Frequent Kidney Infections After Hysterectomy
Dec 26, 2013
In Jan '09 I was diagnosed with cervical cancer. I opted to have a hysterectomy due to I was done having kids. I had it done in feb '09. Doctor said that everything look fine and sent me home. I called the doctor's office daily complaining of pain. They told me I was being lazy and needed to get up and walk around more. They said I was having gas pains. Finally the doctor told me to get gas ex that would help. I went back to work about 6 weeks later. While I was at work I started leaking urine. The next day I went back to the doctor (OB) and all he could say is I don't know what is wrong. they but a catheter on me and I was still leaking around that. They ran test after test. Finally when that day was over they sent me home with a catheter and said get some rest come back tomorrow and talk to the urology department we have no clue. I had 3 kids husband out of town working and I am in severe pain. My mother in law took me to the doctor the next day and he said oh your ureter was damaged during surgery we just need to do a minor surgery to put a stent in there and you will be as good as gold. They did the surgery that day. When I woke up they told me that I had 15 mins to get my head on right cause I had to go to the hospital to have a nerostophy tube put in my ureter was actually cut in half. I had no clue what was going on. My mother in law took me over there where I was admitted into the hospital for my 2nd surgery that day. When the doctors there but the tube in they hit my main nerve in my back so every time I would breathe I would get sharp shooting pains up my back. I was sent home with cather and tube for 6 weeks. then in 6 weeks I have a Ureter replacement surgery. The doctor there did wonderful. But to this day I get kidney infections VERY easily and I am ALWAYS in pain in my right side on my back right by my kidney. I was wondering does anyone else have this problem?
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I had the bladder sling done and hysterectomy this past june. The doctor told me he did pull the sling tight since I am just 41. I keep having bladder infections every couples weeks or months. What the heck. I don't have insurance now. The scientific method was used on me (sling). I am scared , don't wanna have no more surgeries. Gotta go see the doc tomorrow or Thursday.
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Hello I am 19 years old I have been suffering with bladder and kidney infections since I was 14. I was admitted to hospital to find out what was wrong with me nothing could be found, I think I have tried every antibiotic under sun...nothing seems to help, I suffer with them every few mounts or so on and off.
When I fall ill with one I'm very ill it puts in bed for days with terrible pain and fever, I'm young and starting university very soon...I don't know anyone who suffers as bad as me and I struggle to get to the doctors a lot with being a full time student, it's so unbearable and frustrating can anyone help?.
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I went to the doctor as i am constantly running to the toilet. I also feel a lot of pressure. I am 46 years old. I am trying to loose weight but can't walk far as i then need to pee. I pee approx 15-20 times a day. Blood tests show no diabetes etc. My doctor examined me and says i have a cystocele, he said it wasn't as bad as he expected going by my symptoms. He did say tho that everything is crammed in there (whatever exactly that means i am not sure) He is referring me to get a pelvic ultrasound and then consult with gynecologist. He thinks i may benefit more from surgery as he thinks the other treatments don't work as well for me.
Anyone had similar symptoms with a mild cystocele?
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My son has been on amiodarone for four months now following an atrial flutter which required DC Cardioversion. He takes other drugs for his heart such as furosemide, ramipril and warfarin. He seems to have frequent throat infections which lead to flu symptoms (hot and cold shivers, aches and pains) these have forced him to bed for 6 days at a time. We have been told that these are not a side effect by the consultant but we were managing to keep on top of infections before amiodarone with some wonderful natural supplements. I am interested that none of the comments that I have read on this site have really mentioned similar side effects. Has anyone experienced the same? He has been free of atrial flutters and has declined an ablation on the grounds that they cannot guarantee a total success rate.
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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 have RA, fibromyalgia, and diabetes II. I have been dealing with kidney stones for 10 years. The last 4 years have involved kidney infections and hospitalization. Last year I was near sepsis and placed in the ICU. Since then I have been experiencing RA/Fibro flare-ups that are worsening. I have had mono 3 times (infancy, twenties, and early thirties). I am wondering if I have it again and whether the kidney infections caused it or were a result of the EBV in my system.
