Insulin resistance symptoms and conditions

I had Mirena inserted about 3 months ago and have been consistently gaining weight since then. I initially wrote it off as anything else besides this drug because the pamphlet is very clear that weight gain is not a side effect and I talked to 2 gyns and they insisted the same thing. So I had my thyroid checked and started eating better and increased my exercising, I am a personal trainer so I already do these things pretty intensely, but I have stepped it up to slow the weight gain. I am up 8 pounds in three months which makes me crazy. Yet I am hesitant to get it out since it was so insanely expensive and not knowing for sure that it is the mirena. So any of you who have had it removed could you comment on if your excess weight that you did put on has come off or not. Besides this frustration, I have loved it, but it makes it difficult to build my business as a personal trainer if I am gaining weight.

I've not experienced any of the horror stories listed here, but I've had two side-effects that I've isolated. The first is the upper respiratory tract infection. That's a known side-effect. The second I believe was caused by an interaction between Januvia and Splenda. I use a lot of Splenda in my oatmeal. I've been having to urinate in the middle of the night (not like me) and I've experienced urinary tract irritation. Since stopping Splenda I've stopped getting up in the middle of the night and my tract irritation is subsiding. But, all this could be incidental and I would like to hear if other people are experiencing these symptoms while on Januvia and using Splenda. It appears, APPEARS, that, while on Januvia, that I experience the published side effect of losing a little bit of my appetite (good!) but that I have an increased appetite (bad!) using Splenda while on Januvia. I did not experience these symptoms while using Splenda before I was on Januvia. Please write to me if you have similar symptoms and situation at ******

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.

you can't seriously think you got PCOS from taking Yasmin. PCOS is a syndrome, and taking the pill is used as one of the treatments for it.
One of the possibilities is the it is genetic, and it can be caused by insulin resistance or problems in your adrenal gland. You can't possibly get PCOS from taking yasmin. And PCOS does in fact increase the risk for cervical cancer, cardiovascular disease, and Diabetes, but has nothing to do with taking the pill or not.

I started taking Yasmin 2 years ago, and after about the first 2-3 months of taking Yasmin, I started experiencing horrendous pains after sex. Once my doctor figured out what was going on, I was diagnosed with Endometriosis. Not long after that, I was diagnosed with Polycystic Ovarian Syndrome. Now I am more than likely unable to have children, and am at risk for cervical cancer, cardiovascular disease, and Diabetes.
If anyone else has recently been diagnosed with Endometriosis, or PCOS after taking Yasmin....PLEASE reply or contact me!!!!!!!!!!!

I have been on NR since July 18 of this year. I was diagnosed with PCOS and Insulin Resistance. I am also on Byetta. My experience with NR has not been good. First of all I was skeptical about constantly having a foreign object in my body especially such a sensitive area. Symptom 1, decreased sexual desire! Symptom 2, burning sensations down there. Then itching, and a horrible discharge and smell!! At this point I kept thinking how much worse can it get. Well it did, I should be loosing weight from the medication finally regulating my insulin levels, after all I work out 5 times a week and follow a healthy eating plan. My lower tummy is swollen as well as my hips and thighs. Not to mention I have pains in my hips, like they need a massage. On top of this all I have an increased resting pulse rate and blood pressure as well as tighten feelings in my chest. I really feel like this birth control is not safe for me. I was previously on yasmine, and loved it. My endo suggested NR due to the PCOS and IR they feel like it works best with Byetta! WRONG!!! I am waiting for the DR to return my call I am requesting AGAIN that my BC be changed.

I just got off yasmin , and now am on alesse. I tried to get off yasmin to x,s before, and actually had extreme headaches and insomnia. I somehow got viral meningitis last summer, just after getting off yasmin,(I had been taking it for a year) . I have no idea if this is relevent or not. I also had bad folliculitis on my inner thigh, and rashes. On yasmin my cellulite would appear much worse. I am only 110 lbs, and 5'5. Now off of it , my cellulite looks better(a lot less) . I am having trouble adjusting to my new pill, I guess because of the hormonal shift. I have insulin resistance , so I am very prone to side effects.