About the Campaign
The Campaign for Patient Access was launched by the American College of Cardiology in December 2009 as a national effort to reverse Medicare physician fee schedule cuts that threatened cardiovascular care. The site provided background on the issue, the ACC's legislative and legal response, resources for patients and practices, a newsroom tracking coverage across the country, and ways for supporters to share their stories and support the campaign.
From the Newsroom
Medicare Meltdown: Access to Health Care in "Critical Condition"
A press release warning that cardiology access was in critical condition due to Medicare payment cuts.
Read more
Cardiology Takes Legal Action Against Medicare
The ACC filed suit against HHS Secretary Kathleen Sebelius over the 2010 Physician Fee Schedule.
Read more
ACC Statement on Health Care Reform
The ACC used the State of the Union address to highlight the need to reverse the Medicare cuts.
Read more
Medicare Patients and Physicians Join Petition Drive
Patients and physicians in Washington, DC joined a petition drive calling on Congress for Medicare reform.
Read moreMake Your Voice Count During a Health Policy Comment Period
A comment period gives patients, clinicians, carers and communities a formal opportunity to influence a proposed policy before it is finalised. It may concern Medicare payment rules, specialist services, hospital funding, professional regulation or access to treatment. A well-prepared submission can place real-world consequences alongside economic modelling and technical advice.
The Campaign for Patient Access showed why this process matters. When physician fee schedule cuts threaten cardiovascular care, the effects can reach appointment availability, practice viability and timely treatment. For an Australian audience, the same advocacy principles apply to consultations involving Medicare, the Medical Benefits Schedule, public hospitals, private health insurance and specialist services.
Find The Decision Maker And The Deadline
Start by identifying which institution is conducting the consultation. In Australia, a health policy proposal may come from the Australian Government Department of Health and Aged Care, Services Australia, the Australian Parliament, a state or territory health department, or an independent body such as the Australian Health Practitioner Regulation Agency. Each has different submission rules and decision-making powers.
Read the consultation paper carefully and record the closing date, preferred format, word limit and submission address. A federal consultation may use an online portal, email or written submission. A parliamentary committee may publish submissions and invite evidence, while a department may seek targeted responses from professional associations and community groups. Sending comments to the wrong office can mean your views are never considered.
Your elected representatives still have an important role. At the federal level, contact your local member of the House of Representatives and relevant senators. State and territory MPs may be more appropriate when the issue concerns hospital staffing, ambulance services or outpatient clinics. City residents in Sydney, Melbourne, Brisbane, Perth or Adelaide may face different access pressures from people in remote communities, so explain the local setting clearly.
Turn Personal Experience Into Useful Evidence
A strong submission connects a policy proposal with a specific effect on patients and services. Describe what happened, when it happened and why the proposed change matters. A patient might explain how a long wait for a cardiology appointment affected work, transport or family care. A practice may describe rising rent, wages, technology and compliance costs that influence whether it can continue offering appointments.
Personal stories are most effective when they protect privacy and stay focused. Do not include a patient’s full name, medical record, Medicare details or other identifying information without informed consent. The Privacy Act 1988 and professional duties around confidentiality should guide how doctors and advocacy groups collect and share case studies. Use a pseudonym or a general description where appropriate.
Link the story to a policy request. Instead of simply stating that care is becoming harder to access, explain that lower reimbursement could lead to fewer bulk-billed appointments, longer waits or reduced outreach clinics. In Australia, patients often judge affordability by the gap between a Medicare rebate and the specialist’s fee. That everyday experience can help officials understand how a technical change may affect household budgets.
Use evidence that can be checked. Include relevant data on appointment delays, travel distances, bulk-billing rates, workforce shortages or the cost of maintaining diagnostic equipment. A rural patient travelling several hours for specialist care presents a different access problem from a patient in inner Melbourne, but both may be affected by changes to service capacity.
