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:-
Has anyone found anything to help neuropathy after ALIF surgery? It has been 19 months and the pain is increasing. I cannot bear to wear anything except the loosest of clothing, I cannot walk without a cane or walker, I have new bowel and bladder function problems within the last 3 months. Is there anything that would even work temporarily to allow an airport ride? I buy even groceries online. I am in pain management with a respected doctor. I have have PT, water PT, massage, acupuncture, and narcotic medication. The fusion on L4/L5 and L5/S1 is fine; my life is not worth living.
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For the past weeks I've been getting random bruises around my legs, but now I found one in my arm. I find them weird because I don't bruise easily, plus they are tiny (although there is one that is larger in size) and I don't recall hitting myself with anything repeatedly to cause them. Additionally, I've been feeling increasingly tired, even when I sleep for a long time (i.e. 10 hours). Could this be related?
I've had leg pains for the past 12 years (I'm 20), but the reasons are still unknown. Could the bruises be related to this?
Plus, I get pains around my right-lower back, and around my uterus (like slight cramps. The last time I went to the gynecologist a sonogram was performed and I had an ovarian cyst. I was supposed to return after my period for another sonogram to see if it was endometriosis (it was a huge cyst), but was not able to. Are these pains related to that, or something else?
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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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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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My wife noticed yesterday that I had a very large lump on my right hip. It could have been there a while, I've no idea. I've been looking online and it looks like I may have Hip Bursitis but I have absolutely no pain at all.
I've been taking Ibuprofen and ice packs, which brought the swelling down yesterday but it's grown back overnight.
Can I have Hip Bursitis with no pain?
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I was perscribed the drug before the results of my culture were in. I just learned that my culture is negative, soI stopped taking it. My last dose was close to 24 hrs. ago. How long do I have to wait before having a drink, after just 3 doses?
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I have a 8 year old daughter who i have been worried has Coeliac disease for some time now, She was under a doctor in the first two years of her life as she was not growing at the expected rate, they done many tests at the time including a blood test for Celiac which came back negative. in the end it was decided she was just small. She Is still very small and at 8 years old wears age 6 clothing, she complains often of stomach pains after eating. I have also recently noticed that the enamel on her front teeth is not forming properly, is very pitted and looks very brittle. I requested another blood test last year which also came back negative but i'm still not convinced. We do have Celiac in our family, not her immediate family but grandparents. I don't know if i'm worrying for no reason or if I'm going to cause long term problems for her by not pushing this further.
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In short, I (27) was diagnosed with bladder neck stenosis and underwent BNI surgery 4 months ago. I was unable to pee at all. My urinary symptoms are much improved and although my flow rate is still on the low side (15ml/sec), I can fully empty my bladder.
I was in the hospital for a week before doctors diagnosed the reason for my urinary retention. A CT scan showed I had mild prostatitis.
Now I feel I have recovered somewhat but about 2.5 weeks ago, pain associated with prostatitis returned. I went to a Urologist who told me to get a few tests done: CBC, Urine DR, bladder PVR and uroflowmetry. He also prescribed 10 days of antibiotics. The tests seem to be normal with the exception of 4-6 pus cells in my urine. I have not returned to the doctor since.
The pain went away in about a week but has returned. No fever, just a mild constant pain in by upper buttocks area which gets better in the morning. I also have occasional burning pain between my scrotum and anus. My penis feels sore as if I just ejaculated. Occasionally there is sharp pain in the shaft of my penis. I am also experiencing frequent nocturnal emissions. My libido is almost non-existent but when I try I am able to achieve a decent erection.
I have had these symptoms on and off for a few years but although annoying, I did nothing. My GP just tells me to take painkillers. I have read about the kinds of prostatitis and nobody has been able to tell me what exactly is wrong. I have taken 4 rounds of antibiotics (7-10 days) in the last 4 months. It may be of bacterial origin; I was diagnosed with epididymitis 6 months ago with prostatitis symptoms and it cleared up with Cipro.
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I had one of my thyroid glands removed about 11 years ago and about 18 months ago I was diagnosed with thyroiditis on my remaining gland. I have lot of the symptoms of hypothyroidism but every time my bloods are checked my hormone levels seem to be ok. As anyone else experienced this.
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I have many negative side effects from this drug. I recognise that some may be down to my having Hashimoto's and hypothyroidism but I think I am allergic to some of the medicine's contents. The medicine contains lactose and acacia. I know little about the latter but know that I have become lactose (as well as wheat) intolerant since being diagnosed (9 months ago) and given levo. Some side effects are - hot and then cold 'flushes', burning ears and lips, dizziness, continual headache. I have altered my diet and lifestyle to manage the condition as best as possible but cannot manage these side effects. Any help - or just sharing - very much welcomed. I wonder if there is an alternative drug on the NHS in the UK.
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