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:-



Cyclizine Reaction - Oculogyric Crisis - Involuntary Facial Movements

I had surgery to remove a kidney stone last month, I was given cyclIzine to take home along with pain meds. After a day of taking the cyclizine tablets all of a sudden I felt really on edge and strange and had gone from being quite sedated from pain meds to breathing unusually. I had involuntary movements in my face and neck. It progressed into difficulties talking, my gp told me to stop taking cyclizine immediately. 2 days later the symptoms were worse so my gp gave me procyclidine to stop the symptoms. The following night they got even worse and apparently it's called oculogyric crisis, felt like I was fitting. Being treated with sedatives now which have really helped, it's a month later now though and I had a series of episodes last night of oculogyric crisis. Has anyone else had similar experiences and how long did your symptoms last?

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Ciprofloxacin :: Floaters And Flashes Vision / Eyes

anyone else have floaters and flashes in formerly normal vision since taking cipro?

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Nervous System :: Intermittent Pains In Different Parts Of My Brain/skull For 3 Weeks Now

I've tried about 3 other boards and seems like 100's of site but I cannot find anyone with similar symptoms to what I have. On feb 14, I got a huge euphoric feeling in my head, followed by rapid heart rate, tingling in my fingers and toes, and a feeling that I was going to have a mental breakdown. I went to the ER and got blood pressure/blood sugar/EKG test and a physical test and they determined I was fine and gave me Ativan to take. The next day I started feeling pains in my head that would last for 2-5 seconds and then go away, come back in a different spot later. They hit me anywhere from in my brain, in my sinus (although no sinus pain since Monday), different parts of my skull and on the sides of my head. Most of the pains are on the skull (bone). I mentioned to my doc and he switched me to clonazepam and told me to come back in two weeks to see if I need an MRI.

That appt is next Wednesday and as it has been 3 weeks of the pain not getting better or worse I'm almost positive I'll still have it by then. On a side note, in the past my headaches were in my brain and would be a constant pain for a few hours, and would only come ones a month or so. These pains are not nearly as painful and do not last for more than 20 seconds, but they happen at all times of the day (although in he morning I can lay in bed for a half hour and have no pain, then they come shortly after i get up. I've looked at brain tumour symptoms and I don't really have any of them, the pain is light, my cognitive skills are the same, no nausea, dizziness, etc. The only thing I have is chronic anxiety because of the pains and the fact that they could be something serious. So basically, should I try to get an MRI before meeting my family doc next week? I live in Canada so everything is covered.

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Thumping Sounds In Head

For years now, I have been getting a thumping sound in my head. Usually when I am busy at work or on the computer, it doesn't happen at all, but when I am not busy doing anything it happens regularly and usually 3 to 5 thumps at a time and multiple times in a row. What could be the problem?

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Men :: Very Frequent Wet Dreams

im facing too much of wet dreams .... after every one day ... at night i go through this ... sperm comes out in quite good amount ... but this has become very frequent .... and i feel some pain in my penis when sperm comes out ...

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Delirium After Drinking Beer

I need information urgently. My son was on the birthday of his best friend. They have been drinking a lot. He usually drinks beer. But he has drink too much. His friend calls me to say that my son has fallen in delirium after drinking beer. He is hospital now. What will happen?

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Post-Traumatic Stress Disorder? After Sexual Assault

I am too scared to ask my psychologist about this, i have been having flashbacks for a long time now of sexual assault when i was much younger (ages 3 to 5 most likely). they can be triggered by events or come out of nowhere. i am feeling a bit better now, but for about a month it felt like i was having non-stop back-to-back panic attacks because of this.

i can remember the event but i still have a lot of doubt and feel like my mind is tricking me into thinking that it's real. i've told my psychologist, but i don't want to right out ask if this is ptsd. i really just want something to call this.

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No Corneal Transplant Due To Herpes Simplex In Eye?

A doctor from my local eye hospital told me that i could not have a corneal transplant due to the herpes simplex being in my eye. He said there was too much risk of the new cornea becoming infected. Is this the norm? Should I see a different doctor?

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Teenage With Cyclothymia - Scared

I've been going online to try and find an answer to why I have been feeling how I do, depressed for a week or so then hyper for a few days and then depressed again and the most accurate reason for this that keeps popping up is cyclothymia. The websites all say to speak to your gp to get help with a diagnosis and medicines etc. I'm 16 so patient confidentiality applies but the problem is I don't want my mum to find out and she is friends with my gp so would be told by her. But I want help as it is affecting my school and social life. What do I do?

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Parkinson :: Bad Tremors - Sodium Valproate / Lovan?

I suffered severe depression and anxiety and began to get bad tremors around 6 months ago, this was a first for me. My psychiatrist and GP thought it was because I was taking Sodium Valproate which is a mood stabiliser, however I have now come off that (still taking antidepressants, 80mg Lovan daily) but I still have the tremors.

My GP suggested Parkinson's but that I shouldn't have the brain scan now because medicare are not covering them.

Could anyone give me their thoughts on what I should look for in Parkinson's other than the tremors?

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