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:-
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 have been on Suboxone for about 5 years now with a great doctor who was very strict. Measured you levels and if you messed up or tested positive for ANYTHING you are out and the the next person is in. I really have to thank him the most because in the early phases I really had cravings and wanted and would use if I could, but his monthly appointments and drug checks kept me in check. pretty soon the craving went away and a strong urge to get my life back has come upon me. I worked myself from 8 mg at the beginning to 1/8th mg now per day. It still amazes the power of this drug. I still get symptoms when I try and stretch the 1/8 to more than a day. So tomorrow will be my last 1/8th then I am DONE!!
Has anyone on here jumped from an 1/8th and had severe symptoms.? Just want to prepare myself for the next week or so. The worst part for me has been my bowels at this point and can't sleep early in the AM. I have ample Clonidine from DR but can only take that at night cause it makes me sleepy and dizzy.
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After I exercise I get presyncope symptoms which include being dizzy, change in vision, nauseous,hearing loss etc. I'm only 17 which is pretty young for these things to be happening. I got an EKG done and blood pressure test. Everything seemed to be fine, though my BP was fine lying down, the. Lower sitting up, then went higher standing up which is a bit odd. I have fluid in both ears but I'm only really dizzy when I exercise. The doctor doesn't really have suggestions except to get the fluid down and maybe see a ENT, but I don't feel like that is the issue.
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I am facing HBSAG Reactive infected When Blood donated its was detected as HBSAg Reactive, , and even i didn’t face any symptoms till now.
Last month I have taken check-up with Physician doctor suggest test of Heliogram Complete Test, and its result all are normal and fine ...
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Last week I went to the hospital because my stools were black. They tested for blood but found none. Blood tests showed slightly elevated liver enzymes so they did an US and diagnosed me with fatty liver. That evening I began to notice swelling/faint pain in my upper right abdomen. I thought it was because of all the pressure from the US. It's been a week and it seems it's only gotten worse. Pain/swelling feeling extends from below the rib cage, don't my right side and i also get intermittent pain in my right lower back.
Once I got the diagnosis I changed my diet and stopped drinking. I'll be honest I used to eat horribly. Fast food, frozen meals, high fat, sodium and sugar. I became almost addicted to minute maid lemonade and drank 1-2 liters a day. All that HFCS is what I think mostly contributed to the fatty liver. I don't drink all that often (although when I did it was usually heavy). 2 years ago I used to drink a lot (though still only on the weekends) but up until my diagnosis it would be maybe few times a month tops.
I'm beginning to worry that they misdiagnosed fatty liver and it's something more sinister like cirrhosis. Other symptoms include fatigue, sometimes when I breathe I can take a full breath but it's like I'm not getting enough oxygen. It's hard to describe, almost as if the swelling in my abdomen is crowding my lungs. Lastly, my stools are now very light brown and loose (I honestly can't remember the last time I had a normal BM). I have a follow up with a GI Dr but that's not for 3 weeks. All of this has triggered some severe health anxiety that I once had as a child after an oral surgery.
Does anyone with fatty liver experience this feeling of swelling, abdominal bloating and pain in the upper right abdomen, right side and lower right back?
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I've been a smoker for 17 years now. I've tried everything and still can't quit. Any methods anyone can recommend that helped you?
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I was put on 15mg of Lansoprazole by my GP as I've been getting interjestion and heartburn from my heart medication. Had a heart attack in August. After taking it for a few days it was making things worse not better so decided to stop taking it. First day ( yesterday ) I felt 'rough' in the afternoon and had to go to bed early. I have felt even worse today and have been having chest pains off and on all day. I have now had chest pain for about an hour and half. It is not the unbearable kind of pain I had when I had my heart attack and I have no pain else where but I have come close to using my GTN spray . I am also constipated and have wind.
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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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How to lose weight after tubal ligation?
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Recently when I find it difficult to begin certain letters, such as 'a', 'v', 'r' and 'd', when I am writing. I am studying Physics, and so write a lot of maths. I have never previously had any trouble writing letters, and consider myself to have neat handwriting. I have tried different pens, pencils e.t.c, and worry this might have some link with Parkinson’s disease, which runs in my Dad's side of the family. I am a male aged 18.
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