I'm a bit worried. I had a urine test at work but forgot to mention that I had some antibiotics about 3/4weeks (maybe more) prior to the test, the antibiotic was penicillin VK.
I've read most antibiotics stay in your system for up to around 4-8 hours, especially penicillin VK. Some other sources reckoned between 7-10 days max. Although most said up to about 8hours max.
So I'm wondering if this would show up in the test at all?
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I've been having bleeding in between periods since July but also had it a couple of years ago for about 6 months. I had smear tests etc back In 2011 all was ok and I was told I Had an erosion too. I also had a pelvic Scan and the uterus lining was 15mm.
But I was told all was ok. Bleeding Stopped but then it started about 5 Months ago it's light and usually starts a few days after my period has Finished and lasts a few days.
I went to the doctors a couple Of weeks ago the doctor looked at my Cervix and she said that was clear then she booked me in for another pelvic Scan I had that 2 weeks ago and the Uterus lining was 19mm I've got to See a gynae tomorrow and I've been Told I'll probably have to have a hysteroscopy or d&c.
I'am 35 I have 9 children 7 normal. Births and 2 by c-section. I have been so worried and keep going Online and that's gets me even more Worried.
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For sometime now I am diagnosed with anxiety. I get some medications and was advised for group therapy. Problem is that I do not feel better at all. I am still "trembling" every time I had to do some things or to go somewhere. Friend of mine told me that Paxil helped her with hers problems. I have no knowledge of hers diagnose, but I wonder, could Paxil be used for my anxiety?
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All of this started a few months ago. I had a really bad phase with a lot of panic attacks and severe depression etc. Shortly after all of this calmed down i couldn't stop flexing my toes for about a month. I had this urge to just flex them, often bad enough to the point where my toes started cramping. It stopped from one day to the other and since then its my eyes. I can't stop squeezing them shut. The urge to do this is unbearable. It feels worse with the right eye. I just have this unbearable urge to squeeze them shut or to blink really hard. I try not to do this which evolves in repetitive blinking all day long. I can't stop. Well, I can, but it's driving me crazy. This awful urge in my eyes isn't going away and I feel like my eyes are burning when I stop. It's horrible. I had people comment on this. Mostly my parents. My mother asked me at least 10 times now what's up with my eyes and she seems really annoyed about it. I tried to explain it to her but she reacted really pissed off. I don't know why. I googled a bit and read a lot about Tourette's and I'm afraid that might be it? I don't know what I'm supposed to do? This goes on all day long and I can't handle it anymore. I don't even want to be around anyone anymore because it's not stopping. To have this urge and this feeling all day is killing me. Is there anything I can do? What happens when I tell a doctor about this? Is there anything they can do to stop this?
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Ok. So i have broken my fifth metatarsal and have been put into a non weight bearing air cast for two weeks.
Due to the break, the doctor has given me a blood thinner Innohep 4500 UI to take everyday to prevent a blood clot.
My problem is: For the past 3 days my calf (same leg as broken foot) has felt like it's been cramping. Elevating it relieves the pain a little but i am required to attend my courses at University - meaning i'm on crutches all day. Sitting/standing makes the pain increase. The pain has gone from mild to severe; i can almost cry from the pain coming from my calf.
It is extremely painful when trying to stretch any of the muscles in my right leg now, Should I be concerned about a potential clot? (I do not show any of the typical signs i.e. the swelling/heat/redness) Or is this muscle related? I have trawled through the net for similar cases but cannot find anything!
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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?
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Over 2months ago in jan 8th, when i took generic benadryl with dextromorphan, acetomeniphen, phenyleprine,(pill. after about an hour, noticed i loss about 99 of smell which in turn made me unable to taste certain flavors. Throughout the whole day i started feeling unusually shivering and cold. and notice i started to get tingling on the left side of my body. the next day my smell hasnt returned, and i went to the ER, was afriad it was a stroke or some brain injury. Spent 5 1/2 hours trying to find out the cause, but was unable, the whole time the doctor did notice my other symptoms i was jerking twitching while on the bed, and felt very tingly, i also have tachycardia. i was eventually discharged, over the next few days, i still had sense of smell loss which went to 50% but went to 90% loss very quickly over the next few days. While i was sleeping, at night my neuro symptoms intensified, my myclonic jerks, twitching increased, and RLS developed, at the same time i realized i also pins and needle show up on the left side of my body.
