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 take Naproxen for Rheumatoid arthritis but as I have high blood pressure I also need to take Losartan 50 mgms daily. My GP now wants me to have 6 monthly blood and urine tests. I think this is because these drugs combined can cause kidney problems. Has anyone come across this before?
View 5 Replies
I am suffering terrible fluttering in both legs below the knee, sometimes the back of the knee too. The fluttering then explodes into a cramp in one muscle which spreads to one or more others as I try to manipulate or stretch the first. The cramps are agonizing and last for up to 10 mins! When they finally subside the fluttering returns and the cycle keeps repeating itself. Rest and cold are sometimes factors. I would say I'm generally healthy and fit, I don't drink much water and sometimes I wonder if coca cola or diet coke make if worse. I have also recently done atkins diet but have been eating normally for a week or more. I can go weeks with no cramps then be plagued for a month! Its driving me mad and keeping me awake! HELP!!
View 1 Replies
I had an accident at work October 2004 (head injury), I complained of hissing in my ears and my hearing was hypersensitive, I had a hearing test at NHS audiology, I was issued with noise generators. I also complained of jaw ache pain, so I visited my Dentist, he had taken an x-ray that shown no problems with teeth. May 2005 after many minor accidents I was referred for neurological examinations and MRI scans. I was diagnosed with Post Concussion Syndrome. Tinnitus and Hyperacusis, I have complained from day one, that my Tinnitus gets louder when I turn my head, it sounds as though it’s from my ears! But I have realised that when I have been talking in a crowded room for a long time this is more prominent. I can live with Tinnitus and Hyperacusis that seems to be in my head due to Neuro rehab CBT, and Tinnitus therapy, could it be I am temporally damaging my jaw cartilage or muscles through raising my voice, I feel discomfort and fullness of ears, the Tinnitus and Hyperacusis that then radiates from my ears lasts for hours or a couple days, but aggravates the Tinnitus and Hyperacusis that seems to be in my head, this is when I am accident prone. I am 58 and my occupation is lorry driver. I feel that when I explain this to the medical profession that they do not listen. My dentist suggested trigeminal nerve, cartilage, TMJD, I have lived with this condition for 4 and half years but would prefer a better quality of life. I would be very grateful for any information.
View 1 Replies
Has anyone found anything to help neuropathy after ALIF surgery? It has been 19 months and the pain is increasing. I cannot bear to wear anything except the loosest of clothing, I cannot walk without a cane or walker, I have new bowel and bladder function problems within the last 3 months. Is there anything that would even work temporarily to allow an airport ride? I buy even groceries online. I am in pain management with a respected doctor. I have have PT, water PT, massage, acupuncture, and narcotic medication. The fusion on L4/L5 and L5/S1 is fine; my life is not worth living.
View 3 Replies
Does anyone else worry they'll never be happy and carefree again? I look at other people who live normal lives (at least what it looks like) and are happy, and I'm so envious. I know everyone has their problems, but it seems like having to deal with these thoughts ALL THE TIME this is on another level. It's like you're trapped in your own mind. I am so scared I'll never be free of this.
I just want to be happy and excited about life, and I'm so far from that. I dread having to deal with this forever. All I can think is, I have a long road of hardship ahead of me for the rest of my life, and this is how life is. No one should live like that.
View 2 Replies
I was taking Sandomigrain for 10 plus years (0.5mg per day – I could not increase the dose as it made me too drowsy to function) and decided to slowly wean myself off as I was still having fairly regularly occurring Migraines that included visual and stomach symptoms. Over a period of a year I slowly cut down the 1/2 a tab in size and frequency till finally in December I was Sandomigran free. For the first 3 - 4 months everything was great, I had less migraines and headaches than I had ever had. Then in March, I woke up with an almighty pain in my head in the front half of my head. My blood pressure and pulse kept spontaneously elevating especially when I was asleep. This intense pain lasted for 2 weeks. Since then, I am left with a permanent Migraine which fluctuates in its severity and my brain (the front half) permanently feels as though it is in a contraction. I also have facial numbness and a sense of cold on my front and back periodically. After many tests (which have all come back clear) I am beginning to think that what is happening is a result of stopping the Sandomigran and of its consequential withdrawal. Has anybody else had these symptoms after stopping Sandomigran and if so, do the symptoms ever go away?
View 1 Replies
I was diagnosed with a large ovarian cyst at the end of March this year (17cm), eventually being given an operation date of 26th July. Unfortunately, this had to be cancelled due to staff shortages - much to my frustration and worry. I let my doctors know of my anxiety as I felt the cyst had grown much bigger and I'd also got new strange symptoms where my legs were very swollen and painful when I walked up hills.
Anyway, a couple of weeks before my rescheduled op one of my legs really swelled up, and started to go a purple colour. Luckily I made the swift decision to go to A&E as I was concerned it could be a blood clot (you're at increased risk on the pill/pregnant and I currently looked 5 months pregnant).
I was admitted with a massive DVT - up to the top of my hip - and at risk of a pulmonary embolism. The cyst had grown so big (20 by 30cm) it was cutting off the blood flow to both my legs.
After 10 days in hospital, 4 in intensive care, I've had the cyst drained of 3 litres of fluid, a catheter inserted into the blood clot to diffuse it and now need to be on blood thinners for the next 6 months. This all could have been avoided if the operation was a bit sooner - or if I was monitored more closely. And I still need to have the actual cyst removed.
Once in hospital the nurses and doctors were wonderful - but the whole experience has been at a huge cost to both myself and the NHS. I just wanted to let people know that if you feel something is wrong, or a cyst is growing at a fast rate - demand to be seen - it would be far better for everyone if these things are prevented!
View 1 Replies
I've been taking anti depression meds for years. now, and none of them have been helping. All they've accomplished to do is cause some bad side effects. I've heard that there are certain type of herbs that can help with many of the same issues as anti depression meds. One of them I've been reading up on and taking is rhodiola root extract. It's supposed to be good for depression, anxiety, among others. What I want to know is if anyone of you ever use any type of herbs? If so can you get away with using just one type of herb to do its work, or do you have to combine it or is it a must that you combine it with other herbs? I hope I can get some feedback from someone that's actually using it by experience. I've learned throughout the yrs. that they are the only ones that can give you a straight answer.
View 1 Replies
I've been going online to try and find an answer to why I have been feeling how I do, depressed for a week or so then hyper for a few days and then depressed again and the most accurate reason for this that keeps popping up is cyclothymia. The websites all say to speak to your gp to get help with a diagnosis and medicines etc. I'm 16 so patient confidentiality applies but the problem is I don't want my mum to find out and she is friends with my gp so would be told by her. But I want help as it is affecting my school and social life. What do I do?
View 4 Replies
I'm 38 years old and this will be my 12th week that I have been diagnosed with bell's palsy. I started with a headache on friday morning and by sunday, I had woken up with my face messed up. I suffered from headaches for the first couple of weeks, and they were gone, but they started back again. My face is getting better and I have slight move movement on my left side. Are these headaches normal?
View 1 Replies
