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:-
I've had GA for 2 years now but was only diagnosed today, It appeared a short time after a skin reaction- Erythema Nodosum. This was brought on by Rigevidon, the contraceptive pill. Has anyone else experienced GA as a consequence of contraceptives?
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i had the flu jab about 6 weeks ago (free from work, not for medical issues). Since then I have had either a constant runny nose or a completely blocked up nose. I've tried cold remedies which, surprise, haven't worked. I don't suffer from hay fever or any other allergies so could this be a reaction to the flu jab? I don't want to be like this for xmas!
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I got diagnosed today by a dermatologist after ten days of suffering and wrong diagnoses by GPs. He gave me some Elocon to apply but did say that steroids usually have little/no affect and keep using calamine. He also gave me Atarax 25mg tablets as I told him I have been taking double doses of Piriton antihistamine at night to help me sleep and stop me itching with no effect. He said that I should also moisturise with E45 on top of any topical treatment.
He did however say something that contradicts a lot that I see on the internet. He said I can continue to take baths, saunas and exercise as this does not affect the condition. The internet is full of warnings against this.
Has anyone had it and continued to exercise? I have become a real gym bunny for once and don't want to stop training til this thing goes.
Thanks for advice re head and shoulders. I just applied some in the shower and then went for 4mins on the sunbed. I am fair skinned and burn easily but seem fine from it. ! I am desperate for this thing to go and have bought an immune-boosting multivitamin.
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I had a high transsphincteric fistula (multiple abscesses). CRS placed a cutting seton with fistulotomy in July. CRS told me that the seton would be in prob 4-6 weeks. It is now 8 weeks later, new CRS (first one moved), told me that he doesn't use these much as they are not tolerated well and that he thinks he will have to go back in and tighten it as it is not advancing. He says this is/can be a long process. Now I am to go back in several weeks to finalize new plan. Problem is, after surgery, I had Augmentin. The fistula track was not draining like it was supposed to and I got another abscess... after the fistulotomy and seton placement. CRS gave me Augmentin which I'm not sure really helped. So, I got a total body rash from the augmentin. I lasted 5 weeks before I was so miserable that I finally took oral steroids from Dermatologist with CRS approval. After I did two weeks of steroids, which helped tremendously, the rash came right back. Derm subsequently gave me a new prescription for prednisone (for one month taper!) and told me that it is a rebound rash after I stopped steroids. CRS says he won't do next surgery until I am off of prednisone for several weeks. Do I take the prednisone? or try to power thru the rash and not tear off my skin? How long will this next seton take to cut thru? wonder if it will get "stuck" midway too? More tightening procedures? Oh.. what to do?
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I had an operation to remove a pilonidal sinus on 24th july. 5 months on and I don't really feel any better off. I didn't say anything when I first discovered the problem as I didn't think anything of it. I only said something once I found out my brother had the same problem! I must have had the sinus for around 2 years before I had the operation, something which I deeply regret now. The wound was a very deep one and I was expecting it to be a long while before it had fully healed, but not this long! I was told by the nurses about 2 months ago that it was only a few weeks away from being fully healed, but it got infected and has set me back a long way. I have to say I do feel a little let down by the nurses I have been seeing. Fair enough they have a tough job but I have questioned quite a few of their decisions during this recovery period. Surely they should be able to see an infection developing on a nearly recovered wound. The fact I was the one who had to push for antibiotics to cure the problem is worrying. I feel I have been palmed off in other ways too. Since the infection, there seems to be little or no healing, and despite persistence from myself to either see the surgeon again or visit a wound clinic they have been very reluctant to do anything. The inconsistency with the nurses has also been a major concern of mine. One day I will see a nurse who says it's not looking great, and the next, I will see someone who hasn't seen it for months, which gives me no idea of how it's doing.
In the last few weeks, I have discovered a lump at the base of my spine, and looking at information on the internet, I'm pretty sure it's a cyst. The annoying thing is that I have told the nurses 3 times about this lump and they either say they don't think it's anything to worry about or they simply don't know what it is. I need closure on this issue and have booked another appointment with the doctor to get to the bottom of it. (I saw him 3 weeks ago with the nurse and he said the wound was looking ok, and that I should give it another few weeks to see if there has been any improvement). There is also a pretty strong odour which is embarrassing. I've got to do something to try and cure the problem. It's driving me crazy and I can't see an end to the problem right now. I'm going to request either being referred back to the surgeon or to a wound clinic. Have any of you been to wound clinics that you would recommend? What are the processes involved? Are they effective?
