I had the procedure done in June 2009. This month my menstral started like normal, but when it came time for it to end, it didnt. It did get lighter, and no cramping, but i was concerned so I made an appointment to see my dr. She put me on hormone pills for a week thinking that was the problem. During the exman of my abdomen, it was tender and hurt, so she decided to do an ultrasound. 2 days later, (this past friday) I went in for the ultrasound. It revealed that 1 of the coils had come out and lodged itself in the Endometrium. My dr called me friday evening with the results. I was scared, and with my husband out of state (OTR driver) I had no one here, besides my children. They are making an appointment to see the Ob/Gyn with the recommendation for a hysterectomy.
After hearing this from my Dr. I called Essure about this, they told me that out of the 700 woman who had this done during the trial phase, less then 2% had this same problem that I am. BUT because its less then what FDA requires, us as woman patients are not told about this. I was disgusted when I heard that. I started screaming at the woman on the phone. I was so angry that I wanted to throw my phone across the room.
What it comes down to, is us woman standing up to these people and telling them that we have the right now know ANY & ALL side effects and complications..REGARDLESS OF WHAT THE FDA REQUIRES!!!
Thanks,
Worried in AZ