Posts - Children's Liver Disease Foundation | HealthUnlocked

Children's Liver Disease Foundation

2,003 members703 posts

All posts for September 2012

CLDF's Leeds Bowling Day - continue the conversation!

Thanks to everyone who came to our Leeds bowling day on Saturday. It was great t...
Caitlin-CLDF profile image
Partner

Living with Biliary Atresia

Andrew is 10 years. He's only had a Kasai. He has portal hypertension, a big sp...
courage profile image

Hollywood Bowl Good Day

Really enjoyed bowling and was nice to meet new people.Staff at Liver foundation...
reuben profile image
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Alagille Syndrome

Any information from others that may have being affected
reuben profile image

Is anyone familiar with the diagnosis Alagille Syndrome and what affect does it have long term?

reuben profile image

Anyone got any thoughts/advice/experience on testing siblings for A1ATD?

It seems to be a bit of a moral/ethical/clinical/delete-as-appropriate minefield...
zedgirl profile image

who here is going to the staines event for under 5's in november?

nicky1986 profile image

Choledochal cyst/biliary atresia

Hello, My name is Vickie. I was born in New Zealand but have lived in both Engla...
Victoria2 profile image

Biliary Agenesis

My son Reuben was born 20th March 2012 and was diagnosed with biliary agenesis a...
reuben profile image

Alpha 1 ATD

Hi, My name is Christine, my son Reece was born with Alpha 1 ATD. He was diagnos...
ChristineB profile image

Bowling at Hollywood Bowl, Leeds - 22nd September

Have you got any plans for Saturday 22nd September - IF NOT get yourself down Ho...
Hidden profile image

Lacey was diagnosed with Autoimmune Liver Disease last year.

In June last year my eldest daughter Lacey became jaundice, I took her to the GP...
xtabbiex profile image

frustrated

really frustrated as we have to come down to Birmingham Childrens Hospital to ge...

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