Sanofi US

We’re an R&D driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. For U.S. residents only. FOR U.S.

https://www.sanofi.com/en/chasing-miracles RESIDENTS ONLY. Interactions with our Sanofi US page must comply with our terms: http://bit.ly/US-terms. This page is intended to provide a forum for discussions regarding Sanofi US. If treatments are discussed, we can only allow messages that are in accordance with the FDA approved use. This page is not intended as a forum for reporting Sanofi US or other company's products' side effects associated with the use of prescription drugs. For more information on our products, please visit https://www.sanofi.us/en/products-and-resources. For questions relating to our products or treatments, please visit https://www.sanofi.us/en/contact-us. MAT-US-2510212-v1.0-09/2025

03/11/2026

During , we’re proud to spotlight stories of three people living with autoimmune Type 1 Diabetes, including how they find strength in shared experience. Read more: http://spkl.io/6186AIp0K

03/10/2026

This Myeloma Action Month, we are proud to stand with the International Myeloma Foundation. We're empowering patients and their care communities to embrace More Than Myeloma – proving that their lives are defined by more than just this challenging disease.

Learn how you can join the action this March. 🔗 http://spkl.io/6184AIya2

03/02/2026

Misconceptions about kidney donation and transplantation may leave patients waiting longer for a second chance. This , we’re sharing the facts that can help save lives ⬇️

02/27/2026

In celebration of , we're taking a look back at the impact of the and the individuals whose advocacy and leadership help move the rare disease community forward. Nominations for the 2026 TORCH Awards are now OPEN: http://spkl.io/6187AaT97

The TORCH Awards celebrate those making a difference in the rare disease community and beyond. Who do you know whose dedication and advocacy deserve recognition?

Let's continue to amplify these vital voices in our community. Learn more and nominate your rare hero today!

02/25/2026

Rare diseases are complex, and every journey is unique. awareness matters.

02/18/2026

Rare disease impacts more than many imagine. This , we’re raising awareness.

02/17/2026

From a leukemia diagnosis to a bone marrow transplant and then chronic graft-versus-host disease ( ), Amanda turned adversity into advocacy — taking control of her health, connecting with others and becoming a voice for those impacted by this condition.

This , we celebrate the GVHD community and the strength it takes to face this challenging condition.

Discover Amanda’s story and learn more about GVHD: http://spkl.io/6186AQjO4

02/12/2026

Better health starts in our communities.

With our Healthy Futures Solution Fund, we're making a multi-year commitment to empower community-led solutions and build meaningful partnerships in historically under-supported areas.

Together, we're driving long-term change by tackling root causes and creating lasting impact.

02/11/2026

Xavier is re-writing the script on what life can look like with autoimmune type 1 diabetes (T1D), so that people with T1D can be the star of their own story.

02/03/2026

From athletics to the arts, Xavier is now a writer and filmmaker, inspiring others to live authentically. His story proves chronic illness doesn't diminish ambition!

We’re chasing the miracles so people like Xavier can continue to chase their dreams.

01/28/2026

Xavier is chasing his dream of becoming a filmmaker and advocate, determined to bring diabetes representation to the screen.

Keep chasing, Xavier. We’re right beside you.

01/21/2026

Type 1 diabetes (T1D) changed Xavier's life, but it didn’t limit his dreams — it redefined them! 🎬

We’re leading a new era in T1D care, chasing the miracles of science so people like Xavier can continue to chase their dreams.

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