My boyfriend and I just got a confirmation on the 11th that our baby boy has a cleft lip on the right side and the doc says more then likely will also have a cleft palate. We are due around March 26th but from my latest measurements it is anywhere between the 22nd and 26th. This news has been a total shocker to us and I know I'm having a hard time processing all of the information given to us. I'm just so sad and confused on why this is happening to our sweet little baby. I think my family is all thinking that I'm only upset because that he is going to come out looking different then other babies but this isn't the case at all....he is perfect already in my eyes. The stuff I'm most upset about is knowing my baby will have to go through surgeries already at such a young age.  And I know I've heard it already a million times..."At least he will be young and not remember." "Cleft lip/palate is so common and easy to be fixed." "Well, at least this is the only thing you have to deal with." Yup! I'm over all of that "nonsense" talk....I still feel like crap and like it was something I did wrong (I know I did nothing wrong) And all of the other complications that can come from this is sooooo overwhelming! Special feeding techniques that not only do I and bf have to learn, but teaching other caregivers, grandparents, aunts, uncles and anyone else wanting to help out. Just a lot to take in already at only 21 weeks in to the pregnancy and just more to come! Right now I'm just feeling so lost in all of the talk from the genetics team and then knowing not only will I be seeing my ob dr. on the regular basis but also added in appointments with the docs at the hospital as well (my work has already not been the most supportive when it comes to me having appts.) Along with the surgeries after he is born and hospital stays with that and follow up appts. I feel like my job might be in jeopardy after baby is born and I HAVE to work...there is no way around it.                 
                             
        
Re: Confirmation :(
You have learned that your baby is going to be dealing with a serious issue and you have every right to feel overwhelmed, concerned, worried, and stressed out. The comments about "at least this is all you have to deal with" or "it's common and easily fixed" are in no way helpful. It's ok to not be alright and to struggle with processing and dealing with this news and how it alters your plans.
I am also sorry work is only adding to the stress. Sending lots of good thoughts your way!
Can you find a support group of other mothers/parents who have gone through this already? Maybe your doctors or the hospital where the surgery will take place can point you in the right direction. It might help to talk to folks in the same circumstances, and get a real sense of what's needed and how you can schedule it around your work and other life circumstances and also how to cope with the anxiety and feelings that come up around it.
BFP with #1 (twins!) 11/18/2011 - missed m/c at 8weeks3days; d&c 1/19/2012; myomectomy to remove 18cm+,10cm & 5cm fibroids 4/2012; TTC again 7/2012; BFP #2 (twins) 11/13/2012; missed m/c at 7weeks;
BFP #3: baby girl born 3/5/2014
Balaustine: an anthology about wanting family
Proud Cloth Diapering, Babywearing Mommy to Desmond (5.30.2011) and Evangeline (2.26.2014)
Loving wife, best friend and teammate to Babywearing Daddy, Kelly (7.27.2000)
Volunteer Babywearing Educator at Babywearing International of South Central Pennsylvania
Ts and Ps for you and your LO
Married my love 6/11/11 | MMC 10/11/11 | Eliza Frances born 9/18/12 | Rhett Garland born 2/24/14
I'm sorry you have to go through this. Hearing that our babies might have to suffer or go through anything all, no matter how common or easy to fix it may be, is hard and stressful. I hope you can find support.
My Pregnancy/Parenting BLOG TTC since 5/2011, BFP #1 12/3/11, M/C 12/7/11 @ 4wks 2d. Began seeing RE Sep 2012. October 2012 Metformin 1500 mg= ovulation on CD34 BFP#2 11/14/12 9DPO, EDD 7/26/13, DX Gestational Diabetes @14 wks, our angel born sleeping 3/24/13 @ 22wks 2d. BFP #3 7/4/13 8DPO EDD 3/22/14, DX Gestational Diabetes @14 wks. started insulin @16 wks. Our rainbow, born 3/19/14 @ 39wks 6d., we're so in love!
Hugs!
TTC since December 2012, BFP 6/25/13. EDD 3/2/14. Baby Elias born 2/21/14 (38w5d)!
Heck, I cried when my daughter got a "lazy eye." It's just hard to think of anything wrong with our sweet little babies.
I am sure you have been bombarded with info, and if you you don't want to hear anymore, just ignore the rest of this post and tell me to FO. I am a surgical resident and am on a surgery team that provides care for patients with cleft lip/cleft palate. I work with a group of healthcare providers including plastic surgeons, oral surgeons, dentists, orthodontists, speech pathologists, occupational therapists, nurses, and dieticians who coordinate care for kids from birth to adulthood. We meet each month to evaluate and discuss the patients on our team so that each child gets the specialized care they need when they need it. I can tell you from professional experience that it is a long road ahead, but I just want you to also know that there are teams of people who dedicate their lives to treating and caring for kids with CL/CP. I hope you can find a CL/CP team in your area to be there for you every step of the way.
At the same time, I relate more with the other people. Try not to get upset with them. I have just found out my baby has a significant congenital defect requiring surgery at birth, and I will have to stop working. It's terrifying, but the only way to get through for me is to be positive. It's not a negative thing until it actually is. I can't handle the opposite where people try to give you sympathy and make a big deal.
Anyway, I'm rambling. I'm really really sorry you are dealing with this. I hope the palate isn't affected or is minor. You are a good strong mama and I know you will do everything necessary to take care of your baby. Best of luck with it all!