitz bones (ischial tuberosity), upper thighs, lumbar region and feet (calcaneum) for almost 2 years now. I'm 26, have always been healthy, but I have to say this condition is affecting my quality of life SEVERELY.
I have researched a lot about my ailment, read many scientific articles, have been to almost 50 doctors and still I haven't received a proper diagnose. I have already done many exams to investigate the source of my pain, namely: MRIs, CT scans, electroneuromyography of the perineum/legs, dozens of urine and blood exams, etc.
I (together with some physicians and physiotherapists) have come up with some diseases which are compatible to the symptoms (burning pain on the pelvis, ischial tuberosity, perineum, pubic bones, upper thighs, calcaneum), such as:
1. Pudendal nerve entrapment (negative result after an ANGiography)
2. Ischial Bursitis (negative after a MRI scan, no bursas inflamed)
3. Hamstring Tendinosis/Tendinopathy (negative on MRIs)
4. Prostatitis (no bacteria detected whatsoever, although I have taken antibiotics - PSA normal)
5. Autoimmune diseases (Reactive Arthritis, Ankylosing Spondylitis - negative)
6. Lyme Disease (inconclusive, took doxycycline for 3 weeks though)
7. Irritable Bowel Syndrome
8. Sciatica/Piriformis Syndrome (hypothesis ruled out after intense physical therapy, pilates for over 11 months)
The only exam that showed something not normal was a discreet enthesitis on both heels (calcaneum). That's why rheumatologists thought it could be some autoimmune disorder. Apart from that, everything seems pretty normal. My vitamin D levels are low too, but I have started taking vitamin supplements and my vitamin levels (not only D) are almost close to normal.
I was wondering if someone with similar symptoms have already received a light on that. I have visited a lot of forums on the internet with ppl complaining about the same things, but never read/learned about someone who received an ultimate/precise diagnose., nor did I found anybody who actually recovered from that.
Medication taken to date: Lyrica, Prednisone, Cymbalta, Ciprofloxacin, Doxycycline, Arcoxia, Sulphasalazine, Fluoxetine, Naproxen, Cyclobenzaprine
I have recently started a new treatment called Prolotherapy. I've read it is a helpful technique for chronic tendinopathy.
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I've had this nasty problem for almost 5 years now. I was in a severe vehicle collision where I fractured my L1 vertebrae, and then about 6 months later, I started getting this nagging pain in my left sit bone and down my leg.
I was misdiagnosed for the first 3 years of it. At first they thought I had piriformis syndrome ( which is most doctor's first diagnosis since it sends pain down the sciatic nerve. I did 6 months of rigorous physio/chiro/needling to attempt to fix the pain, but nothing helped.
Then they thought it was a bulging disc radiating pain down my back from the injury.
All the while, my pain was getting worse and worse. Taking more and more pain medication. Getting heavy into the opiates. Then after losing my career in the military, and after a year of wasting time. I finally got in to see a spinal specialist. one who teaches around the world and after 5 minutes of asking questions and a couple of manipulations, he diagnosed my with Ischial Tuberosity bursitis.
While I was happy to finally KNOW what it was. It hasn't been fixed. I get cortisone injections every six months, and unfortunately the relief is is not the best. I am taking a Fentanyl patch for consistent pain relief.
It sucks that a pain in my butt is a constant in my daily life. It's depressing and it makes it so i can't live like a normal person....doing normal things....movies, dinners, socializing, driving... etc.
All I do, is try to keep on moving......moving....trying to stay flexible...doing my stretches....trying to keep in decent shape and health.
If anyone wants to chat about their issues with Ischial Bursitis, I'd be glad to. Or if anyone wants to know about treatments etc....ask away.
