Kidney Stones - Diabetes - Constant Urge To Pee And Nausea


Nov 12, 2013

Since last Weds evening, about 5-6 days ago, I felt like I was getting a UTI. Had persistent urge to pee, every 20 mins or so, all night, and sometimes I really had to go and sometimes just a dribble but felt like bladder not empty and I'd pee and immediately feel like I had to go again. Had some burning and general discomfort. I also felt like I might have a yeast infection - I have type 1 diabetes (24 years, am almost 45 yrs old, female) and get them often. So on Thurs symptoms still were there so went to gyno to do a urine sample that they said they'd send for culture. They gave me prescription for antibiotics, which I did not fill till the next morning - on Fri morning, still had frequency to pee and also some on and off left-sided flank pain, some lower back pain, some twinges on and off way low in my urethra area - that was all new. Started antibiotic on Fri. felt a tiny bit of relief but had reaction to Macrobid (sp?) so doc called in Cipro, which I started on Sat. By Monday still no better, was still peeing constantly and having the flank pain and back pain on and off. Went back to gyno who said my urine culture came back clear - no bacteria so this was not a UTI or kidney infection. He did say there was a trace of blood in the sample - but I have not seen any blood in my urine myself. Doc performed a pelvic exam to rule out ovarian cysts and uterine fibroids and all was normal. So he suggested it could be a kidney stone, to see the urologist so that is where I am. Still miserable and peeing constantly.

I have never had kidney stones ever. Today still peeing all the time and some on and off back pain, hip pain and even some mild thigh pain - all both sides although flank pain is more left sided. It all comes and goes and is not excruciating and when my husband had a stone, he was in terrible pain and rushed to ER and ended up passing stone that night.

So here's the weird thing - since Sept I was experiencing upper right stomach pain, right under my ribs, nausea after large or fatty meals, constant burping, on and off constipation. So I had an ultrasound done to check for gallstones by my regular dr - everything was normal. They checked kidneys and no stones showed up on ultrasound. I am scheduled for a HIDA scan for gallbladder next week bc still having those symptoms but this urinary stuff is new. All blood work normal. Upper GI endoscopy normal also.

I am a mess! And I just want answers. Not sure if it's all related or I may be dealing with 2 separate conditions or maybe what I've been experiencing as gallbladder pain has been kidney-related all along.

Do all kidney stones show up on ultrasound or is it possible to still have them and have them not show up? That only a CT scan will catch?

Could the constant peeing still be a UTI/kidney infection without bacteria showing in urine culture?

I now have a yeast infection from the antibiotics and treating it. Could it worsen the peeing problem?

Has anyone ever had kidney stones that showed symptoms like this for a long period of time before the excruciating pain of passing happened? Or could this be a problem w/my kidneys and function? Being type 1 diabetic, I worry about this but all my regular kidney blood tests are always normal - I see doc ever 4 months for that.

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Diabetes In Relation To Kidney Stones

I just learned I am diabetic, A1C is 9.0 with an average blood sugar of 211.

Likely I was thrown into a higher diabetic state due to a low purine diet for about a year now which was necessary due to uric acid kidney stones. I was eating more foods that was bad for a diebetic such as bread and potatos since I could eat those on a low purine diet. Note I was likely high in blood sugar already which may be a contributing factor to kidney stones as I found one study that indicated a 40% increase in uric acid kidney stones with diabetics.

Of course now I'm really messed up as foods I can eat on a low purine diet I can't eat on a diabetic diet and foods I can eat on a diabetic diet I can't eat on a low purine diet. So that leaves hardly nothing that I can eat.

It's only been 5 days since the change in diet due to diabeties. I can't seem to get it regulated by diet. It goes up overnight as I sleep which doesn't make sense, I'm not eathing anything!

Readings before meals at different times of day have been 189, 159, 161, 160, 138, 132, 168, 138, 236, 182, 150, 142, 193 taken at different times to the day. The 236 reading was 2 hours after a snack. Mid-day seems to be the lowest. I'm eating so little I'm having trouble maintaining weight. Over the course of the low purine diet I've lost 30 pounds. I could stand to loose a tiny bit more but not much.