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I have never really posted on any board before, so I don't know what to do or what to say. But. I am currently experiencing my 6th UTI and the pain is beginning to radiate to my back already; I believe I have a kidney infection. I just turned 18 years old during the holiday and I never really had a problem with UTIs until 8 months ago when I had my first kidney infection. It was the worst pain I had ever experienced. I had the UTI for a week prior and I was just using monistat since that had worked for me the one other time I had one, and when the pain reached my back I didn't tell my mom until three days after and I was taken to the hospital right then. Anyways, they gave me strong antibiotics and sent me on my way home after hours of IV tries and ultrasounds. The antibiotics worked wonderfully and I finished the bottle like instructed. After a few weeks I had another UTI, so I went to see my doctor and I was given more antibiotics. I didn't think anything of it and I just took my medicine as instructed.
My third and fourth UTI snuck up on me about three and a half weeks after my second and that was when I was kind of worried. I know something is not right, but I don't have an ob/gyn to consult with as I'm not sexually active (but I will be making an appointment with one and getting a referral for urologist). So I went to my doctor again and I was diagnosed with a kidney infection and sent off with more antibiotics and that single pill that clears up the uti (i don't remember the name). I thought that it had finally worked and I was going to be a-okay until Dec. 23rd when I got my fifth UTI. I went to the hospital, was given a shot (a steroid, maybe? All I know is that it burned) and it cleared up until the day after my birthday on the 28th. I haven't been able to get out to my doctor yet for antibiotics and I'm not a fan of hospitals so now I'm beginning to have flank pain all the way up to beneath my right shoulder blade.
This was rather lengthy but Is there anything that could be causing these recurrent UTIs and kidney infections that I should bring up to my doctor? Because whenever I go there, I pee in a cup and get sent home with antibiotics and "this will nip it in the bud!" but it's back within a month. I'm probably not wording myself right (it's 2AM) but I just want to know if anyone else has had this and what worked for them/their diagnosis?
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I'm 23 and have had trouble with Kidney infections all my life.
When i was little i had trouble with wetting the bed until i was 8years old.
All my life i've had infections, some urine but mostly kidney. When i was 20 I developed acute pyelonephritis which overnight turned into septicaemia and i was rushed into theatre with suspected internal bleeding.
I've seen specialists in Dorset, Somerset and Gloucestershire and have had loads of scans and xrays which all confirm there is nothing wrong with my kidneys.
The only symptoms i get are pain (always always my left kidney only) and cloudy urine. I seem to get these about once a fortnight - i'm so sick of antibiotics (which don't even work that well anymore) that i've stopped going to doctors and just try to cope with it on my own by drinking loads of water and taking painkillers.
Its been suggested that i take a permanent antibiotic which i take everyday for the rest of my life - but i'm only 23 and i hate taking drugs for anything.
I worry that when i'm older i will get kidney failure. I just CANNOT believe that a normal healthy person can get this many infections and nothing be wrong? Or that there is nothing that can be done about it. The specialist in Gloucestershire told me "It's very common and unfortunately technology hasn't advanced enough to deal with the disorder, so there's nothing we can do".
I feel sick, tired and emotional everytime this happens and its so hard to cope with work, university, keeping a house and being a single mum to a 2 year old when i feel this ill. I manage but it makes me cry a lot.
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Can wearing panties cause the uti's?
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I am a 19 yo male and I've been suffering from burning bladder feeling and frequent urge to urinate, I drink a lot of water daily because on December 21 15' I passed my first kidney stone, however the urgency and burning has not gone away. I've been on multiple antibiotics to treat (suspected) prostatitis however to no avail. There is no blood, nor have I ever had blood in urine, it doesn't hurt to masturbate however sometimes after masturbation (masturbation) I feel like I have to use the bathroom followed by burning. I'm scared that this feeling will not go away, will it go away in time? To heal? I've had tests done, ultrasounds show perfect retention and passing of fluids.
