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 2016 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:-
Hallo - my husband was taken into hospital a few days ago with a ?heart attack - but that (thank God) was not proven. They said it could be angina. But the next day after having been given Amitriptyline he showed the symptoms of a mini stroke and I couldn't understand what he was saying because of slurred speech. The GP (when he was discharged) said it was highly unlikely to be a stroke and he blamed this drug - as did all the hospital doctors.
This is very odd to me and can I ask whether it could be true? He hadn't been on the drug prior to admission, so I don't know why on earth they gave it to him in hospital.
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I have this problem- I have bowl movement and then I have to lay down on bed, and massage all over my head for 10 minutes. When I take probiotics, this feeling gets worse. I do take olonzapine for sleep and have been on several anti-depressants before. This annoying thing began happening summer of 2009 and is not healing by itself. I do suffer from constipation time to time and sometimes it is chronic. I discussed this issue with my GP and she doesn't know what's going on. She says take fiber supplements for constiaption like Metamucil, but they make me worse.
I have not had bowl movement for 2 days now. I discussed my resting after bowl movement with someone not a doctor and he said that it maybe little high blood pressure and it goes down after bowl movement.
Also does probiotic supplements increase or decrease blood pressure. Probiotics claim they reduce high blood pressure. I am getting mixed information from what I have searched on web. About.com says it can also increase chances of sepis- blood infection and diverticulitis. I don't know if this is true.
On some probiotic supplement, like Udo's, I think, not sure that probiotics can increase blood pressure. When I take these I have to rest more and massage more after having bowl movement.
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Does osteoarthritis generally cause an elevated Sed Rate and and elevated C-Reactive Protein? Anyone have these tests elevated with your condition?
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I would like to share with the community that unless your Bartholin cyst is a real problem in your life, don't do it. From my own experience, and from what I have read from others on forums and sites, it seems pretty safe to say that many women who have had the surgery regret it. Ladies, it is not worth the pain. Many doctors completely play down the surgery and pass it off as being minor with little pain, fast recovery.
Here is my story: I had a small to med. size cyst, not bothersome at all..it was just there. I went to my yearly exam and the doc said, let's remove that. He explained that is was a simple, common surgery. So, I went in to remove it , expecting to be able to work the next day (ha!). I was given some shots of anesthesia, and then some more, during the surgery I felt pain...was administered more shots. I became completely nervous and entered panic, pleading for something to calm me down. Well, I went through it and I noticed there was a lot of blood and the doctor asked the nurse to help me up, the doctor left the room and I was bleeding so much, like all over the place. To make a long story short, the doctor found my out in the hospital hall and rushed me into surgery again (this time they put my ass to sleep). Come to find out, there was a vein behind the cyst that got cut during the surgery. Later on through research I discovered that this could cause the need for a blood transfusion! Thank goodness I didn't. I completely regret the surgery.It's been 8 days and I still can't drive or sit with both cheeks down in a chair, I'm still walking funny and my vagina looks weird. I love to run and swim and I would NEVER EVER have done this if I had known it was this painful and debilitating. So girls, unless it is a complete necessity and it is totally ruining your life, don't do it. And for those of you who do do it, demand an ultrasound to make sure there aren't any veins behind it, its your right. A lot of veins run through this area and if the doc cuts a vein, its a bad surprise and there is a chance you would need a blood transfusion if you loose too much blood and the doctor isn't prepared. Oh, and I was prescribed tylenol with codeine for the pain every 12 hours...I ended up in the emergency room the next day so they could give me something much stronger. Today, day 8 I didn't have to take any pain meds, but I still can't work/drive/sit normal/walk normal.
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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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This started around late November 2013, I started getting my normal Winter allergies and then came down with what I now believe was a sinus infection. Non-stop mucus, post nasal drip, face hurting, head throbbing etc.. This lasted for about two weeks. During the end of this and soon after, my ears slowly became more and more congested. I attested it to these allergies/sickness and thought it would slowly go away.
