
At The AIP BIPOC Network, our mission is rooted in equity, access, and support for those living with chronic illness. Whether navigating autoimmune disease, cancer, or other serious conditions, our community members often face high out-of-pocket costs, confusing systems, and limited culturally competent support.
To help change that, we’ve partnered with the Patient Advocate Foundation (PAF), a national nonprofit that provides free case management and financial assistance to patients with serious and chronic health conditions.
We are proud to serve in two official roles with PAF:
Patients can qualify for help with prescription co-pays, deductibles, and treatment-related costs if they meet income and insurance criteria and have a confirmed diagnosis.
Since 1996, PAF has worked directly with patients to ease the burden of medical costs and treatment access. Their services include:
🟡 Case Management for insurance denials, billing issues, and access to care
🟡 Co-Pay Relief of up to $7,500/year for qualified patients with open disease-specific funds
🟡 Education and Navigation Tools in multiple languages and formats
🟡 Support for Treatment Plans tied to serious or chronic diagnoses
Patients can qualify for help with prescription co-pays, deductibles, and treatment-related costs if they meet income and insurance criteria and have a confirmed diagnosis. Patients can qualify for help with prescription co-pays, deductibles, and treatment-related costs if they meet income and insurance criteria and have a confirmed diagnosis.
As an Equity Partner, The AIP BIPOC Network is part of a national collaboration aimed at reaching communities historically left out of traditional care models.
Together with PAF, we are working to:
🟡 Expand awareness of trusted, free support for patients
🟡 Ensure that resources are culturally responsive and accessible
🟡 Center community voice in the national conversation around healthcare equity
🟡 Strengthen care pathways for chronic illness populations nationwide
This is a long-term investment in how support systems engage the communities we serve, not just temporarily, but sustainably.
In addition to our Equity role, we are now integrated into the PAF Non-Profit Patient Partner Portal, a secure, referral-based platform that allows our team to:
🟡 Directly refer patients to PAF using a HIPAA-compliant system
🟡 Track the outcome of referrals so we know people are receiving help
🟡 Ensure warm handoffs, not just links or information
🟡 Identify barriers through real-time data to better serve our community
This makes a huge difference for patients who are already exhausted from navigating chronic illness. Instead of starting from scratch, we help streamline the process and walk with them.
Our PAF partnership is woven into both our in-person and online outreach. We:
🟡 Share co-pay relief opportunities at community outreach events
🟡 Highlight the program as a trusted resource for our virtual community
Whether someone meets us at an event or online, we ensure they know support is available, and we help them take the first step.
To be eligible for PAF’s disease-specific funds, individuals must:
🟡 Have active health insurance that covers treatment
🟡 Have a confirmed diagnosis and treatment plan
🟡 Live and receive care in the U.S.
🟡 Fall within income limits (typically under 400–500% of the federal poverty line)
Example (2025 Estimates):
*Eligibility varies by fund (400%–500% of federal poverty guidelines)
Approved patients can receive up to $7,500 per year for:
At The AIP BIPOC Network, we believe no one should miss out on care because they can’t afford it or don’t know where to start. That’s why we’re proud to partner with the Patient Advocate Foundation—because equity doesn’t happen in isolation. It takes trusted networks, practical tools, and the power of real-time help.
This is what support looks like in action, and we’re committed to making sure our community has access to it.
If you or someone you know is living with a chronic illness and struggling to afford treatment, co-pays, or medication, you don’t have to navigate it alone.
Through our partnership with the Patient Advocate Foundation, we can help you:
🟡 Start here: Email us at info@aipbipoc.org
🟡 Follow us on Instagram @aipbipoc for updates, deadlines, and outreach events
🟡 Visit patientadvocate.org to learn more about available programs
We’ll help you take the first step, and stay with you along the way.
Jamie Nicole is the Founder and CEO of The AIP BIPOC Network. She is a Certified AIP Coach, patient advocate, and fitness instructor living with multiple autoimmune conditions. Jamie is committed to advancing equity, access, and representation for Black, Indigenous, and People of Color navigating autoimmune and chronic illness. Through education, advocacy, movement, and community-driven initiatives, she works to ensure BIPOC voices are centered in healthcare conversations and solutions.
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