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I've been dealing with sit pain for almost 4 years. Mostly feels like on the bone on my left butt cheek but from time to time moves to the outside of iT (along panty line) or to the inside between bone and groin. I can't pinpoint any particular event that caused it. Been mis-diagnosed as piriformis syndrome, have had tons of injections, PT for SI joint issues, sciatica injections, ischial bursitis injections, when pudendal nerve (but didn't pursue that) & today I had RF ablation oF L2, L3, L4, L5 and S5. I've not had back pain except once in awhile an ache in lower back & hips feeling out of alignment (probably self inflicted trying not to sit on my left butt cheek). Anyone else having the same issue or found a solution?
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Findings: -
AC Joint: There is mild AC joint arthrosis present.
Osseous Structures and Articular Surfaces: The glenohumeral cartilage is normal. There is fibrocystic change in the greater tuberosity. There is normal signal in the glenoid.
Rotator Cuff: The supraspinatus, infraspinatus, subscapularis, and teres minor are intact. There is no retraction or atrophy. No fluid in the subacromial/subdeltoid bursa.
Labral-ligamentous Complex: The biceps anchor is intact. No definite labral tear present.
Additional Findings: No mass lesion in the quadrilateral space or suprascapular notch.
I was in a bad car wreck Feb 15th , luckily i didn't get hurt to bad, just banged up pretty good with alot of bruising , i really didn't have pain in my shoulder until 2-3 days later i started feeling a sharp stabbing pain in my collar bone, i kinda ignored it and went about my business thinking ok its just from being banged up. I then went to work on a saturday and noticed that the pain started to get worse and noticed a bulge in between my collarbone and shoulder , i proceeded to put ice on it and just kept working, then i went into work sunday and still same thing but i started to feel very weak and ill . so i told them sorry i am unable to come back to work the next day and made a doctors apt . he scheduled an MRI i got it done and that was in march 9th , he said they didn't see any tears or broken bones, but i do have Mild ac joint Arthrosis , he sent me to an Orthopedic surg. and i have been doing physical therapy since then and he did give me some shot in the shoulder. the pain in my shoulder is a deep ache pain with a burning sensation in my upper arm, then i lift my arm or turn it it pops, clicks , crackles and crunches, the pain stays mostly at a lvl 3 and some days can go to a 5 . If this ac joint is causing all this my god i just want it to go away . I already have degeneration in my spine with herniated and bulging discs in my lower back . Mild bone spurring in my middle back and neck . he wanted me to do 4 more weeks of therapy but so far its not helping the burning sensation seems to be getting worse I also feel like i have a tennis ball in my shoulder (scapula) area when i sit in my car or lean back in my chair . the areas are very tender to touch . I am taking diclofenac for the inflammation . i am supposed to be going back to my DR. may 24th to possibly have him clean and scope my shoulder to see what is causing all this !
also what does this mean ? The glenohumeral cartilage is normal. There is fibrocystic change in the greater tuberosity. There is normal signal in the glenoid.
" There is fibrocystic change in the greater tuberosity." ?
I am just wondering if anyone else has had the same problem with there ac joint doing that ?
bc i am to a point lifting anything real heavy, sweeping and mopping my floors, drying or combing my hair , mixing or stirring anything with that arm ( left ) side .. just makes it worse ! i've heat it iced it , but it gives a very short relief
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I had an exposure around 3 months ago, I got a rapid blood finger-prick test at around six weeks and a little more, and it came back negative. However, starting from this month, I kept having mouth ulcers in my mouth,they are small, I'm getting a new one maybe like a week or so, then it goes away about a week. It's been a month and i have a new mouth ulcer each week after the old one heal.
My question is, how much can I trust my 6 weeks rapid test? I know its not conclusive and I'm getting another test soon, but just really wanna know its accuracy.
Also, is keep having mouth ulcers related to HIV?? is it damaging my immune system and cause such situation?
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I used to have recurrent utis about 5 years ago- trimethoprim used to work as a charm and they disappeared after i had my tonsils out (linked?)
