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News and Press Releases
Advocacy Tax Reform Bill Expected to Be Signed Into Law

The package of tax reforms expected to be signed into law includes several provisions that will impact some people with cystic fibrosis.

| 3 min read
In the Spotlight | Advocacy Cystic Fibrosis Foundation Awards Sen. Susan Collins the Breath of Life Legislator Award

The Cystic Fibrosis Foundation awarded U.S. Sen. Susan Collins (R-Maine) the Breath of Life Legislator Award on Nov. 3 for her leadership in ensuring that people with cystic fibrosis have access to the adequate, affordable care they need to live full and healthy lives.

| 3 min read
Health Care Reform | Advocacy CF Advocates Convene on Capitol Hill for Teen Advocacy Day to Fight for Adequate, Affordable Care

As part of the Cystic Fibrosis Foundation's ninth annual Teen Advocacy Day, 162 advocates from 38 states met with elected officials in Washington, D.C., to tell their stories and make sure the cystic fibrosis community is heard in ongoing health care reform discussions.

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Health Care Reform | Advocacy | Our Advocacy Work Senate Health Care Bill Fails to Adequately Protect People with Cystic Fibrosis

Today, the U.S. Senate released its version of the health care reform bill, titled the Better Care Reconciliation Act, and in response, the Cystic Fibrosis Foundation affirmed its opposition to the legislation.

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Health Care Reform | Advocacy House of Representatives Passes Health Care Reform Legislation

The U.S. House of Representatives has passed the American Health Care Act (AHCA), legislation that fails to adequately protect people living with cystic fibrosis.

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Advocacy Cystic Fibrosis Foundation Participates in HHS Roundtable on Drug Pricing

Yesterday, the Cystic Fibrosis Foundation met with HHS Secretary Tom Price and seven other patient advocacy groups to discuss drug pricing and the needs of the CF community. President Trump has identified drug pricing as a top priority, and this meeting was the start of a listening tour by the Secretary.

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Health Care Reform | Advocacy | Insurance Cystic Fibrosis Foundation Joins 86 Organizations to Call on Congress to Protect Medicaid

On March 20, the Cystic Fibrosis Foundation and 86 other organizations called on Congress to protect Medicaid, a critical source of coverage for people in the cystic fibrosis community. 

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Health Care Reform | Advocacy Cystic Fibrosis Foundation Issues Statement on House Health Reform Bills

This week, House committees released legislation to repeal and replace the Affordable Care Act. The Cystic Fibrosis Foundation issued a statement consistent with our ongoing work to promote policies to help ensure that people with cystic fibrosis have access to high-quality, specialized care and adequate affordable insurance.

| 3 min read
Health Care Reform | Advocacy CF Advocates Convene on Capitol Hill for 2017 March on the Hill

As part of the Cystic Fibrosis Foundation's 11th annual March on the Hill, more than 100 advocates from 44 states met with nearly 300 elected officials or their staff to help ensure that everyone with cystic fibrosis has access to high-quality, specialized care and adequate, affordable health care.

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Health Care Reform | Advocacy Congress Approves Budget Resolution: First Action Step Toward Health Care Reform

This week, Congress approved a budget resolution that will allow lawmakers to make certain changes to the Affordable Care Act and Medicaid.

| 2 min read