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.
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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.
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Recently Indexed Messages:-
I was recently diagnosed with Complex Post Traumatic Stress Disorder. The difference between C-ptsd and PTSD is that Complex happens over an extended period of time, and usually originates in childhood. Whereas PTSD is typically a one-time traumatic event (such as rape, war, etc).
After spending my entire life in pain, confusion, and emotionally abusive relationships, I finally have an answer. While it is a big relief, the process of recovery is not easy. I feel like there are two versions of me: The chameleon who has put on a good act and adapted for the sake of everyone else, and the real me, who has been hidden all these years. I'm just now starting to get to know the real me.
This is a relatively new diagnosis, and it didn't make it into the new DSM, but I read where someone said that Complex PTSD is at the core of a great many mental health issues.
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I had surgery to remove a kidney stone last month, I was given cyclIzine to take home along with pain meds. After a day of taking the cyclizine tablets all of a sudden I felt really on edge and strange and had gone from being quite sedated from pain meds to breathing unusually. I had involuntary movements in my face and neck. It progressed into difficulties talking, my gp told me to stop taking cyclizine immediately. 2 days later the symptoms were worse so my gp gave me procyclidine to stop the symptoms. The following night they got even worse and apparently it's called oculogyric crisis, felt like I was fitting. Being treated with sedatives now which have really helped, it's a month later now though and I had a series of episodes last night of oculogyric crisis. Has anyone else had similar experiences and how long did your symptoms last?
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I have had rt thigh, calf and hip edema since 1/14 (8 months). It came on out of nowhere. No injury. Neg for DVT, neg MRI for mass, neg mass on abdominal CT scan. Multiple hypodense, Ill defined nodules were identified on spleen and a few on liver. CT scan of chest identified multiple hilar lymphadenopathy. This prompted bx. Dx: Sarcoidosis. Had 2 unsuccessful rounds of prednisone. Now getting Remicade tx. I feel better overall, but the edema. Has not changed. My sarcoid dr (pulmonologist ) thinks this may be totally unrelated to the sarcoid.
I'm desperate for an answer. Vascular consult was neg. any clues?
I was originally told this could be a spinal compression issue. I do have a hx of lower back pain/spasms.
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Since I was 13 I've been plagued by Candida. I told my mom about it when I first found out what it was and asked her to take me to the doctors. She never did so I thought it would go away on it's own. 2 years later I was sick of it and went to my school nurse for help. She had given me the cream that's inserted deep into the vagina and I had started treatment, but then after one dose, I got my period so I had stopped treatment. I went back to my school nurse and she gave me the pill telling me it would get rid of the symptoms but it never helped. Unfortunately I moved to the country where I was then taught at home and I had no one to go to for help. And so I read online that Greek yogurt helps alot and so I started eating one pot a day like it said as well. That helped with the symptoms but it never got rid of it. I'm 18 now and I have moved back to the city and I have tried the creams twice, but every time I've started bleeding, which is unusual because I had the Jadelle inserted. I am literally stuck on what to do next
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Has anyone used melatonin to help them fall asleep to any great effect. It has yet to work for me
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I have had this condition where when I am bit by something, may it be mosquito or ant bites, a small blister forms around it. It is extremely itchy, and when popped, the blistered area is ulcerated. Now it does not become painful at all, but becomes more itchy. when scratched, it rarely bleeds, but becomes itchier even when the skin is obviously more damaged. When I stop scratching, the area releases clear, very slightly yellowish liquid (i'm assuming it's some sort of antibody the body releases), and it takes a VERY long time to heal.Now when i do leave it alone, it heals up and becomes brown, but the scar is still very, VERY itchy, even if fully healed.I have been researching the internet to what it may be for days now, and I have not found what it is. I have used anti-bacterial creams but it does not help. I am not sure if this could be a parasite, or could be fungal.
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Hi everyone! I am totally new to this group and excited to get input from everyone! I'll try and give you a quick synopsis of the past year and a half for me when I gave birth to my first child....