This problem has kept me from doing some of the things I love, such as playing football, for almost half a year now and will inevitably be longer. There's only so many jokes you can make about it before the depression and annoyance kicks in. It's really getting me down at the minute. Luckily I'm taking a gap year this year and will be going to uni next year, which will hopefully give me time to recover from this nightmare. (Hopefully being the major word!!)
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Are there diseases that can sort of "mask" as mono, yet be something else? Can something else other than EBV test you positive?
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I have small bumps on my penis and a larger one which seems to by a cyst i have had the itchy sensation for almost a year now w/o going to a md. No insurance is on reason other is embarrassment. Are the two connected my scrotum will itch unbearably almost all the time. My palms will itch the same why with rough skin on the hands just the palms. This my seem weird but guys when we pee we usually use our left hand to hold our pants down and my left thumb will usually touch my scrotum or penis that is where i have gotten a itch rash before that went away after washing hands and using hydrocortisone 1% cream. No weird discharges but it seems to be spreading to my anus area and around the bottom or my buttocks by my legs. I also will get small blister type bumps that when i pop them will bleed like crazy. I have used hydrocortisone and it stops the itchy almost 100% for a few hrs. I thought maybe a fungus and I am trying tinactin creme on my penis and hands seems to be very itch after the tination creme has been on for a few hrs.
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Is there anyone who has both these conditions? And if yes, do they flare at the same time?
I have had raynaud's since a child (am now 57). I think erythromelalgia has been gradually getting worse since perimenopause began in the early '90s.
But only over recent years has this gradually gotten so bad that I'm relatively lame and housebound
My feet, hands and face are affected. The feet are worst. The NHS rheumy tried my on low dose vasodilator which had to stop cause it made all my symptoms much worse, apparently permanently.
When both conditions flare together my feet are sort of the colour of raw meat. This has been happening daily for nearly 1 year.
The erythromelalgia association website is v helpful, but even on the raynaud's & scleroderma org website it's hard to find anyone with EM, let alone both EM & RP.
If you are out there and have any tips for how to manage these 2 conditions.
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A doctor from my local eye hospital told me that i could not have a corneal transplant due to the herpes simplex being in my eye. He said there was too much risk of the new cornea becoming infected. Is this the norm? Should I see a different doctor?
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I just learned I am diabetic, A1C is 9.0 with an average blood sugar of 211.
Likely I was thrown into a higher diabetic state due to a low purine diet for about a year now which was necessary due to uric acid kidney stones. I was eating more foods that was bad for a diebetic such as bread and potatos since I could eat those on a low purine diet. Note I was likely high in blood sugar already which may be a contributing factor to kidney stones as I found one study that indicated a 40% increase in uric acid kidney stones with diabetics.
Of course now I'm really messed up as foods I can eat on a low purine diet I can't eat on a diabetic diet and foods I can eat on a diabetic diet I can't eat on a low purine diet. So that leaves hardly nothing that I can eat.
It's only been 5 days since the change in diet due to diabeties. I can't seem to get it regulated by diet. It goes up overnight as I sleep which doesn't make sense, I'm not eathing anything!
Readings before meals at different times of day have been 189, 159, 161, 160, 138, 132, 168, 138, 236, 182, 150, 142, 193 taken at different times to the day. The 236 reading was 2 hours after a snack. Mid-day seems to be the lowest. I'm eating so little I'm having trouble maintaining weight. Over the course of the low purine diet I've lost 30 pounds. I could stand to loose a tiny bit more but not much.
I'm starting to exercise some and plan on increasing it as soon as I receive excersise equipment...
I just don't understand the changes in sugar levels, can't seem to attribute it to any particular food necessarily. We are trying diet first before meds. I'm taking Urik-K for the kidney stones.
Just trying to figure out why the rise overnight when it is basically fasting and it rises which I would think it would lower since I didn't eat anything for a period of time?
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