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 was diagnosed with SVT years back and have had 2 ablation ops with no success. Too near my AV node. Exercise is the main catalyst for an episode with myself(rapid heart,sweating,have to stop, feel faint) but have the odd flutter and increased heart rate at any time. However i have stopped drinking Caffeine and what a difference. I have not had any episodes whilst out running for about 3 months now( used to be every other run) and have confidence in entering 10k runs and completing them without having to stop. I am going to start playing squash again and really test out my hypothesis.Also, i am not noticing my heart jumping or bouncing during the day now. Just wanted to share this with others as stopping caffeine as really benefited me. I check all labels on soft drinks and obviously no coffee or tea.
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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 suffer with Rheumatoid Arthritis and so have been on all sorts of painkillers and medicines, opiate based seem to be the only ones that genuinely work. I have struggled with addiction until finally learning my tolerances and tapering etc. etc. so I can take them safely without doing myself in.
I tried Tramadol, they stopped me sleeping and effected my mood. I am also on an SSRI, they interacted and caused weird symptoms so I have stopped them and gone back to Dihydrocodeine so physical symptoms are pretty mild.
I am however suffering severe mood swings still; depression, insomnia, RLS, muscle pain...
It has been exactly a week, does anyone know how long these issues might last? As I am struggling at the moment, struggling to keep up with work and responsibilities. I know it will end, I am positive about this, just looking for a time frame!
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My son has been on amiodarone for four months now following an atrial flutter which required DC Cardioversion. He takes other drugs for his heart such as furosemide, ramipril and warfarin. He seems to have frequent throat infections which lead to flu symptoms (hot and cold shivers, aches and pains) these have forced him to bed for 6 days at a time. We have been told that these are not a side effect by the consultant but we were managing to keep on top of infections before amiodarone with some wonderful natural supplements. I am interested that none of the comments that I have read on this site have really mentioned similar side effects. Has anyone experienced the same? He has been free of atrial flutters and has declined an ablation on the grounds that they cannot guarantee a total success rate.
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I've been prescribed the orlistat pills today and I was wondering if it's true about the rumours about the liver damage
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For the past years, I've been taking 5 tabs of Methocarbamol 750 mg. along with 600 mg.(6 caps) of Gabapentin during supper and right before going to the bed, because I have not only leg cramp and spasm but also nerve pain on my legs. Those two meds. have been alleviating my pains that mostly occur during sleep, ... specifically during early morning hours before getting up from the bed.
Prior to those two meds. I had an excruciating and unspeakable pains that waking me up in the middle of the nights lasted about 10 minutes or so. Furthermore, the pains made all over my body sweat like taking hot bath, because of excruciating and unspeakable pain. Those nights, I self-exercised stomping, and often back and forth legs on hard floor in trying to subside the pains.
However, despite maximum doses of two pain meds., I still have been experiencing 'stiffness' along with 'pain' on my legs, some mornings before getting up from the bed.
Is there any good meds. for me more to manage and first of all control muscle spasms and cramps on my both legs?
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I have been battling with anorexia and bulimia for a year and a half now, and I just really wanted to share my thoughts and feelings about my recovery hoping some of you can relate.
I was diagnosed about a year ago when my family finally convinced me to get help. I've been in therapy since, but still battling with my eating disorder every day. I often feel extremely guilty about it, like this is all my fault, or that I'm doing this to myself. I know deep down that having anorexia isn't something that I would ever CHOOSE, in fact some nights I pray that I will wake up and be well again. But it will never happen like that, not without hard work. I want everyone to know that YOU DIDN'T CHOOSE THE EATING DISORDER - IT CHOSE YOU.
My ED voice has been winning most of the battles recently, and I've hardly eaten anything for the last week or so. I don't want to be unwell, and I'm trying so hard to fight this but I feel so out of control. Which is strange because some may say that I'm completely in control - in terms of controlling not eating. But I feel the opposite. I feel completely hopeless.
I want to be happy but I feel awful after everything I eat. One day I will feel free to eat what I like whenever I like without regretting every bite. And I'm going to fight hard to get there.
If anyone has anything to share, please post. And if you are reading this and able to relate, then know that you are not alone!
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After 5 weeks of waiting, i finally received a letter in the post yesterday fromt he Hospital regarding my MRI scan. It states in the letter that everything was normal APART from "a incidental 14mm calcified, extra axial lesion in the left frontal region, probably menigioma". It goes on to say "no further action will be required but a copy of the letter will go to visiting neurosurgeon for further clarification in this regard".
i've just googled menigioma and it comes up with brain tumor - should i be worried about this do you think? :-( i honestly didn't expect the letter to say this as i have waited over 5 weeks for these results. Can anyone advise? thanks
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I was recently diagnosed with Hemochromatosis. I am waiting for the genetic testing result before they do treatment. One of the issues I have been having is hair loss, which led to me getting my iron tested. Have others of you experienced hair loss? Once you started getting treatment (blood drawn) did your hair grow back? Did you have to do other treatment for the hair loss?
I should probably be more concerned about other aspects of this disease, but as a woman in her 40's, losing half your hair is very disconcerting. I also feel like my scalp is burning or tingling quit a bit. That and the hair loss started about 6 months ago.
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My friend and I smoke cannabis occasionally and whenever we seem to be getting pretty high my friend starts feeling sick and turning a yellow, pale color and loses color in her lips, also her stomach starts churning, she starts twitching, and she feels as if she's about to puke or pass out, is she allergic or is this just caused by dehydration or not being used to the substance?
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