Urology :: My Pee Smells Like Asparagus But Didn't Eat
Sep 20, 2013
My pee smells like asparagus but didn't eat any, can something you eat cause this besides asparagus?
About two weeks ago, I noticed a pain in my back together with the asparagus smell, I took an antibiotic for a few days, the pain cleared within a day but the asparagus smell did not clear.
Two years ago my pee smelled like asparagus too and since I was convalescent from a physical injury and had antibiotics I took them and the smell cleared. Am a celibate person with clean health habits so it could not be an std, and I don't have any of the symptoms of a uti. Can something you eat besides asparagus cause this?
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Basically in april 2015 i went to consultant for pile treatment, he advised me to have them treated by injection, i went ahead with this procedure, for a week i was fine then i noticed the itching and pile/pain had returned went back to my consultant he told me he thinks it was a fissure and to take creams and come back to him in 3 weeks time for further consultation.
alas 2 weeks later i was in severe pain and discomfort and phoned the consultants office that i was in bad pain and was told the consultant was on holidays and would not be back for a further week!
at this stage i was told by my doctor to attend hospital a+e for emergency
treatment ,this i did and was told to present myself at the hospital fasting from night before to see a new consultant---Phew it gets worse!
arrived at the hospital new consultant in fairness said he would put me under a full GA and see what is going on there
the following morning he told me yes indeed the piles were back there was one internal and one external and that i was better off going for the laser treatment called THD, which i booked in for the following week this was at this stage mid may had the procedure and for 2 weeks felt great
however on the third week i was in severe pain in the anal area and knew something was wrong (bearing in mind i was told the THD procedure has a 90%success rate..presented myself back to the consultant in hospital had to go under a full ga again he told me afterwards that the procedure had not worked for me for fu..s sake i was one of the 10% that it did not work for so i was booked in for the following week to have the piles which i was now told one of them was thrombosed removed by surgery so have had this done in mid june and have been in terrible pain since, especially after bm to the point where all i could do is sit/lie in the house all day taking pain killers stool softeners and baths every day. every time i phoned the consultant i was told it takes time to heal so after 7 weeks of severe pain id had enough, i went to my doctor got a letter of him to see the consultant urgently as i was in severe pain meet with the consultant am now booked in again for early next week this is what he said the wound is healing however it is a time thing, he will have a further look at me to see if there is something else causing this awful pain he said there is no fissure but wants to give me a botox injection in the anal area to help with the healing, can anyone please advise with this as i do not want to get any worse pain than i am in presently sorry for the long rant but this is actually what happened to me it has changed my life whereby in the last 6 months being in terrible pain and discomfort and am now wary about this botox injection
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I've had worms since last September which is almost 7 months. The worms are white and small. I've take ovex about 10-15 times in the past 6 months. I've taken pripsen about 4 times. Neither have worked.
My nose has been itching and really bad itching anus which is depressing me. Could this be anything other than threadworms(which I've sent a stool sample and sticky tape test off and all come back negative).
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I am healthy non smoking 65 year old, very active physically and overall healthy. I had the urolift procedure done May 23 2015 at which time the surgeon installed 5 clips. Prior to surgery I was on 8 mg of flomax which made it possible for me to urinate.I did wear a catheter bag for awhile then. After surgery I was on 4mg of flomax for approx. 1 month. I was able to urinate adequately for about 8 weeks. Never but once what you would consider a flow. At about the 9th week I started slowing down again until it got to the point (about 11 weeks) where it took me 8 minutes to start peeing and then it took two more times in the next half hour to finally eliminate somewhat completely. Now in the 14th week of post op I'm on 8mg of flomax right back where I was before surgery.I am now considering what options are available to me now.
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I'm 17 years old I've played volleyball basketball and track my whole high school career and I've always had problems with my knees and ankles but I've been going to the doctor for my knees for like 2 years now and I've had like 3 MRIs they never tell me anything I've tried braces but they don't work. My left knee is way worse than my right but they both hurt. It started out feeling like I just had to crack my knee like if you straighten your elbow and it cracks but then it progressed and know it hurts extremely bad when I start running and I can't stand up after sitting like straightening them hurts horribly bad. Sometimes while I'm sitting they ache and I feel like it's on the inner side of my knee and on my left knee it's on the left side inside and if I go on my tip toe it hurts really bad like a shooting pain kind of it's like a line kinda. And it's also worse when they're cold like I have to drive with the heat on them even when it's 80 degrees outside.
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Degenerative discs and spondylolisthesis,had injections worked well for 5 days now all back ...
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I was diagnosed with low B12 levels and further tests revealed that I had intrinsic factor.
I was given the 6 injection course and was told I would have another in 12 weeks then again and then blood tested again. 6 weeks since my last injection and my symptoms are back. Feeling vague, tired, lethargic, irritated etc. How can it be that I have intrinsic factor but obviously have low B12?
is it likely something else is going on? - any ideas/suggestions?
