Bub requiring gastroschisis surgery
too much pressure on us financially, please Keep our baby in your prayers, I hold onto alot of hope xx
We are 1000$ away from being able to buy a reliable family car we have been aiming for, if anyone could help, it would be greatly appreciated xx
I just want to say everything will be ok!!!.. I am 36 years old and was born with gastroschisis.. you will be fine and so will she.. I have three beautiful children.. zero complications while pregnant.. and outside of being in the NICU for a few weeks after I was born, along with a couple of surgeries and no belly button all is well ( ok.. really ugly scar.. but again it was 36 years ago..surgical technologies are so much better now.. I bet she will even be able to have a real belly button..) Try to stay positive and not let all the "what if's" make you crazy!
Hey guys! Just a quick note: Keep fighting and stay positive. My daughter's story in on youtube called Hannah's Gastroschisis Story Part 2. It's old, but relevant. She's 6 years old now and doing amazingly. Every year she gets better and better. We were told that she had a range of issues and offered termination a few times. Check out the video if you can :) From one gastroschisis family to another; You are in our thoughts.
My Daughter had this 13 years ago, the is on the dance team at her junior high.. no problems, have faith in God, and everything will be fine. You will spend about a month in NICU.. waiting for baby to recover.. be patient.. after it is over it will be a little scar.. and he can do anything he wants later in life..
My first-born daughter was born in 1987 with gastroschisis, 5 weeks early (once her lungs were developed) via C-Section and stayed in NICU for 5 weeks. This is survivable. There will be things you'll always need to watch for, but with great medical care, you're baby will survive and thrive. Prayers to your family.
Hi, I just wanted to wish you guys all the best. I know it's hard but try and stay positive and strong. My son was born with gastroschisis 5 years ago, and after 2 operations and 8 weeks in NICU he finally made it home and is doing perfectly fine today. Can you ask to speak with a social worker from the hospital? We had a lovely one in Sydney who helped us out with finding accommodation close to the hospital (as we also had our 2yr old daughter at the time) There is a scheme called IPTAAS which you might also be eligible for to help out with travel costs. Sending prayers your way xx
My daughter was born with this 25 years ago. Please feel free to reach out to me if you have any questions. This is very hard to deal with but please know you are not alone. Lisa
Keep up with the good work darling, our prayers are always with you, great to see the donations coming in! Lots of love cousin maria and Auntie Militsaxxx
All the best for tomorrow darling. We love you and have you in our prayers, love cousin Maria and Auntie Militsaxxx❤️❤️❤️❤️
My daughter who is 5 months now has larger omphalocele which is liver and intestines on the out side these babies are the strongest babies and they truely are fighters ... and I was told to terminate at 20 weeks ... my little girl won't be getting surgery until she's 4 so she'll have a everything on the outside till then and she stayed in rch for 2 months and now where back and forth due to infection hope everything goes well with ur Bub n stay strong xx