I got a uti 4th of nov- got cephalexin. it got better but i still couldn't have trousers on due to uncomfortability which i assumed meant that the infection was there- 2 weeks later i got test results from gp saying i had a resistant form of e.coli and got new set of antibiotics- as i was on them i took a pregnancy test- which was positive (very happy news). last period date being 3 november.
my symptoms for uti are insane- my clit gets uncomfortably stimulated and i feel like i have to rub it to release the tension but if i do that the same feeling comes back with a vengeance. i have to keep pushing in the toilet and if i stand up there's a horrible sensation over my vaginal area which makes me want to jump out the balcony. so this is a major problem for me unlike the symptoms of "i pee a lot with a burning sensation".
i can't bear this feeling anymore. its been 4 days since i finished the last course of antibiotics, and mornings are horrible followed by symptom free nights. luckily i gave another urine sample on friday (waiting for results). can someone help me? starting to think uti came with the pregnancy.
or maybe i have screwed up genital area that needs to be fixed or something. i got the same symptoms when i was little around 4/5- i used to rub myself back then and remember how bad it used to get - my mum had to sit with me in the toilet to help me get through it. and now i just cry in the toilet for a hour before i force myself up and into bed.
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OK, so the problem started at night...
During sleep, I noticed my right ear became blocked. My hearing from this ear became impaired and there was a feeling of fullness. (If I slept on my left ear, it was like I was deaf!). During the morning however, the problem would disappear.
Anyway, this problem kept recurring night after night. After a bit of google research, I figured it was just excess wax in my ear. I went to a local grocery store and picked up some ear drops, claiming to remove excess wax. ("Debrox"). After administering, the feeling of fullness came back...and has now stuck!!
I read in one article, that gently placing your index finger in the ear and moving it up will create a vacuum that will open up the ear. However, within seconds, this whooping sound occurs in my ear and it closes up again. I repeat the process over and over and the same thing keeps happening.
So should I have put the drops in my ear? Is the problem more serious? I also read it could be Middle ear pressure- how can I hear properly through my ear again?
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I have suffered for a few years now with my kidneys, first starting off with when I drank alcohol. A few days later I would get really ill with a kidney infection and given antibiotics. It then became more common to get them without drinking. I would also inbetween this get recurring bladder infections.
I am 19, a female, and have had various tests (ct scan, dye put in my arm through a drip to see any problems clearer and a few ultrasounds) done to check the structure of my kidney is all okay and that there isn't any obstructions ( all seems to be okay, and they didn't think that it would be worth looking with a cystoscope just yet.) However something worth noting is that I always seem to have invisible blood in my urine that is discovered through dipstick tests. And recently my brother has been having the same kidney problems (kidney infection, especially after drinking alcohol).
I am also now on medication called 'Hiprex' it has antiseptic qualities to try and prevent getting UTI's/kidney infections however doesn't seem to be working as I still get them.
Really getting fed up now, as when I get ill with it I get super achy, all of my glands swell up, a dry mouth so constantly thirsty and weeing loads, especially at night, and dull aches in my back.
Once when passing urine I passed out from a pain in my right lower side. But like i said, no kidney stones or any problems structurally.
Has anyone else been going through this too? Any ideas what could be wrong?
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I am 26 years old with no children yet..Two year ago i had an operation and my bile was removed because i had stones in the bile.Last year i had an operation and removed two chocolate cyst with laparoscopy,one on right ovary 4.5 cm and one on the left ovary 8cm.After the operation i had 3 injections ,one every month named arvekap,they stop the blood for three months.After for six months i was taking pills named qlaira,birth control pills.In December i went for check -up and i was cleared.In April when i went for check -up we found out with ultrasound that i had again two chocolate cyst one 8cm in right ovary and one 4cm in left ovary.some doctors told me that is better to make laparoscopy and others laparotomy(Iopen surgey) and i need a surgery quickly because the cyst might broke.some other doctors told me that i have to make injections to stop my period or to take pills made visane and the cyst may get smaller or dissapear and after to do surgey.what you suggest that is the better treatment to do and if i need to do a surgery now or later?if i don't do surgery now there isn't a risk that cysts might broke?