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After meeting someone on a dating site (getting along very well) a month later I started to itch and little lumps with a white centre started to appear. I thought I had been bitten by mosquitoes and treated them as such. Another few weeks past and they were getting worse not better. That's when I realised what they were. I told the person who I had met and they would do nothing about it so I discontinued the relationship. However I was left with this mess. So far i have used 20 tubes of lyclear and a bottle of tea tree oil. All to no avail. I am at my wits end now especially after reading a lot of the stories. This is horrific. I desperately need help in getting rid of this curse.
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I've had a brown fairly flat mole on my left cheek since as far back as I can remember. It started to annoy me so I decided to get it removed. I saw a dermatologist who said a shave excision might not work but he would give it a go.
Everything has healed now but I am left with a small 'crater' where the cut was made but the coloring of the mole is still there. If anything, it looks worse than before. I'd really like to get rid of this.. what are my options?
I've attached 2 images of how it looks from the side and also front-on (which shows how it caves in now). I know it's not a huge thing and is purely cosmetic.
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Is there any natural medicine to cure fibroids?
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I started taking birth control pills two months ago. I completed one pack of the pills. I had a menstrual cycle last month but I didn't have one this month. Is it possible that I might be pregnant?
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I opened a heavy window at work in April this year 2014 (twice in a matter of a few days) I've had 11 sessions of physio to which this didn't respond to. I've had horrendous pain over the months and now had a scan to show a prolapse disk. On Thurs 27 November I had an epidural injection which doesn't seem to have made any difference and I am currently off work this is my 5th week off. Prior to this had four weeks off intermittently. I am due to see the Neurosurgeon again on 17 Dec to discuss surgery that he said he can offer me. I keep as active as possible but to walk sometimes if really painful and I can't work with this. This has gone on for so long, any advice on how to treat this? Should this have gone off for this long? The L5 S1 disk is prolapsed.
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I was diagnosed with SVT from an early age, and spent most of my childhood going to and from appointments at the children's hospital. Eventually, after many many episodes (and of increasing length!) I was suitable for an ablation. I had the ablation at aged 17, however, unfortunately it did not work and I had an episode 6 weeks later - frustrating! However, it has somewhat modified it and my episodes are less frequent and the length of episodes has decreased substantially from 3 hours to just 5 minutes! So I would definitely recommend the ablation surgery, although it didn't quite have the desired effect for me it has improved the condition and the effect on my life. I now control my episodes through the various maneuvers suggested (and with success thankfully.
My question is, how do people with SVT get on with exercise? I have always been keen to compete in sports, especially during school - however the severity and frequency of my episodes before the operation meant that this tailed off a little. I am now 22 and I am keen to get back into running, moreover, running distances for charity etc.! I am just a bit apprehensive about overexertion and effects on my heart! I would thoroughly appreciate any help/advice about how much exercise people tend to do! especially those who have been diagnosed with SVT from birth or a young age.
I am due to run the race for life in a few weeks, and have been running a little in preparation for that. But I am keen to get back into running longer distances with a view to doing half-marathons/marathons. Has anyone run these kind of distances with SVT?
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I'm not sure if anyone else experiences this? I tend to find something will work for me down there, then it does not. For example: coconut oil has been quite soothing in the past, lately it just irritates me no end.
I tried Olive Oil but it wasn't that great. The Doctor prescribed Sylk vaginal moisturizer and that can either be Okay or not.
Has anyone else got other 'comforters' for LS? Mine gets sore and stingy as opposed to itchy.
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I have got lichen planus on arms very bad, legs, vulva, oral and now starting on my chest. I have used cetraben, dermovate, dermal, doublebase cream, hydrocortisone, calamine lotion, aqueous cream..my GP been excellent.
Also Tramalgin, betnovate for below and am now tearing my hair out with sleepless nights with itching.
I go to work like a zombie and it's so embarrassing having to scratch, they say the monkeys here as a joke.
This has gone on for 6months nearly...am waiting to see the dermatologist. I had a vulvar flare 4 years ago and was ok up until early this year.
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I have diagnosed with IBS for nearly 2 years now and have tried a number of medicines (including Fybogel Mebeverine, Colpermin, Wind Eze, Buscopan hyoscine butylbromide, and VSL#3). This has been complimented by cutting out gluten and following the Fodmap diet. Nothing has changed and I’m an in constant discomfort i.e. every day, with peaks of pain (stomach pains, wind, need for toilet etc.) and troughs of just simple discomfort in the stomach. I have lost count of the amount of times I have gone to the doctors and I’m now being broadly told: “you have IBS, deal with it”. Does anyone have any similar experience of this and has anyone got any suggestions as to what I can try next? I feel that I am stuck.
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I'm only 27 and had an appendectomy a few weeks ago for perforated appendicitis with peritonitis. Following removal of the catheter, I couldn't urinate. They said it would get better, but three days later I went home with a catheter. 1200ml urine was drained. The surgeon suspected urethritis with a spasm of the bladder sphincter.
I was hospitalized 2 days later, and a Urologist told me to wait a few more days. We waited 4 days and there was not much improvement following catheter removal. Further diagnostics were performed. Urodynamics showed a severe obstructed flow and bladder outlet obstruction. CT showed a mildly heterogeneous prostate: prostration and urethritis.The Urologist concluded I had a stricture considering I was having a split urine stream for as long as I could remember and an epididymitis episode 3 months prior.
