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:-
I have been taking escitalopram for over two years they were prescribed for severe panic attacks, i feel i got my life back while taking this drug, but have recently started to reduce the dose on my doctors advise, i have been feeling very weepy, vulnerable and the old feelings are coming back i am down to 5mg every third day but i am frightened i will revert back to how i was and this scares me i wonder if i will ever be able to stop altogether
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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've been dealing with severe sciatica pain that radiates from my lower back down to my calf. It sometimes gets so bad I cannot move. I've been seeing a chiropractor for the past two weeks and we've discovered I have a tilted pelvis and curvature of the spine; aside from my dx, the adjustments don't seem to be helping.
My question is, should I still be exercising with this pain or is it worsening the pressure and inflammation of the nerve?
**I am a gymnast and athlete so I spend a lot of time at the gym do hardcore lifting and HIIT. My chiro said to focus on stretching but it hurts so bad I can barely manage it.
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I was just recently diagnosed with cellulitis. It started with feeling a lump on the side of my neck down to my shoulder and I thought it was a muscle knot, so I proceeded on trying to rub my neck trying to get the knot out. I went to bed not feeling too well - woke up in the middle of the night with a fever, sweats & chills, and no energy. I went to the doctors and he sent me right away to the emergency room. I was admitted to the hospital with IV and antibiotics. The emergency room doctor, nurse, and assistant could not find a bite mark, scratch, or anything on the side of my neck and on my shoulder. I have eczema on my back and neck, but I did not have a bad break out of the eczema the time that this has happened. Is there anyway that this eczema created my cellulitis ? I am very concerned about this and do NOT want to get this back. what precautions can I take so that I don't get this back ?
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I am 8 weeks pregnant tomorrow, yay! I had 2 miscarriages last year and this would be my first baby so every little thing is making me panic slightly! I had an internal scan at 7 weeks and we saw a little jellybean with a heart beating it was amazing! Sonographer was very happy with how everything looked so that took a weight off my shoulders.
However for the past 2 days I have been getting these slight cramps/muscle spams in my right Lower back.. I'm not sure if it's where I sit at a computer all day or where I've been driving or maybe even slept funny but it's starting to worry me. It feels as though my muscle just along my waistline on my back is being pulled and stretched. It doesn't happen all the time just every now and then.
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Okay so I'm 17 and I've never been sexually active . I would never be comfortable with just wearing underwear so I would wear party liners all the time but then I noticed a smell on my liners so I started using a Summer's eve spray for down there to cover up the smell. That worked but I got tired of wearing the liners so I stopped . Throughout the day I start to smell weird almost like the ph of my vagina is off . It's disgusting and embarrassing . My first boyfriend tried to go down on me and he said he didn't like the sent . It's was so embarrassing . What do I do to get rid of the smell . I wash with summers eve wash down there as well . I take care of myself but everything I've tried isn't working . Is it possible that I might have an infection ? But from what I've never done anything . I looked online and it said sitting in baking soda for 20 minutes helps balance your ph so I tried that and it worked for a few days then the smell came back . PLEASE HELP ME ASAP
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Is it possible to have CKD or kidney failure without protein in urine?
Last week my masseuse found a knot in my back that she suspects could be inflammation in my kidney. I've had some weird symptoms popping up over the last month like foot/ankle swelling, profound fatigue, leg cramps and blurry vision. This last week though I began developing SEVERE flank pain (like 9 on a 10 scale), back pain (started out lower, now entire back), horrible nausea, horrible headaches, shooting pains down my legs, metallic taste in mouth, dizziness and loss of appetite. Not to sound melodramatic but I feel like I'm dying. The pain is constant but the intensity seems to be moving in 24 hour cycles. Today I feel awful but I was able to shower/get dressed. Yesterday I couldn't even get out of bed. I slept for 16 hours. It's been going in that pattern for the last week and a half.
My doc did a urine culture last week, got results today and there was no protein in my urine, but I had 3+ ketones and a large amount of leukocytes. Blood work from a month ago just came in and my kidney numbers were off a month ago: BUN (32), Creatinine (1.8), eGFR (33). Between the symptoms and the blood test I'm thinking it sounds like renal failure, but could it be CKD without protein in the urine?
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I am 44 years old. I just stopped bleeding 4 days ago after having my regular period which usually lasts a week. I started again today. this has never happened before. Very concerned
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I was diagnosed w/ Metabolic mitochondrial myopathy over 10 years ago. Right now I am struggling with the worst illness I have ever had. Started about 5 weeks when I woke up I noticed every time I breath in it stinks. Since then I have gotten weaker and very sick. I have bouts of vomiting, diarrhea, constipation, my head feels full, burning pressure in my ears and sinuses. My shoulders hurt so it feels like my arms will fall off. I also am having problems with this weird pain in my back & stomach, it feels swelled and I feel raw all the way down to my bladder. At times it feels like burning raw sensation all over. My face feels numb and my left foot. I know this makes me sound crazy, it is making me crazy but I just can't seem to will myself to get better. Every day I wake up with some hope and it's the same thing every day. All I have had was a z pack of antibiotics witch seemed to help a tiny bit,(I am able to sit up a little longer)but I can't stop feeling horribly sick & weak.
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None of the medications that I have taken are helping with fatigue and energy, and are causing a lot of side effects. So I'm thinking about going on Dr. Teitelbaum's protocol for fibro and CFS: D-Ribose, Acetyl-L-Carnitine, Co Q10 and 5-HTP. Has anyone tried these supplements and did you have any results (good or bad)?
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