
Foundation for Children With Atypical Hus
Official page of The Atypical HUS Foundation. We are here to support and provide resources for patients and their families.

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Home - aHUS Foundation The aHUS Foundation fosters sharing of informationand inspirationfor anyone looking to gain insight into atypical hemolytic uremic syndrome aHUS. We connect people with the resources and opportunities they need to help improve the lives of those dealing with this rare and complex disease. Learn More Weve Been There. Weve spent the evenings in hospitals worrying and bracing ourselves for the worst.
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🌟 Don’t miss your chance to join us at the 2025 aHUS Family Conference. 🌟 We’ve had a few cancellations, which means a handful of spots just opened up — and this is your opportunity to grab one. This year’s conference has something for everyone: yoga to start the day, inspiring talks from leading doctors and mental health speakers, a fun night out at Top Golf, and our can’t-miss music-themed party 🎶 It’s more than a conference — it’s a chance to connect, learn, and celebrate together.
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