Hi Ladies,
My name is Francesca and I am looking for mom's out there with Congenital Heart Disease who are pregnant or have given birth. I just found out that I am pregnant and would like to talk with other mom's who may be going through the same experiences.
Thanks,
Francesca
Re: Congenital Heart Disease Mama's
Hi Francesca I'm Elle and I guess I kind of fit into this category. I was born with a bad mitral valve and multiple septal defects. Last year I had my third heart surgery to replace my mitral valve with a biosynthetic valve just so I could have children. It was recommended that I not get pregnant unless I got my valve replaced. Right now I'm 29 weeks pregnant with a baby girl. So far my pregnancy has been uneventful, but I am being closely monitored by my MFM doc and my cardiologist.
Hi,
My name is Lise, I have Tetrology of Fallot and am pregnant with my first child (I'm 25 weeks). It's been an interesting ride so far, lots of out-of-town appointments (I live 5 hours away from a decent perinatal clinic). I have an excellent OB here in town though, feel like I am in good hands.
No problems so far, just tired all the time
I still work full-time, but am eager to get off work so I can focus on baby things
I work at a college, so we'll see how the September rush treats my already-weary body 
Cheers!
Hi!
My name Beth I am newly pregnant; I'm 10 weeks. I was born with a Tetralogy of Fallot. I have two heart surgeries as a child, and had a pacemaker put in at 22. I have always been active and healthy and never really considered my heart condition as as an obstacle in my life...until I got pregnant. I have an ever list of growing doctors and appointments. I will hopefully know at my next appt at 12 weeks with my high risk baby doctor if I have passed on my hear condition or not.
If anyone has any advise about how to deal with a high risk pregnancy please let me know.
Take Care!
Hi There,
So this is better late then never, maybe it will help someone in the future. I was born, 30 years ago, with a Tetralogy of Fallot. I had two corrections as a child and was able to not have a pacemaker until I was 22. I lived a very happy and healthy childhood.
My advised for anyone who children have the condition is to not focus on it. I was always aware that I was special, but I was not allowed to use it an excuse not to do something. My parents put me in dance lessons at 3 to help me be active; I did not have my first correction until I was 5. I danced all the way through college, played basketball in high school, and even ran a few 5ks...much to my cardiologist?s dismay.
I am newly pregnant, I?m 10 weeks, and will know at my next high risk doctor visit at 12 weeks if I passed on my heart problem or not. If I pass it on or not will not change how I feel about him or her.
If anyone has any questions, please email me. Bethanylynn97@gmail.com
Take Care,
Beth