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For the past few years now i have suffered with constant water infections, its always pain in my right side, sometimes i'm sick with it and my back feels like it could break. It can also go into my groin area and down my leg also. I've had CT scans and another type of test which all came back as normal which was last year. I don't understand how it can be nothing as the pain is horrendous and all they do is take a urine sample and give me antibiotics. Does anyone else suffer with this? I wasn't sure if it was when i drank alcohol which is very rare but sometimes i get a water infection and sometimes i don't. The hospital put me on antibiotics for 6 months changing them every 2 months and i still managed to get a water infection on them. I am now having blood tests again and will presume i may have to go for all scans again but just wondered if anyone has had the same problem and had any advice on what it could be or what i could do?
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I recently had outpatient gynecological surgery, following which I had frequent urination, burning, stinging when urinating and side and back pain on the right side. Went back to my doctor, and she diagnosed a UTI and put me on doxy and Cipro. Took them a few days, but the side and back pain persisted, on and off, in waves. I also became debilitated with extreme fatigue and weakness--i went back to the doctor, and couldn't even fill out a simple form in the office, simply couldn't think or have the energy to write. She sent me to the ER, saying she thought I had a kidney stone. They did a CT scan and said I have stone in my kidney, but that normally when it's in the kidney it doesn't cause pain. They couldn't explain my other symptoms (included also sweating, fairly frequent urination, low grade fever, confusion). They gave me 2 rounds of pain meds (& fluids) in the ER and I felt better for a couple hours. The next day I felt so rotten and weak I could barely sit up, i couldn't talk, check email or texts, read, move, shower, etc. over the past 3 days it has gotten slightly better. The pain has virtually subsided since the ER, but the fatigue is debilitating. Two friends described their experiences with kidney stones as similar--has anyone experienced the same? Does anything help?
I have heard water and beer help a kidney stone pass, but is that only once it's descended? I'm not really in pain, so my doctor thinks it may have shifted around in the kidney (she thinks my symptoms are something else). Anyway. I don't know if it would do any good to try to flush it out at this point or just wait and see. I simply can't go on for much longer feeling this extreme weakness and cloudy head, feeling rotten, etc. I continue to have a low grade fever, but my labs came back after the antibiotics clean. I do have similar symptoms when I get bad sinus infections, but that's clearly not the case now. Thanks!
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Is it me or is this stuff a waste of time?
I've had obout 20 lithotripsy's in 15 years of having continuous stones. They've never gotten my kidney completely empty of stones ever. I've had lithos, ureterscopy, PCNL. On meds but they can't seem to stop them from growing. I avoid alot of the things that cause stones or limit them. Got to have the 1 cup of coffee in the morning
On the day before litho, your suppose to eat light ( nothing that leaves residue in bowl) but they say you can have white bread or boiled chicken. (Why bother?) I usually only eat jello, gatorade, and just broth. Plus tons of water. The instructions say to drink the magnesium of citrate after dinner. Well to me dinner is after 6/7. But I thought this time I would take earlier since last time didn't start to move the bowels until i was in the hospital. Plus this stuff is awful- taste bad- even refrigeration like they suggest doesn't really help. Twice in past I threw it up.
So I took at 5 pm thinking it would work earlier. Nope. Nothing. Just stomach cramping and it finally started around 5 am after me getting up every hour during night. Still was working again while in hospital.
There has to be something better (tasting) and work faster. Plus less side effects. Or they should change instructions & say take a noon. Next litho (in 2-3 months) I'm taking a 1/2 day off day before and taking at noon. Maybe then can get a little sleep the night before procedure.
Sorry- felt like ranting as frustrated as its been two full days since litho and nothing passing yet. Plus I have a bad back (2 surgeries) which makes it hard to do the exercises where you drink 2 cups water, wait 30 minutes, then elevate kidney @ 45 degrees and stay like that for 30 minutes to try and get the pieces to move.
