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CLDF HIVE - Welcome

Hive is a social network run by Children's Liver Disease Foundation. It is for the use of children and young people aged between 11-25 who have been diagnosed with a liver condition, or who have had a transplant. This is your site's landing page.

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CLDF HIVE - Welcome | cldfhive.co.uk Reviews
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Hive is a social network run by Children's Liver Disease Foundation. It is for the use of children and young people aged between 11-25 who have been diagnosed with a liver condition, or who have had a transplant. This is your site's landing page.
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CLDF HIVE - Welcome | cldfhive.co.uk Reviews

https://cldfhive.co.uk

Hive is a social network run by Children's Liver Disease Foundation. It is for the use of children and young people aged between 11-25 who have been diagnosed with a liver condition, or who have had a transplant. This is your site's landing page.

INTERNAL PAGES

cldfhive.co.uk cldfhive.co.uk
1

CLDF HIVE - The Help Hub

http://www.cldfhive.co.uk/pages/helphub

Need someone to talk to? Want to make friends on Hive but not sure who to start with? Or maybe you just need to know more about how Hive works. Our Hive Ambassadors are trained peer mentors who are here to help you. They log in regularly, so send them a friend request, or drop them a private message. They're all lovely. Olivia P: Hive Ambassador. Scott M: Hive Ambassador. Katie B: Hive Ambassador. Zainab B: Hive Ambassador. Stuart T: Hive Ambassador. Catherine B: Hive Ambassador. Joanna H: Hive Ambassador.

2

CLDF HIVE - Forgot Password

http://www.cldfhive.co.uk/user/auth/forgot

If you cannot login because you have forgotten your password, please enter your email address in the field below.

3

CLDF HIVE - Badges - Badges Home

http://www.cldfhive.co.uk/badges

Rich Wall: Young People's Officer. Emma P: Hive Ambassador. Zainab B: Hive Ambassador. Stuart T: Hive Ambassador. Joanna H: Hive Ambassador. Katie B: Hive Ambassador. Catherine B: Hive Ambassador. Paul R: Hive Ambassador. Scott M: Hive Ambassador. Elle W: Hive Ambassador. Olivia P: Hive Ambassador. Jordan S: Hive Ambassador. Michael J. A. Heather Rose G R. Michelle k r w. Tue at 4:33 PM. This Badge is given to a member who is on Default Member Level. Given to members who write several blog entries. This ...

4

CLDF HIVE - Welcome

http://www.cldfhive.co.uk/members/home

The social network for young people living with a childhood liver condition.

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cldf-focus.org cldf-focus.org

CLDF Focus

http://www.cldf-focus.org/links.aspx

Keep up to date. Living with liver disease. Holiday / Travelling (2). Hygiene and puberty (6). Rights and legal stuff (2). Tattoos and piercing (6). Useful bodies and organisations (6). Work and Your Career (4). Registered Charity Number: 1067331. Registered Company Number: 3431169.

cldf-focus.org cldf-focus.org

CLDF Focus - Stories

http://www.cldf-focus.org/Meeting-and-sharing/Stories

Keep up to date. Living with liver disease. These stories were all written by young people who have a childhood liver condition. Once you've read some of their stories, we would love to hear yours. Use this form to send us your story. I do not remember being diagnosed with my illness as I was 3. All my friends go to parties and get drunk. I go with them and still have fun. Only recently my scar has made me feel a bit self conscious as i'm worried what boys will think of it. I have learnt to live with it.

cldf-focus.org cldf-focus.org

CLDF Focus - Talk, Tell, Transform 2015

http://www.cldf-focus.org/Talk-Tell-Transform-2015

Keep up to date. Living with liver disease. Talk, Tell, Transform 2015. These digital stories were created by the wonderful young people at CLDF’s Talk, Tell, Transform residential in 2015. They all discuss an aspect of their liver disease journey and we're very proud of the bravery and courage they have shown in sharing their story with us. You can find out more about Talk, Tell, Transform here. They got me through the darkest times where I thought that nothing was going to help me, so I’m so grateful a...

