AminoChain

Building trust in science and healthcare through a transparent, decentralized research ecosystem. Visit our site for more info!

07/24/2026

Some of our best ideas happen off screen. For our summer onsite, the AminoChain team came together to strategize, collaborate, and remember why we do what we do.🙌

07/20/2026

Chronic illness doesn't just test your body. It tests who stays. In this clip, Andrea explains how her Myasthenia Gravis diagnosis impacted her former relationships, and simultaneously ushered in new ones within the MG community.

Her take now: "Who wants to be with somebody that's not with you through the bad as well as the good?"

How did Myasthenia Gravis impact your relationships? Tell us in the comments below ⬇️ 💙

Afterwards, click the link in our bio to join our MG study and learn how we're working to raise MG awareness!

04/10/2026

When your muscles stop responding the way you expect, even simple moments can feel unpredictable.

For people living with Myasthenia Gravis, muscle weakness is more than physical; it shapes routines, energy, and independence in ways that are often unseen.

Research should reflect that reality.
At AminoChain, we are building patient centered research that starts with lived experience. From home, on your schedule, you can help bring new understanding to MG and move science forward. 🧪💛

Your experience can wake up MG research.
Join the study today. Tap the link in our bio to learn more ➡️ aminochain.io/mg-study

04/03/2026

What comes after a diagnosis?

On April 9, we are collaborating with to bring together people living with lupus and myasthenia gravis for an evening centered on connection, conversation, and community.

This is not a stuffy lecture. It is a space to hear what is happening in research in a way that actually makes sense, ask honest questions about what participating in our study looks like, and meet others who are navigating similar experiences.

Whether you are newly diagnosed, years into your journey, or supporting someone you love, you are welcome here.

No pressure. No jargon. Just real people and real conversations.

Because research should include you. And community should feel like this.

Join us in Mountain View from 5:30 to 7:30 PM
Save your spot: https://luma.com/aglf9b4v

03/25/2026

“Data sharing is necessary to truly understand MG, which is ‘continuously elusive’ and has many different faces.” — .longoria, Patient Advocate and founder of .supportgroup

Help shape the future of MG care from home.

Amino Chain, in partnership with ImYoo , is launching the Myasthenia Gravis Repository Initiative and recruiting 60 U.S. participants (≈50 with MG, ≈10 comparison) for at home blood collection for whole genome sequencing and longitudinal immune profiling.

Built on privacy first technology, this study keeps participants directly connected to their samples and data, provides regular updates, and gives a clear window into how contributions are used.

Learn more and join: https://aminochain.io/mg-study

03/17/2026

Old samples, new discoveries. Retrospective biospecimens are fast, affordable and great for biomarker or rare-disease work, but only if you check the basics: the sample’s story, how it was stored, provenance, and any consent limits.
Swipe to see what to look for → link in bio to browse de-identified samples via AminoChain’s Specimen Center. 🔬✨

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