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Advocating for Patient Safety: Reaching out to MEPs for improved thrombosis and hemostasis Care

Welcome back to the ETHA blog!

Building relationships with MEPs about thrombosis and hemostasis

In this post, we will explore how doctors, scientists and clinicians in bleeding and clotting disorders can effectively reach out to the offices of Members of the European Parliament (MEPs) in the European Union. Our focus will be on advocating for appropriate patient safety protocols, adherence to VTE risk assessments, and promoting strategies for preventing blood clots. By engaging with MEPs, we can work together to enhance thrombosis and hemostasis care across Europe.

Why Engage with MEPs?

MEPs play a crucial role in shaping healthcare policies and legislation within the European Union. By engaging with these representatives, doctors and scientists in bleeding and clotting disorders have a unique opportunity to advocate for necessary changes and improvements in patient care. Through informed dialogue and evidence-based recommendations, we can encourage MEPs to support initiatives that prioritize patient safety and promote effective clot prevention strategies.

Understanding the MEP Landscape: Before reaching out to MEPs, it's important to familiarize yourself with the key players and relevant committees. Research and identify MEPs who have expressed interest in healthcare, public health, or related issues. Take note of their party affiliations and previous voting records on topics relevant to thrombosis and hemostasis care.

Crafting a Clear and Compelling Message: When communicating with MEPs, it is crucial to convey your message concisely and effectively. Clearly state your advocacy goals, emphasizing the importance of patient safety, adherence to VTE risk assessment, and the implementation of clot prevention strategies. Back your claims with scientific evidence and real-world examples, demonstrating the impact of improved thrombosis and hemostasis care on patient outcomes and healthcare systems.

Building Relationships: Building relationships with MEPs and their staff is key to fostering meaningful engagement. Attend healthcare-related events, both in-person and virtual, where you can interact with MEPs directly or their assistants. Share your expertise, provide educational materials, and offer to serve as a resource for any questions they may have. By establishing yourself as a knowledgeable and reliable source, you can become a trusted advocate for improved thrombosis and hemostasis care.

Collaborating with Patient Advocacy Groups: Working alongside patient advocacy groups can amplify your message and lend additional weight to your advocacy efforts. Collaborate with these groups to develop joint initiatives, raise awareness about thrombosis and hemostasis issues, and advocate for patient safety protocols. The collective voice of doctors, scientists, and patient advocates can be a powerful force in influencing policy decisions and effecting change.

Follow-Up and Continued Engagement: After initial contact, follow up with MEPs to maintain an ongoing dialogue. Provide them with additional resources, such as research papers, policy briefs, or reports, to reinforce your position and keep them updated on relevant developments. Attend committee meetings or hearings related to thrombosis and hemostasis care whenever possible, and seize opportunities to provide expert testimony or insights.

Engaging with MEPs is a critical step towards achieving improved thrombosis and hemostasis care in the European Union. By effectively communicating with these policymakers, advocating for appropriate patient safety protocols, promoting VTE risk assessment adherence, and emphasizing the importance of clot prevention strategies, doctors and scientists can drive positive change and ensure better outcomes for patients. Together, let's make our voices heard and build a future where thrombosis and hemostasis care are prioritized across Europe.

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