Elasticity symptoms and conditions

Wow, who should I believe? Placebo controlled studies which suggest Avelox is a perfectly safe drug or a bunch of crazy people who like to TYPE every OTHER word IN all CAPS who are probably all middle aged women with psychological problems and/or fibromyalgia, irritable bowel syndrome, or other made up diagnoses.

Here's a hint morons: The reason why every drug in existence now lists every possible side effect is because of crazies like you. This way, the drug company can protect themselves from litigious idiots like the poster below who wants to join a class action lawsuit. This only compounds the problem, though, because then more crazies look at the side effect profile and when they see that "Oh my gosh, it says right here it causes x, y, and z" it just validates in there mind that this is somehow a dangerous drug.

I swear, if all of the pampered babies in this country were put to work in a rice field in Cambodia, there would be a lot less nonsense in the world. You would see what true pain and suffering is about.

I have been taking Yaz for six months now, and I'm stopping after I finish this pack. I've been on it this long because I thought at first the side effects caused by it were just the beginnings of aging for me (I'm 25), but the acceleration of my problems has been so noticeable that I can't be in denial any more! Basically, here's what I have:

-thinner hair that comes out more easily and doesn't grow back as fast (it would be nice if this were restricted to "unwanted" hair, but this actually includes my eyelashes, eyebrows and head hair, which have all gotten noticeably lighter and thinner)

-CELLULITE, which I never had before...not only on my thighs but on my bum and CALVES, I didn't even realize it was possible to get cellulite there!

-spider veins on my upper thighs, again, never had this before

-very decreased sex drive

-thinner skin with less elasticity

-memory problems

-much increased vaginal discharge

Now, it's not all losses...my boobs are bigger when I actively take the pills, and my skin has become less acne prone...but is all that other stuff really worth it??? I think not.

I've had Mirena for 6 months and after 3 children. I've always been skinny/underweight (5'6" 100 lbs) and after having my third child I am now a stable 120 lbs. I am very happy about my weight but the only thing I am not happy with is my stomach. I have always been blaming it on having 3 kids and that my skin on my stomach has just lost its elasticity. I have the same diet and I have also even been exercising a lot more compared to never even before Mirena. I walk at least 1-2 miles everyday and along with that I do pilates concentrating on just my abs. My stomach looks like I'm at least 3 months pregnant. I started to think it might be the Mirena so I googled side effects and came across this page. My stomach got weak as I read only 3 posts as there are many side effects. I don't want to believe it is the Mirena doing this to my stomach because I love how there is no more remembering to take pills and no more periods (only very light spotting for 2-3 days). I have three kids so I can easily forget.

Omega-3 is an essential fatty acid that helps to reduce the artery pressure, the sanguineous cholesterol, clots and the cardiac problems, to prevent arthritis, to improve the transmission of the nervous impulses, the health of the skin, the hair, the treatment of the candidiasis and psoriasis, also of reinforce the development and the function of the brain.

Omega 3, 6, 9 contains as Active Ingredients, the Flaxseed Oil or which have several beneficial properties for the health. This product offers aid in the increase of the metabolism, increases the action of the insulin, activates the secretion of the hormone of the growth, helps in the increase of the production of testosterone, aid in the regulation of the sanguineous arterial pressure, is a great hepatic protector, as well as aid in the fortification of the immunological system.

Vitamin C as antioxidant and anti infectious, aid to elevate the immunological system, to maintain the elasticity of the skin and the hair, to avoid the fragility of the nails, to take part in the hormone production anti-stress, interferon and collagen, to participate in the metabolism of folic acid, the tyrosine, the fenilamine and in the repair and growth of weaves.