Match The Message To The Audience
Different officials need different information. A minister or department may want evidence about costs, implementation and health outcomes. A local MP may respond to the number of constituents affected and the impact on a nearby hospital or clinic. A senator may focus on national equity, legislation and the long-term sustainability of Medicare.
| Audience | Useful emphasis | Practical action |
|---|---|---|
| Local federal MP | Constituents, local services and waiting times | Send a concise case and request a meeting |
| Senator | National access, equity and legislative consequences | Provide evidence and a clear policy recommendation |
| Health department | Service delivery, workforce and measurable outcomes | Follow the consultation format and cite reliable sources |
| Professional association | Clinical impact and sector-wide trends | Share de-identified examples and coordinate messaging |
| Community organisation | Affordability, transport and patient experience | Invite members to submit consistent, personal accounts |
Use plain English rather than relying on specialist terminology. Explain a Medicare Benefits Schedule item, reimbursement change or funding adjustment in terms of what a patient may see: fewer appointments, a higher out-of-pocket charge, reduced after-hours care or a longer journey to treatment. Officials can obtain technical detail from departments; your contribution should make the human and local consequences clear.
Keep the central request easy to find. For example: “Retain adequate support for cardiovascular consultations so patients can receive timely specialist care without an unaffordable increase in out-of-pocket costs.” A submission can contain several recommendations, but each should be specific, realistic and connected to the evidence that follows.
Build A Credible Contact Campaign
A coordinated campaign is more effective when every participant understands the issue and communicates accurately. Professional colleges, patient groups, carers and practices can prepare a short briefing sheet with the proposal, key dates, verified figures and suggested actions. That helps prevent exaggerated claims and keeps public advocacy focused on access to care.
Begin with a written submission, then make direct contact. An email gives the office a record of your position, while a phone call can confirm that the message reached the correct adviser. Request a short meeting with the MP, senator or staff member. If an in-person meeting is impractical, a video call can work well for people in regional Australia and busy clinical practices.
Prepare three points before the meeting. State who you are and where you live or work, explain the effect of the proposal, and give a practical recommendation. Bring a one-page summary rather than a large bundle of documents. Offer to provide supporting evidence after the meeting, and send a brief follow-up recording any commitments or further information requested.
Timing matters during a formal comment period. Submit early enough to allow officials to review the material, then follow up before the deadline. If the issue is receiving media attention, avoid treating coverage as a substitute for a formal submission. News articles may raise awareness, but the official consultation channel is where your evidence is most likely to enter the policy record.
Local circumstances should remain visible. An urban specialist practice may face a competitive private market and high commercial rent, while a regional service may struggle to recruit cardiologists and maintain diagnostic equipment. Patients in Western Australia, the Northern Territory or far north Queensland may face air travel and accommodation costs that are invisible in metropolitan policy assumptions.
Follow The Process After Submission
Advocacy does not end when an email is sent. Save your submission, note the date it was lodged and monitor the consultation page for updates. Some agencies publish submissions, summaries of feedback or a response explaining which recommendations were accepted. Parliamentary committees may also publish evidence and later issue reports.
Keep elected officials informed when new evidence emerges. A short update about an appointment cancellation, a clinic closure or a change in patient charges can be useful if it is factual and de-identified. Avoid sending repeated generic messages that overwhelm an office without adding information. One well-supported update is more valuable than a series of identical emails.
Watch for the difference between a policy announcement and an implemented change. A government may accept a recommendation in principle, refer it to another body or introduce legislation that still requires parliamentary consideration. The Health Insurance Act 1973, Medicare arrangements and state health legislation can all shape how a proposal becomes operational, so check the relevant government source before sharing claims.
Thank staff members who provide a substantive response, even when the answer is not what you hoped for. Constructive relationships make future contact more productive. Patient advocates and clinicians who are known for accurate information are more likely to be heard when the next consultation concerns cardiac services, specialist rebates or healthcare workforce planning.
Use the campaign’s patient and practice resources as a model for disciplined advocacy: explain the stakes, gather credible stories, protect confidentiality and ask decision makers to preserve access. The objective is to make it difficult for a policy discussion to overlook the people who depend on timely care.
Send your submission before the closing date, contact your federal and state representatives, and share a concise account of how funding or payment changes affect patients in your community. Encourage colleagues, carers and patient groups to contribute their own evidence through the authorised consultation channel. Clear, respectful participation can help keep cardiovascular care available, affordable and responsive across Australian communities.
Campaign for Patient Access