Cystoscopy was performed and a small incision was made at the bladder neck. I was catheterized for 5 days and after it was removed, the flow was much stronger than I can remember. I had some bloody discharge for the first 10 days. That was followed by lots of bleeding and clots in my urine for the next 15 with burning upon urination. I was given antibiotics. Bleeding stopped at 4 weeks. I have had two wet dreams so I don't have retrograde ejaculation which was a big concern.
Now my only worry is erections. I had really strong nocturnal erections in the first few days (even with the catheter). However, erections were painful in the sense my urethra felt like it was on fire. These erections woke me up several times at night.
The pain at night subsided but now I find that my morning erections are not rock hard. Sometimes, when I touch my erect penis, the burning pain stings. I get erections through stimulation too. But sometimes, especially when I touch my penis it hurts. I really haven't tried to achieve a full blown erection because of this fear. This burning pain occurs when I'm flaccid but that is rare. Sometimes, I also get a dull pain in the tip of the penis. In fact, my whole system feels "sore" as if I had sex only a few hours ago. It's been almost 5 weeks. I had contacted my GP when the pain first started and Urologist a few days later but they don't think much of this. I can't seem to find anything about this online.
Once I can get pain-free rock hard erections, I'll be much happier to have had the surgery since my urinary symptoms have improved. I had never considered a slowish split stream to be a problem before.
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I am a 32 year old female. With Polycystic Ovarian Syndrome, and otherwise very healthy, except for a recent issue this summer with C.Diff/Clostridium Difficile after being given Augmentin antibiotic for bronchitis back in May. It killed all my good bacteria.. and have been on Flagyl and Vancomycin to treat the c diff damage Augmentin did. Back on Vanco a 2nd round.
Anyways, a month and a half later after the cdiff started, I developed this weird "burning" sensation around and inside my urethra. I had no idea what it was. Never had a UTI before that I know of. Then, I noticed these little "specks"/particles that looked like teeny little skin flakes in my pee and sometimes its cloudy with it... and weird little "bubbles". there were 4 occasions.. where something that resembled a shred of lettuce, very small, but looked, like.. lettuce, even the little veiny lettuce leaf things... came out during urination. oddly, i had lettuce the day before 2 of those events. I am pretty sure it came out with my urine, as the toilets were perfectly clear beforehand... and it happened at my work toilet and at home. and i did not do a #2 during any of these incidents. these were all in afternoons/evenings. and i normally only have BM's first thing in the morning. even with cdiff. i never saw such a thing in my pee before. then again, i never exactly looked all the time at my pee. until the burning thing started... then yeah, i was paying attention.
So, I do not have insurance, and was under the care of a Gastroenterologist at the main city hospital for the cdiff and he was letting me see him for free for 3 appointments as a courtesy thing. So, I told him how I thought I had a UTI, and if I have a UTI, I am in BIG trouble because that means I would need an antibiotic.. and I cant be on any other antibiotics as it would cause me to have a major c.diff setback or even kill me.
So, he ordered me to get a Urinalysis by Microscopy and Urine Culture test at the lab downstairs to their office. The urinalysis came back all normal/negative.. except trace ketones and trace mucus. everything else was fine. Urine culture came back and no Leukocytes, etc. BUT... it had 3 bacterias.. but within "normal limits". it just said "#1.. gram negative rods 2,000 count #2. gram neg rods 3,000 #3 Lactobacillus species 50,000. colonies per ML. Lab paper just says most likely sample collection contamination due to the mixed bacterias found. repeat if they wanted to. and that was it. doc said they don't treat unless its over 100,000 colonies. and they considered it a non-UTI. is this correct?
So... question is... is this actually even an "infection"??? The burning went away for several days, actually.
BUT I am currently taking probiotics.. for the cdiff treatment. LOTS and lots of Lifeway Kefir...which contains.. lactobacillus.........
so, could this be that its somehow getting into my urine? or... vaginal contamination how i did the sample collection? just funyn how it happens to be.. just that bacteria.
I know docs thought perhaps I may have IC back in 2007, but was never tested for anything. That was after I was having chronic urination... im talking 20-30 times a night. AFter they ruled out other problems and diabetes.
Also, can baking soda help fix this "problem"?
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I found blood in urine yesterday (Saturday) So today I went to urgent care.
The following tests were performed:
"CBC With Differential"
"Comprehensive Metabolic Panel"
"Urinalysis With Microscopic"
"XR Abdomen AP."
Doctor said that everything appeared normal, but my GP may follow up with a CT scan. Why? I'm really scared about this, but I thought something really serious like a malignancy would show up in blood work.
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feeling lot of pain while urinating most frequently. Sometimes the pain is less sometimes very high. i had habit of masturbating. One day after masturbating the pain started and is continuing now. Please can u say any remedy for this. any medication.
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I've had PBNO - primary bladder neck obstruction and been self cathing for 6 years.
anyone with any experience with PBNO or the recommended TUIP?
I just spent an hour writing a post and but disappeared when I tried to preview it so this is the abbreviated version.
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