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While I was in the hospital, the creatinine level in my blood was 1.42. I was on strong diuretic at this time to help get rid of the fluid. I am out now and take 80mg of Lasix. I am trying to make sense of what this all means. Is there mild heart failure and does it affect the kidneys?
Thanks for any help.View Thread
I just got back from a trip to Guatemala. The weekend back I did have a pretty big 'party' day with some friends in which there was quite a bit of drinking. When I woke up on Monday I felt a dull pain in this area of my back/kidney. I figured this was just due to the extra work I put on the kidneys with the drinking. Well, later that day I sneezed and the pain that shot through me from that area was debilitating. I literally had to just stop for a few seconds while the shock worked out of me. The 'ache' seemed to stick around for about 10-15 minutes. Now it seems I've been sneezing a few times a day and this pain shoots back through me each time.
I've been flushing myself with a lot of water and vitamins. I usually drink a minimum of 3 liters per day (I'm very active and work out 5x per week).
Also, turns out I did get a sore throat and a bit of an infection while I was away. I am on antibiotics which I started pretty quickly to head it off before it got too bad. The mucus is a bit thick and yellowish in color. I could feel the infection starting to spread from behind my nose down my throat - to the chest, but breathing is clear.
I take synthroid, advair and omeprazole.
Thoughts? ... (and I already know, so no need to repremand on the partying over the weekend)View Thread
Thank for any adviseView Thread
Can you help me with these results. I do not drink alcohol either, which I keep getting asked by these results. I also was told I have unspecified granuloma supeorior to my bladder dome and up my pertoneal walls. I kept being told, that these symptoms are in "my head", and there is nothing wrong with me. My nepherologist, said I have no "real", kidney issues. My health has went down rapidly in the last year. I lost my health insurance, and am at stand still. I am so confused. My PCP doc stands by his diagnoses with Polymyotosis, Dermamyotosis, and because my RA doc will not confirm Lupus(even though I have all the signs and symptoms), he is calling it unspecified myotosis. Can you please help? Sometimes I feel like ripping my kidneys out because the pain is sooo bad.View Thread
I have now been doing chelation therapy for some thirteen months, without interruption. I have been having a number of "issues" with my health, some symptoms having attenuated, while other symptoms seem to have come to stay.
The thing that concerns me most, and what brings me to this board, are my vague symptoms that are very much like kidney issues, albeit without the expected hypertension, extreme swelling, chem-7 problems, and protein in the urine ( I checked by way of dipstick several times over the last six months, with no color indicator changes)
Right now, my blood pressure remains very good, even low at times. However, I still have polyuria, albeit a bit less than when I first embarked on my treatment regimen, and now, my feet and hands often feel-and appear(?)-somewhat swollen. I wake up fatigued, and there is always some swelling under my eyes.
I am taking Synthroid, and the endo said that my numbers are quite good, so I rule out hypothyroidism.
I do notice that my morning urine voiding as been reduced to a little more than a trickle and very concentrated!
Lastly, and most confusing, are the darkened spots on my fingernail ends, along with white spots, sometimes looking like "half and half" rings.
I cannot-and will not-go to the doctor again for some time, however, it is difficult to believe that all these symptoms could be pointing to serious renal issues, given my otherwise favorable blood pressure measures, and blood test results over the last couple of years!
I do suspect that I have neurogenic Diabetes Insipidis, as I have a pituitary adenoma. Oh, yes, I have started burping constantly, but not hiccuping, the latter of which seems to often accompany CKD.
Sorry for the rambling account, but I have been suffering these symptoms for over a year and the docs say that everything is normal!View Thread
I have also heard that it may be possible to change from one transplant hospital to another for care. What are the guidelines to accomplish this?View Thread
I am contactable at janaki2869@gmail.comView Thread
Concerned MomView Thread
Right side pain in kidney area, front and back right below the ribs. past 2 months getting worse over the past 2 weeks.
penis tip and urethra pain, 2 months off and on and getting worse over the past 2 weeks. also recently noticing aching in between anus and testicles, in the prostate area.
some bladder discomfort when bladder is full, urinating a little more then usual but i have been drinking a lot of fluids lately.
went to my PCP and urine tested positive for Protein and leukocytes, Tested negative for any STD's. Also got blood work done and apparently all my liver/kidney functions are normal.
High blood pressure, Headaches, and waves of slight vision change, seeing tiny black dots.
Waves of confusion and anxiety rising heartbeat, when this happens i get a racing feeling in my chest and slight chest pain. this happens once a day, over the past 3 days.
I am curious if i had a UTI but it spread to my kidneys or the possibility of kidney disease or Prostatitis
fatigue, been sleeping more than usual.
