Mp symptoms and conditions

I just recently had the mirena iud inserted. Oct 30 2008. 3 months after having my first child under a normal vaginal delivery. When I have asked my doctor regarding any side affects he stated that women may have heavy bleeding the first 6 months/ and that after those 6 months that your periods will actually disappear.

The first week that I had the mirena in, I began bleeding almost instantly. Blood clots the size of my closed fist came out of my body from the uterine wall I suppose. I went through a super tampon/ and a pad in an hour and a half. ( I am one of those women who normally use a super tampon maybe once in a while/ normally a reg. size does the job) This bleeding has not stopped since the mirena was inserted.

Looking at a computer screen is part of my daily routine at work. It seems as though my eyes feel blurry through out the day as I am working. Towards the end of the day I can barely stand to look at it. This has never happened to me before. It is almost like I want to turn all lights off and sit in the dark, with no noise(headaches).

Of course sex drive is at the all time low. Who is in the mood to go for it when you are bleeding with a terrible headache?

The first few nights I had a horrible time falling asleep and staying asleep.

Well... at this point I have had headaches... all day for a week now. My head hurts like someone is pounding it against a wall. I have not had a headache in years. My stomach has been upset/ feeling as though I may have to throw up.

I am afraid that I may start seeing the other symptoms that ladies have talked about.
When you had the symptoms did they all happen at once or one at a time over different time periods?

I have Crohns and had a flare up so I'm back on 40mg of Prednisone. I've been on 40mg now for 3 weeks and I start to tapper off in another 3 weeks. Well every time I start the prednisone again I get new side effects. This time, my gum are bleeding all the time and the pain in my knees are horrible! I still get the regular side effects, ie: Mood swings, joint pain, sleeplessness, sweating, swelling of my legs and hands, wanting to eat everything under the sun, moon face and my hair falls out! I wish the drug manufactures could develop a drug that would not be so hard on our bodies. I have to struggle with the pros and cons with every flare up. Do I want the weight gain, mood swings and hair loss or do I want to look good and be very sick! I'm 37 and was 16 when I found out I had Crohns.

Hi my name is Jessica an I was diagnosed with Chrohn's on 3/4/08. I started with the Entcort for two weeks and that did nothing for all the pain and suffering that I had been going through since November. The put me on Prednisone at 40mg a day. I have been on it for about 3 weeks. After 3 day I noticed the moon face because I had lost so much weight because of being so sick for so long. I still hardly eat and am still losing weight. I can't sleep more then 3 hours at a time unless I take something to strong enough to help me fall asleep and if I sleep for more then 5 hours I will be up for the next 20 before I can even try to lay down. I have OCD which I have never had and cant stop cleaning when I feel up to it (kinda like this side affect). I have been haveing awful leg cramps and walking into stuff all the time. I forget what Im doing or were Im going. BUT the WORST PART is the ACNE... I am an Esthetician and I never had anything like this. I mean I have breakouts during the normal times ect... But this is bad an everyday there are more of them. I use really good stuff on my face to begin with an the things I would use on a client are not the same for treating acne that is caused from this drug so those things are not helping either. Right now my makeup covers it ok, but Im going to be on Prednisone for 3 more months before they will start weening me off and then going on 6-MP drug. I cant go 3 more months if this is going to get worst. PLEASE IS THERE ANYONE WHO KNOWS WHAT TO USE TO CONTROL THIS ACNE ????

I have never taken Prednisone, but when my daughter was 18, she was stricken with ulcerative colitis and was on prednisone and then 6-mp for quite some time. She nearly died from the 6-mp and even after 8 years, she has horrible "growing" pains in her shin bones from the prednisone. She had psychotic reactions to the prednisone almost a year after she was weaned from it - such a severe reaction that she spent a week in the psychiatric ward of the hospital. Of course, the doctors said there was no connection btwn the episode and the steriods, but I know better.
She eventually had her colon surgically removed, and was fortunate enough to have a j-pouch created at the end of her small intestine so she does not have a "bag"! I am afraid that she will always suffer some residual side effects from all of the drugs she was on, and may, in fact, be sterile.
She has not yet attempted to get pregnant, so we will see.
anyone on these meds for more than a couple of weeks needs to research their condition and find some alternative treatment! These drugs should only be a last resort!