Resource the Source, BigResource
Since 2005, our team is working 24/7/365 to maintain one of the World's largest resource center for webmasters and programmers, bigresource.com. The idea is simple ... crawl, validate, format, trim and prioritize similar programming related issues on a single page from hundreds of resources over web. A time saver for overburdened programmers and also provides focused solutions to their problems.
Finally, after 12 years of expertise, feedback and developing a consistent team of top notch editors, we are expanding horizontally towards General categories e.g. health, autos, business, finance, pets, gardening etc. A bit diversion from our core project of programming and languages in the form of bigresource.org.
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Just crawling and building a database of questions/issues/problems is not an art. The success of this unique project lies in the human editing of these messages by professionals for content validity and definitive solution. Compare and see the difference between an original post on a forum and the same edited message added to our index (by clicking categories above). No unanswered posts, salutations, lengthy code lines, images, avatars, attachments, closing remarks, reference URLs, signatures etc., just the core issues and solutions to them. We ONLY index the issues/questions, to find a qualified solution, our visitors have to visit respective sites.
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Recently Indexed Messages:-
I'm a bit worried. I had a urine test at work but forgot to mention that I had some antibiotics about 3/4weeks (maybe more) prior to the test, the antibiotic was penicillin VK.
I've read most antibiotics stay in your system for up to around 4-8 hours, especially penicillin VK. Some other sources reckoned between 7-10 days max. Although most said up to about 8hours max.
So I'm wondering if this would show up in the test at all?
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I have been on a gluten free diet for about 4 weeks now. I had originally went on this diet because I am having the same symptoms and someone that may have a gluten sensitivity bad headaches, feeling very fatigued, joint pain, depression, numbness and foggy brain I was to a point where I couldn't get the word out of my mouth that I was trying to say and that's the point where I really started to research some things. I went to a neurologist and had an M.R.I. done all came back negative the Dr. said there is nothing wrong with me. Quite frankly I can't believe this so I started doing my own research since I wasn't going to get help from that Dr. I do plan on getting a second opinion done here soon, But none the less frustrating. So I found that pretty much all the symptoms that describe a gluten sensitive individual is everything I felt as well, so I thought I might as well give this a shot. I started this diet 2 weeks in I noticed that the numbness went away for the most part the pain still lingered the foggy brain hasn't shown its ugly face still fatigued and still had the headaches. So now 4 weeks in the numbness and the pain has been coming back more frequently and the headaches are still around foggy brain is still gone for now. But as the numbness and pain intensify and start showing up more often now it kind of makes me think am I really having to do this diet, and for the record I am not one of those people that cheat diets nor thinks its okay to cheat a diet especially with this kind of health dependency. I have been very strict with this hence why the frustration with it seeming like its not helping so high. I have done my research on the hidden gluten what to look for etc I actually try to buy only certified gluten free foods that say on the packages. I mean if all I have to do is change my diet to a gluten free one and it changes my life for the better because of this i'm all on board not just half way. Some places I read 6 weeks others say 6 months before you start to add wheat back into your diet to see if it affects you in a negative way, of course only if you feel like its not working for you. I definitely don't want to do this to soon because any chance that this is helping me I would hate to ruin that. At first I thought it was helping me, But not so sure anymore.
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Broke fibula and tibia Feb 17, 2016. Had surgery March 1, and had 2 screws put a n fibula and a plate on tibia. After 8 weeks in cast and NWB I am now in a boot. I am doing exercises for therapy but after walking on it for about an hour leg hurts and ankle and foot swell. Also get sharp twinges now and then in ankle area. Has anyone else had these problems and how long before you can put full weight on it and be able to work. I'm a waitress and have to be on my feet for 4 hours or longer without sitting.
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Hi, my daughter was just diagnosed less than a week ago with DA. I am heavily in the research phase and would love all the input I can get. I am wondering whether to skip our local cardiologist and go straight to finding a specialist, which I am not have much success with yet. She has been symptomatic for a long time on and off again. Recently, in the last 1.5 mos her symptoms have worsened. She was have "spells" of dizziness, feeling faint, extreme weakness and tired. Over the past week she has gotten worse and has not been able to go to school for 2 weeks now., She gets really faint, very weak and exhausted with ambulation. She has difficulty getting out of the bed.
So my questions are: Since we have seen a progression does this mean it is getting worse and worse? Anyone know any specialist in SC or NC or close by to those states? She was started on Florinef. How long before we see improvements? Her doctor said 1 or 2 weeks? feeling sad and overwhelmed by this diagnosis. This is my 15 yr who was a competitive gymnast and looking forward to team sports in HS. I am sorry for all who are having to deal with this. Thank you in advance for your input.
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I've been taking duloxetine 30mg for 2 weeks for anxiety. I've been noticing my feet - mainly my toes will go numb for no reason. Also, if I'm cycling to work and it's cold they will get very cold and stay numb for a long time afterwards (very unusual - the weather's much better now than it was a month ago). I've also got chilblains on my toes. Also I get burning feet at night time which drives me crazy! It keeps me awake and I have to sleep with my feet out of the duvet.
These side effects aren't as bad as sickness and insomnia etc (which I got with citalopram) but I'm worried as they are not on the side effects list I was given. I noticed that duloxetine is actually supposed to treat numb and burning feet in diabetics with nerve damage. So I'm slightly worried that this drug is having adverse effects on me and actually giving me nerve damage!
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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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For the past 10 years I have had really sensitive lips and have only been able to use one type of lip balm. As anything else - lip sticks of glosses give me little sores on my lips and cause them to puff up and get little scabs and peel constantly - i also get dry patches under my eyes and eye lids. When I visited a doctor they told me I may have an allergy to nail polish and an ingredient in lip glosses/balms its also happens when I were nail polish. After removing it it usually clears up within a week.
Recently I haven't even be able to use my usual lip balm as my lips react to that as well and my eyes are puffing up and getting extremely itchy and stinging. I was heading overseas for 3 weeks and the doctor have me some tablets to take to clear up my lips as she said they looked like they had a staff infection. Whilst I was OS all my symptoms cleared up completely and within 2 days of returning home everything started up again!
A week after I had been back,I woke up in the morning and my eyes were completely closed over and extremely swollen. I visited a doctor and they said I might have hives or some type of allergy. I was put on antihistmines and a course of panafcortelone, which worked with the eye swelling and the lips a little. but now i have reduced the amount of panafcortelone I take daily as I am at the end of my course, as have been told it isn't something I can take long term and my eyes are becoming more irritated and puffy and my lips sore are getting worse. I haven't changed any make up lately or products like toothpaste, washing powder.
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I was told I had cyst in my ovaries before, but I received a shot that made the bleeding and blood clots stop and I was getting regular periods.
Now I haven't gotten a period for almost 2 months now and I'm starting to bleed again like before. Should I be worried that the cysts may have came back? What is my best option?
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I'm not particularly worried about this but I'd rather know what it is. I quite commonly will get, after stretching or getting up suddenly, flying black dots in my peripheral vision. These tiny black dots just appear, fly in a direction, then disappear. A bit like a swarm of flies in the corner of my eye except they keep appearing and disappearing individually. It might last up to five seconds or so. Then it's gone and I feel fine. I'm pretty sure I've had this for years.
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I've been diagnosed with ulcerative colitis yesterday and was given 30 x 500 mg suppositories but the consultant said I would have my next appointment in 3 months time.I have to use one per night.Do I use them just for 30 days or should I ask my doctor for some more after 30 days ? It's all very new to me.
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