It never did. Instead, it started getting worse. Towards mid-December, I began to get slight ringing and more fullness in my ears. Soon the tinnitus grew worse and worse. My tinnitus during this point was extremely loud high-pitched noises, sweeping in and out. Coupled with 24/7 hiss, like an air conditioner was on in my room. Can't hear high frequencies anymore. A loud tea kettle-esque whistle in my right ear if I hear something of a certain pitch or something too "loud."
I saw my primary care doctor on two separate occasions, who said he saw a little liquid in my ear but that my eardrums appeared fine. He gave me Prednisone. No help. I got recommended to the Head and Neck specialist.
The first specialist I see, he doesn't really care to listen to me to say the least. He does get me a hearing test within a few days though. The hearing test shows a curve that they say can be attested to sensorineural hearing loss that someone my age (23) shouldn't have, and that since my hearing dropped with the timeliness of my sickness, that it was odd.
I see a different specialist next trip. He attests it to allergies and says that my eustachian tubes seem to be blocked up. He looks in my ears, up my sinuses, etc.. He recommends I just use a sinus rinse and to not get my ears drained because that will probably make things a lot worse.
I began to do so for the next week or two, and my symptoms did not seem to change at all. I had already been taking flonase and allergy medication as well, to not much help for my ears.
Lastly, I saw another specialist about a week or two ago. He told me that my hearing test showed what he typically would cite as congenital hearing loss, and kept implying that I had been born with bad hearing (That's definitely not the case, this has been a HUGE shift!) He had me do bloodwork for environmental allergies and other tests and a CT scan. I also asked for antibiotics just to rule things out- those have been used up now.
To say the least, I had to call back a few times as a follow-up. They didn't even bother to get in touch for my results, and all I learned was that I did have mild allergies (something I've known my whole life) and that the CT scan was "fine." I ordered those results to be sent to me to see for myself, but either way I guess he hasn't much interest in seeing me again. Do I see ANOTHER specialist now?
Right now, my tinnitus is not as bad as it was then (I could barely sleep then) but still extremely irritating. The tinnitus is still like that of an air conditioner, and there is still a constant ring that goes on, although it is a bit quieter than before. My hearing is still congested and full, and I can hardly hear someone talk a few feet away from me, I'm afraid my hearing may be permanently damaged or getting worse. I can no longer hear certain frequencies. Sometimes I feel like there is liquid in my ear, but maybe not. Wouldn't the CT scan or other ear examinations show that? Is this actually ETD?
I've done all the advice shown around (Proper Flonase spray to the tubes, Sudafed, (extremely careful) Afrin use, etc. I feel like I'm not getting better. My passion is music and I'm afraid I'll never be able to hear things "right" again.
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For the past 3 months I have thoughts of death and dying, almost everyday I feel a choking feeling around my throat and neck area and I keep thinking that I would suffocate. It's gotten to the point where I panic on a daily basis thinking that I'm going to die.
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I have diabetes for 10 years and recently got diagnosed with Hypertension. I am not overweight and i got these genetically.
Can you please suggest how to lead a healthy long life with these two deadly diseases.
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I got the implant a week ago and have nocked it a few times. I'm a little worried that it will break. Any advice?
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On Thursday I had my meningitis C vaccine in my left arm, and diphtheria, polio and tetanus in the other. I've been feeling a bit off since.
Basically- my arms hurt(which I know was to be expected) but they hurt more than everyone else's seemed to...
Then on Friday I completely lost my appetite, I just didn't want to eat at all, I felt like crying all day(not out of pain though?) I had a really bad headache, my arms still hurt...mainly the meningitis arm, I felt exhausted, all throughout the day, especially in lessons, and I was really irritable and moody towards a few people then today I've been feeling a bit better, although I think the vaccine gave a me a cold? My voice at the moment is husky and I'm worried I'll lose it...
Is it normal for those vaccines to make me feel like this? If so, what can I do about it?
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