Practice nurse symptoms and conditions

I had the Mirena fitted in May 08, and boy did I see hell before heaven, I wished I had seen this website befork agreeing to the Mirena. It was very painful on insertion with lower back pain that I almost passed out. I began to notice a slight tingling in my breasts, this increased as time went on and felt like a thousand hot needles attacking my breast with terrible pains and sweating. .I have restless nights and gets moody very quickly, my joints aches and pain tremendously, I move at the pace of a 100 year person, my movements are slowed down and its an effort to get out of bed on mornings. I haven't even got the energy to play with my grandson.I saw the practice nurse and told her I want this out of me ASAP, I can't wait for the two weeks to come.I had the Mirena implanted in me because I became anaemic with heavy periods and not for contraception-- Ladies BEWARE, read and think carefully about the harm you might be putting your body through, the Mirena might not be for every on, I think there should be more research carried out on new products, who knows the manufacturers are only interested in selling their products to earn a quick buck. I sympathize with all of you who had the Mirena coil.

I've been taking Levaquin for about 3 weeks. Last week, suddenly, every joint in my body started aching. I mean from my neck, hands, hips, knees, ankles, feet, everything. For the past week, when I wake up, I can't even make a fist without experiencing excruciating pain. I've always been very active, running, basketball, soccer, skiing, you name it, so this is scaring the heck out of me. I'm 47 years old, and up until a week ago, I was hiking with my family, running everyday with my dog. Now I feel like I'm 100 years old. It hurts to walk, stand up, etc! I have an appointment with my doctor tomorrow! I'm ticked about this!

I felt and acted like an invalid, being helped out of bed, up from a chair. Struggled with the toilet. Had very little energy. Was very surprised when Doctor advised to come off the drug and shocked when I read the side effects on the advice sheet as these could have just been written by me from experience. Started taking December 2007 and stopped, after the practice nurse referred me to the Doctor, 9th July. Already feeling 99% better.

PREDNISONE.... a word that is unknown to the naive and despised by the the knowledgeable. Before i begin i want to tell you that prednisone for lack of better word F***ed me up. So heres my story with the pill. About a year ago i was officially diagnosed with Minimal Change Disease, now remember i am eighteen at the time, and was prescribed prednisone to cure the disease. Now being unaware of the severity of the drug and disease i casually continued life while taking 80mg per day of prednisone. Well this was good and all because it did in fact put me in remission, but the side effects were starting go surface. My face ballooned up "moon face", started experiencing random series of depression, became insomniatic, and unfortunately gained several pounds. Well this was not the end of side effects as for me. I continued with the medication and after 6 weeks of 80 mg i began my 5 week course of 60mg. Then after that i started 4 weeks on 40 mg and began tapering 5 mg every 2-3 weeks afterwards. Toward the middle of 60 mg the drug started taking its toll on my body as my skin lost its elasticity so i started getting gruesome strecht marks all over my body. I also became constipated for whatever reason most probably prednisone was at fault. I became very frightened actually terrified so i started to research about the drug in hopes of finding ways to avoid some side effects. In doing my research i found out very disturbing information regarding prednisone. Along with all the side effects that i mentioned above, prednisone also causes cateracts, glacoma, diabetes via insulin resistance, and osteoporosis. Now these i consider as the more severe permanent side effects as the list unfortunately is much longer. Finding out about the side effects i became extremely paranoid and started a very strict diet to hopefully avoid some permenat side effects. I admit reading about the information on prednisone created my paranoia and/or possible phycosis which ultimately led to my stress which led to my severe depression. Now this wasn't any old type of depression, i was sersiouly in need of some help. Everyone around me could tell something was wrong and really i dont blame then for in fact i felt as if my soul had died, the very essence of my being. Now magin if you can someone taking away your youth from you, sucking the very life out of you... thats exactly how i felt. To add along with the depression my grades became a wreck in college as i dropped several classes, lost a friend, developed problems with my parents as they tired to help me, and disrespected family relatives with my uncontrollable mood swings. A few weeks in of dieting and exercising i lost a lot of weight (15-20 pounds). As far as side effects non had changed i still had to deal with all that was mentioned above especially with the fragile skin that was a real burden as i had even a few stretch marks on my face from sleeping on my side. At this point of my long and what seemed to be a never ending journey i become exteremly weak. My body had no energy to run on as i refused to eat and when i did eat it was either foods that are considered free foods or protein nothing else. Everything at this time had been taken away from me including smoking marijuana (marijuana drops blood sugar as this would cause me to start feeling faint and lightheaded), alcohol (same as marijuana drops blood sugar), and the fact that i was not comfortable in my own skin (literally). I was driving myself insane. Everyday i was behind the computer searching for more and more. I was obsessed and became my worst nightmare. Oh by the way half in the medication therapy i showed 1+ grams of protein in my urine which my doctor possibly thought it could have been a relapse. This news i did not take lightly i had lost it and was prepared of comiting suicide. I cant lie, i really did not want to live anymore i just wanted to end this and suicide seemed like a very real and convienent possibility. If it had not been for my parents talking to me giving me a 3 hour speech and lecture i do not know what i would have done. Suicide at that point became out of the question because i could not do this to my family. So i went and purchased urine dip sticks to monitor the protein. The doctor had given me a 2 week window or chance to get back into remission or else he was going to prescribe me cytotoxic agents aka chemo therapy drugs. This was horrible news to me. So as i monitored my protein i found out of a very interesting trend. I noticed that my protein levels in the afternoon were in fact positive for protein and were usually up and down as far as how much but in the mornings i noticed i was always negative. Now this give me a huge bit of hope because when in researching about MCD months earlier i found out that there is a coniditon called orthostatic proteinuria which affects mostly young adolecent males and is a condition described as for some unknown reason there is protein loss in the afternoon when the person is upright and active then when they are supine or laying down the kidneys do not allow any portein loss. This condition is in fact harmless. I was very happy from then news and i told my doctor, he was somewhat doubting, but i don't blame him he is looking out for my best interest, but sure enough after the 2 weeks had past i went in again for my appointment after testing and i was negative for protein as i had expected. We began tapering after that point and i continusouly monitored my own tests at home and eventually i got off the steroid, actually today is that day after a 9 month period of heartache and distress. You know people say that they went to hell and back in a hard moment in life, well i went to hell stayed there for 9 months then came back. I feel so everyone who as ever needed to take steroids for long periods of time, i know its tough but believe it as it is indeed a potent drug and in most cases a miracle drug. It gave me a second chance at life and no matter how hard it was or how much pain it put me through i cannot complain for it did in fact cure me and thats why i can never hold any grudges. So thats my story i kno its not pretty but what can i say it is indeed mine whether i like it or not.

