18 year old reoccurring kidney pain/problems

Posted , 3 users are following.

I am an 18 year old girl. In 2013 I had been suffering from many urine infections which I thought nothing about, took antibiotics and moved on. In June 2013 I suffered terrible pain in my right side, conviced it was appendicitus and called for an ambulance. I was told this was not he case and to make an appointment at my gps. I went there and was reassured it was not my appendix but my kidneys were swollen and my urine suggested another infection was present. Not to be too graphic but oh ad blood in my wee and it was slightly cloudy, the pain in my side was unbearable, but would come and go as time passed. I was given painkillers to take and was told to take it easy for a week or too. After my course of painkillers the pain went and I was back to normal. About a month later the pain came back and I was again put on painkillers and sent to have an ultrasound for suspected kidney stones. Te ultrasound found nothing, and I had a blood test to check renal function which came back high but I had high proteins in it. Since then I have had another urine test and another go thought I had a kidney infection that hadn't been treated therefore the pain was not going. After a course of antibiotics the pain went however I keep getting short blasts of pain only sides and I am wondering if anyone has had the same? GPS keep putting me on tablets but I'm getting no real answers apart from this could be something that happens throughout my life- with no reason or explanation for it. Please help!!!

0 likes, 5 replies

5 Replies

  • Posted

    Male and 60 years older than you I have had a similar worsening problem to yours since around February when I had a bad kidney infection. At the time I was waiting for laser prostate surgery and was prone to

    bladder infections. I kept on going back to my GP with urine samples and complaining of pain in the right

    kidney area. Several time my samples were positive for a bladder infection and had more antibiotics. After my prostate operation in late May I got an infection from the catheter that took three lots of antibiotic to

    clear.

    I have been back several times with kidney area pain but urine samples were negative. This made my GP

    say that it was back or muscle pain. I disagreed as bending, lifting and stretching were not painful and the

    pain came on when in bed or sitting. Recently it has spread to the other side and is now mostly constant.

    Last week I went to A&E, only three others there as it was around 10am but I was still there for five hours!

    The doctor felt around my stomach and kidney area without finding anything suspicious and decided the

    pain might be from my back,,, He sent me for an X-Ray that did not show anything wrong.

    He suggested that I go back to my GP for him to arrange for ultrasound scans and other tests. I don't know why he could not have arranged for them while I was there. If I go to my GP he will tell me that he has to

    refer me to a consultant to authorise the tests.

  • Posted

    Hi Courtney , I suggest you go and ask for a second opinion and to see a consultant urologist , you obviously aren't getting your problems sorted and theres something going on , ? Have you seen a consultant , and asked for further tests ?
  • Posted

    It always surprises me that when hospitals find nothing at A&E they send you back to your GP rather than

    pass you on to another department. My wife once had very bad pain on the right side of her stomach late

    one Thursday night. She was very pale and sweating. I phoned 999 and paramedics and a doctor arrived. They took

    her BP and did some other checks at home and took her to hospital. One paramedic said that the pain

    seemed similar to what he had with a duodenal ulcer. I agreed that it was similar to duodenal pain that I

    once had.

    At the hospital their first thought was a pulmonary embolism and they gave her aspirin and heparin

    injections while she insisted that the pain was in her stomach not her chest. They did a chest x-ray and an

    ultra sound scan the next day. Finding nothing they sent her home still in pain saying that the majority of

    chest pan presented never has a reason found for it. While we still protested that it was in her stomach.

    Still in on the Monday she went to her GP. He prodded her stomach, she squealed and he said, duodenal

    ulcer and sent her for an endoscopy. It was , plus a cluster of gastric ulcers.

  • Posted

    Hello Courtney. I agree with Helen. You definitely need to see a consultant urologist. Your GP needs to organise this without delay. 35 years ago a GP fobbed me off for 7 years. I was back and forth to him like a yo~yo. Eventually a locum LISTENED to my symptoms and within weeks I was having a massive staghorn calculus removed from my left kidney. If I'd have seen a urologist, sooner it would never have arisen. Please ask your GP Best wishes Dorothy
  • Posted

    I want to tell you my story with a similar problem because I scoured these forums for an answer but never found one until very recently. I'm 20 years old and starting Spring 2013 I would have severe attacks of kidney pain about once an month with very similar symptoms as yours including blood and protein in my urine. I went to 8 different doctors/hospitals over the year and was told everything from kidney stones to muscle spasms to a doctor just blankly staring at my chart and concluding "I dont know". I was given constant pain killers as a band aid but every month it would come back with severe pain and vomiting and really disrupted my life. They kept saying kidney infection but I did NOT have an infection every time I had symptoms so I was getting very frustrated. Finally a urologist with half a brain suggested maybe I have endometriosis that is pressing on the kidney causing pain and infections. Endometriosis does NOT show up on any scans or tests the only way to find out is a laparoscopy where they actually go into your body cavity and search for it. She was right! I had the laparoscopy done yesterday and they found and removed the endometriosis causing my symptoms! To all the girls with similar problems as me who are creeping these forms for answers: highly consider endometriosis as an answer! And dont give up I had to go through 8 s***ty doctors who didnt want to put any work into finding the correct answer to find the one doctor that actually thought outside the box.

Report or request deletion

Thanks for your help!

We want the community to be a useful resource for our users but it is important to remember that the community are not moderated or reviewed by doctors and so you should not rely on opinions or advice given by other users in respect of any healthcare matters. Always speak to your doctor before acting and in cases of emergency seek appropriate medical assistance immediately. Use of the community is subject to our Terms of Use and Privacy Policy and steps will be taken to remove posts identified as being in breach of those terms.