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:-
It started out with some swelling in my perineum. Eventually my anus become swollen shut (now constipated for 5 days), and my anus has balloons around it, mucous, and it's puffy and purple. Preparation H makes the swelling decrease a little bit, but I'm worried because I cannot flex my perineum so I have erectile dysfunction. It feels like my perineum is disappearing.
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I have just read about a new procedure for surgery of the CMC joint in the thumb. It's a much smaller infusion, doesn't involve removal of a whole bone and is supposed to have a much faster recovery time and little loss of strength. It involves an implant called the Bio Pro thumb implant.
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I'm 30 years old and have suffered back pain and knee pain to an almost debilitating stage and the fatigue can be immense. I've had this since I was 17 ish. Quite often out of nowhere my knees will 'pop' or 'crack'. This can be when I'm walking, starting to sit, try to kneel or even stand still! Sometimes the pain is horrendous. I've also noticed my back has become less flexible over time (in fact my whole body). My calves feel heavy and my feet hurt like crazy. I find it hard to sit for very long without my spine hurting. My wife has tried massaging my back, but she hates it because she sees the pain I'm in. I have been to a Chiropractor, but I seemed only to get worse! I have been to the Dr and they seem to only want to look at one thing at a time rather than collectively. However, I do get some violent jolts or shakes which has been diagnosed as Myoclonus. It has been suggested by one Dr that I may have Fibromyalgia, however, I read through the literature and although some of it sounds familiar I'm not so convinced. By chance I then read an article in my local newspaper drumming up awareness of AS. I'd never heard of this before so I googled it and I would say the symptoms described struck a chord with me. I'm yet to discuss this with my Dr. Has anyone else found the same awkwardness in regards to getting to the bottom of what their suffering from? I'm convinced my mother also had it, although it was never confirmed. I can remember how much of a struggle daily life was for her. One Dr even tried telling her she was a bored housewife and that she needed to get out of the house more! Unbelievable. Anyway thanks for reading this, just trying to build up more of a picture of what it is I have :'
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I dont know i have cervical spondylosis , but MRI said i have a cervical spasm < now even after eating food my heart rate increase some times and there are weird feeling all day long in the chest ,pain in arm .. i feel tingling numbness, in legs ,arms , shouledrs some time. disbalance when i just stand up
Mty Doctors are sending me to neurologist,Cardio , Rheumatologist,Internal medicine .
nothing solved . Heart is ok , ECG is ok, x-ray of heart is ok.Blood test was ok ...
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I'm a new member to the board but I have found it very useful reading as I have been trying to understand my own hormone imbalances. I was diagnosed with PCOS but I am not done ruling out everything else, yet.
I took the ACTH stim test (high dose) recently to test for NCAH. These were my levels:
Cortisol Levels:
Base: 11.9
30 M: 29.7
60 M: 32.6
17 OHP levels (luteal):
Base: 124
30 M: 112
60 M: 91
In all of my research, healthy women and women with PCOS get elevated levels of 17 OHP during the ACTH stim test. Mine, on the other hand, went down. At an earlier point, during my folicular phase, I took a base 17 OHP that showed me at 35. And another serum cortisol (AM) was at 10.9.
If anyone knows a reason why my 17 OHP would go down so much in response to ACTH, I would really like to know. Also, I've taken several hormone tests before this, so if there are other levels you think are relevant, I might be able to tell you.
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I lost 50% hearing in right ear after having wax removed by irrigation with syringe. Seems like the water pressure was excessive. Now, hearing is muffled, nasally and distorted. MRI of brain was OK. Must use hearing aids now to hear anything. Have not used hearing protection in drum and bugle corps. Previous violin player 7 years ago so left ear shows 35% in audio test.
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I am hoping to find other parent's that also have an adult with Down Syndrome. I am finding that there is several subjects for baby's etc. but very little groups that focus on "adults with Down Syndrome".
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They were massive, Dr said she could barely get them all inside the tube They use to do the stapling. The recovery was horrible, but i I am feeling better now. Still can't eat anything to Hardy just because out will make me bleed when it comes out.
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I have recently been diagnosed with IBS, but my main symptoms are not so much the spasms / pain, but a nasty cough associated with acid reflux, and the sore throat that goes with it. It is worse in the mornings, and if I lean forward. Eating / talking / stress also bring it on more. Does anyone else have this, and, if so, does anyone know if Mebeverine helps with this too, or is it just the spasms that it helps ? I see from reading some other posts that it does seem to help diarrhea.
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I am a 30 year old mother of two and I've been a migraine sufferer since I was 16, where this used to be occasional a few months ago they became more frequent, occurring about 3-5 times a month with headaches in between. Up until this point in my life I never felt the need to be on any kind of medication for them, at this point I was desperate. I was popping Excedrin, Ibuprofen, Tylenol, Advil, whatever I could get my hands on just to function. After a trip to the ER to receive a nice little "migraine cocktail" to relieve my pain, I scheduled a visit with my PCP who sent me to a neuro.
This is my second trip to a neuro. Two years ago, I had an incident where out of the blue, my speech became garbled, I couldn't make any sense out of what I was saying and moments of my memory were erased. I was sent to a neuro then too (a different one) by the same PCP who did a quick little physical to be sure I hadn't had a stroke and sent me on my way. At this appointment, the doctor attributed my migraines to stress given I'm a single mother, prescribed me Topamax in addition to Imitrex to take PRN. She started me on 25mg to take twice a day for two weeks. After two days I started noticing weird side effects, tingling down my left arm and feeling like I didn't have full control of the arm. My index finger would move by itself, twitching (which is frustrating when you have to type for a living). The next side effect was my inability to form a sentence, again, very frustrating! I knew exactly what I wanted to say but for the life of me could not spit it out! I called the doctor's office, the doctor was out but they said they would relay the message and call me back. When they did they said she wanted me to stay on it but take it at night to reduce the side effects. Two weeks later it was time for me to double my dose, now I was taking 100mg daily.
I have now been on Topamax for a month and I am having tons of bruising on my arms, legs and hips with no explanation, hair loss and today I noticed my eyes are yellow. I went to E Care and they are running tests on my liver functions and have ordered me to stop the medicine cold turkey, hoping for no bad side effects of that because I can't take any OTC medications.
Has anyone else experienced liver damage from Topamax?
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