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:-
I am 34 year old NZ mum and I had CES about 3 years ago, after 3 operations and lots of physio and exercise I returned back to work, bit by bit, slowly working my way up to full time over the period of 8 months. I actually feel pretty fortunate and feel that Iv made a pretty amazing recovery, I got the mobility of my right leg back (it was dragging) although this is still very numb and weak, it appears normal to those around me, and I no longer walk funny, and my bladder only seems to play badly up certain times of the month (by play up I mean weakness and high frequency) the pain is pretty good too....compared to what it use to be like. The night before my first urgent operation I had hot cold sensations filling my legs,it felt like they were being dipped in warm or cold water, it was one of the strangest things I have ever felt, I hadn't realised that going to the bathroom every few min was a warning sign (I actually thought I must of been pregnant). Anyway recently I'm getting cold patches (large patches) and weird almost pleasant cold tingling around the butt and the back of the legs and wondered if anyone else gets similar sensations?, I hate rushing back to the docs and don't want to live in fear that the CES will raise its ugly head again, I also want to avoid too many more MRIs as I have already been exposed to far to much radiation from these. Was really just hoping that another CES patient could tell me their ongoing symptoms and issues that they have just managed to live with.
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I'm having a lot of pain on the outside bottom of my left foot. It came on pretty suddenly and has gotten worse over the past three days. It's not that swollen, but I do have very poor circulation to my hands and feet. I now have some bruising on ankle and shin that are specific to the areas that start feeling pain when it really starts hurting. In the morning it feels better but it only takes a little bit of walking for all the pain to come back.
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My mother is taking dialysis on a regular basis but off late she is having breathing problem even after dialysis. Not sure what is the cause of this
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Does any know natural to lower high blood pressure and cholesterol? I'm trying to stay away from all the doctor prescribed medicines.
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I took the drug for High BP for many years at max dose 5mg/day.
Can cause awkward need to pass water at inconvenient times- but effective against high BP - in my case used in conjunction with ACE inhibitor Trandolapril with some success.
However, if you have a familial tendency to Gout (ie Arthritis in family- as a precursor) then this drug type will make Gout pretty likely.
You will not want to experience the pain of Gout, believe me!
At the first sign of joint reddening (esp. with alcohol usage) then review use of this drug. Certainly reduce alcohol intake.
It took me 6 weeks to adjust to cessation of this diuretic -with some fluid retention problems and BP surging up again.
I've talked to many people over the years about this -and the link between any diuretic and Gout seems very common.
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I have struggled for a long time with candida. I've tried a few cleanses and better diets over the years, but haven't stuck with them.
Recently, I began taking a good "Living Green" multi-vitamin, three times a day as directed, along with more water and less unhealthy food. But instead of feeling increased energy, I felt more fatigued. I stopped the vitamin for a few weeks, then started it again a few days ago. The deeper fatigue returned, and my body feels stiff and sore, feet are always cold.
These symptoms match those of die-off. Can a vitamin/supplement have this great of an effect?? if it is die-off, should I muster through or back off?
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Is there anyone who has both these conditions? And if yes, do they flare at the same time?
I have had raynaud's since a child (am now 57). I think erythromelalgia has been gradually getting worse since perimenopause began in the early '90s.
But only over recent years has this gradually gotten so bad that I'm relatively lame and housebound
My feet, hands and face are affected. The feet are worst. The NHS rheumy tried my on low dose vasodilator which had to stop cause it made all my symptoms much worse, apparently permanently.
When both conditions flare together my feet are sort of the colour of raw meat. This has been happening daily for nearly 1 year.
The erythromelalgia association website is v helpful, but even on the raynaud's & scleroderma org website it's hard to find anyone with EM, let alone both EM & RP.
If you are out there and have any tips for how to manage these 2 conditions.
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I was diagnosed with a large ovarian cyst at the end of March this year (17cm), eventually being given an operation date of 26th July. Unfortunately, this had to be cancelled due to staff shortages - much to my frustration and worry. I let my doctors know of my anxiety as I felt the cyst had grown much bigger and I'd also got new strange symptoms where my legs were very swollen and painful when I walked up hills.
Anyway, a couple of weeks before my rescheduled op one of my legs really swelled up, and started to go a purple colour. Luckily I made the swift decision to go to A&E as I was concerned it could be a blood clot (you're at increased risk on the pill/pregnant and I currently looked 5 months pregnant).
I was admitted with a massive DVT - up to the top of my hip - and at risk of a pulmonary embolism. The cyst had grown so big (20 by 30cm) it was cutting off the blood flow to both my legs.
After 10 days in hospital, 4 in intensive care, I've had the cyst drained of 3 litres of fluid, a catheter inserted into the blood clot to diffuse it and now need to be on blood thinners for the next 6 months. This all could have been avoided if the operation was a bit sooner - or if I was monitored more closely. And I still need to have the actual cyst removed.
Once in hospital the nurses and doctors were wonderful - but the whole experience has been at a huge cost to both myself and the NHS. I just wanted to let people know that if you feel something is wrong, or a cyst is growing at a fast rate - demand to be seen - it would be far better for everyone if these things are prevented!
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I have a golf ball lump under my right armpit that has been there for almost 5 years and is slowly getting bigger. Your now able to see it when I lift my arm ... The lump is not painful but lightly pressing down from my armpit to my breast with your fingers is painful. What could it be and how worried should I be?
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Burning vagina constantly like sensitive burning bit itchy in vagina. No thrush no infection. One test bit blood under microscope. Pressure to pee and good flow each time. Doc referred to specialist. Very worried. Postmenopause.
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