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I was so worried about having treatment but its been much easier than I expected

  Glad I saw my Doctor

HCUK Support & Support Groups

One of our aims is to ensure consistent support is available to everyone affected by Barrett’s Oesophagus, regardless of who they are and where they live. Information and advice is available to all those affected by the disease and to the people who support them on our website or by telephone.

We need your help to bring this to the attention of your employees, friends & family or indeed anyone who might suffer from Persistent Heartburn!

You can make a difference. Perhaps you know someone who has suffered from Persisitent Heartburn, Barrett’s Oesophagus or Oesophageal Cancer. Perhaps you run an organisation and would like to help, why not make it your company’s corporate responsibility?

NEW GROUP BEING SET UP - WE NEED YOUR HELP
North Hampshire Support Group for those diagnosed with Barrett’s Oesophagus or Cancer of the Oesophagus. If you would like to take part in this group or would like to help with its running

Please contact caroline.sutton@heartburncanceruk.org or call 01256 338647

Currently we have two very active Support Networks in:- 

HCUK East Anglia

East Anglia - based in Cambridge
Alastair Reid - Chairman


HCUK London

London - based in University College London Hospital (UCLH)
Jane Bellamy - Chair


Through the Support Network we aim to provide support, raise awareness and fundraise.

Through our website fellow Barrett’s sufferers and like minded people can find information from previous sufferers which can be very helpful when you are concerned about your condition.

Fundraise in any way you wish. We have had marathon runners, beard growing initiatives, trekking to Everest Base Camp. Not only does this raise money but also raises awareness, which is just as important.

We have leaflets, posters and flyers for distribution in gastroenenterology departments, GP surgeries and pharmacies. Perhaps you could help distribute them?

Please support us in any way and make a difference to other people’s lives. Raise awareness so the rise in oesophageal cancer is stemmed.

Mimi McCord (Chair of Heartburn Cancer UK) is either a phone call or email away and she can help guide you in the right direction.
Tel: 01256 338 668
Email: mimi.mccord@heartburncanceruk.org


Setting up a regional network

If you do not have a Support Network near you, have you thought about starting one up? Your gastroenterology department would hopefully help by contacting others with a similar condition to you. We could also provide them, or you, with posters and flyers to help raise awareness.

Ideally you need the support of your gastroenterologist or specialist nurse. They have the database of Barrett's sufferers and they will have to send a letter on your behalf advising their patients of what you are doing and why. HCUK can provide the letter for your consultant/specialist nurse to send.

You should now have a group of people (a minimum of three but there is no maximum) who are as keen as you are to work along the following lines:

Raise public/medical and political awareness in your local area of heartburn and/or reflux and its link with Barrett's and oesophageal cancer.

Provide support to local sufferers and those connected with them.

Raise funds to make these aims possible and for local initiatives such as a piece of equipment for your gastroenterology department.

Raise funds to enable HCUK to achieve its objectives.

At this point you might like to consider forming a committee with a Chairman, Vice Chairman, Secretary and Hon. Treasurer. HCUK will provide you with the 'Terms of Reference for Regional Groups' which as a charity we have a legal responsibility to follow.

How you raise awareness and funds is entirely up to your members, as long as you follow the charity branding and that it is legal! We will offer you support, publicity information and anything else you might need, just ask.
 

Why Heartburn Cancer UK Exists


As a recognised and trusted authority in the field of Cancer of the Oesophagus, we know that with your help we can make significant inroads in the Prevention, Detection and Treatment of this disease by focussing on 5 key areas of action:  

EDUCATION

Education leads to a lasting change. We are working hard to influence public and social policy, to lobby politicians, to campaign for change, to promote greater collaboration amonsgt the medical profession, the public and the government. We are already in the process of developing a network of effective partnerships with businesses, the pharmaceutical industry, medical professionals and other like-minded groups. We intend to affect change and influence how this disease is perceived, detected, diagnosed and treated.

RESEARCH

Our aim is to significantly reduce incurable oesophageal cancer in the UK.

Our renowned medical professionals, all experts in the field of oesophageal cancer, will continue to play a key role in research and trials designed to reduce the incidence of this appalling disease.

AWARENESS

Early detection rates are vital to ensure a positive outcome. We are creating a communication network to facilitate greater awareness of the importance of diagnosing the disease early, identifying the symptoms associated with the disease and seeking medical help quickly. Oesophageal cancer affects everyone regardless of their race, gender or age.

SUPPORT

We will ensure consistent support is available to everyone affected by Barrett’s Oesophagus, regardless of who they are and where they live. Information and advice is available to all those affected by the disease and to the people who support them on our website or by telephone.

We need your help to bring this to the attention of your employees, friends & family or indeed anyone who might suffer from persistent heartburn!

You can make a difference perhaps you know someone who has suffered from persisitent heartburn, Barrett’s Oesophagus or Oesophageal Cancer. Perhaps you run an organisation and would like to help, why not make it your company’s corporate responsibility?

EVOLVE

We are not content with standing still, we are determined to develop and grow a sustainable UK charity which continually re-invests to maximise the impact of its resources.

Working with UK businesses and voluntary organisation’s, our outward facing collaborative approach will ensure we are the first place to come to for reliable up to date information about Heartburn, Barrett’s and Oesophageal Cancer.

HCUK - Information Centre


All you need to know about Heartburn, Barrett's Oesophagus, Oesopageal Cancer. If you need support we can offer advice, please contact us on the "Ask our Doctor a Question" form, or you can join one of our Local Support Groups. You can also buy Heartburn Cancer UK Clothing and other HCUK Merchandise to help Raise Awarness and of course we would very much welcome a Donation to keep the charity able to carry on offering free advise and Raising Awareness, Changing the Future and Saving Lives.

HCUK - USEFUL INFORMATION BOOKS TO DOWNLOAD