I'm starting to exercise some and plan on increasing it as soon as I receive excersise equipment...

I just don't understand the changes in sugar levels, can't seem to attribute it to any particular food necessarily. We are trying diet first before meds. I'm taking Urik-K for the kidney stones.

Just trying to figure out why the rise overnight when it is basically fasting and it rises which I would think it would lower since I didn't eat anything for a period of time?

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I'm not sure where to put this and I'm fairly certain I do not have enough space for all of this. But I will try anyways.

I am 27 years old and male. And my life right now is not great. I have a long list of medical problems most of which have gone untreated for years and are all more or less working together to ruin my life. Since I do not have the appropriate length here to explain all of this a simple list will have to do for now.

Current Issues:

Chronic Pain left and right flank

Chronic Nausea (will result in vomiting)

ADHD (untreated)

Anxiety (Untreated)

Depression (untreated)

Sleeping problems

Eating/Weight problems

Chronic Kidney stones

UPJ obstruction and Hydronephrosis of the Left Kidney (3 surgeries to repair)

What I NEED help with is Identifying what I need to do to make this better. I have been seeing doctors for the past 23 years of my Life. I honestly need A LOT more space to explain all of this.

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I have a lot of prescription pain meds in my medicine cabinet because I have had 2 c sections and another surgery within the last couple years and I hate taking pain meds... I took an oxycodone.  That along with a vibrating massage mat under my back seems to be helping with the pain for the moment, but the nausea is even worse now. Any suggestions for that? I just need to make it to morning so I can go to an urgent care clinic. There is no one to watch the babies right now and of course o would get sick on Sunday when my primary care doc is closed.

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I have been out of work since oct 5th 2015 i had sinus surgrey done then had high blood pressure coming out of surgery kept up with the family doctor they refused to put me on bp medicine they sent me for an ultrasound to check the kidneys and they found out i have gallstones and then a week later i was in the ER with horrible stabbing pain in my back and right side loss of appetite and nausea and when i would eat i would take a couple of bites and then i would feel full right away they did another ultrasound and then they found out that i had a kidney stone i passed that kidney stone but still are having the stabbing sharp dull pain in my back and right side, loss of appetite, nausea, when hungry i take a couple of bites and then i feel full and sick, and i started getting chest pains and the pains hurt worse when i breathe and also am constipated. They just did a CT SCAN but haven't heard anything yet on it. Could it be my gallbladder or could it be something else?

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For the last couple of days I don't seem to be peeing much out, just small amounts at a time. Constantly feeling I need a pee most of the time. I did have a small TURP back in 2013 as was having problems then.

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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've had a constant headache since September 20, 2015. It started in the middle of the night and increased in severity throughout that month. The pain is at the front of my head varies from a 2-9 typically getting worse throughout the day and into the evening.  Other symptoms include dizziness and nausea, lightheadedness-- sometimes extreme and debilitating.

After 1 month, I went to the doctor who had a MRI done, several blood tests, a nerve block, a hospital DHE treatment, every painkiller and triptan/migraine drug in the book. I went on a course of Phenergan and diclofenac, and also had IV antibiotic in the hospital. I started taking magnesium supplements. I assessed the stressful elements of my life (at home and at work), began meditating, and lowered my overall stress. I did yoga and stretched did neck exercises which both reduced some of the pain. Nothing worked, and they recommended Topamax, but as nothing made a dent before, I decided to question their diagnosis of intractable migraine.

Since then, I had my Nexplanon implant removed (received it July 11th, 2015, removed it November 22, 2015). And started acupuncture. The acupuncture achieved some considerable relief, but after a month of treatment twice a week, I went on a business trip and took charcoal several times during the trip to work with a hangover (I don't drink much). During the end of the trip and the 5 days following it, I didn't have a headache. At the time, I concluded that the acupuncture had worked.

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When i was little i had trouble with wetting the bed until i was 8years old.

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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.

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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".

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