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.
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Recently Indexed Messages:-
Has anyone experienced a recurrent cholesteatoma in one ear and now a cholesteatoma in the other?
I experience chronic pain and chronic migraines as a result of the 3 surgeries I've had in my right ear. I have severe tinnitus. So severe, that there are times when I literally cannot hear anything around me. Another thing is that sound gets extremely distorted should a voice or sound be too high or too low - you can imagine how difficult this is being a PreSales IT Architect who speaks with a number of people every day.
Also, my right eyelid and right side of my face fall a little lower than my left. In addition to this, I feel pain outside the ear as well and in the muscle that has been relocated three times for each surgery. This causes me pain when I simply move my head in any direction...even when I make facial expressions. Dizziness and vertigo are almost a daily occurrence with some days worse than others...It feels like the room is in a blender. Driving is also becoming increasingly difficult as I often feel like the car is still moving when I come to a stop and vice versa....It's a laundry list of things, I know.
I now have a cholesteatoma in my LEFT ear with my 1st surgery on that is on 11/13/15.
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This is all very new to me so I hope I'm doing this right but I'm just looking for some reassurance. I'm 26 years old and was diagnosed with a parapharyngeal space tumour in late 2012. 2013 my surgeon attempted to remove the tumor by cutting my jaw and going through the back of my throat into the pps, unfortunately he was unsuccessful and didn't remove any of the tumor. We decided to monitor it over two years and see if a change in growth was noted. I should mention that for the last 4 years I've had pain in my left ear and face which has been gradually worsening, and around 10 months ago I lost hearing in the same ear which is now joined by a high pitched ringing. A mri in early December 2015 showed a growth in tumor so my surgeon decided to remove it, however he would need to take a wider approach to ensure he would get the tumor this time, he is concerned that it's involved with my lower cranial nerves so we may need to remove or damage them which would greatly alter my quality of life. Currently I'm looking at other options or other ENT over the world for more opinions.im desperate to find someone else who has been through something similar or if anyone has a suggestion of surgeon or alternative treatments. They are unsure the nature of my tumor so time is of the essence for me. Any help would be greatly appreciated. I have a 1 year old baby who I need to be around for to watch grow up.
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Does anyone know if hair removal is available on nhs for Folliculitis?
Suffered with with this for nearly 3 years and nothing works. Suffer with it on my genital area which is now spreading to my inner thigh. Ive been prescribed washes which don't seem to help and umpteen amounts of antibiotics. Antibiotics help for short while but then just comes back. Sick of this horrible condition which leaves me in a lots of pain as well as intense itching. In process of using pure tea tree oil which seems to have helped on a few of the spots but not on others. Would really like an end to this condition but have been told there is not much else i can do. Doing lots of research online has told me that laser hair removal is very effective for folliculitis but ive also found out it can be quite expensive. I hope one day i will be rid of this condition but until then i guess i will just have to suffer and battle on.
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Does anyone out here have any experience with using progesterone to help regulate the function of the Sphincter of Oddi?
My history: I am a healthy and active 132lb, 42 year old female, but I have been having pain in my upper right shoulder, neck and collarbone for three years now that has really curtailed my life and work. I have tried massage, acupuncture, physical therapy, drugs, strength training, chiro, all with no results. Recently a chiro noticed that my gallbladder area was tender and mentioned that gallbladder problems can refer pain up to the right shoulder area through the phrenic nerve. When I started tracking my pain and food I did notice a connection with pain in my shoulder and my right lower ribs as well (which I had been hiding with lots of ibuprofen). An ultrasound, blood work, and HIDA came back normal (at least that's how the doc reads it), but I'm still having pains when I eat oily foods. So now I am thinking I might have problems with the sphincter and with bile backing up creating pressure on the phrenic nerve. Another symptom is that I am now also having pains on my left side which could be the pancreas being impacted, which shares the common duct and sphincter.
So my question stems from the fact that I had a hysterectomy several years back and have only been on estrogen replacement. I've recently found out that progesterone is important for relaxing the Sphincter of Oddi muscles as well as gallbladder function (as well as many other things). When my nutritionist suggested a few months back to use Progonol, a progesterone cream, it did have a positive effect on the pain within two weeks, but it also caused acid reflux (it also loosens the valve between the esophagus and the stomach), so I had to stop taking it and now we are trying to figure out the best way to introduce it back into my body.
