PAN Foundation

PAN Foundation

Non-profit Organizations

Washington, District of Columbia 7,896 followers

Helping underinsured people with life-threatening, chronic and rare diseases get the medication and treatment they need.

About us

The Patient Access Network Foundation™ is an independent, national 501 (c)(3) organization dedicated to helping federally and commercially insured people living with life-threatening, chronic and rare diseases with the out-of-pocket costs for their prescribed medications. Partnering with generous donors, healthcare providers and pharmacies, PAN provides the underinsured population access to the healthcare treatments they need to best manage their conditions and focus on improving their quality of life. We also work to educate policymakers about the long-term solutions needed to improve healthcare access, affordability, and equity for all. Since our founding in 2004, we have provided more than one million underinsured patients with $4 billion in financial assistance.

Website
http://www.panfoundation.org
Industry
Non-profit Organizations
Company size
51-200 employees
Headquarters
Washington, District of Columbia
Type
Nonprofit
Founded
2004
Specialties
Patient Assistance, Co-Pay Assistance, Financial Assistance, Chronic Diseases, Rare Diseases, Oncology Disease, Out-of-Pocket Costs, Healthcare, and Healthcare Access

Locations

  • Primary

    1032 15th St NW

    Suite 413

    Washington, District of Columbia 20005, US

    Get directions

Employees at PAN Foundation

Updates

  • View organization page for PAN Foundation, graphic

    7,896 followers

    Last year, we had another impactful year of helping people access their treatment, championing healthcare policies that put patients first, and equipping people with educational resources to help navigate complex healthcare topics. Read more in our annual report: https://bit.ly/4fAGPYI Thanks to your support, in 2023 we: ✅ Provided more than $255 million in direct financial support to 110,520 people across all 50 states and U.S. territories ✅ Hosted our inaugural in-person Advocacy Action Day, convening 40+ advocates from 16 states and one U.S. territory in Washington, DC ✅ Expanded our educational footprint by providing resources about the Medicare Part D reforms, copay accumulators, alternative funding programs, health equity, and more Together, we can continue to save lives and champion access to care. Thank you for being a part of our community!

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  • View organization page for PAN Foundation, graphic

    7,896 followers

    Did you know most adults living with chronic illnesses are open to participating in clinical trials? The biggest barrier to participation is lack of information 📋 Our new clinical trials initiative, launching in fall 2024, will provide patients with the information, resources, and support they need to navigate the complex world of clinical trials. Read more about the initiative here ➡️ https://ow.ly/9ZJp50SQhiB

    • Tan background with teal text that says “79% of adults with chronic illnesses say they are open to participating in a clinical trial in the future.” Underneath are five people icons. Four of the five icons are light teal, and the last one is dark text. The PAN Foundation logo is in the bottom left corner. The bottom right corner says, “Source: PAN Foundation.”
  • View organization page for PAN Foundation, graphic

    7,896 followers

    August is Spinal Muscular Atrophy (SMA) awareness month! SMA is a rare disease that impacts the nervous system by progressively destroying motor neurons that control essential muscle activity. Do you have a patient or know someone living with SMA who needs help paying their out-of-pocket prescription costs? Our SMA fund is currently open, and eligible patients can receive up to $3,800 per year in financial assistance. Learn more at: https://ow.ly/ovbg50SJCNy

    • An image of a young woman in an electric wheelchair with pink hair on the phone. Along the bottom right corner of the image is white text that says, “Financial assistance for Spinal Muscular Atrophy. Eligible patients can receive up to $3,800 per year for their covered medications!” The PAN Foundation logo is in the top left corner of the image.
  • View organization page for PAN Foundation, graphic

    7,896 followers

    For Karen Lewis, the first half of 2021 was a blur of phone calls, letters, and documentation as she and her neurologist’s office tried to get her insurer to approve a drug that would be safe for her to take. Time after time, the request was denied. Time after time, Karen appealed the decision. She had encountered a step therapy, or “fail first,” policy, which requires patients to try and fail an insurer-preferred medication before covering the medication that was originally prescribed. This harmful practice can lead to delays in care, severe side effects, and irreversible disease progression. Read more about Karen’s story and urge Congress to support the Safe Step Act today: https://ow.ly/6iSi50SJB7g

    • A tan background with a large quote in teal text that says, “I was trying to take care of my health, and a panel who knows nothing about me or my health was making decisions about my care.” In the bottom right corner of the graphic is a photo of Karen Lewis, PAN grant recipient, with transparent blue and teal circles behind her headshot. The PAN Foundation logo is in the bottom left corner.
  • View organization page for PAN Foundation, graphic

    7,896 followers

    📢 We’re thrilled to announce our new disease fund for Myelodysplastic Syndromes (MDS)! MDS are conditions that can occur when the blood-forming cells in the bone marrow become abnormal and are considered a type of cancer. Eligible Medicare patients can receive up to $6,800 in financial assistance for their covered medications! Learn more about our new MDS fund here: https://lnkd.in/eud_Vxar

    • An image of an older white man smiling with his wife and daughter on both sides of him, smiling and embracing the man. The image has a purple overlay with the PAN Foundation logo in the top left corner and “New fund launch: Myelodysplastic Syndromes Fund” in white text along the bottom left of the graphic.

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