April 27, 2026

Recognizing the Signs of a Bleed and Knowing When to Act with Angie Farrar

Today on Beyond the Bleeds, Heather is joined by stand-in co-host Erica for a conversation with Angie Farrar, lead nurse coordinator from our Wausau clinic, about recognizing the early signs of a bleed and why acting early matters.

From joint bleeds and muscle bleeds to injuries that may seem minor at first, Angie shares what patients and families should watch for, including pain, swelling, warmth, tingling sensations, and changes that just don’t feel normal. The conversation also explores why early treatment can help prevent complications and why calling your HTC sooner rather than later is always the best approach.

Heather, Erica, and Angie also discuss how bleed symptoms may show up differently in young children, why some symptoms can be easy to overlook, and how patients can become more aware of changes in their bodies over time.

This episode is a reminder that when something feels off, trust your instincts and reach out. Early detection can make all the difference.


“If it doesn’t feel normal, call us. We’d rather talk through it together than have someone wait too long.” — Angie Farrar


This episode of Beyond the Bleeds explores:

  • Early signs and symptoms of a bleed
  • How joint and muscle bleeds may feel different
  • Why early bleed detection matters
  • What parents should watch for in young children
  • When to call your HTC and why “wait and see” can be risky
  • How awareness and education support better outcomes

Find an HTC Near You:

If you are not connected to a Hemophilia Treatment Center, the CDC’s Hemophilia Treatment Center Directory can help you locate specialized bleeding disorders care near you. Search by state, city, or center name to find an HTC and care team in your area.


Looking for practical tips, expert advice, and a sense of community while living with or supporting someone with a bleeding disorder?

Subscribe to Beyond the Bleeds, the podcast that explores life with hemophilia, von Willebrand disease, and other rare conditions. Hosted by Heather Hansen and John Mazzariello, we share real stories and helpful conversations to support families at every stage.

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