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WE SUPPORT KIDS, TEENS, ADULTS AND FAMILIES@HEART WE PROVIDE PRACTICAL AND EMOTIONAL SUPPORT WE FUND EQUIPMENT WE EDUCATE WE INFORM WE FUND RESEARCH WE LISTEN, WE LEARN, WE ACT WE MAKE A DIFFERENCE
@Heart, we know what life is like living with a childhood heart condition. We have been providing support services to children with heart conditions and their families since 1984.
The needs of those with a childhood heart condition are different from the needs of those who acquire heart disease later in life. Whilst there are other organisations that focus on promoting healthy living and the prevention of heart disease acquired through lifestyle choice, @Heart’s focus is on those who are living with a childhood heart condition that has existed from conception or as a result of rheumatic fever, cardiomyopathy, or Kawasaki disease. We are the only organisation in New Zealand dedicated to supporting all those affected by a childhood heart condition.
@Heart primary goal is to reach and improve the lives of everyone living with childhood heart conditions. Our mission is to provide life long support for all affected by the world's most common birth defect or heart disease acquired during childhood.
We're here to help every step of the heart journey - from when it is diagnosed through childhood, the teenage years and into adulthood.
Our practical and emotional support is vital for those affected, helping them cope with the day-to-day challenges of living with a childhood heart condition.
@Heart is registered with the Charities Commission, registration number: CC20102. |
Scars are for Fighters Awareness Campaign
This year, we are privileged to have well-respected rugby legend Tana Umaga starring together with heart kids Johnny Grimstone and Georgia Delmonte in our Scars are for Fighters Awareness Campaign.
  
Our heart kids show tremendous strength, fighting spirit and resilience, much like Tana has shown throughout his rugby career. His presence in the @Heart Awareness Campaign has helped us tremendously in raising awareness of the scale of childhood heart disease in New Zealand. We are extremely grateful to Tana for his time and wonderful support in helping our heart kids fight their battle with childhood heart conditions.
The Awareness Campaign started on 5th August. It ran on billboards, radio, our website and our Facebook page. Heart families and @Heart were profiled in national media such as the Good Morning show on TV One, the NZ Herald, and AdMedia as well as in many local dailies and weeklies.
During Awareness month, many activities took place in different parts of the country including the Heart Stopper Challenge in Auckland’s Takapuna, memorial services for our heart kids who have lost their battle, an online appeal, and a national street appeal.
 
The national street appeal held on Friday 10th August saw hundreds of volunteers shaking their buckets in shopping centres and on street corners all over the country. In recent years, many charities have struggled to reach street appeal targets as much of New Zealand has become a cashless society. Kiwis have embraced plastic as their favoured method of payment, and are generally leading a much more ‘online’ lifestyle.
In the face of this, @Heart trialled an online street appeal this year at www.scarsareforfighters.co.nz with great success. We are excited about further developing the potential of this new fundraising pathway. Everyday Hero were instrumental in helping us develop the appeals (direct giving) side of the site, as well as offering fantastic support as we went through the building process, and for this we are hugely grateful. They have also helped us extend the campaign further with the inclusion of a Donate Now tab on our Facebook page.
We have received much positive feedback showing that this was the strongest and most well-received Awareness Campaign that we have produced in some years. Scars are for Fighters could not have come about without the tireless help and expertise of many – (Georgia’s dad) Warwick Delmonte, Quent Pfizter and the talented creative team at Zephyr WPD, advertising guru Greg Eichmann who led us to Zephyr and offered much support and insight during the process, Stephen Roke of Stephen Roke photography and Glenda Hughes.
Our thanks also go to Georgia’s mum Sarah, Johnny’s mum and dad Kelly and Chris for their wonderful help; Roadside Attractions, APN Outdoor, AdMedia, Crew News Magazine and Oliver Lee Publishing for advertising space; Kalamazoo for printing support; Telecom Foundation and the many volunteers for collecting on the streets for us; and the generosity of donors and supporters that makes our work possible. Thank you to all of you from the bottom of our hearts. |
In 1980, Linda Davies and Michelle Mann met in Greenlane* Hospital. Their newborn babies were suffering from major heart problems, and sadly both children died in 1981. From their experiences, Linda and Michelle realised there was very little written information for parents of a heart child and they felt a book was needed.
When they left hospital Linda and Michelle spent a great deal of time finding information and surveying other families with a heart child. In 1983 the book "Heart Children" was published and made available free to parents of children who had a heart condition.
