I visited a hospital on 5/15/14 with symptoms of a swollen and severe sore throat (a lot of pain when swallowing) and a 100 f temperature; my throat also had white patches on it. When the doctor saw my throat he said it looks like you have strep. Then he did the 5-10 minute strep swab test but it came back negative. Nevertheless, he still thought I most likely had it and that I should start treatment. We also tested for mono on that day and since then they haven't called back for that (if they don't call back assume negative they say).
He prescribed Amoxicillin 500 MG X2 daily for ten days. So far I have taken 2,000 MG (over the course of 2 days) and my throat still seems the same in regard to pain. The only thing that consistently seems to help my pain is Ibuprofen.
Should I worry? Should I go back to the hospital to see what's going on?
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had a red patch of skin under my eye for at least 3 months now.
i think it gradually appeared and has slowly been getting bigger ever since it does not itch and is not sore it goes dry and flaky after a shower and sometimes gets white head spots
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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 would like to share with the community that unless your Bartholin cyst is a real problem in your life, don't do it. From my own experience, and from what I have read from others on forums and sites, it seems pretty safe to say that many women who have had the surgery regret it. Ladies, it is not worth the pain. Many doctors completely play down the surgery and pass it off as being minor with little pain, fast recovery.
Here is my story: I had a small to med. size cyst, not bothersome at all..it was just there. I went to my yearly exam and the doc said, let's remove that. He explained that is was a simple, common surgery. So, I went in to remove it , expecting to be able to work the next day (ha!). I was given some shots of anesthesia, and then some more, during the surgery I felt pain...was administered more shots. I became completely nervous and entered panic, pleading for something to calm me down. Well, I went through it and I noticed there was a lot of blood and the doctor asked the nurse to help me up, the doctor left the room and I was bleeding so much, like all over the place. To make a long story short, the doctor found my out in the hospital hall and rushed me into surgery again (this time they put my ass to sleep). Come to find out, there was a vein behind the cyst that got cut during the surgery. Later on through research I discovered that this could cause the need for a blood transfusion! Thank goodness I didn't. I completely regret the surgery.It's been 8 days and I still can't drive or sit with both cheeks down in a chair, I'm still walking funny and my vagina looks weird. I love to run and swim and I would NEVER EVER have done this if I had known it was this painful and debilitating. So girls, unless it is a complete necessity and it is totally ruining your life, don't do it. And for those of you who do do it, demand an ultrasound to make sure there aren't any veins behind it, its your right. A lot of veins run through this area and if the doc cuts a vein, its a bad surprise and there is a chance you would need a blood transfusion if you loose too much blood and the doctor isn't prepared. Oh, and I was prescribed tylenol with codeine for the pain every 12 hours...I ended up in the emergency room the next day so they could give me something much stronger. Today, day 8 I didn't have to take any pain meds, but I still can't work/drive/sit normal/walk normal.
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well at the end of December 2011, i entered a psychosis that came from my cannabis use. before the psychosis i wasn't the brightest kid or even the most social or happiest, but i knew how to keep myself busy.
So anyway, i was taken into a mental ward for my psychosis and i remained there for 11 weeks. during thins time i was put on the medication risperdal and oxazepam. my psychosis lasted for about 2 months and after i was just left with emptiness. needless to say this was the start of my emotions going blank. in this type of place there a quite an amount of people and it just seems to be polite to talk to one another. However i never felt the need to converse and i was emotionless. i could never find the right words to respond to someone and even now i'm having trouble finding words to type.
after the almost three months in the ward, i was finally released home. shortly after i began see a psychiatrist for medication and status checkups. he took me off oxazepam but kept me on risperdal he informed me that i would have to take the medication for about two years.
anyway, my real reason for being here is i wanted to know if my emotions will ever return after i am taken off the medication. i did some research and some say the emptiness stems from negative symptoms of psychosis, and some say its the effect of the medication. Furthermore i read that some who were taken off the risperdal have yet to return to how they once were. this is very frustrating. I just feel a lack of pleasure and even things that are supposed to bring pleasure, such as smoking cigarettes, are currently doing nothing for me. i don't even get lightheaded from smoking them anymore. i also have no sexual cravings or do i get pleasure from sexual intercourse anymore. i would also like to know how many others are in a similar situation.