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I was just wondering if anyone has protein in their urine with Chronic Kidney Disease and what did your doctor do about it if anything. I am trying to keep my GFR stable. The last time it went up a bit but am worried about the protein causing more damage quicker.
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Is it possible to have CKD or kidney failure without protein in urine?
Last week my masseuse found a knot in my back that she suspects could be inflammation in my kidney. I've had some weird symptoms popping up over the last month like foot/ankle swelling, profound fatigue, leg cramps and blurry vision. This last week though I began developing SEVERE flank pain (like 9 on a 10 scale), back pain (started out lower, now entire back), horrible nausea, horrible headaches, shooting pains down my legs, metallic taste in mouth, dizziness and loss of appetite. Not to sound melodramatic but I feel like I'm dying. The pain is constant but the intensity seems to be moving in 24 hour cycles. Today I feel awful but I was able to shower/get dressed. Yesterday I couldn't even get out of bed. I slept for 16 hours. It's been going in that pattern for the last week and a half.
My doc did a urine culture last week, got results today and there was no protein in my urine, but I had 3+ ketones and a large amount of leukocytes. Blood work from a month ago just came in and my kidney numbers were off a month ago: BUN (32), Creatinine (1.8), eGFR (33). Between the symptoms and the blood test I'm thinking it sounds like renal failure, but could it be CKD without protein in the urine?
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Thursday morning I spent the night in the ER with a kidney stone in the left kidney -- when they did a CT Scan - they came and told me that they made an "incidental finding" in the right kidney that is a problem -- they have discovered that I have a "Staghorn" kidney stone that has attached itself and almost completely filled the right kidney. He said that I will not pass it and now my GP has made me an appt. with a Nurse Practitioner at the urologist's office for Tuesday morning to discuss my options. What are my options going to be?
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A while ago I had kidney stones, I was sent for a scan after, upon returning to my GP for the results of my test, he told me there were calcium deposits in my kidney that could mean I have another on the way, I've been trying to keep well hydrated and doing all I can to prevent a recurrence, because they're damn right evil, I've got away with it for quite a while now, last night I was woke up with the same pain I had when I had kidney stones, I sat on the toilet and waited for the pain so subside, it seems to have gone again for now, I was just wondering if I'm supposed to avoid eating foods rich in calcium, I'm also lactose intolerant and with all this I'm starting to wonder if I'm going to en up deficient in calcium.
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In the last week of Jan I was diagnosed with a bad kidney infection and given a weeks antibiotics (can't remember the name). After 2 weeks feeling no better I went back to docs with a sample and the infection was still there and given 3 day course of antibiotics (naturfranton (not sure of spelling)) and was told to come back again the next week with a sample. This time the sample was clear but a week later I was back with flank pain and generally feeling unwell, there was no infection in urine but I was sent for blood tests to test my kidney function etc and sent for an ultrasound. All of these tests came back clear. 2 weeks later back again feeling unwell, nausea, pain around bladder, upset stomach and received 3 day course of trimethoprim. I finished this course and finally felt normal only ten days later to be back with nausea and kidney pain and I am currently on a 5 day course of amoxicillin.
I'm not sure if this infection is one that will just not go away or recurring infections.Has anyone else ever had this problem and what did it take to get rid of the infection? I,ve never had kidney infections before and never had antibiotics before this ( I am 18 ) any help is welcome, I am sick of being sick at this point.
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I'm now almost 4 weeks post abdominal and it still hurts to wee. It's not severe but I definitely feel it, especially if I don't go immediately. Is anyone else experiencing this?
I don't have any symptoms of infection and everything seems to be going well with my recovery. I even laid on my stomach in bed last night...for about 10 minutes lol
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Off to Endo tomorrow to see what they say, I was wondering if anybody is taking Carbimazole with HRT. Had complete hysterectomy last year so taking HRT and just wondering if this has anything to do with my over active thyroid, a few people spoke to know of women who have had hysterectomy and gone on to have OA thyroid.
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