Always happy to help: My name is Rachel... - Children's Liver ...

Children's Liver Disease Foundation

2,041 members710 posts

Always happy to help

OMGPinkJello profile image
6 Replies

My name is Rachel I'm 24 years old and I've had not one but two liver transplants!

My first transplant was on May 14th 1992 at Birmingham Children's hospital and I had my 2nd liver transplant on 14th of January 2015 (both on the 14th! what a coincidence!) if anybody needs a question answered please let me know as I have been through an awful lot in my 24 years as a liver transplant patient and I would be very happy to be able to help anybody with any qualms wether it's about my transplants or anything else related

Written by
OMGPinkJello profile image
OMGPinkJello
To view profiles and participate in discussions please or .
Read more about...
6 Replies
Caitlin-CLDF profile image
Caitlin-CLDFPartnerCLDF

Thank you Rachel :)

YBiliaryAtrecia profile image
YBiliaryAtrecia

Hi Rachel, appreciate your time and help. My little girl is on the list for transplant. She had BA and had Kassai done in 5weeks, she is not doing great. Thankfully she is not worse either. She is sticking to her growth and meeting milestones. But a transplant has become inevitable in the next 6months to 1 year.

What was your experience like in the early days post your first transplant and how much did it have an impact on your school and activities?

Thanks, Omer

OMGPinkJello profile image
OMGPinkJello in reply toYBiliaryAtrecia

Hi Omer, I apologize for the late reply.

From what I can remember from a young age post transplant was that although I did miss quite a lot of school (due to infections,hospital appointments and vaccines) I've had a pretty normal life. The only thing that used to temporarily stop me was the fatigue but from an early age I was encouraged by both parents that if I was feeling tired in any sort of activity that I can stop , rest for as long as I had to (have a drink) and carry on if I felt that I could do. I even came 1st in one of my sports days at primary school in the running competition.my advice is to encourage your child (which I'm sure that you already do! :) ) and let her know that although she is poorly and is doing activities of any sort that it's perfectly ok to want to stop if she's feeling tired. I did struggle through high school but that was from my own personal experience which was in no way related to my transplant .encouragement and praise is key. since leaving school in 2008 I've been to college and passed my course with distinction, worked with small children and in several places serving food with no trouble to my health (minus the odd sniffle and appointment) and I've also been engaged for 5 years now

YBiliaryAtrecia profile image
YBiliaryAtrecia in reply toOMGPinkJello

Hi Rachel,

It feels so great to hear your story and I write this wiping off my tears of joy. I am so pleased to hear your experience and I pray for your good health and happy life.

My little girl is very active and joyfull as like never before. She is so loud too. Thankfully she is still holding on to her appetite for food so things are little easy for us. We are still waiting for the call for the transplant.

Penguin8 profile image
Penguin8

Thank you for sharing x

sameerudeen profile image
sameerudeen

Hi OMGPinkJello,

My daughter had a kasai at 8 week, and it was not successful. She is in the waiting list for the liver transplant. Her blood group is AB.

Can you please tell me , how long (approx) I need to wait for the donor to be available considering her blood type which is rare)

Not what you're looking for?

You may also like...

After Kasai Procedure

Hi, my son was operated 02/06/18. He have shown no physical signs of improvement or signs of...
Twiin profile image

Query for liver transplant

My daughter had kasai at 52 days but seems like that has failed and now doctors are insisting for...

Would love to hear Some positive stories from people with Alagille Syndrome ...

Hi everyone! My daughter is most probably having Alagille syndrome, can't stop reading things on...
Dina1986 profile image

Hi I am new to this''' I would like to talk to some people who are goin or been through same situation as I am goin through now.

My daughter was diagnosed with billiary atresia at 8 weeks had the Kasai at 9 weeks. Everything...
leather profile image

Biliary atresia

Hi everyone, my name is Louise Currie, I was born with Biliary Atresia and was given the kasai...
Loooooo profile image

Moderation team

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.