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.
BigResource, always blammed for spamming and infriging copyrights by collecting and putting together content from other sources. Rest assured that this content is being added by due permission of respective sites. People say it SPAM, we say it an ART, resource the source. Click here to view a detailed Copyright Policy.
Recently Indexed Messages:-
I have a problem and need advice! My family is known to have history of arthritis. I am 34, male and I am afraid I have this disease too. I feel tingling in my temples. Is this a symptom of arthritis?
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After fighting this for four months I have had no spots or itching for several weeks now. I have however kept applying the cream (lyclear ) every second day. For the past three days i have not applied cream. Tonight checking my skin (as i do every night) to my horror i have found a spot with a white dot in the middle. I am devastated. I have not been in contact with anyone who has scabies. Do i have to go through all this again. Can i ever be free of this.
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I have been dealing with the first few months of CRPS which started as burning hot and has changed to a freezing foot that turns blue or purple. Lately I have noticed the bottom of my foot will be ice cold but the top of my foot is normal temp, my toes are like ice. Is anyone else experiencing this? I am battling the workers comp nightmare right now and I hate to tell them about this as it may complicate an already horrible experience dealing with them.
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October of 2014 my primary doctor discovered that I had endo after 6 years of painful periods. I had a laparoscopy on may 13th to gain a better idea on how bad it was. they found fluid floating around from a cyst that was on my right ovary that had ruptured. my left ovary was huge, filled with fluid and its also completely attaches to my bowel. now my GYN said that they just cleaned up the fluids and did not want to remove my left ovary because i am so young (20yrs old). she put me on a BC, camrese to calm the endo and I started taking it on may 17th. for a few days now i have been having symptoms like when I am about to have my period. since yesterday I have been feeling nauseous and both of my ovaries started to hurt. By today the pain has gotten worse. it feels like my ovaries are about to explode. I notice that when I urinate or move my bowel, a little bit of pressure is relieved. the pain is getting unbearable and I don't even have an appetite. I still have 32 more active pills until its my break week. anyone have any idea what could it be? I am scared that its something serious.
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Since college and then 7 years afterwards, I was lacking a period. Then one day it came back. Wanting to know what happened, a gyno doc diagnosed me with PCOS. Also, the years without a period causes hyperplasia(crowded cells in the uterine lining, the form I had has a slight risk of cancer.) I was treated with provera pills to force a period for a while and the hyperplasia was reversed. I was also diagnosed with mild diabetes and I'm on metformin. When my doc found out I was sexually active and on metformin he encouraged me to be treated by depo provera. Also affecting things I take a drug called trileptal. Trileptal prevents most hormonal birth control from working and it is suggested depo to be given more often while on trileptal.
Anyway the problem is I'm started to get periods when I didn't before on depo and I'm acting all hormonal when I am not suppose to. It's so bad I'm getting breakthrough bipolar symptoms right before these periods. But my gyno says there is no way that is happening and my psych symptoms have nothing to do with the depo because hormone fluctuations are impossible on depo.
I want to go off depo, but my doctor is insistent that if I go off it my periods will stop again and I'll get hyperplasia again and get cancer. But there is no sign of my PCOS and I'm bleeding on depo, now that my pcos is treated why would my periods stop and the hyperplasia come back? I didn't take the depo and a main reason is I'm thinking about a child. Why would he push depo so heavily? Should I get the shot?
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I've been told i have a cervical erosion and have been bleeding non stop for 10 days and lots of watery discharge.. can the erosion do this?
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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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My sister in law, a very good doctor who has always given me sensible advice when I have asked, suggested I get my CRP checked. CRP is apparently a marker for inflammation in the body, although lupus and rheumatoid arthritis do not always trigger it.
I know I sound like a broken record, but I really think a lot of post-interferon syndrome can be explained by body-wide inflammation - chronic fatigue arises from an inflamed brain; psoriasis is inflamed skin; arthritis is inflamed joints; fibromyalgia is inflamed muscle tissue; vasculitis is inflamed blood vessels, etc.
Our immune systems were amped up by the drugs, and they never settled down again quite right. The drugs induce autoimmune disorders that can effect every system of our body.
If I eat bagels and cream cheese (I love bagels and cream cheese) for two or three days in a row, and throw in a pizza, all my inflammatory symptoms get worse, including depression and fatigue. My ankles swell. My psoriasis gets worse. My joints start aching worse. My fingers start trembling and twitching spastically. I had nothing like this before treatment.
So anyway, if anyone cares to follow this theory, it means eating a non-inflammatory diet - no pizza, no fast food, skip the sugar, read In Defense of Food. The more you want to live, the better you will eat. If anyone cares to follow this theory and is having their blood drawn anyway, be sure and get CRP checked. My sis-in-law says it's very inexpensive test. I'd love to hear of any correlation or thoughts on this subject.
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Most postings here are asking about symptoms of stomach cancer, as we all worry we have got it. I suppose I worry more because my mother had it. I have had constant nausea for 3 weeks and loss of appetite for about 3 months. I have lost quite a bit of weight.
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my boyfriend and i are Muslims and he believes very strongly on the method that if a girl does not bleed then she has lied and is not a virgin! i should not be worried because i swear i am a virgin and that should be ok.. apart from during foreplay activities we have done like fingering.. nothing happened there was no blood.. so does this mean the hymen has already been broken?
i am a virgin, and have never had full sexual intercourse yet! now me and my boyfriend (of 11 months together) we are getting to the time we are ready, but the problem is, i am worried i will not bleed!
i know that it is possible without intercourse and can be broken by tampons and strenuous physical exercise. but i don't want this to shadow the first time sex, as i know he will not believe i am a virgin! so what should i do?
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