Okay, I've been thinking about this for awhile. Being on Soul Cysters I've seen a lot of loss. IC is pretty common amoung the women with PCOS, yet there does not seem to be any verifiable information reguarding a link. There has been some research to indicate that it is related to progesterone levels, which would make sense. What I want to do is start a letter writing campaign to University Hospitals and see if we can't get one of them to do a study about IC as it relates to PCOS. I think that a study of this nature could help save the lives of babies. If they knew for sure that there is a link between women with PCOS and IC then they could do more to prevent it. Women with PCOS could be monitored closer. Right now most of our doctors aren't watching out for IC and many of us don't discover we have it until we suffered several 2nd term losses. I want to try and stop this.
If anyone can tell me their stories, I'd greatly appreciate it. These stories will be repeated and sent to anywhere I can think of to try. If anyone feels comfortable sharing or has any ideas where I should send letters please let me know. I have no experience at trying a campaign like this, so any advice is appreciated.


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Sparky, our emergent cerclage baby, born at 23w1d on 3/4/07 through his cerclage. 



