💙 New to Blau? Start Here.
We know how overwhelming it can be to face a rare disease diagnosis like Blau Syndrome. You are not alone — and we’re here to help guide you, connect you with resources, and empower you to take the next steps with confidence.Here are a few ways to get “on-boarded” into the Blau community:
Download our Physician Guide
📘 What’s Included in the Guide:
Your physician will find a high-level overview of the following:
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What is Blau Syndrome?
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Genetic Cause
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Classic Clinical Triad
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Expanded Systemic Involvement
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Diagnostic Workup
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Treatment Overview
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Monitoring Recommendations
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Resources & Contact Information
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Watch: Expert Webinar
Start with our introductory webinar featuring leading Blau researchers and clinicians. Learn how Blau Syndrome presents, progresses, and what current treatment and research options look like.
▶️ Blau Syndrome: A Monogenetic Granulomatous Disease
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Explore Our Website
Take your time browsing through our site to learn about:
· What Blau Syndrome is
· Research news and opportunities
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Join the International Patient Registry
Help drive progress in research by enrolling in the Blau Syndrome International Patient Registry.
Your experience matters — and contributing your data can help shape the future of care.
👉 Learn more and register here
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Follow Us on Social Media
Stay connected and informed by following us on social media. We share updates, stories, events, and resources just for the Blau community. Connect with others in our private facebook group "Cure Blau Syndrome Foundation Community Group"
🔗 Instagram | Facebook | TikTok
