For many families, vacations and travel are some of the most meaningful parts of life. Time away offers a chance to explore, recharge, and create memories together.
For families living with congenital heart disease (CHD), travel can also come with an added layer of planning.
Questions often arise:
Having answers to these questions can make all the difference. For heart families, peace of mind often comes from preparation.
In a medical emergency, healthcare providers will always act quickly to provide care. However, having access to a patient’s full medical history can help ensure that care is as informed and personalized as possible.
Congenital heart disease is complex. Each patient’s anatomy, procedures, and care plan are unique. Having key information readily available – such as surgical history, medications, and care notes – can help providers make more informed decisions, especially when care is needed away from home.
While laws like HIPAA protect patient privacy and ensure that only authorized individuals can access medical records, accessing and transferring those records between health systems can take time. In some cases, records may take up to 30 days to be provided and may involve additional steps or fees.
In moments where time matters, having information readily accessible can provide reassurance and clarity.
At HeartWorks, we recognize that families living with CHD navigate more than just clinical care – they manage a lifetime of information, decisions, and preparation.
When The Co-op @ HeartWorks was created, it was designed to be more than a platform. It was built as a supportive, patient-centered resource that reflects the real needs of the CHD community.
Rather than placing the burden on families to organize everything on their own, The Co-op brings key tools and information into one connected space.
The Co-op is a patient-powered initiative designed to help individuals and families living with CHD stay organized, informed, and connected.
It offers tools that support both day-to-day care and long-term understanding of health.
This combination of tools allows families to move from reacting to care…to feeling more prepared and informed at every step.
Whether preparing for a routine cardiology appointment or planning a family trip, having information in one place can make a meaningful difference.
Members can:
These small actions can help create a greater sense of confidence – not just in clinical settings, but in everyday life.
The Co-op is not only a tool for individuals – it is part of a larger effort to strengthen the future of CHD care.
By choosing to share their experiences and insights, members are helping build a resource that can:
Every entry, every shared experience, and every data point contributes to a broader picture of what it means to live with CHD.
For those interested in joining or learning more, support is always available.
Emma Hofmeister, a member of the HeartWorks team, is available to guide families through The Co-op and help them explore its features step by step.
The Co-op is open to:
Whether you are just getting started or looking to better understand how to use the platform, support is available every step of the way.
Living with congenital heart disease requires strength, organization, and ongoing care. Tools like The Co-op @ HeartWorks are designed to support families not just in moments of need – but in everyday life.
Because when families feel prepared, connected, and informed, they are better equipped to navigate whatever comes next.
And together, those shared experiences are helping build a future where care is more connected, more informed, and more personalized for every heart.
Living with congenital heart disease means managing more than appointments – it means navigating a lifetime of information, decisions, and unknowns.
The Co-op @ HeartWorks was built to help make that journey more connected, more organized, and more informed.
Create your free account today and:
Every experience shared helps move the field forward.
If you’d like help getting started, Emma is here to guide you step by step and answer any questions along the way.
Because congenital heart disease is complex, having access to medical history helps ensure more informed care – especially during emergencies or when traveling.
Access may vary by provider, and records can take time to transfer. Tools like The Co-op help bring information into one place for easier access.
The Co-op is a patient-powered platform where individuals with CHD can track their health, organize medical records, and contribute to research.