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Am a male aged 35 I've been having pains in my penis when passing urine for while but yesterday when I was urinating the pain became Unbearable so I paused a bit when I started again a clot of blood came out there after I couldn't pass urine anymore cause of the pain,as I tried to slowly release the urine blood continued to come out I've since been to the hospital where I was examined but was told it was not because of any std, what I want to know is what could have caused it
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I had mirena IUD for five years and in those five years I never had a period I was not regular before mirena and now that I got it removed in 4-14-15 I have only had 2 periods and i haven't been on any kind of birth control I have been TTC for 2 months now and I begin to worry that I can't conceive BC I haven't been using any birth control for 7 months now and I haven't gotten pregnant and now that I am trying to for two months I feel like its not going to happen I'm just worried,is it that I'm just being impatient? should I just relax and keep on trying?
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The attacks described on this forum are exactly the same as what i've been experiencing for 4-5years now. I get a stabbing/pressure pain in my butt that feels really deep inside and like something in there is about to burst!
It lasts for minutes at a time and comes without warning although i can usually feel the pain building seconds before the sharp pain begins. When the pain starts it renders me motionless and unable to speak and am often frozen in pain with a cold sweat and faintness. In Between attacks i have no pain at all.
I first experienced it when i was about 24 years old and the pain was unlike anything else that i had ever felt.
Unlike most of the other people on here my attacks occur during the day and hardly ever at night - usually when i feel the need to go to the toilet or pass wind and it always happens when i'm on my period. It can be very embarrassing when an attack comes on when i'm at work or walking around Tesco's as i can't hide my pain.
I approached my doctor and he did an internal examination and said that it wasn't piles or anything like that so then he thought that it was Endometriosis and told me to put 2 packets of my contraceptive pill together to clear it - that didn't work. They then sent me for a scan to see if i did have Endometriosis and that came back clear.
It is now thought that i am suffering from IBS but reading this site it seems that my symptoms are related to Proctalgia Fugax although my doctor has never mentioned it before.
As i said before the attacks only seem to happen when i'm on my period so for the last year i have been controlling it by putting two packets of my contraceptive pill together therefore only having a period (and the pain) every 2 months. The problem is that i want to come off of my pill in order to start a family but i'm petrified of being in constant pain.
Does anyone out there have the same symptoms as i do?
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So I'm 8 months into my latest debilitating 24/7 dizziness. After a clear MRI, a neurologist suggested my imbalance might have a migrainous element to it. There is such a thing as vestibular migraine.
At this point, I'm willing to try anything, so the Dr has out me on Amitriptyline as a migraine preventative. I've been taking 10mg per night for the last 5 days (I can go up as high as 60mg by gradually dosing up).
I know it can have side effects that take a while to wear off and that it might not become effective for several weeks. But honestly, it's making me feel much worse already. I wake up every morning with a pounding head as if I'd drank a bottle of vodka, which is worse than the cannonball-head feeling I had already. Plus, I think it's making me woozier and dizzier than before (which was already so bad I've been off work for 3 months).
Has anyone tried it? Does it get better? I'm finding it really hard to cope with the side effects on top of how I'm already feeling. Many thanks.
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I'm having a first colonoscopy soon, and am concerned at the pain aspect, Doctors tell me it is virtually pain free, and I have a history of poor reactions to anaesthetics with previous hospital procedures and Dentists, where they just don't work, anybody else have this problem and how do you overcome it.
I have always told the Doctors who tend to just ignore what I say, I have to assume that any pain relief I get will not work until much later in the day, is this manageable?
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