I'm very sorry. How is she moving though, if she's brain dead? Not trying to be snarky, purely curious. Maybe it's something to ask the doctor about. I was under the impression that brain dead meant nothing but basic life-sustaining actions. I didn't think movement was included in that. Some cases of fetal hydrocephalus are also treatable. Are they sending you to a specialist first, to be 100% positive of the diagnosis?
Im so sorry you are having to go through this, but I was thinking the same thing as krptcmschfmkr128. I think that seeing a specialist is worth a shot.
Again, I am so sorry, and I will be praying for you, baby girl and your family. Sending you lots of hugs.
I'm so sorry. I know how you are feeling as I am in a very similar situation myself. It's heart-wrenching. my husband and I decided that we will do our best to treasure those movements because they are our boy and for now, he is all ours. They do hurt like crazy, but he's still in there and I don't take that for granted. I suspect there will be times when he's gone that I just want to feel him move again.
And I do second the girls saying get a second opinion. I'm surprised he would suggest termination without sending you to a high risk specialist. He deals with everyday pregnancies, well, every day, but a specialist might be able to see hope or a treatment plan that he doesn't even know about.
I am so sorry you are living this right now. Hang in there and take care of yourself and your husband. You will be ok, hon. Praying for your baby girl.
Trigger Warning (LC and loss) --
Married May 2008
Beautiful daughter Alyssa born April 23, 2011
Precious son Isaac born at 34 weeks in April 27, 2014 with Potters Syndrome Type 4 and Down Syndrome - trusted into the arms of Jesus after 3 hours.
Pregnant again! Due August 8, 2015 please be healthy, little one!
(results on 2/4/15 showed no Down's and it's a girl!)
Thank you all for the thoughts and prayers. This had been
such a long weekend for my family and I. Today we went to a specialist who did
another ultrasound and a few tests and the news is even worse than before. At
first, I was told there was fluid in the baby's brain which most likely
is Hydrocephalus. Depending on the level, this can be treated and the baby
does have a chance at a normal life. This information is what has kept me sane.
I have joined support groups who are familiar with hydrocephalus and the women
have helped me so much. Today at the ultrasound we learned the baby does
not have hydrocephalus, but instead has Holoprosencephaly which is basically a
much worse brain deformation. The baby's brain never split into the two
hemispheres. Most babies do not make it through birth yet alone anytime after
that. We have made the decision to terminate and have begun the process to do
so. It was our decision to do what we felt was best for our baby. I have
reached the acceptance stage of my grief and look at this situation as a
learning experience. I learned how much I can love someone before ever meeting
them, I learned how amazing and strong my husband is, and I learned I can count
on my support system for just about anything. Once again thank you all for the
concern and help. I truly wish you all the best of luck. Hopefully I will have
the family we have been dreaming about the past 5 months someday.
Yelena + Rubere Married: 05/13/2011 TTC since 2012 BFP#1~ EDD: 06/21/2014 ~ TFMR --Holoprosencephaly Said goodbye on 2/10/2014 at 21 weeks.We miss our baby girl "J" My Chart
I'm so sad and sorry, Kitty. You have an amazing perspective on the situation and I admire your courage and strength. I will pray for you and your family.
My heart is breaking for you. Lots of prayers coming to you and your DH as you go through this very difficult time. Don't hesitate to talk/vent to any of us.
I'm so, so sorry for your loss. When you are ready the loss board as well as TTCAL will be waiting for you with open arms. Please make sure you lean on your support system however you feel most comfortable. If you need anyone to talk to, cry to, yell to...I'm here.
I am so sorry you are having to go through this. I am glad you are getting the support you need, and have found some peace with what I am sure was a gut renching decision. Due to my job, I am very familiar with both holoprosencephaly and hydrocephalus.
The loss board was a great support when I had my miscarriage, and I too would suggest it, when you are ready.
Again, I am so sorry.
PgAL (MC@7w 29/10/11 - lost you before we knew we had you)
I am so sorry to see this update. Hugs and prayers to you.
DS 1 Alex born May 28, 2007 7lbs 14oz DS 2 Aiden born November 29, 2011 9lbs 1 oz DS 3 Lucas b/d February 26, 2013 at 18w6d Forever our angel DS #4 due June 13, 2014
Im so sorry for everything you are going through right now:( I wish I could reach through this computer and give you a huge ((((((((((( HUG)))))))))))))
Its so wonderful that you have such a strong loving & supporting husband and you can lean on each other through this awful experience. You are in my prayers.
I truly lack words to properly express how so sorry I am to hear the news of this diagnosis. Your loss is unimaginable and I wish you all the best in your physical and emotional healing. If you need anything...you know we are here.
Re: Grieving A Loss While Baby Is Still Here
2nd BFP 9/20/13, EDD 6/1/14 -- hoping for our sticky baby!
BFP#2: EDD 2/11/14, MMC confirmed 7/15/13 (growth stopped at 6 weeks), D&C @ 12 weeks 7/25/13
Pipsqueak born 6/9/14
Im so sorry you are having to go through this, but I was thinking the same thing as krptcmschfmkr128. I think that seeing a specialist is worth a shot.
Again, I am so sorry, and I will be praying for you, baby girl and your family. Sending you lots of hugs.
DD 3/15/12
DD 6/3/14
#4 Due 10/26/18!
Thank you all for the thoughts and prayers. This had been such a long weekend for my family and I. Today we went to a specialist who did another ultrasound and a few tests and the news is even worse than before. At first, I was told there was fluid in the baby's brain which most likely is Hydrocephalus. Depending on the level, this can be treated and the baby does have a chance at a normal life. This information is what has kept me sane. I have joined support groups who are familiar with hydrocephalus and the women have helped me so much. Today at the ultrasound we learned the baby does not have hydrocephalus, but instead has Holoprosencephaly which is basically a much worse brain deformation. The baby's brain never split into the two hemispheres. Most babies do not make it through birth yet alone anytime after that. We have made the decision to terminate and have begun the process to do so. It was our decision to do what we felt was best for our baby. I have reached the acceptance stage of my grief and look at this situation as a learning experience. I learned how much I can love someone before ever meeting them, I learned how amazing and strong my husband is, and I learned I can count on my support system for just about anything. Once again thank you all for the concern and help. I truly wish you all the best of luck. Hopefully I will have the family we have been dreaming about the past 5 months someday.
TTC since 2012
BFP#1~ EDD: 06/21/2014 ~ TFMR --Holoprosencephaly
Said goodbye on 2/10/2014 at 21 weeks. We miss our baby girl "J"
My Chart
DS #1 born January 2010. DS #2 due June 2014.
The loss board was a great support when I had my miscarriage, and I too would suggest it, when you are ready.
Again, I am so sorry.
DS 2 Aiden born November 29, 2011 9lbs 1 oz
DS 3 Lucas b/d February 26, 2013 at 18w6d Forever our angel
DS #4 due June 13, 2014
О Привязать! Z!
DD 3/15/12
DD 6/3/14
#4 Due 10/26/18!
I'm so sorry for your loss. Thoughts and prayers are with you for peace and healing.