I have been on prednisone since November 2007 for minimal change disease, 65 mg, in May I started to decrease the dosage (per Drs. orders) and by the time I got to 15 mg all my symptoms came back and I swelled up again. I was again put on a higher dosage of prednisone and put on Cytoxan 75 mg. I am now decreasing prednisone, back to 15 mg every other day and will be off Cytoxan next month. Hopefully this will work. Right now my main complaint of side effects is chest pressure, anything I eat or drink makes my stomach swell and I feel like I can never take a full breath. I recently had chest and abdoman xrays and an ultrasound, all negative. Does anyone have this symptom? I also have moon face, weight gain, hump on back, insomnia, headaches, digestive problems ,shakes, night sweats, vision problems, extreme tiredness and hair loss. How long before all this goes away?

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.

I'm feeling really scared now because I've had the Mirena, well 2 of them, in for around 8 years. In all that time I've experienced really debilitating back problems and I thought at one point i would end up in a wheelchair. I just didn't connect it to the mirena even though my back problems worsened after having it fitted. I've also developed swollen ankles and fluid retention generally. Over the last three years I've had migraines and throughout I've been irrational and impossible for two weeks around my period.
My skin is awful now and seems to have lost most of it's elasticity.

I am finally booked to have this thing removed but I fear it could be too late to reverse much of the damage. I'm sure that skeletally my back is just too messed up. My skin hangs now like a 60 year olds because of the excess weight I'm carrying but if I could just get some energy back I'd be so happy.

I am a 25 year old female who has been on and off prednisone for 5 years for ulcerative colitis. The first time I was on it, I was taking 30 mg for about three months and then tapered down 5 mg a week until I was done. I have always been super thin and athletic and I gained about 20 lbs in 2 months. My face used to be very defined, but I lost my cheek bones and my chin. This is what they call moonface I guess. And I wanted to eat all the time, even when I was full. I had never had bad acne before either, but I had breakouts constantly. I also had more hair growth in places hair shouldn't grow like on my chin and my nipples. I got stretch marks all over my hips and stomach area because the prednisone apparently makes your dermis lose elasticity and that was combined with the weight gain. I also became very moody and depressed and part of it was because my physical appearance had drastically changed. The next few times I was on the pred, same amount, I learned from my mistakes and exercised constantly, watched my diet and drank more water. It helped but it's hard to fight the hunger pangs and you still get moody. If you can, try to use something other than pred. In my opinion, it's poison. I'm now off it for good and I'm taking another immunosuppresant called azothioprine and so far so good. Good bye prednisone...forever!

I have been on Lipotor for several years. I am almost 60 years of age, It is easy at my age to put "changes" in your physical being down to "old" age. Could some or all of these changes be symptons of Lipitor damage?

Gradually I seem to be losing the ability to walk. My legs feel as if they are encased in cement. Getting up from bed or a chair, I stumble around until my muscles seem to get moving. Sometimes I seem to get vibrating spasms in my legs.

My whole body has become stiff. I walk from side to side with my arms bent like a wooden soldier. I have lost my elasticity of movement. My wife looking at me walking has wondered what is wrong with me.

Stepping up onto a step ladder one step at a time, I feel like my legs are too weak to handle my body weight. I thought it was due to my increased weight. I had not considered that it was a breakdown of muscle caused by Lipitor. I continue to go to the gym and do not think that my eating habits have changed but I seem to be putting on more weight.

I had a bit of arthritis in my knees before Lipitor but it did not stop me from running for miles. Now I find if I walk on the treadmill for a mile or two that I am stiff and sore all day. I live with joint pain, muscle ache and a weakness in my legs that makes getting up a real struggle. I put this down to having put on weight but maybe I am putting on weight because of Lipitor and that is causing the problem.

I now seem to have a perpetual nasal infection which I have been putting down to the smog. My skin is so dry, at times, it hurts but I was putting it down to the dryness of central heating in winter. I too have floaters in my eyes but have been told they are common at my age whether I was on Lipitor or not. Sometimes my vision is so blurry I have geat difficulty reading.

I am also taking Cozaar, Allopurinol and Gen-Doxazosin.

I am looking at this web site because I am worried. I will now see my doctor.