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.
BigResource, always blammed for spamming and infriging copyrights by collecting and putting together content from other sources. Rest assured that this content is being added by due permission of respective sites. People say it SPAM, we say it an ART, resource the source. Click here to view a detailed Copyright Policy.
Recently Indexed Messages:-
Am a male aged 35 I've been having pains in my penis when passing urine for while but yesterday when I was urinating the pain became Unbearable so I paused a bit when I started again a clot of blood came out there after I couldn't pass urine anymore cause of the pain,as I tried to slowly release the urine blood continued to come out I've since been to the hospital where I was examined but was told it was not because of any std, what I want to know is what could have caused it
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I'm 34 years young but my body is aging faster than I am. In 2007 I separated my shoulder joint while at work. It wasn't diagnosed until 2013 when I finally got a dr who listened to me. I did PT and also had surgery that year. Surgery also cleaned up my partially torn rotator cuff and got my bone spur that was fraying a ligament out. Last year (a year after surgery) I started having issues again. My dr wanted to throw me into PT as well as ortho but I refused because I'm so over PT after spending 6-9 months before & after that surgery. I just found out that nearly half of my collar bone was removed to repair that joint separation and because my shoulder/joint is lacking support the muscles over my scapula are basically permanently strained. PT would've been a waste of time. I can do range of motion exercises & meds. I need to check into NSAIDs because I have stage III kidney disease so I'm supposed to limit my NSAID use. Right now I have to go in 1-2 times per month for Toradol to treat migraines. We think the kidney disease is because prior to being diagnosed with my separated shoulder in 2013 and until surgery I was taking 800mg of Advil 3x/day (max dose). At one point I won't be able to lift my elbow to my shoulder. Once that happens I can get steroid injections. As it is, I can't lift my arm above my head for more than 1-2 minutes without extreme pain. I suspect the steroid injections could be in my near future. So...can that collarbone be replaced? Do I have any surgical options or any options? Or are these really it?
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This is all very new to me so I hope I'm doing this right but I'm just looking for some reassurance. I'm 26 years old and was diagnosed with a parapharyngeal space tumour in late 2012. 2013 my surgeon attempted to remove the tumor by cutting my jaw and going through the back of my throat into the pps, unfortunately he was unsuccessful and didn't remove any of the tumor. We decided to monitor it over two years and see if a change in growth was noted. I should mention that for the last 4 years I've had pain in my left ear and face which has been gradually worsening, and around 10 months ago I lost hearing in the same ear which is now joined by a high pitched ringing. A mri in early December 2015 showed a growth in tumor so my surgeon decided to remove it, however he would need to take a wider approach to ensure he would get the tumor this time, he is concerned that it's involved with my lower cranial nerves so we may need to remove or damage them which would greatly alter my quality of life. Currently I'm looking at other options or other ENT over the world for more opinions.im desperate to find someone else who has been through something similar or if anyone has a suggestion of surgeon or alternative treatments. They are unsure the nature of my tumor so time is of the essence for me. Any help would be greatly appreciated. I have a 1 year old baby who I need to be around for to watch grow up.
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I experienced impetigo for the first time about 4 months ago which was treated with antibiotics(flucloxacillin)-it appeared again & treated with antibiotics & a 3rd time-I thought this had cleared when i got it again 1 day before my hols last week & when i returned home this week--I have been prescribed 1 months supply of antibiotics again 4 a day for 2 weeks then 2 a day for 2 weeks also i use fucidin cream----I am 56 yrs old very clean & very fed up & upset--what am i to do about this?
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I'm a 48 yr old lady who has UC now for 25 years. I was diagnosed when i was 6 months pregnant and the flare lasted until my daughter was 2 years old. I have had several episodes over the last 20 or so years, but all have been controlled with rectal Mesalazine. Sept 2012 I had a major flare up while on vacation in USA and hadn't brought any meds with me. I have been bad ever since. I have had the 10 weeks of steroids which cleared it up, but as soon as i stopped them it started all over again. I was put on 200 mg of Azathioprine, 400 mg Ferrous Sulphate, 4 g of Mesalazine oral as well as the supositories. Grim.......so tired, so low. Jan I was put on Adacolumn for 8 weeks of dialysis. This gave me a months break, but the symptoms returned along with leg ulcers (pyoderma gangrenosum) and an amazing pox, warty virus all along my abdomen, and thighs. The skin Dr said it was all due to the Azathioprine. Weighing up the pros and cons, My consultant and I have decided to stop the Azathioprine and start me on Arsenic suppositories.....sounds gruesome. Has anyone else been down a similar path?
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I have a problem and need advice! My family is known to have history of arthritis. I am 34, male and I am afraid I have this disease too. I feel tingling in my temples. Is this a symptom of arthritis?
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This morning at my rheumatologist's office we made the decision to not do any further fibro meds. I can't stand the side effects and eventually quit taking them all anyway. She went more in depth with me about helping myself with healthy diet and exercise and recommended low gluten.
I was doing research on how to limit gluten in my diet and started reading about celiac disease. Like a lot of other health issues, the s/s are very close to fibro. I'm not sure if I've ever been tested and am waiting on my family doc to call me back to tell me.
My question is, have you tried gluten free? Did it help any symptoms? Were you diagnosed with celiac or just experimented on your own?
This is a pretty big difference in diet and a big commitment. I also kind of feel that gluten free has become a bit commercialized and a bit of a fad thing. I would just like more information before jumping into something I don't understand.
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This took place about 2 months ago now and started with loss of appetite, I could go all day without even getting hungry. when i would realize how long it had been seine i ate i would make myself eat, but it would cause stomach cramps and pain so i started just not eating. i felt fine never getting hungry or even feeling weak. I am sure this wasn't good but eat became quite painful. it progressed to if i would eat i would burp literally constantly the rest of the day. So now i am back to not eating at all and still burping constantly. I know i need to eat but don't know what i can do to help this, tums and over the counter meds have done nothing so far.
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friends i am eating slate pencils for 2 years and nowadays also eating ice cubes .is these habits are harmful for my health?
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After fighting this for four months I have had no spots or itching for several weeks now. I have however kept applying the cream (lyclear ) every second day. For the past three days i have not applied cream. Tonight checking my skin (as i do every night) to my horror i have found a spot with a white dot in the middle. I am devastated. I have not been in contact with anyone who has scabies. Do i have to go through all this again. Can i ever be free of this.
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