Increasing access to treatment in Georgia

| Amy Prentice

At the beginning of 2017, the National Psoriasis Foundation, in partnership with the Crohn’s & Colitis Foundation, targeted the state of Georgia for the introduction and passage of step therapy legislation. 

Step therapy, also known as ”fail first,” is a health insurance mandate that restricts spending on prescription drugs. This mandate requires patients to fail first, often multiple times, on certain medications before they are able to receive the treatment originally prescribed by their physician. All too often, step therapy delays access to optimal treatment, while potentially exacerbating a person’s condition.

Georgia’s step therapy bill, HB 519, was introduced in the Georgia House of Representatives in 2017 and carried over to the 2018 session. As a carryover bill, HB 519 will fail if not passed by the end of this session. The proposed legislation ensures that step therapy protocols are based on sound clinical guidelines, establishes a basic framework for when it is medically appropriate to exempt patients from step therapy, and creates an exceptions process that is transparent and accessible to patients and health care providers.  

With a very strong coalition in place – a diligent and motivated group of patient and provider advocates – we have made considerable progress this year. On Jan. 23, more than 20 coalition partners and advocates joined at the Georgia State Capitol in Atlanta for our 2018 Lobby Day. The morning was spent meeting with legislators, followed by a lunch briefing highlighting patient stories.  

Our voices were heard. On Monday, Feb. 12, the House Life and Health Subcommittee held a hearing on HB 519. Bill sponsor Rep. Sharon Cooper opened the hearing with an introduction to our legislation followed by five strong advocate testimonies. There was no opposition testimony. Now committee members must consider the legislation and vote on whether to support moving the bill to the full Insurance Committee. As these members weigh their decision, coalition members and advocates continue to reach out and express the importance of passing HB 519. 

Your help is needed!

We continue to look for new patient and provider residents of Georgia interested in supporting our efforts. Support can be shown through various avenues, from posting on social media to contacting your representatives to sharing your story for our media efforts. It is the voice of patients and providers that make these campaigns a success. Please contact Amy Prentice at [email protected] or 503-546-5551 if you would like to learn more about step therapy or get involved with our advocacy efforts across the country. 

Above: Our advocates on the steps of the Georgia State Capitol. Photo credit: Amy Prentice
 

Driving discovery, creating community

For more than 50 years, we’ve been driving efforts to cure psoriatic disease and improve the lives of those affected. But there’s still plenty to do! Learn how you can help our advocacy team shape the laws and policies that affect people with psoriasis and psoriatic arthritis – in your state and across the country. Help us raise funds to support research by joining Team NPF, where you can walk, run, cycle, play bingo or create your own fundraising event. If you or someone you love needs free, personalized support for living a healthier life with psoriatic disease, contact our Patient Navigation Center. And keep the National Psoriasis Foundation going strong by making a donation today. Together, we will find a cure.

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