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.
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Recently Indexed Messages:-
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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Ok. So i have broken my fifth metatarsal and have been put into a non weight bearing air cast for two weeks.
Due to the break, the doctor has given me a blood thinner Innohep 4500 UI to take everyday to prevent a blood clot.
My problem is: For the past 3 days my calf (same leg as broken foot) has felt like it's been cramping. Elevating it relieves the pain a little but i am required to attend my courses at University - meaning i'm on crutches all day. Sitting/standing makes the pain increase. The pain has gone from mild to severe; i can almost cry from the pain coming from my calf.
It is extremely painful when trying to stretch any of the muscles in my right leg now, Should I be concerned about a potential clot? (I do not show any of the typical signs i.e. the swelling/heat/redness) Or is this muscle related? I have trawled through the net for similar cases but cannot find anything!
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I am 23 years old, college student in adderall 20mg 2 x days. I am taking adderall primarily for weight control. I don’t think I have eating disorder, but I think I became depended on this drug. I was wonder is anyone else here on adderall or some amphetamine and how does feel. I think that I am severely depressed when I am not on a drug. I can restrict my food and I have a constant fear of getting fatter. I did try to stop once but I put on 10 kilos in 2 months.
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I've been taking duloxetine 30mg for 2 weeks for anxiety. I've been noticing my feet - mainly my toes will go numb for no reason. Also, if I'm cycling to work and it's cold they will get very cold and stay numb for a long time afterwards (very unusual - the weather's much better now than it was a month ago). I've also got chilblains on my toes. Also I get burning feet at night time which drives me crazy! It keeps me awake and I have to sleep with my feet out of the duvet.
These side effects aren't as bad as sickness and insomnia etc (which I got with citalopram) but I'm worried as they are not on the side effects list I was given. I noticed that duloxetine is actually supposed to treat numb and burning feet in diabetics with nerve damage. So I'm slightly worried that this drug is having adverse effects on me and actually giving me nerve damage!
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currently my creatine 205.
can take enalapril or losartan? will it affect or worsen kidney function.
well, i have been taking enalapril since 2008 . my creatinine was hopping around 150-180 in these 7 years till 2015.
However, due to chronic diarrhea , vomiting. acute renal failure. creatinine shoot up to 400 in Jan and urine infection in march.
creatinine now hopping around 200-250.
doctor stop my enalapril and replace with amlodipine 5mg
once i stop the enalapril , my urine protein is back. from march 0.17g to 0.61g. i am worried.
i didn't have any urine protein over those few years since 2009 to 2015. i guess this is the reason which i can keep well in my condition with creatinine hopping around 150-190.
i am worried that the urine protein my cause my kidney worsen and dialysis may starts soon.
Posts: 11
Joined: Tue Apr 19, 2016 5:03 am
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From time to time I feel this burning sensation in breasts (both). Feels like tingling and burning sensation, but doesn’t hurt or anything. I am examining my breast regular and can’t seem to find anything. Does tingling mean anything?
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Last week I went to the hospital because my stools were black. They tested for blood but found none. Blood tests showed slightly elevated liver enzymes so they did an US and diagnosed me with fatty liver. That evening I began to notice swelling/faint pain in my upper right abdomen. I thought it was because of all the pressure from the US. It's been a week and it seems it's only gotten worse. Pain/swelling feeling extends from below the rib cage, don't my right side and i also get intermittent pain in my right lower back.
Once I got the diagnosis I changed my diet and stopped drinking. I'll be honest I used to eat horribly. Fast food, frozen meals, high fat, sodium and sugar. I became almost addicted to minute maid lemonade and drank 1-2 liters a day. All that HFCS is what I think mostly contributed to the fatty liver. I don't drink all that often (although when I did it was usually heavy). 2 years ago I used to drink a lot (though still only on the weekends) but up until my diagnosis it would be maybe few times a month tops.
I'm beginning to worry that they misdiagnosed fatty liver and it's something more sinister like cirrhosis. Other symptoms include fatigue, sometimes when I breathe I can take a full breath but it's like I'm not getting enough oxygen. It's hard to describe, almost as if the swelling in my abdomen is crowding my lungs. Lastly, my stools are now very light brown and loose (I honestly can't remember the last time I had a normal BM). I have a follow up with a GI Dr but that's not for 3 weeks. All of this has triggered some severe health anxiety that I once had as a child after an oral surgery.
Does anyone with fatty liver experience this feeling of swelling, abdominal bloating and pain in the upper right abdomen, right side and lower right back?
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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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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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I had high ALT, high cholesterol, Triglycerides and Non-alcoholic fatty liver for last 1 year (as i know). I was trying to control these for last 6 Months.
I had my liver function blood test results back today as follows:
Serum Albumin: 43 g/L
Serum Alkaline Phosphatase : 77 iu/L
Serum ALT level 34 iu/L (it went upto 110 last year same time and slowly decreasing since then, in December 2014 it was 65 iu/L i am glad that it is back to this level )
Serum Bilirubin level 9 umol/L
Serum Lipids
Serum Cholesterol 5.3 mmol/L (In December 2014 it was 5.8)
Serum Triglycerides 1.95 mmol/L (In December 2014 it was 3.96)
HDL Cholesterol level 1 mmol/L
LDL cholesterol levels 3.4 mmol/L
Total cholesterol:HDL ratio = 5.3
It is clear that i have improved my ALT and Triglycerides with diet control and sports/exercise. However, still my cholestrol is high and recent Ultrasound scan suggested NAFLD, i.e fatty liver.
I would appreciate expert's suggestions regarding my cholesterol and reducing NAFLD. I am worried as i did not have these issues just about 1 year ago. I am playing sports 2-3 times a week, controlling my diet (no cheese/butter etc), what else i can do to lower my cholesterol and Fatty Liver.
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