Initially I felt fine, until about 4 months after I gave birth. I had initially lost all the baby weight and then I started gaining again, had major brain fog, dry skin, cold, crazy water retention and bloated face, unmotivated, etc. all the usual symptoms. In February I was diagnosed with Hashimotos by my regular doctor and here are my levothyroxine dosages and blood results since...
Feb 2015 Tsh 269. T4. <0.11. T3. <20. (No meds yet...initial blood work)
Apr 2015. Tsh 156. T4. 0.45. T3. 42. (25 mcg)
May 2015. Tsh 6.69. T4. 1.83. T3. 96. (75 mcg)
Sept 2015. Tsh 2.89. T4. 1.59. (100 mcg)
Oct 2015. Tsh 8.61. (75 mcg)
Nov 2015. Tsh 1.21. (100 mcg)
Feb 2016. Tsh 2.36. (100 mcg)
So my original Doctor began my levothyroxine regimen at 25 mcg for 6 weeks. I immediately felt much better even though my numbers were still going crazy. He upped my dosage twice then sent me to an endocrinologist. Both agreed that my numbers were so bad it could not be postpartum hypothyroidism and I had probably had this for a long time undiagnosed and the pregnancy made it officially just turn off. In October we lowered the dosage to double check this theory and I felt terrible and my numbers changed right away so my endo put my meds right back up.
Now, hair loss was actually never one of my initial symptoms and I am convinced that it began when i started my medication, but both doctors insist that it's my body getting used to the meds and my levels getting better and better. My endo thought perhaps it's was especially bad because I was also experiencing postpartum hair loss. But at this point it is now a full year since I have been diagnosed and on medication. Coupled with the hair loss I also started getting serious joint pain, but again my endo said I was adjusting and this was a common symptom of hypothyroidism.
So basically, I am wondering how after a year of medication I would still be experiencing symptoms with levels that are now perfectly fine? Unless it was related to the medication??....I feel very guilty bringing it up all the time to my doctor because I know I should be glad that the huge issues of brain fog, concentration and mood are generally good (I still say I am not exactly myself yet). I feel silly bringing up something cosmetic but it is so depressing to look in the mirror. I hate doing my hair, washing it, sometimes just running my fingers through my hair I get five more. Even though now I can say it's less, it's definitely still happening and I don't see any new growth. But, on the flip side, hair loss is associated with adjusting to armour and I am terrified to lose any more.
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I have suffered with plantar fasciitis in my right foot for about a year now.
It originally started after a knee operation and a torn calf muscle after an accident.
The pain in my right foot is so unbearable that I opted for a steroid injection last year. I watched some of the youtube videos to see that some numb the area first then inject.. Not my GP...Straight in with the steroid and it was so painful I kept saying "Oh my god oh my god". Well it didn't work and I know that I will NEVER have another one. The pain is more than before.
My left foot has now got a pain across the top of the foot.inferior extensor retinaculum I think it's called.
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Well I had a small boil on the inside of my nose for months and it just wouldn't go away. I visited my NHS Dr who prescribed some cream, nothing happened - he advised to continue using it and suggested perhaps getting it cut off. Anyway I visited the Dr at work who advised getting it cut off which I thought would be end of it. But to my dismay they did a biospy on it and found out it was Sarcoidosis. My mum has this so I was aware of it. I was devasted. This followed with CT scans, lung test, blood test which confirmed Sarcoidosis on the lungs and enlarged nymph nodes. After a long consultation it was decided not to treat it yet as I had no other systems. But a couple of months later I developed a cough, two months later I am still coughing and on exertion (netball albiet quite a bit of running around) I end up having a sort of ashtma attack. Anyway to cut a long story short this is all related and have been prescribed steriods and some other stuff to counteract the side effects. I am really reluctant to take them but after reading the different views on this site with all the different effect I feel I should start taking them (waiting for the NHS to reluctantly prescribe them) before it gets worse. I am wondering now if I have had this for ages as the symptoms of tiredness, aching neck and shoulders I have always had but just thought it was me. My mum was diagnosed 20 years or so ago and it has only just flared up again but in the bones of her ankle. She has trouble breathing which they have said is asthma...
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Have glue ear anyone else got it? I am a 56 female in distress.
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