After about 1 week, the pins and needle came back on my left hand and feet. Then a few weeks later i noticed i had loss all internal sensations(full or empty bowel,stomach,bladder, eye movements) Any internal movement you can think of is loss. Actually about 99% gone, because i can still have a bowel movement, pee, and stomach sensations only when its overwhelming and prolonged stimulation. i do not have loss of bowel movement, no loss of bladder control.
The pins and needle came and went and move around my hands feet above the ankles. this is over the weeks as its now.
The pins and needles eventually started to appear more frequently on the right side, but not as frequent as left.
In feb 2 i went to the pcp, for possible diagnosis, but i hit a wall, as the pcp kept insisting that my conditions were mental, or genetic in nature.
Within the week, my pins and needles progressed to cool feeling(randomly but not frequently), now im experiencing random joint pains(1-2 sec bursts, not frequently or constant). Also the twitching is more prevelant when i am still.
I have been diagnosed with vit d deficiency, i am taking 2k per day(i dont know how long i have to be on) but she wanted 4k but was scared it causes itchyness, i already have itchyness from the so-called rashes i got, she diagnosed me with atopic dermatitis, which i dispute, as some other doctor said was contact.
Due to me being on welfare(MEDI-CAL ) i am not able to see my medical tests or records online, as they do not have this technology, but the medical center i go to seems to have it integrated into thier database. I do not have to acess to it, unless i pay for copies of medical record, they dont accept cash.
Furthermore, my specialist appt is in aprl 30th, which cannot be changed to earlier, because of me being a mED-CAL patient. i did not go the pcp appt last week because its across the city from where i live, and the pcp is already losing favor, because my previous visits with her was not finding whats wrong with my present conditions, but trying to make up a diagnosis related to mental health issues, hypochondriac, and i felt like i was going to get the same answers as b4.
i was tested for b12 and cbc blood count, but i do not have access to those results. when i requested other vitamin tests, she refused, i also requested lyme(because my symptoms only fit the neuro portion, now that i have limited joint pain). The parasthesiasins and needle, spider web on arm and leg feeling, tickling,prickling, pin priks, coldness feeling,some joint issues) these are constant everyday, there were days where they subside, and when i wake up. loss of sensations prevents me from feeling (if im about throw up acid). abnormal sensations of my right hands. i do not have numbness, loss of pain or itching, but i am certain thats coming next. Any ideas its lupus.i am in college, and i had to drop a class so i can deal and try to find out what my mysterious neurological condtions is..
My pcp thinks this is also hypochondria, because i stupidly told her i had kaiser records, before turning to WELFARE.
You wouldve think that sudden loss would warrant an immediate red flag, but she/they are not taking my condition seriously i am currently taking 4000IU, (2x2000Iu) per day. and taking b12 (1000IU prophylactic, i don't have test results for this yet.
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I took the drug for High BP for many years at max dose 5mg/day.
Can cause awkward need to pass water at inconvenient times- but effective against high BP - in my case used in conjunction with ACE inhibitor Trandolapril with some success.
However, if you have a familial tendency to Gout (ie Arthritis in family- as a precursor) then this drug type will make Gout pretty likely.
You will not want to experience the pain of Gout, believe me!
At the first sign of joint reddening (esp. with alcohol usage) then review use of this drug. Certainly reduce alcohol intake.
It took me 6 weeks to adjust to cessation of this diuretic -with some fluid retention problems and BP surging up again.
I've talked to many people over the years about this -and the link between any diuretic and Gout seems very common.
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Just got my results after 6 months on atorvastatin:
Total cholesterol; 129 (down from 185)
LDL: 66 (Down from 117)
HDL: 40 (down from 44)
Triglycerides - 96
My cardiologist is very happy with these numbers, but I'm wondering if they could get too low. My total has never been below 150 until now.
I'm a 42-year old male in good health but with a family history of heart disease and borderline high BP.
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