Edgewise Therapeutics

Edgewise Therapeutics On a mission to improve the lives of people facing serious muscle disease.

At Edgewise, we view caregivers not as a sign of lost independence, but as bridges to independence itself. Caregivers ar...
05/28/2026

At Edgewise, we view caregivers not as a sign of lost independence, but as bridges to independence itself.

Caregivers are the unsung heroes who make everyday life possible for many individuals living with serious diseases. They are the advocates, navigators, and anchors who provide vital support, both emotional and physical.

To the caregivers within our community: thank you. We recognize and celebrate the important, often-unseen work you do to move us all forward.

Meet our Director of Cardiovascular Patient Advocacy, Jasmine Patel!Jasmine's passion for patient advocacy was shaped ea...
05/21/2026

Meet our Director of Cardiovascular Patient Advocacy, Jasmine Patel!

Jasmine's passion for patient advocacy was shaped early in her life while volunteering in rural parts of the world. Those experiences guided her toward a career built on a single belief: People most affected by a problem should be at the center of solving it.

That belief has been the driving force throughout her career. Jasmine has worked for various cardiovascular patient organizations dedicated to raising awareness and ensuring access to transformative treatments. Her most profound moments have been training hundreds of people to share their stories, advocate for change, ensure research and innovation is shaped by patient experiences, and foster a sense of shared purpose among all stakeholders to ultimately improve health outcomes.

At Edgewise Therapeutics, she instills that same mindset into her work every day, ensuring that the voices and perspectives of individuals with lived experience inform and guide decision-making across our early and late-stage cardiovascular clinical development programs.

Many people are taught that their value is tied to physical strength or independence. For those living with Becker muscu...
05/15/2026

Many people are taught that their value is tied to physical strength or independence. For those living with Becker muscular dystrophy, those messages and expectations can weigh as heavily as other symptoms.

We’re here to remind you that your worth isn’t only about what your muscles can do. It’s about the courage needed to show up each day – both for yourself and the ones you love – and to ask for support when you need it.

Light up the Becker Power Map with a message of support here: https://beckermusculardystrophy.com/power-up-community/

The impact of living with a serious muscle disease extends far beyond the physical. From the anxiety of a new diagnosis ...
05/08/2026

The impact of living with a serious muscle disease extends far beyond the physical. From the anxiety of a new diagnosis for some, to the emotional resilience required every day for others, maintaining one's mental health is as important as taking care of your muscles.

This Mental Health Awareness Month, we recognize that these conditions can sometimes feel isolating. If you’ve felt unseen in your experience, please know that you are not alone. Your concerns matter.

Our commitment to cardiac health extends beyond the lab. We look forward to attending the following events in May that w...
05/05/2026

Our commitment to cardiac health extends beyond the lab. We look forward to attending the following events in May that will be joined by industry peers, patient advocacy groups, patients and caregivers, researchers, and more!

- Abby Bronson, VP Patient Advocacy - Partnership to Advance Cardiovascular Health CV Health Policy Summit: May 14

- Jasmine Patel, Director Patient Advocacy - World Heart Federation World Heart Summit: May 16-17

We hope to see you there!

When it comes to May events in the muscular dystrophy community, we have a full agenda. Find our team at the following c...
05/01/2026

When it comes to May events in the muscular dystrophy community, we have a full agenda. Find our team at the following conferences this month:

- Nick Mastrandrea, Field Medical Affairs - Jett Foundation’s Family Workshop

- Joanne Donovan, Sarah Tencer, John Wing and Danielle Pelletier - Cure Duchenne FUTURES Conference

- Katherine Krieger, Patient Advocacy - Parent Project Duchenne España International Congress

We hope to connect with you!

We're excited to share the date for the 2026 Becker Education & Engagement Day (BEED)! This annual event brings together...
04/29/2026

We're excited to share the date for the 2026 Becker Education & Engagement Day (BEED)! This annual event brings together individuals and families living with Becker to connect, learn about the latest in Becker care, research and daily living strategies, and support one another. Through their participation as speakers and sites, clinicians, healthcare professionals, and researchers share their expertise, and strengthen their connection to the Becker community and share their knowledge.

We hope to see you at ! Learn more about the event at beckereducationandengagement.com.

04/23/2026

Today, we’re celebrating the critical work happening in laboratories around the world. From early discovery through clinical development, lab research powers every step forward in the development of therapeutics for serious skeletal and cardiac muscle diseases.

We’re grateful for our research scientists for your expertise, your brilliance, and your precision. Your work drives progress every day.

04/22/2026

Hearing from others navigating similar realities can be profoundly impactful, offering perspective, validation, and a sense of connection. Mike shares words of encouragement From The Heart, part of our series that reminds us that the most important insights about Hypertrophic Cardiomyopathy come from those who experience it on a daily basis.

Our work in developing investigational therapies for individuals like Mike is fueled by these perspectives.

Explore valuable resources: https://edgewisetx.com/patients-families/support-for-hcm/

04/21/2026

Abby Bronson, VP of Patient Advocacy, shares why we created Becker Power Up Community, a visual reminder that no one navigates the Becker muscular dystrophy path alone. Finding people who share your diagnosis can transform your outlook, inspiring hope for a brighter future together.

Add your message of support and light up the Becker Power map: https://beckermusculardystrophy.com/power-up-community/

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1715 38th Street
Boulder, CO
80301

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+17202627002

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