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Yesterday after having intercourse with my boyfriend of a year and a half, i noticed that some of the sperm came in contact with my hand and broke me out in a small rash on the area that was infected. I automatically assumed i may be allergic to my partners sperm and began looking online for answers as i think it might be related to why i get recurrent cystitis. I have been tested for Thrush and UTI's in the past 6 months and also underwent a bladder/kidney scan and a cystoscopy which all came back negative. After that i was completely baffled as to what could be causing me so much pain and misery. I know i don't have any evidence that this could be the cause to all my problems but when i visited the doctor yesterday he said it is a possibility that they are connected some how.
I really just want to know if anyone has suffered from a sperm allergy before who has maybe been affected with recurrent cystitis because of it and if so how you were diagnosed to find out if you were allergic to your partner's sperm and what you did to treat it?
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I have been dealing with recurrent yeast and bv infections for several years. I have been to a handful of doctors, they cannot tell me why my symptoms won't go away. Doctors have tried to grow cultures of the yeast, but it never grows. I have tested negative for diabetes and do not have anything that would otherwise compromise my immune system. I have tried the yeast free diet - all I did was lose 5 pounds (and on my 100 lbs. body that is saying something). Now my Dr. says that I have BV and a yeast infection. I have tried eating yogurt, inserting yogurt with a probiotic powder, taking probiotics, nothing seems to work. He is giving me Flagyl (500 mg for 5 days) then he wants me to take a Diflucan pill once a day for 20 days. I am not having sex during this most recent treatment plan, in hopes of getting this under control.
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I have only had a primary outbreak about 3 months ago now. Twice since then I have had a sore throat similar to the one I had in the first 3-4 days of my outbreak. My question is, do you think my recurrent sore throats are in relation to my herpes? I have not had another sore since then.
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I've just moved to a very dry climate and have spontaneously experienced a corneal erosion. I had a recurrent corneal erosion many years ago. Is it possible that this is the same injury returning or is it more likely that I have scratched my eye without realising it?
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I had this condition undiagnosed for many years its frequency has increased from once a year to twice a month or so. Eye drops such as chloramphenicol and chloromycetin make it worse. Chloramphenicol ointment Chloromycetin ointment and Simple eye ointment seem to be the only treatment that works. I have to sleep on my back to avoid my eye burying into the pillow if I sleep on my side. To ensure I wake up and have no problem I have to apply a blob of chloromycetin and a line of simple eye ointment into both eyes at bedtime.
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I’m a 28 year old male. I’m 5”11, 10st 4lb and have been a vegetarian for about 10 years.
I’ve had an on and off problem with erectile dysfunction in the past 7 years or so. Towards the end of a 5 year relationship when I was 21 and an undergraduate, I experienced problems with getting an erection and with a low libido (I can’t recall now whether the latter just came from anxiety about the former). The relationship ended, I began a relationship with a then friend, in addition to seeking advice from my GP. The GP prescribed a 4 cialis 10mg tablets, and things relatively quickly recovered.
Fast forward another 5 years (with no problems), and that relationship ended. After about 5 months, I went on some dates with a girl. As we started getting a bit more physical, I became a bit anxious about my ‘response’, and again had trouble getting an erection (again, I don’t know which came first). I got another short course of 10 mg cialis, though we never had intercourse and that ended. I was wary that the performance problems might impact upon future relationships, and wanting to not have to worry about it, I got a longer course (28 tablets) of 5mg cialis. I began a relationship with a new partner, which has now been going for about 7 months. I moved for work relatively early on in the relationship, so we mostly saw each other at weekends. A single 5 mg tablet would allow me to achieve erections without problem for 2 days.
Realising that it was probably not good to become reliant on these tablets, I started trying to wean myself of them by breaking tablets in half. One weekend recently, I took half a tablet on Saturday, and was fine for the day, but could not achieve an erection on Sunday morning when we became physical. I sometimes wake up with erections, and sometimes achieve one whilst masturbating, though both seem less frequent and less strong than they used to be.
