CLDF National Conference: The CLDF... - Children's Liver ...

Children's Liver Disease Foundation

2,050 members710 posts

CLDF National Conference

Caitlin-CLDF profile image
Caitlin-CLDFPartnerCLDF
1 Reply

The CLDF National Conference is closing for entries tomorrow (Thursday 22nd) at 5pm.

As well as hearing top liver specialists talk about new developments, you'll get the chance to ask questions about your child's condition and chat to other families.

We're looking forward to seeing lots of families there! childliverdisease.org/confe...

Written by
Caitlin-CLDF profile image
Caitlin-CLDF
Partner
To view profiles and participate in discussions please or .
1 Reply
Penguin8 profile image
Penguin8

We can't wait!

Not what you're looking for?

You may also like...

Suggestions on how to include my 3 year old now my baby has been diagnosed with biliary atresia please?

Our worlds have just been turned upside down... Thought our son had breast feeding jaundice went...
Blazer profile image

Alpha 1 ATD

Hi, My name is Christine, my son Reece was born with Alpha 1 ATD. He was diagnosed at the age of 7...
ChristineB profile image

Introduce yourself...

It's great to see so many of you have joined the community. Why not leave a short comment below...
Caitlin-CLDF profile image
Partner

Allagille syndrome

My son is 3,5 months diagnose with this waiting for final confirmation in a way I am relieved that...
Zuhal 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.