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I am also a survivor of AFE. I am so glad that you are okay.
Another survivor has started a foundation focused on researching AFE with the hopes of finding a better understanding of the causes of AFE. The foundation will also help support those who have been affected by AFE. We are currently building a database of AFE survivors.
I would love to share more information with you about the foundation and tell you about a research study that will soon be underway that will focus on AFE survivors.
Please contact me at for more information about the AFE Foundation. I would love to chat with you about your experience with AFE. Also, if you are interested, I can help see if there are any other AFE survivors in your area. I have recently met a few survivors and it has been an incredible experience. We are a rare and special group!
Many thanks,
Amy
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Amy, I would love more information about the AFE foundation for research, and the AFE survivor database you mentioned.
Thanks so much.
Shana
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Melanie
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I would love to share more information with you. It looks like I can't post my e-mail address here (it was removed from my original post-oops!) but you can contact me via the AFE Foundation website at . It is a work in progress but the home page is up. There is a place at the bottom to send an e-mail. The e-mail will go to Miranda who is the survivor that started the Foundation. She can either respond or forward your message to me and we can go from there.
I am so glad you are okay. We know of several survivors go on to have uncomplicated second pregnancies. This is one of the reasons keeping a survivor database is so important-we are able to track things like this. I have never heard of the 10% chance of that recurrence.
We also have a group on Facebook. The group name is Amniotic Fluid Embolism (AFE) Foundation if you belong to Facebook then you can find us that way too.
I look forward to hearing from you and any other AFE survivors out there.
Take care,
Amy
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I had a AE in 96.
I had a grand mal seizure, was cyanozed, thrombocytopenic and had a cardiac arrest during it all.
I'm pregnant again now, hence why I'm also checking these sites. There is about a 10% higher risk of recurrence. My Dr has alerted the maternity hospital and they have a specialist team that will take care of me.
They'll probably just want to monitor you, as you're now what is considered 'high risk'. But better safe than sorry they say.
As for your C/S bringing it on, its more like the labour that actually did it. Although there are some Dr's who advocate C/S in case of AE.
Anyhow, hope this helped:)
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I am also a survivor of an AFE and I would also like more information and / or research on this. I am now pregnant again and my husband are I are being really positive but and would like to take the necessary precautions to avoid a recurrence. Please let me know how I can access more information.
Regards
Claudette
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I had an Amniotic fluid embolus (AFE) with disseminated intravascular hemmorrhage in 1980 during the birth of my third,and final child. We both survived, and without any neurological damage which is pretty rare. I needed 14 units of blood and blood products.There is a facebook page for AFE survivors, their families, and for the familes who have lost a loved one due to AFE. New members have to be added by current members, so I'd be happy to add anyone, just email me at puubatcomcastdotnet.
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