Website: https://www.kidscape.org.uk/

Email: info@kiscape.org.uk

Telephone: 020 7730 3300

Parent Advice Line call 020 7823 5430 (Monday-Tuesday, 10 am-5 pm)

Address: Kidscape, 2 Grosvenor Gardens, London SW1W 0DH

Our vision is for all children to grow up in a world free from bullying and harm, with adults who keep them safe and help them to reach their full potential.

Our mission is to provide children, families, carers and professionals with advice, training and practical tools to prevent bullying and protect young lives.

Our values

• We believe that every child has the right to live life free from bullying and harm
• We believe that all adults have a responsibility for creating safe and nurturing environments for children
• We value the role of parents and carers and work with them to keep children safe
• We believe that by working together we can protect more young lives and actively encourage partnership work

Find us on Face Book @KidscapeCharity and Twitter @Kidscape

Registered Charity Number. 326864

Website: https://www.hopeagain.org.uk/#

Email: helpline@cruse.org.uk

Contact Form: https://www.hopeagain.org.uk/hope-again-contact-us

Telephone: FREE phone helpline on 0808 808 1677 Monday-Friday, 9:30 am – 5:00 pm

Address: Local Office The Roy Fletcher Centre, 12-17 Cross Hill, Shrewsbury SY1 1JE

Hope Again is Cruse Bereavement Care’s website for young people.  Cruse is a national charity that provides support, advice and information to children, young people and adults when someone close to them dies. We also work to enhance society’s care of bereaved people.

Some people find that talking about what’s happened, or how they’re feeling, is helpful, even though it can be really hard.

Hope Again is another place where you can talk about your grief.  When you send us your message by clicking the ‘Talk To Us’ button on the homepage here https://www.hopeagain.org.uk/ a young person will personally reply to you, and the messages and stories you send will be monitored by young people. Find out more at this link https://www.hopeagain.org.uk/hope-again-talking-about-it It tells you how talking may help you.

What is Cruse Bereavement Care?                                                                              

Cruse has been offering bereavement support in England and Wales since 1959 and in Northern Ireland since 1984. 

Cruse is a national charity that provides support, advice and information to children, young people and adults when someone they love dies. We also work to enhance society’s care of bereaved people.

Cruse services are provided free of charge and are dependent on the generosity of the local community and statutory support to deliver the service.

Cruse services are provided by dedicated and skilled volunteers in local communities who support children, young people and adults through grief.

Someone to turn to for young people

At Cruse we can offer a safe, youth friendly space where young people can work through their grief in their own time and own way accompanied by a trained and experienced volunteer who will work individually with the young person over a period of 6-8 weekly sessions.

Find us on Face Book Cruse Bereavement Care and Twitter @CruseCare

Cruise Bereavement Care is a Registered Charity No. 208078 

 

 

Website: https://www.glaucoma-association.com/

Email: info@iga.org.uk

Email: sightline@iga.org.uk (For general enquiries, including advice about glaucoma or membership) 

Telephone: 01233 64 81 64 or 01233 648170

Helpline-Sightline glaucoma : 01233 64 81 70  Monday – Friday 09:30 – 17:00

Member support: 01233 64 81 64  Monday – Friday 09:00 – 17:00

Address: Woodcote House, 15 Highpoint Business Village, Henwood, Ashford, Kent TN24 8DH

We provide information for everyone who is interested in glaucoma, people who have just been diagnosed, or anyone living with glaucoma. 

IGA are a UK based charity, committed to preventing unnecessary loss of sight through the condition, which is one of the most common eye disorders.

We provide support to thousands of glaucoma patients; arranging meetings in the UK through the year and providing a regular newsletter to members and friends as well as overseeing a network of support groups and fund research.

Glaucoma is the name given to a group of eye conditions in which the main nerve to the eye (the optic nerve) is damaged where it leaves the eye. This nerve carries information about what is being seen from the eye to the brain and as it becomes damaged vision is lost. This results in misty and patchy vision, with eventual loss of central vision, although this is rare.

IGA can provide leaflets, they have support groups, have a helpline, provide a buddying system. They also raise awareness and have a membership that you can join.

Find us on Face Book @internationalglaucomaassociation and Twitter @TweetIGA

Charity Registered: in England & Wales No 274681 in Scotland No SC041550

Website: https://www.nopanic.org.uk/

Email: info@nopanic.org.uk

Contact Form: https://www.nopanic.org.uk/contact-us/

Telephone: 01952 680460 (Office open Monday-Friday 9 am-5 pm)

Telephone: 0844 967 4848 (Helpline)

Youth Line: 0330 606 1174 *For 13 to 20 year olds, 
Opening times-Monday, Tuesday, Wednesday, Friday: 3 pm to 6 pm,Thursday: 3 pm to 8 pm and Saturday: 6 pm to 8 pm

Address: Jubilee House, 74 High Street, Madeley, Telford TF7 5AH

No Panic is a registered charity which helps people who suffer from Panic Attacks, Phobias, Obsessive Compulsive Disorders and other related anxiety disorders including those people who are trying to give up Tranquillizers.

No Panic also provides support for the carers of people who suffer from anxiety disorders.

Severe anxiety and phobic disorders are a major and widespread problem. Recent surveys indicate that they affect up to 18% of the population of the United Kingdom.

It is a voluntary organisations that provides professional support and specialises in self-help recovery and our services include specialist help with:

• panic attacks
• phobias
• obsessive compulsive disorder (ODC)
• related anxiety disorders
• tranquilizer withdrawal

We also provide support to sufferers, their families and carers.

Providing people with the skills they need to manage their condition and work towards recovery, enabling them to lead more fulfilled lives.

Find us on Face Book  and Twitter @charitynopanic

Website: https://www.barthsyndrome.org.uk/index.php

Email via contact form: BST Email Contact Form

Telephone: 01794 518 785

Address: Barth Syndrome Trust, 1 The Vikings, Romsey, Hampshire SO51 5RG

Barthe Syndrome is a rare genetic disorder that mainly affects boys.

Barth syndrome is a rare, often life-threatening genetic disorder that affects boys.  Look at our logo and you’ll see a heart at its centre: this is because most of our boys have heart failure and a risk of sudden cardiac arrest.  However, the heart at the centre is also a powerful symbol of who we are as an organisation: we are a strong, caring and positive force.

The swirl around the heart encompasses the many symptoms which are caused by Barth syndrome – immune system problems, muscle weakness, extreme and debilitating fatigue, growth delay and feeding problems.  But again, our swirl means more to us than just a collection of symptoms – for us it symbolizes unity, collaboration and inclusion.

Main symptoms:

• Heart muscle weakness (cardiomyopathy)
• Neutropenia (lack of white blood cells needed to fight bacterial infections)
• Fatigue and general muscle weakness
• Growth/feeding issues

The Barth Syndrome Trust is a well-established community of families, medical professionals, scientists, donors and volunteers with links to other affiliates all around the world.  We provide the most comprehensive source of reliable and current information about this condition and we invite you to visit our pages to find the information you seek.

We are dedicated to saving lives through education, advances in treatment, and finding a cure for Barth syndrome – a sometimes fatal, often debilitating genetic disease.

 Working together we are making a difference in the lives of children and their families. One day there will be a cure; please join us and help us make that day come sooner. Find out more on our website. https://www.barthsyndrome.org.uk/index.php

Find us on Face Book and Twitter.

Registered Charity No:1100835