While they had set out only with the intention of writing a book, Linda and Michelle soon found themselves acting in a much needed support role to other families "going through" Greenlane Hospital. Over a period of time, as families returned to their own part of New Zealand, a network of support groups was established.
This network was co-ordinated by the Auckland group who formalised themselves as Heart Children Incorporated in 1984. The organisation continued to grow and in August 1994 a national board was elected. A new constitution was adopted in 1995 and the organisation renamed Heart Children New Zealand Inc.
Visit our Contact Info for your nearest group.

Left: Michelle Mann and Linda Davies,founders of Heart Children and co-authors of the book cutting the cake at the 15 year celebration of Heart Children New Zealand in Auckland.
*In December 2003, the Paediatric Cardiac Unit was relocated from Greenlane Hospital to Ward 23B at Starship Children's Hospital as part of the Auckland District Health Board's health delivery plan and the building of the new Auckland Hospital. @Heart’s work continues on in its support to families in the same way as when the PCU was housed at Greenlane Hospital. |
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Membership
Heart Children, Parents of Heart Children and Whanau of Heart Children can apply to become members of @Heart.
Membership is free and it comes with benefits such as:
- opportunities to attend heart camps, @Heart Conferences and Seminars, - provision of specialised equipment for Heart Children as required, - opportunities to attend local Branch activities and to connect with other heart families, - regular news updates via our Heartline newsletter, and much more.
To enable this service we will need to keep your personal records on file, please complete and return the Membership Form by post to @Heart, PO Box 108-034 Symonds Street, Auckland 1150; or you can scan the form and email it to
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Please email
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if you wish to inform us of changes in your circumstances such as contact details and family members.
Membership@Heart application form
Membership@Heart for whanau application form
A warm welcome to the @Heart family!
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Heart Children are defined as those who are born with a Congenital Heart Disease or who acquire a heart condition before the age of 18. |
Constitution
Board Nomination Form 2013
Roles & Responsibility of a Board Member 2013
Map NI Regions & Towns
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Upper North Island
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Donna Jujnovich, Chairperson
Lives in Auckland and is married to Malcolm with two children, Daniel and Nicholas and is the daughter of Nana Marie, volunteer Family Support Worker on Ward 23B. Nicholas, the youngest was born in 1991 with Tetralogy of Fallot. Nicholas had an emergency Blalock Shunt at 2 months and a major TOF repair in 1993. In September 1997, because of arrhythmia he had a pacemaker inserted. In 2004, Nicholas had a Pulmonary Valve replacement, Tricuspid Vale repair and an upgraded dual chamber pacemaker inserted. In 2005, due to a broken wire, Nicholas had a new pacemaker inserted. He will require further surgery in the future.
Donna has been an active committee member of Heart Children Auckland since 1991 and Chairperson from 1993 to 2007; an Inaugural Board Member of @Heart representing Auckland since 1994 and Chairperson 2008 to 2010 and a Trustee of Heart Children (1995) Trust since 1998. Donna has held the HR Portfolio for HCNZ Inc. since 1999. This Portfolio is responsible for the hiring and managing of the CEO and assisting with the employment of senior staff at HCNZ Inc. Donna is a Procurement Manager at Fisher & Paykel Finance Limited.
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Central North Island
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Sheree Dodson
Lives in Papamoa and am married to Bryan with two children, Mikaela born July 2000 and Nathan September 2004. Daughter, Mikaela was diagnosed at 5 months with an ASD and pulmonary stenosis; at 8 months she had surgery to repair the ASD and a PDA. Mikaela has an amazing outlook on life and loves to get out there and give things a go.
Sheree was part of a very enthusiastic group from the Bay that set up Heart Children Bay of Plenty (now Bay of Plenty@Heart) as an affiliated branch of @Heart, holding the Chairperson role from 2001 until March of 2005. She has been on the Board since 2005 as representative of the Central North Island. Prior to this she was involved in the Shaping our Future working party and has seen some significant growth and development of our organisation, and is very proud to be part of such and inspirational group.
She works in the banking industry and has done so since 1986. |
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Lower North Island
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Rob Lutter
Rob is married to Maureen, who was Chairperson of Hawkes Bay@Heart for eight years and they have three boys, youngest of who is Zac, their heart child. Zac was born with multiple heart defects. The major faults were L-TGA, Pulmonary Atresia. He has had multiple heart surgical procedures including Pacemaker replacements and many months in hospital, Hawkes Bay, Greenlane and now Starship through the years. At this moment he is going really well but will require ongoing surgery in the future. Rob is a Director of Bay Business Solutions, a business consulting firm which provides business planning for companies and organisations in Hawkes Bay. He also currently serves as a Napier City Councillor. What he brings to the Board are skills and passion to make a difference in shaping an organisation that provides a great service to you and your children when you need it most.