cldf-focus.org cldf-focus.org

CLDF Focus - Fundraising

http://www.cldf-focus.org/Fundraising

Keep up to date. Living with liver disease. Get your school, college or uni involved. Contact CLDF's Fundraising Team. Share your fundraising story. There's lots of ways you can raise funds for CLDF and it can be great fun. If you've already started fundraising, click here to set up a JustGiving page. A great way to get support from your friends and family. There's lots of ideas below to get you started, but please get in touch with the fundraising team. If you have any questions or need some help.

cldf-focus.org cldf-focus.org

CLDF Focus - Get Involved

http://www.cldf-focus.org/Meeting-and-sharing

Keep up to date. Living with liver disease. Talk, Tell, Transform. CLDF National Conference and Family Weekend. You may find it useful to chat and share with others growing up with a liver condition. How about coming along to a CLDF event and meeting other young people and families living with liver disease? There are events all over the country, as well as two residential projects; Talk, Tell, Transform. Formerly Closer to the Edge). Contact CLDF's Young People's Team. You can also read stories.

cldf-focus.org cldf-focus.org

CLDF Focus - Living with liver disease

http://www.cldf-focus.org/Living-with-liver-disease

Keep up to date. Living with liver disease. Taking your liver into adulthood. Making the most of an appointment. Living with liver disease. Growing up with a liver condition or transplant can bring some additional challenges to life. This section can help you think about some of these challenges and how to tackle them. CLDF's young people’s team are here. If you want to chat about any aspect of living with a liver disease. Taking your liver into adulthood. Making the most of an appointment.

cldf-focus.org cldf-focus.org

CLDF Focus - CLDF Breakaway

http://www.cldf-focus.org/ctte

Keep up to date. Living with liver disease. Talk, Tell, Transform. CLDF National Conference and Family Weekend. CLDF Breakaway (formerly Closer to the Edge) is a residential for 12 to 15s with a liver condition or transplant. Up for a challenge? CLDF Breakaway includes team building games and woodland challenges, aerial ropes adventure course and a 24 hour 'bush-craft and survival' challenge. Check out the full programme here! Date for the next CLDF Breakaway:. Tuesday 18th to Friday 21st April 2017.

cldf-focus.org cldf-focus.org

CLDF Focus - News

http://www.cldf-focus.org/News

Keep up to date. Living with liver disease. Missing Type campaign 2016. This August, Children’s Liver Disease Foundation is delighted to be a charity beneficiary of a BBC Radio 4 Charity Appeal. /span " /. BBC Radio 4 Appeal. This August, Children’s Liver Disease Foundation is delighted to be a charity beneficiary of a BBC Radio 4 Charity Appeal. Visiting the hospital for an appointment or attending the ward this month? Find out when well be there /span " /. August Hospital Visits 2016.

cldf-focus.org cldf-focus.org

CLDF Focus - Medical stuff

http://www.cldf-focus.org/Medical-stuff

Keep up to date. Living with liver disease. Information on liver diseases. Follow the links below for information about the liver, liver diseases, signs and symptoms and transplant. All the information is on our main website, but don’t forget that you can contact the young people’s team. If you would like to talk about anything you read. Information on liver diseases. Registered Charity Number: 1067331. Registered Company Number: 3431169.

cldf-focus.org cldf-focus.org

CLDF Focus - Events

http://www.cldf-focus.org/events

Keep up to date. Living with liver disease. CLDF runs events all over the country where you can meet other young people and have fun. Take a look below to see when we'll be in your area. Make sure you're the first to find out about new events by letting us know your details. Learning more about ourselves and the world around us is what Cardiff Discovery Day is all about, including 2 special workshops. Manchester Festive Family Day. Talk, Tell, Transform. Northern Ireland Family Weekend.

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The social network for young people living with a childhood liver condition.

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