Frequently Asked Questions

• What does a patient advocate do?
  A patient advocate helps you make sense of the healthcare system, so you feel less overwhelmed and more in control. I offer support with things like preparing for appointments, researching providers, understanding a new diagnosis, and coordinating care, always with compassion, clarity, and your voice at the center.

• Do you accept insurance?
  No, I don’t bill insurance for my services. As an independent patient advocate, I work directly for you, not a hospital or insurance company. This allows me to support you without restrictions or limitations, so everything I do is centered on your needs, not what insurance allows.

• What doesn’t a patient advocate do?
  While I’m a nurse by background, I do not provide hands-on care, make medical decisions, or offer medical advice. My role is to guide, support, and help you feel more informed and empowered, not to replace your healthcare provider.

• Why would I need your services?
  Healthcare can be confusing, time-consuming, and stressful, especially if you’re dealing with a chronic illness, facing a new diagnosis, or helping a loved one from a distance. I’m here to walk with you, simplify the process, and help you feel seen, supported, and prepared every step of the way.

• Can you help me if I live in a different state?
  Yes! All of my services are provided remotely, through phone or video, so I’m able to support clients and families anywhere in the U.S.

• How much do your services cost?
  Fees are based on your individual needs and situation. Once I understand what kind of support you're looking for, I’ll create a plan with recommended services and pricing that reflects the level of care that’s right for you. You’ll always know what to expect before we begin.

• How does the process work?
  It starts with a free consultation. If we decide to work together, I’ll create a personalized Advocacy Support Plan tailored to your situation.