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Upper South Island
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Ross Blackler
Lives in Christchurch with wife Suzie and Children Bradley and Grace. After many years in Auckland, Suzie became homesick and the family moved to Christchurch, where they enjoy a relaxing lifestyle. Grace was born with Hypoplastic Left Ventricle. Grace has had a Norwood Procedure, a Bi Directional Glenn and a Fontan Procedure. So far Grace is doing very well and enjoying life to the full. Ross works in Credit Management for MARAC Finance Limited and is actively involved with Canterbury@Heart both on the Committee and the Business Committee.
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Lower South Island
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Theresa Smith
Lives in Dunedin and married to Brynley. She has one son Alexander, who is now eight years old. Alex was diagnosed at eight days with Complex Congenital Heart Disease which includes Complete Heart Block, Single Ventricle, TGA, Pulmonary Stenosis and a few more. Alex has undergone five lots of cardiac surgery which has included two trips to Auckland on Child Flight as a result of him breaking his pacemaker wires. Much more excitement than she really needed. Theresa is a Registered Nurse currently working in General Practice as a Nurse Administrator. Her background is in Infectious Diseases, ICU and post Cardiac Surgery ICU. She has been on the committee for Otago@Heart for six years, previously as Secretary and now as the Chairperson.
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By Appointment
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Graeme Mann
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By Appointment
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Jenny Cresswell
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Heart Adult Representative
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Scott Murray
Scott has been appointed to the Board to represent the increasing number of congenital heart adults supported by @Heart. Scott lives in Wellington and has been working as a corporate travel consultant since 2007. He was born with transposition of the great arteries, hyper plastic right ventricle, large VSD and complete heart block. After many operations as a youngster he was given the gift of life - a new heart. He has had no issues since the heart transplant surgery and has been able to concentrate on giving back to @Heart. His involvement with @Heart includes participating in fundraising events such as street appeal and the annual Heart Stopper Challenge, serving as a Leader at Camp Brave Hearts as well as being a member of the Adult Heart Team in the Lake Taupo Cycle Challenge. Scott has been serving on the Wellington@Heart Committee for the past few years. He has been actively involved in the Wellington Youth Programme, helping to organise events where heart youth can get together and connect with one another.
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@Heart Inc Annual Report 2011
The @Heart Annual Report 2011 covers the financial year from 1 December 2010 to 30 November 2011. This Annual Report is extra special because it is our first Annual Report under our new brand @Heart, produced by award-winning design company gardyneHOLT.
We are extremely grateful for gardyneHOLT’s generous donation of time, expertise and resources to design this beautiful publication for us. It has been a real pleasure to work with Fraser Gardyne, partner of the firm, and his talented team.
Paper copies are available on request by email to:
This e-mail address is being protected from spambots. You need JavaScript enabled to view it
or mail to @Heart, PO Box 108 034, Symonds Street, Auckland 1150.

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@Heart's 2010-13 Strategic Plan focuses on the following areas of importance:
Awareness, Membership, Funding, A Unified Organisation and Credibility
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Mission
"@Heart provides lifelong support for all those affected by the world's most common birth defect and heart disease acquired during childhood".
Aims
The chief objective of @Heart is to provide the parent and families of children with congenital heart conditions the appropriate and timely support they need. @Heart aims to:
- reduce the suffering, stress and premature death of these children and the emotional strain on their families;
- reduce the financial burden and stress placed on families taking a child to Starship Children’s Hospital;
- encourage, develop and implement programmes for a child's rehabilitation following surgery;
- promote awareness and conduct and publish research about children with heart conditions.
- It is also responsible for the publication and distribution of the practical handbook for parents.
@Heart Values
- Heart children and their families first
- Education and empowerment
- Passionate and professional
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Stay up-to-date with @Heart news
The ‘Heartline’ newsletter gives you an update of @Heart news, events and ways to get involved. You can download and read our latest copy below.
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Heart Forum, designed for young adults (18-25 years old) with a congenital heart condition or a heart condition acquired during
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| Stay up to date with @Heart news, events and ways to get involved. Sign up for our quarterly newsletter and email updates below and we'll deliver it straight to your email inbox. |
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