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PPCM is very serious. When were you diagnosed? Are you seeing a cardiologist? What's your EF? How symptomatic are you? Are you on any medications like a beta blocker? Sorry for all the questions but that stuff is what you need to be aware of. You'll need close monitoring during deliveryC-section Delivery presentations Infant care following delivery, a cardiologist should be on handHand or foot spasms Hand tremor because of the volume load your heart gets after delivery - it could be potentially very dangerous.
Now I'm going to be worried about you until I hear from you, so please send a message, ok? I'm a survivor, and I know a bunch of great women who have gone through this too. You need good medical professionals on your side, it's vital.
You've been getting some really good advise here. The fact that you have a diagnosis means your seeing someone. Follow their advise, every single word, this is VERY serious for both you and your baby. Please let us know how you do, and Good Luck
gail
Babies actually fare very well in moms with PPCM. The only complications they typically face come up if they have to be delivered early for mom's sake. Even then, they usually do very well.
Thank you all for you replies,I think they have called it Dilated Cardiomyopathy. I'm 19years old and only got diagnosed in june, a few months after finding out i was pregnant, but they say i have had this for a while but not sure how long or what has caused it.. Ive been seening a cardiologist since day dot they sent me away for lots of test which was a bit scary.. My EF was 39% it is not as low as some other people but is still not normal. My resting heart rate is about 90+ bpm, making the bed or walkin up to catch the bus it goes to about 140bpm.Get very breathless at times. Ive been takin meds for it but a low dose cause im pregnant, Metobrolol which has been helping. Ive been told that when i go into labour they want me there so i will be monitored and have a slow and long does of epidural and use the forceps thats what they think is best atm, and than ill be in intensive care for 12+ hrs. Still have to find out more
I am a mom with a 25yr old son who has conjestive heart failure with cardiomyopathy he is going to have his first baby in may, he is worried about all the drugs his has had to take causing birth defects. his EF was 14 and we just about lost him. I just wanted to tell you to keep your thoughts positive!! and wish you and baby well. Listen to your doctors and do everything they tell you to do. YOU both are in our prayers. Good Luck and God bless!!! Dianai
I have Idiopathic Dilated Cardiomyapathy and I am 29 yrs. old. I was diagnosed with this 7 yrs. ago, after I had my daughter, who is now 7, of course.
I was pregnant twice by new husband and my cardiologists told me, I would not make it into the 4th month of pregnancy without dying !
I NOW WONDER if I could have found special doctors that could have allowed me to carry and maybe, possibly, have a c-section, for less strain on my heart ?
Also, when I was diagnosed 7 yrs. ago, I was life-flighted in a helicopter 1 month after my daughters` birth and nearly needed a heart transplant.
My ejection fraction was only 10% and I had congestive heart failure. with 8 liters of fluid on my lungs. I was literally drowning to death. I was given a catheter to drain the fluids off of my lungs, and my skin changed every color as I was slowly able to breathe again. With meds, I am holding stable now, and EF is nearly 50%.
Also, my heart has gotten a bit stronger.
But, I still cannot live without the meds.
Question being....Could I have had those babies, or is it impossible to have a baby with such severe heart problems ?
PPCM is very serious. When were you diagnosed? Are you seeing a cardiologist? What's your EF? How symptomatic are you? Are you on any medications like a beta blocker? Sorry for all the questions but that stuff is what you need to be aware of. You'll need close monitoring during delivery, a cardiologist should be on hand because of the volume load your heart gets after delivery - it could be potentially very dangerous.
Now I'm going to be worried about you until I hear from you, so please send a message, ok? I'm a survivor, and I know a bunch of great women who have gone through this too. You need good medical professionals on your side, it's vital.
Sending good thoughts and prayers your way.
gail
I was pregnant twice by new husband and my cardiologists told me, I would not make it into the 4th month of pregnancy without dying !
I NOW WONDER if I could have found special doctors that could have allowed me to carry and maybe, possibly, have a c-section, for less strain on my heart ?
Also, when I was diagnosed 7 yrs. ago, I was life-flighted in a helicopter 1 month after my daughters` birth and nearly needed a heart transplant.
My ejection fraction was only 10% and I had congestive heart failure. with 8 liters of fluid on my lungs. I was literally drowning to death. I was given a catheter to drain the fluids off of my lungs, and my skin changed every color as I was slowly able to breathe again. With meds, I am holding stable now, and EF is nearly 50%.
Also, my heart has gotten a bit stronger.
But, I still cannot live without the meds.
Question being....Could I have had those babies, or is it impossible to have a baby with such severe heart problems ?