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:-
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 used Flonase for 10 days. And I know that it is not a side effect listed by the company by have had really terrible anxiety every since. It started as nervousness then a feeling like I had drank about 20 cups of coffee in a sort time. I could not relax, i was overly emotional - crying... Which is SOOOO not like me. I couldn't eat or sleep...Then my body started tingling all over - especially the feet and legs. All of this is constant... not in waves.... At the ER they attributed it all to anxiety and said that I possibly had a reaction the steroid. That anything was possible. They gave me some good anti anxiety meds and sent me home to ride it out. So the good news is i can now sleep because of the meds but each morning when I wake up I can still feel the tingling starting to come back. And every morning I am hopeful it's just going to be over and I won't have to take more drugs. Can anyone who has experienced the similar tell me how long it was until you felt normal? I stopped it 5 days ago! I'm getting worried I am never going to feel normal again.
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I've had this problem for a number of years. Has anyone had operation to cure this?
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A couple of years ago, I went into hospital for a routine operation on my tongue. After the procedure my tongue was very swollen, so they decided to put me back to sleep until the swelling went down. Unfortunately I then contracted sepsis and pneumonia, was on life support for a week or so. It took me a long time to recover physically and mentally from this experience. I had the most horrendous hallucinations whilst in ICU. I felt like I had been buried alive, embalmed, some of the nurses were from hell and some were from heaven and they were both trying to take me. Even though this was a long time ago now, I still remember it like it was yesterday. Has anyone else had similar experiences?
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Been off Gabby for two months. Most all withdrawal is gone except my chest still aches right around my breastbone.
Anyone else have this?
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This is all very new to me so I hope I'm doing this right but I'm just looking for some reassurance. I'm 26 years old and was diagnosed with a parapharyngeal space tumour in late 2012. 2013 my surgeon attempted to remove the tumor by cutting my jaw and going through the back of my throat into the pps, unfortunately he was unsuccessful and didn't remove any of the tumor. We decided to monitor it over two years and see if a change in growth was noted. I should mention that for the last 4 years I've had pain in my left ear and face which has been gradually worsening, and around 10 months ago I lost hearing in the same ear which is now joined by a high pitched ringing. A mri in early December 2015 showed a growth in tumor so my surgeon decided to remove it, however he would need to take a wider approach to ensure he would get the tumor this time, he is concerned that it's involved with my lower cranial nerves so we may need to remove or damage them which would greatly alter my quality of life. Currently I'm looking at other options or other ENT over the world for more opinions.im desperate to find someone else who has been through something similar or if anyone has a suggestion of surgeon or alternative treatments. They are unsure the nature of my tumor so time is of the essence for me. Any help would be greatly appreciated. I have a 1 year old baby who I need to be around for to watch grow up.
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I have completed 3yrs after liver transplant. My creatinine level is ~1.7 for last 1.5year. Prograf dose is reduced to 0.5mg BD, and tac level is 6.3. Mycophenolate can not be used because it causes leucopenia.
Doctor is thinking to switch to Sirolimus. But with Sirolimus I see this warning.
The safety and efficacy of Rapamune (sirolimus) as immunosuppressive therapy have not been established in liver or lung transplant patients, and therefore, such use is not recommended [see WARNINGS AND PRECAUTIONS].
Liver Transplantation – Excess Mortality, Graft Loss, and Hepatic Artery Thrombosis (HAT)"
Do you think it is safe to use sirolimus?
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I've been diagnosed with ulcerative colitis yesterday and was given 30 x 500 mg suppositories but the consultant said I would have my next appointment in 3 months time.I have to use one per night.Do I use them just for 30 days or should I ask my doctor for some more after 30 days ? It's all very new to me.
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I'm a 19 year old female. In May 2013 I gradually started to become nauseous. It got worse and by June 2013 I was throwing up almost daily. I saw a gastroenterologist who (in November 2013) found celiac disease through an upper endoscopy. I started eating gluten free but the nausea and vomiting continued. Since then, he's done a gastric emptying test, results were normal. I had a HIDA scan of my gallbladder which showed it didn't contract normally. I then had an ultrasound of my gallbladder, which showed tons of stones. Last month, I got my gallbladder taken out. (because my gastroenterologist was sure that was the cause of nausea and vomiting) The first couple days after surgery I felt no nausea, but by the 4th day post surgery, I had the exact same nausea and vomiting I had before. Does anybody have ANY idea what could be causing this? Or what tests I could ask my gastroenterologist to run when I see him next? And before anybody asks, I'm not pregnant.
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I am a 41 year old mom of four and a foster son. I was diagnosed with sarcoidosis of the lungs about 10 years ago and soon after began experiencing numerous cardiac symptoms. I experience extra beats, which I have had occasionally since I was about 21, but have also experienced incredible pounding and pressure in my upper belly, chest, neck, and up into my ears. It is similar to feeling like someone turns up the pressure of my blood vessels like turning up a hose or something and you feel every heart beat so strong and powerful. This would happen with any slight exertion (sitting up, standing, trying to walk up a slight incline etc.) My blood pressure and heart rate would rise drastically (once documented in the hospital my bp. went from normal 114/70 to 167/100 and hr. went from 70 to 160s just from standing slowly) My husband, for a while, had to carry me up the stairs because of the pounding and pressure. I would have to do a little bit of exertion and then stop to let the pounding up my throat, neck, head etc. die down some and them take some more steps. or whenever I stood/stand up have to wait for the rush of pounding pressure to lessen and then start to walk. I have been on metoprolol for about three years now to help extra beats and also to control the surge of my bp. and hr. The docs can't figure out why its happening. The meds have helped a little so that I can walk around now but not much more then that. Thing are worse around my period and that's the only pattern I have figured out. The extra beats make me feel like I'm a slave to them . I feel like they control what I do and I don't do. I don't want to leave the house so I won't experience them when I'm away from where I feel the most safe and comfortable(home) My life has changed so much. I use to play volleyball and be active and miss it so much. I stay at home and my family goes to hike. Even when I'm having a better day and Id like to try and do some activity I'm so petrified that I'm going to do too much and something is going to happen. I'm so tired of feeling this way. I feel like I don't have a second that I'm not thinking about my heart and is it going to stop, or should I try to walk up the stairs cause I know that it makes me feel worse and leads to extra beats, pounding etc. I tend to notice that lifting, bending, sitting up from laying down tend to bring on extra beats, but sometimes its just after I sit or lay down. It makes it so hard to just relax cause I'm always wondering when the next one will come and how bad will it be and how bad will it make me feel. I tend to yawn and burp more when I having more pvc's/pac's
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