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Blog Posts

Tag: Health Policy

The Cost of Convenience - Why Administrative Hurdles Should Never Block Newborn Screening

The Cost of Convenience: Why Administrative Hurdles Should Never Block Newborn Screening

In policy meetings and committee rooms across the country, newborn screening conditions are regularly scored, debated, and weighed. Leaders evaluate analytical validity, treatment efficacy, and system capacity. But every so...

Published September 2, 2026
Why Health Policy Belongs in Patient Engagement Strategy

Why Health Policy Belongs in Patient Engagement Strategy

Patient Engagement Does Not End With Understanding Patient Needs When organizations think about patient engagement, the conversation often focuses on insights. What are patients experiencing? What barriers are they facing?...

Published July 9, 2026
A man and woman pose with their baby in front of a beach. The sun is setting in the background

Recognizing Rare Disease Month Through Newborn Screening Advocacy

A Rare Diagnosis My husband and I both agree that Friday, February 13, 2015, was the worst day of our lives.  We had endured a six-week diagnostic odyssey for our...

Published February 18, 2026
MLD and DMD Added to the Federal RUSP - a Victory for Newborn Screening

MLD and DMD Added to the Federal RUSP: A Victory for Newborn Screening

Today brings exciting news for the rare disease community, born from immense effort, patient advocacy, and a refusal to back down. In a historic move, Metachromatic Leukodystrophy (MLD) and Duchenne...

Published December 16, 2025
Lesa, Brennan, and Tori Brackbill

Newborn Screening – Going Beyond Awareness

Newborn Screening Awareness Month is here, but it's time to shift our focus from awareness to action, and to take the time to listen to state Newborn Screening programs so...
Published September 5, 2025
Listening matters - especially in health policy

Listening Matters – Especially in Health Policy

“Advocacy is key to the effective functioning of a democratic society and a free market economy.”1 Listening to Understand  One of our core values at Patient Advocacy Strategies is listening...

Published March 7, 2025
words related to treatment access

Deciding Access to Treatment for Rare Disease

Imagine this: You and your child are in a cold, sterile examination room where motivational posters on the wall preach empty platitudes of encouragement. You’re anxious about getting bad news...

Published March 4, 2025
rare disease

Why NIH Funding Cuts Matter in Rare Disease

It’s Rare Disease Month – a month typically set aside for awareness, advocacy, and recognition of the estimated thirty million Americans living with a rare disease.  But this month has...

Published February 12, 2025
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