I realise that at my age it is likely to be psychological, especially given the history. That’s in part why I used the medication for so long, hoping it would eventually just blow over again. I also realise that I have probably not handled it in the best way, though I still feel pretty helpless and frustrated at it all I guess.
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I had to share my story in hopes of helping someone else. I had BV for about 3 years and when I did not have BV I had a yeast infection. I was a mess! I had tried absolutely everything you could read on the internet I was obsessed in curing myself. The doctors did not help all the stuff they gave me made me so much worse and I was back to square one. This is what has worked for me after my three years of trying everything and anything. Months later I have no symptoms. What I can tell you that has actually worked for me was: Stop taking baths (only showers). Do not let your partner finish inside you (use your imaginations on this one there are other ways. Do not insert anything into your vagina (NOTHING). Do not douche. Do not wash your vagina with anything but warm water. Do not wear underwear all day (let it breathe when you get home). Drink lots of water. Drink unsweetened cranberry juice. Do not let anything inside you that will change your PH of your vagina. Cut out sugar, and all junk food. Do not use scented tampons. Be patient for symptom relief for about 10 -14 days when taking these supplements. I now take a probiotic, cranberry pills, garlic pills, vitamin D, B complex, and vitamin C. Yes that sounds like so much stuff but I am telling you all the things I listed have a good reason behind them. The supplements are 100% needed to cure you from the inside out and the vagina when left alone will do what it needs to to cure itself. I hope this helps someone to weed threw all of the info online and finally be free from this horrible problem that ruins your self esteem.
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After 6 months and 2 weeks, I am having what appears to be protracted recurrent withdrawals, which are withdrawals that all of a sudden seem to return after a period of getting better. I am having severe abdominal cramps, general sick feeling, sleeping problems, and I have to force myself to eat. I have gone from 204 to 167, but have been at 167 - 168 for 19 days. I have significant fatigue, no stamina, feelings of doom, wondering if this is ever going to end. Also, thoughts of going back on the drug. This has been horrible. If you are Christian, please add me to your prayers to Jesus. I need His help. I have been to the Emergency Room several times for chest pain, abdominal pain, and stroke symptoms, all of which were negative, including the labs (blood work).
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I was diagnosed with recurrent BV and was given a treatment of antifungals for it. Now my original symptoms are gone but I have a whole new set of them. My vagina and the insides of my labia majora are ridiculously itchy, they burn like no other, are cinnamon red, extremely hot to the touch, and have a smell that is simply rank, I've had to change my underwear twice today because it's so strong. I don't have unusual discharge or large amounts of it, it's quite the opposite, it's unusually dry.
Does anyone have any idea what's happening? Should I schedule a pelvic exam with an OB GYN?
If you need to know, they had me take a fluconazole pill every other day, three pills total. I'm turning 19 soon, and I'm not currently sexually active.
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For about 3 months now, my fiance has had an intensely itchy area on the left underside of his scrotum. We tried numerous powders and creams, both medicated and unmedicated. Some would work for a few minutes to a few hours but nothing "cured" it. The area is very wrinkly and dry looking. He scratches and itches it so much that it starts to get raw. I stopped using any laundry detergent at all on his boxers and just washed them in water. He said it helps, he isn't as itchy as he was before, but its not going away.
My crazy mind is now going all over the place to try to solve this and I began to wonder....
I, myself, have been suffering from recurrent episodes of bacterial vaginosis for about 2 years. I treat it with vaginally inserted metronidazole and it goes away. Then, sometimes weeks, sometimes months later, it comes back. I just did some research and am going to try some home remedies for myself.
I find conflicting information online about men and a bacterial infection. I read that it is uncommon for men to get this and if they do they USUALLY have no symptoms. Is it possible that he got it from me and is now starting to show symptoms? And I only treat myself so are we just passing it back and forth? Maybe these are two completely different issues but I have to wonder and ask. I hate to see him so uncomfortable all the time, and I know I hate the symptoms I get with my BV.
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