By: Matt Werbach In 2018, when psoriasis lesions began to show on Seritta Frazee’s face, she decided it was time to take her disease seriously and to find the right treatment. Before then, she’d gotten away with covering her skin, but no one wants to live life in a ski mask. With some other diseases…
DetailsLegislation puts common sense guidelines around insurance industry practice of “step therapy” WASHINGTON, D.C. – April 13, 2023 Today, patient and health care provider groups from across the country applauded the reintroduction of legislation aimed at putting reasonable parameters around the insurance industry protocol known as “step therapy” or “fail first”. The bill (S.652) is…
DetailsCalifornia native Jennifer Pellegrin shares her story on the importance of getting the treatment you need, when you need it. By Jenn Pellegrin Editor’s note: Jennifer Pellegrin is a National Psoriasis Foundation volunteer advocate who is sharing her experience, in her own words, on how detrimental step therapy was to her treatment journey, and why state…
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By Taruja Karmarkar, Patrick Stone, Jennifer Graff The COVID-19 pandemic has exacerbated Americans’ challenges in accessing much-needed and effective care. One such hurdle, step therapy, requires patients to try a clinically recognized, lower cost first-line therapy before reimbursement for an alternative therapy prescribed by the physician and can delay access to care. Pre-pandemic, experts expressed…
DetailsRecorded June 14, 2019 Learn more about step therapy and current protections that took effect January 1, 2019, that offer patients and physicians a clear process to obtain a step therapy protocol exception. Our webinar will provide a synopsis of those protections and guidance on how they can be best utilized.
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At NPF, we often get the question, “Does my voice really matter?” The answer is without a doubt, yes. Your voice absolutely makes a difference for patient advocacy! Your voice can be shared effectively in so many ways – for example, through a call, email or text to your lawmaker. Your voice can also be…
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We didn’t know what to expect in 2018 because our elected officials were so focused on the midterms. But it turned out to be a rewarding year for our volunteers, who wrote to and met with their legislators in state capitols and on Capitol Hill. In Minnesota and New Mexico, we focused on reforming step therapy, which occurs…
DetailsOn October first, 40 national patient and provider organizations sent a letter to the Department of Health and Human Services (HHS) in response to the recent announcement that Medicare Advantage plans can require step therapy for physician-administered drugs starting in 2019. In the letter, the organizations urged HHS to implement a robust exceptions process for…
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Our volunteers made waves visiting Congress and learning firsthand how elevating the patient voice can make a real difference. NPF’s annual Capitol Hill Day is one of the most rewarding and productive events held each year by the Advocacy department, and this year’s event was no different. Advocates from our patient and researcher communities met…
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A group of eager volunteers descends on Congress for our 14th annual Capitol Hill Day Fly-in. On Sunday, March 18, 24 volunteers from 16 states along with six doctors and scientists arrived in Washington, D.C., to prepare for our annual trip to Congress. Our dual mission: to persuade our elected representatives to devote more funding…
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