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I have a problem of having very fast ejaculation during sex with my partner. Please advise me how to control it in order make late ejaculation
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Also what is a half life of a medication like paxil? i don't even know what half life means can someone please explain it?
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My girlfriend and I recently started having sex. She was a virgin. During our first time, I found it a little odd how easily I penetrated her and also that she wasn't in pain and didn't bleed, but I understand that all girls are different and so that's not so unusual.
We'd probably had sex around 6 times or so by last night, and we didn't do anything differently (we had been rather rough before and I had gone all the way in quite easily), and she wasn't in any (or at least very little) pain, but when we finished and turned the lights on she had been bleeding. She does not have her period.
Just sounds like I've broken her hymen but it seems a little unusual that it would have broken so late, when we really hadn't done anything differently this time to what we'd done previously.
I should also bring into the situation the fact that we had both basically just recovered (maybe 95% recovered) from what we had presumed was thrush (symptoms being slightly red/blotchy head of penis beneath foreskin, itchy/sensitive, no discharge as far as I noticed but she said she had experienced it and had had thrush before and it seemed like it).
I suggested the bleeding could have somehow been related to inflammation inside her vagina from the thrush but she insists that she is past the point in healing where inflammation would have been an issue - plus it shouldn't have made her bleed like that anyway.
Ah, I should also point out that it's not a weird STI or anything since she was a virgin and I have only ever been with one other person who was ALSO a virgin, so nothing could really have been passed between us (as far as I know?). I know that STI's can be passed on through oral sex and stuff as well, and my current girlfriend had never done it before me but had given handjobs and had been 'fingered'.
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On Dec 6th i had a protected sex with a sex worker. I read through Google and found it is a low risk.
But what am worried is the symptoms or the things happening.
On the 10th day after the incident, i had a sudden huge dehydration and from there mild fever, fatigue, Throat pain, Pain in my groin, Arm pits as well, Loss of appetite, felt a lot of tiredness. I don't know if the lymph nodes were swollen or not, Nausea, Oral thrush, Blood red spots inside the mouth for a day. I felt all disappeared yesterday. But from today morning, i feel nerve tickling or blistering in my legs and frequency is slowly increasing with a mild joint paints as well.
Tests taken
13th day PCR DNA - Negative
28th Day - Antibody screening (finger prick) - negative
30th day PCR DNA - waiting for results.
my questions are
1) Do you think i will be hiv + ?
2) How good is a 13th day PCR DNA test?
3) 30th day PCR DNA test results are expected to come by this weekend.. If it is negative, then do you think i still need to do the testing after 84 days or 3 months?
I know symptoms cannot diagnose HIV, but i m really worried confused and keep thinking of this always. Please help me with any possible information.
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I had my lips augmented with the Silikon-1000. I had one treatment and the Dr. didn't even use full amount for both lips but I feel things are turning for worse...recently the silicone seems to be forming a bigger lump on my upper lip on the left side. I notice it now in pictures and videos of myself. Especially smiling and talking. Not too bad when I have a closed smile or closed mouth. A little worried it'll just get worse. Do you know if there is anyway to surgically remove just the one lump and not affect the rest of my lips? Or do you think that may be too risky?
I contacted him for his opinion and he suggested to inject the steroid in there, but I have also read very bad things about that stuff and how it can make things even worse. I think perhaps my lump was always there but almost 2 years after injections I have noticed it more...maybe the collagen around it increased a little bit. My mouth is just really asymmetrical and unbalanced and I fear people are going to hyper focus on it and judge me. I wanted a subtle natural result and lately is not looking like one.
Ugh, it's terrible, as much as I like more lip volume I hate the imbalance soooo much! I've had social anxiety and body dysmorphic symptoms for ages and this issue is really just too hard for me to deal with on top of those things....I'm always worried that not only I'm going to say something wrong out of nervousness people are focusing on my mouth when I talk. My pupils are two diff sizes due to an accident but now I don't even worry about that like I used to. I'm clueless about how to proceed and also I can't talk about this sort of thing with husband bc I don't him then focusing in too much as well. He already hates that I got the treatment in the first place since I came back n surprised him with it two years ago now.
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I'm 31 weeks and just started getting stretch marks, any good remedies or something I should use?
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