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.
Every single step of indexing of resources being monitored by professionals (of respective fields), who have already indexed 5 million plus qualified Q&As by humans, not bots.
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.
As of Jan 2025 stats, 50,000 unique visitors visit us every day to get benefited from this index. We are working hard and striving harder to provide programmers an unmatchable resource index to their unanswered questions. On average, 1000 messages per day are edited, validated and added to our index by a team of 18 members.
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Recently Indexed Messages:-
I recieved super bad feelings when i got under 100% dose of olanzapine and couldn't sleep and up-ed my dose to 10mg (from around 6mg i guess). the feelings came when i was falling asleep.
it came like 3 times, like 70% of my cells were being pressured together.... (i'm describing the super bad feelings) it scared me A LOT when it happened and i am very scared to up my dose again because i think then these super bad feelings might come again...
they came for like 7 seconds these 3 times combined, these 3 times happened in like 1 minute. it would not surprise me if these super bad feelings were Life-threatening but i told my psychiatrist about it and he didn't know what it was but said that it was not Life-threatening.
so now i am trying to quit very slowly so i never have to up my dose again. lowering my dose by 0,625 mg each time.
i was hoping that someone here knows what these super bad feelings were and could shed some light on it. it would help me ALOT if i knew that these super bad feelings were not dangerous.
i'm not 100% certain that these feelings were caused by me uping my Olanzapine dose alot but i think so.
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I have a problem of having very fast ejaculation during sex with my partner. Please advise me how to control it in order make late ejaculation
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For the past 3 months I have thoughts of death and dying, almost everyday I feel a choking feeling around my throat and neck area and I keep thinking that I would suffocate. It's gotten to the point where I panic on a daily basis thinking that I'm going to die.
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I was at the mall yesterday and Nivea went around offering these free skin tests, so I got one. I have pretty dry skin. I'm 36. I have read quite a bit about hyaluronic acid and think that perhaps it has the potential to hydrate my skin, so I asked whether they had that at Nivea. The lady said yes, they have a serum, but it should only be used from age 40. They recommended some other anti-age range for dry skin to me, not hyaluronic acid.
So this leaves me being baffled really. Is there any truth to the idea that hyaluronic acid is not for people under 40, or was the lady wrong?
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I was recently diagnosed with Hemochromatosis. I am waiting for the genetic testing result before they do treatment. One of the issues I have been having is hair loss, which led to me getting my iron tested. Have others of you experienced hair loss? Once you started getting treatment (blood drawn) did your hair grow back? Did you have to do other treatment for the hair loss?
I should probably be more concerned about other aspects of this disease, but as a woman in her 40's, losing half your hair is very disconcerting. I also feel like my scalp is burning or tingling quit a bit. That and the hair loss started about 6 months ago.
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I recently had a Lipoma in the middle of my back to the left of my spine, which was pea sized but noticeable to the touch. Over a period of about 5 years it grew to become about the size of a golf ball or slightly larger (things always feel larger inside don’t they!)
I was annoyed because a doctor at my surgery explained that it couldn’t be removed by the NHS, only private as it was classed as a 'cosmetic' operation. I sought a second opinion from my own doctor who said no, it should be removed and could be removed on the NHS; as it was causing such discomfort. I couldn’t believe the first doctor could even think that something ‘about the size of a tennis ball’ (as she put it), which was obviously causing discomfort and could be seen through clothing, could be was classed as cosmetic! (If this happens to you, demand to go on the NHS or see another doctor!)
It was uncomfortable, not really painful, but it certainly felt like someone had left a tennis ball inside my back! I could feel it as I leaned back in a chair and with deep breaths, it felt like it was pushing against my insides (not very pleasant). By now it has also started to be visible when wearing a T-Shirt (as a bump), so I decided it was time to get it taken out.
Within 2 weeks of visiting my doctor I was in surgery. The operation was no problem, even though the anesthetic did hurt!!! (but I’m a man so I’ll soldier on!) After the op I was in Tesco’s shopping … but about 8 hours later, when the anesthetic had worn off, it bloody hurt! It was hard sleeping – I had to sleep on my front for weeks!
It still feels like something remains – its like a 6th sense and I can still feel something in there, but that may either be my imagination or, as I was told, part of the Lipoma that couldn’t be removed.
At the end of the day though, there’s no need to worry about the op (and I’m the biggest coward going when it comes to hospitals!) – it was simple and not too painful … and the hospital staff were very friendly.
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I'm 13 and tried to finger myself but I can't find my clitoris. Any help of how to find it
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I'm a 26 yr old male, I've been peeing cloudy for months now, not every time I pee, usually just once a day, and the rest seem normal. Lately it seems like it's more cloudy than before. Also at night i have to get up alot to pee, but its usually just a few drops each time. Just recently two things happened, on two different occasions. First, I was peeing and it seemed to be normal color, but at the last end it turned white/cloudy and right at the last drop or two it looked like white flaky particles in it. Since then I've been noticing the particles more often. Second thing, almost two weeks after noticing the particles I was peeing one night and it seemed to burn quite bad at the last few drops, and when I was done it didn't feel like a finished, felt like I still had more. I went to outpatients the other night, did a urine sample and the test come back negative for UTI, so they sent it to a lab, next morning they did blood work and another urine sample. Waiting for the results now. Dr thinks it could be a prostate infection (prostatitis) caused from chlamydia so he put me on Ciprofloxacin. I dont think its from chlamydia because the two girls I've had unprotected sex with both been tested recently and come back clean. He also said its possible it could be stones.
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What are the survival rates for ovarian cancer?This discussion is related to Ovarian Cancer.
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I'd been taking 25mg of Sertraline every day for two years for depression. My doctor and I were planning to try to wean me off this summer. But I moved, and so I found a new doctor. However, this one wanted to keep me on the meds and increased my dose. I've been taking 50mg once a day for about two months. But now the new doctor wants me to switch to Wellbutrin. He says I can stop the Sertraline immediately and switch over because I'm on such a low dose. But I'm wondering if that's a good idea. My original doctor had wanted to wean me off the 25mg, and I've noticed that I get really weepy if I miss a dose accidentally.
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