Hi all,

I am 53 and from the UK. I was on Lisinopril for 13 years. First 5mg, later 10mg then a few weeks ago 20mg as my BP was 169/90. Afetr 8 days of taking this dose I felt strange and felt as if I was about to fall down when walking. Also had a feeling I was kinda walking sideways if that makes sense. Anyway, went for check-up with health worker at docs surgery and after 8 days on this stuff instead of my BP being reduced it was up to 210/120. The health worker took my BP 5 times and looked cncerned while trying to reassure me not to be concerned. She went of to consult the senior practice nurse and made me an appointment for the next day to see my GP. The next day I told my GP how I was feeling and he said he didn't know why my BP had gone higher on the double dose of Lis but to continue taking it along with nother drug he prescribed called Amlodipine 5mg, a calcium channel blocker. After another couple of days I felt very ill. Palpitations, dizzy, and a feeling every ten minutes or so as if my chest was puncched from the inside, a very uncomfortable feeling indeed. I decided on a process of ilimination and stopped the Lis but kept taking the latter drug. Almost imedietly I felt better even though my BP was round about 146/85. I started to realize that symptoms I had for 13 years were probably due to the Lis. Symptoms including, waking suddenly, literally choking on acid as my throat closed in a spasm, Strange nightmares, food sticling halfway down my gullet causing extreme discomfort etc. On top of this, nearly two years ago I was diagnosed with auto immune disease and had radioactive iodine treatment on an overactive thyroid, an overactive thyroid that instead of making me lose weight, made me put it on. A while later I was diagnosed as having type two diebetes which I tried to control with diet. Now since stopping the Lis my blood sugar readings have never been better, in fact I wonder now if I was ever diebetic at all. The most upsetting thing is, I now wonder if the thyroid malfunction was caused by the Lis. I feel much better like a veil has been lifted from my mind, no longer moody or having foggy thinking. I hope I have not gone on too long. I wish you all luck with your meds. I have started taking Hawthorn berry capsules which it's claimed help to lower BP naturally. My BP today is 140/80 but does fluctuate.
Lawrence