Dark hair symptoms and conditions

Happy to have Mirena out of me! I had Mirena inserted in 7/07. I had it removed on 7/13/09—YEAH!. My sister, who is a Sonographer (she does ultrasounds), noticed my weight gain and that I haven’t been myself for a while (moody). She said that so many women complain to her about Mirena when she is doing ultrasounds for them. Most of them tell her about the weight they have gained and their moodiness. My sister said… “You workout all of time and watch what you eat. You shouldn’t be gaining weight.” I was 150 lbs when Mirena was inserted and two years later, I weigh 168 lbs. I workout intensely five or more days a week and earned the 2008 Olympian title at my gym (which took a year of hard work to acquire), but my weight keeps creeping up no matter how hard I try. My workouts keep getting harder because my body is heavier… it’s so frustrating! Following my sister’s advice, I decided to do some research on Mirena and found this site. THANK YOU! I was so relieved to know that I wasn’t crazy and that others have experienced the same symptoms as me. Here are some of the other symptoms that I experienced from Mirena: constant bloating, I ached from my hips down to my knees (which I attributed to my hard workouts, but was wrong), mood swings, hot flashes in the middle of the night, acne on my chin, dark hair growth on my chin, dull cramps in my lower stomach, back ache, fatigue, fluttering in my stomach (which felt like a baby), sensitive breasts, pain during intercourse, spotting after intercourse (almost every time). I’m not sure how long it will take me to get my body back, but am so glad that I’m on my way. I’d like to thank everyone who posted symptoms on this site, you’ve changed my life.

I can't believe how reading all of your horror stories make everything "come together" for me too. I have been on Mirena for almost a month and had side effects from day 3 on. It started with this overwhelming fatigue and what I assume was depression. I am the happiest, most vibrant person and all of the sudden I was fighting back tears for no reason at all. Then around day 5, the cramps started. I thought I was going to die. I couldn't work, couldn't sleep, couldn't play with my kids. It was awful. They subsided after about 4 days. Then the worst happened. I started losing hair...I mean clumps, not just natural shedding. I have long dark hair and when I showered it looked like I was on chemo or something with the amount of hair hitting that shower floor. So scary! Then the headaches, OMG! Awful! Remember, all of this happened to me in just a few weeks time. So I'm freaking out crying last night because of my hair and I call the doctor and they think its my thyroid so they're sending me to an endocrinologist. Then my mom found this website and it all came together for me. MIRENA! So needless to say, I am having it removed tomorrow morning. Oh yeah, and I've gained 7 pounds in 3 weeks...nice.

Hi everyone,

I am a 25 year old female who was diagnosed with Crohn's disease one year ago. I stumbled on this website and wanted to share my experiences to let others know they are not alone and that their side effects due to Prednisone are completely normal.

In Nov of 2007, I was in the hospital for a Crohn's flare up and was put on prednisone through IV (240mg/day). After a three days I was released, but one week later, had another flare up and was back in the hospital in December of 2007. This time, I stayed for 6 days and was on 240mg/day again through IV, along with taking Flagyl and fluids for my flare up and infection.

At first, I lost about 10 lbs due to the flare up and all of the medication I was on. However, within 3 weeks time, I gained 28 lbs and was a complete mess. I looked different, felt different and was emotionally and mentally drained.

My side effects included: Severe moon face, buffalo hump, increased appetite, hair thinning and severe hair loss, night sweats where I would have to change pajamas 3-4x a night, OCD to the point where I would have to clean my entire apartment (even if it was already clean), restlessness, anxiety, no sleep and sometimes I would go days without sleeping, increased thirst and dehydration, swollen eyes and headaches, depression and mood swings, upper and lower abdomen swelling and weight gain (28 lbs in 3 weeks), suicidal thoughts, unbearable muscle and joint swelling and aching, forgetfulness and memory loss, blurred vision and dark hair growth on my face near my sideburns and underneath my chin and on the bottom portion of my face. Bottom line: it was unbearable and nobody warned me about the harsh side effects of the drug.

When I left the hospital, I was put on 60mg/day and eventually weaned off Prednisone over the course of 2 1/2 months and took my last 5mg dose in mid- February 2008.

It is now 2 months since I have been off Prednisone and as of now, I have only lost 7 lbs, but much of the moon face has gone away and I don't seem as swollen in my chest. My appetite returned to normal the day I stopped taking the drug and my mood swings subsided one week after stopping Prednisone. I still have the buffalo hump, but it stopped hurting and I am now able to sleep through the night. The fluid retention seems to have moved south towards my legs, arms, and lower abdomen. My doctors say that within about 6 months after stopping Prednisone, most of the fluid retention should go away and they recommend walking for 45-60 minutes/day to help with the fluid/weight gain.

Overall, prednisone helped to save my life and put my Crohn's into remission, but is one of the WORST drugs I have ever taken. My heart goes out to anyone who has had to take this drug and trust that you are not alone--and the side effects are real and they are harsh. I am slowly seeing that it takes time for the prednisone to leave your system and my doctors say that every day there is less and less in my body.

Stay positive, stay active & stay Healthy!!