I was perscribed Bactrim and was diagnosed with a UTI by my PCP but i wanted to get another opinion. i have been taking it for 24 hours now with no change in symptoms. I am shedueled next week for an ultrasound on my abdomin, bladder pelvis etc... but am worried that i waited too long to get help and waiting longer might put myself at danger. i went to the ER last night and they told me to just keep taking my antibiotic and if symptoms get worse to call my PCP or come back in.View Thread
To give you a little background, I went to the hospital in November for what i thought was my appendix. It was in fact my kidney. I have two ureters in my right kidney and one is partially blocked causing me constant back pain, uti's etc. I wanted to see how common this was and if anyone else is going through this. I have seen a urologist however I no longer have insurance so I am unable to have the necessary x-ray done to further my treatment. Is anyone else dealing with a situation similar to mine and if so how was yours resolved.View Thread
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Does anyone have any information related to these symptoms that might assist me?View Thread
I am a 37 male, 170 lbs, 6 foot tall was in good health until this episode happened. I do not exercise much and eat a lot of junk food.Social smoker and drinker. Very moderate though. No history of diabetese or high blood pressure. Some times anxiety causes high bp around 140 by 90 in doctor's office. At home the bp is around 130 by 80.
Ok here is my story. In Nov 2011, I had some pain on my right flank side, just below the kidney area and lower back. The pain was more like spasm than an actual pain. It used to travel down the thigh as well. I went to see my PCP and he ordered routine tests with CT scans. All came normal. Creatinine was 1.0. The pain sort of went away after a few weeks and I was too busy with life to think about this and thought I am being paranoid.
In Jan 2013, I had the same exact episode and continued for a few weeks. I went to my doctor and he ordered the same tests and this time all was normal again. CBC's, LFT's, All Kidney functions such as Urea, Uric Acid, eletrolytes etc. The only thing that was not normal was a creatinine of 2.1. My Doctor could not believe that this is a correct reading. So he re ordered same day. He also asked me to stay in hospital. I was now in the ER room with my blood being monitired every 8 hours, bp checks.New CT scan, Ultra sound ....ECG...TSH, ...H1B1(diabetese I guess(...I mean they did all the basic tests required at that stage. Only thing that was abnormal was a creatinine of 2.1. It stayed at 2.1 for 1 week. I was asked to go home and come back in 1 week. Next week the creatinine was 1.6 and a week after that 1.3. 1 Month after this episode the creatinine went back to 1.0. All possible causes such as rhabdomylosis, drug induced injury, dehydration were discussed but finally no diagnosis was given. It was stated that I had an acute renal injury and no cause is found!! They also did creatinine clearance test and found my GFR around 62% with creatinine serum of 1.3. I was told to take break from work and enjoy life....
Well, I was not well after all these episodes. Even though no cause was found, I started to feel that my BP was high. I bought a home BP kit and checked my BP daily. Its always around 130/80 at rest. I sometimes again have these pains on both flanks and lower back. Doctor in the hospital suggested it was muscular pain. Anyways, I got another test done 2 weeks back in early Feb and found that my creatinine was holding at 1.0. Then suddenly last week I did another test(was sooo paranoid as I had this back pain again) so I found my creatinine now at 1.3. I did not share this new information with my Doctor as he thinks there is nothing wrong with me. All lab tests were done from one lab and it is considered one of the best labs in town.
Has anyone ever gone thru this kind of kidney disorder *if its is a kidney disorder*??? I am soo worried that this could really be a PKD. By the way I have seen 3 nephrologists and 2 PCP's. All seem to have no clue as to why this has happened, Response will be appreciated.View Thread
When I was a much younger man I had henoch-schonlein purpura and it was causing my kidney function to deteriorate. I was put on a large dose of prednisone and my kidney function was fully restored.
About 8 years later started noticing blood in my urine whenever I have a cold or stomach related problems. Nephrologist today diagnosed me with nonprogressive berger's disease (bloodwork came back good and urinalysis showed no traces of blood or protein).
I'm 6'3 weigh 95 kg. I consume about 150-180 grams of protein each day. I tend to eat 5-6 meals a day with each meal having an equal share of the protein. I usually drink about a gallon of water each day. My blood pressure is usually ~120ish/80.
I'm wondering if switching from eating mostly animal proteins to plant based proteins like soy, tempe etc would be lower the risk of my disease from entering a progressive state. I recently started getting into good shape and would hate to ruin my progress.
View Thread
First post here - I am at my wits end and completely desperate for some help!
Thursday evening I was diagnosed with a kidney infection, prescribed antibiotics (Amoxycillin & Calvulanic acid) and have been taking them since - it is now Saturday morning here (I am in Australia) and the pain is still as it was on Thursday, if not edging on the worse side of things.
For pain relief I have been alternating between Panadol (Paracetamol) and Nurofen Zavance (Ibuprofen) and using a heated wheat bag on the area.
My main concern is that I cannot get a full, restful sleep - I'm sleeping in two hour stints and waking up in agony. I have found that I can only lie on my back and if I roll to either side, the pain is just too much. I have tried propping myself up with pillows everywhere but we are also in the middle of summer here at the heat is an issue too!
Being a Saturday, my GP is closed - the only options are the Hospital and the After Hours Doctors (both which has impeccable waiting times) ...so I was wondering if any of you have any tips or hints or suggestions for pain relief, natural or otherwise and keeping in mind that I am in Australia (any drugs please mention their full pharmaceutical name)
I have a low grade temperature of 38.1 C and keeping up as much fluid as possible.
Thank you in advance!
SophieView Thread
I just found out that my daughter has mild left kidney hydronephrosis and was wondering if someone can help me understand what it isView Thread
I just found out that my daughter has mild left kidney hydronephrosis and was wondering if someone can help me understand what it isView Thread
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