Tank tops symptoms and conditions

The first time I heard the word prednisone was late Dec 07 when I was hospitalized for severe pneumonia. I started off with a bad sinus infection that quickly advanced into pneumonia in a matter of a couple weeks. I tried 3 courses of antibiotics but I continued to get worse and got to the point where I was unable to breath on my own. Within a day of being at the hospital I felt like I was living in a dream world and from there I continued to get more stoned by the minute. I had no idea I was being pumped full of prednisone intravenously, along with my antibiotics. I was given a dose of 250 mgs daily, and obviously it was way too much for me. As I progressed into my dream world, I had a couple of “episodes” where I acted completely out of character, and got really paranoid and highly emotional. I pulled my IV out of my arm the one night and sat and watched the blood dripping from my hand, not really understanding where I was or what was going on. Later on I got really paranoid that the nursing staff was conspiring against me and talking about me behind my back (lol) , which I normally would not care about, but for some reason it made me really upset and I sobbed uncontrollably at times. I also tried to leave my room in intensive care a few times, as I was convinced that I was not supposed to be there and wanted to go home. My doctors were really freaked out so they gradually lowed my dose over the last few days I was in the hospital, even sent me for a CT scan of my brain in case I was going crazy. Prednisone is an extremely strong and evil drug – that is why I had the adverse reaction!! Not because I’m crazy! And one should never be given a drug like prednisone without their knowledge!! A few weeks after leaving the hospital I started going down hill again and the doctors realized that what I had was an immune disorder and not just pneumonia per se. After a few months of on again off again prednisone (never longer than a week at a time), I was put on a daily regiment (50 mgs) of it starting in May. Since then I have experienced all of the same side effects noted by everyone on here, weight gain, sleeplessness, anxiety, hair growth (the worst is on my face and fingers!!) dizziness, confusion, trembling hands, tooth aches, and the worst of all , big time MOON FACE! I feel like a complete freak most days. I am now tapering and am down to 10 mgs. So far I have seen no improvement in the side effects, accept now I have withdrawal side effects on top of everything - nausea, headaches, flu like symptoms and trouble breathing. I HATE this drug, even though I know it ultimately saved my life in the hospital and my kidneys – as I had complications caused by the autoimmune disorder. I see my doctor next week and I want off this drug completely. I am not sure the benefits out weigh the side effects to be honest. I want to feel normal again and be able to recognize my own face in the mirror  People should use extreme caution when using this drug and it should only be used to save people’s lives, not used for minor things like poison ivy. That is unconscionable!!!! Good luck to all who are on this drug.

My Mirena Removal....
So i posted here a few weeks ago after I found this site. I had EVERY side effect listed and was so freaked out that i immediately made an appointment for removal.
For those of you reading and wondering what the removal is like..
Well, NOTHING like the insertion. I was so so nervous and it was over before we actually started. The DR was surprised that i was back in his office to have this removed. He then proceeded to do an ultrasound to be sure it was placed properly before removal. And yes, all was OK on the position of it. I explained to him my reasons and he looked at me like he had never heard this before. I honestly can not imagine with all the women he sees that NONE of them have complained. But...as I was getting dressed afterwards, I took a good look in his office. There was Mirena literature ALL over the place. In fact, that was the ONLY thing he was advertising. Not to mention...they made me pay up front with the insertion back in Nivember...billed my insurance and I still have yet to receive my reimbursement. Oh yeah, and that...they charge more than the actual Mirena costs, then they bill your insurance for the price they know they will pay and the DR then makes about $150 profit. Nice.
Ok, back to my side effects post Mirena. The removal was not painful at all. I did spot for about a week- nothing too heavy but it was clotty and def there.
A couple of days after the removal it felt like I was coming out of my skin something terrible. I figured this was my body adjusting to the lack of hormones. I also had some headaches.
It has now been 2 weeks and the spotting has disappeared. I also can see the bloating of my stomach is starting to go away. It looked like I was about 4 mos preggo while I was on it. I also have an increased sex drive. And sleep-- well let me tell you, I have not slept this good in a very long time. I am actually sleeping more than 6 hours now and the night sweats have also discontinued.
I can't believe EVERY time I come to this site and look up Mirena ALL the people that have posted their experience as being negative. Yet, the DR looks at me like I am crazy! I have been seeing him for years and I have never complained about something like this. I really am so happy that I have it out and wish I would have done my research on this prior to insertion (which was one of the most painful things ever!)
So..for those of you out there that are either contemplating having it inserted...I say NO WAY. And for those of you out there that are nervous about the removal or not sure..I SAY YES, DO IT! For our bodies to be reacting this way, it is clear to me that it should not be inside of us. Listen to your bodies...they really do speak to you and let you know when something is not right. Forget about the DR saying it is safe or he has not heard of any of these side effects...YOU be the judge.
Good luck! And I promise it gets better once you get that lil' demon out!
Mona

I had a small dose of Kenalog injected into a hypertrophic scar on my upper back, and also several doses to a small hypertrophic scar on my chest (both from mole removals). The scar on my chest improved - got flatter and softer, but the single shot to the scar on my back made it sink in. Now there is a huge hole in my upper back, between my shoulder blades. Pretty unattractive for a 27 year old female who enjoys wearing tank tops and things.