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It's Time to Listen to Rare Disease on YouTube!

mlincoln214

Sep 7, 20211 min read

This Missed Opportunity of a Bill

mlincoln214

Aug 30, 20212 min read

Infusion Centers: Are They the Future of Sickle Cell Crisis Care?

mlincoln214

Aug 23, 20211 min read

It’s a Tough Time…but It’s Even Tougher for Rare Disease Patients

It’s a Tough Time…but It’s Even Tougher for Rare Disease Patients

It’s a Tough Time…but It’s Even Tougher for Rare Disease Patients

mlincoln214

Jul 6, 20213 min read

Online Survey Debuts to Discover Effect of COVID-19 on Rare Disease Patients

Online Survey Debuts to Discover Effect of COVID-19 on Rare Disease Patients

Online Survey Debuts to Discover Effect of COVID-19 on Rare Disease Patients

mlincoln214

Jul 6, 20212 min read

First Do No Harm: An Open Letter to Administrators Crafting Policies for Ventilator Allocation

First Do No Harm: An Open Letter to Administrators Crafting Policies for Ventilator Allocation

First Do No Harm: An Open Letter to Administrators Crafting Policies for Ventilator Allocation

mlincoln214

Jul 6, 20216 min read

See Me, Not Just My Diagnosis

mlincoln214

Jul 6, 20211 min read

Why Does My Doctor Have That Look on Her Face?

mlincoln214

Jul 6, 20212 min read

The Rare Life, Part I

mlincoln214

Jul 6, 20212 min read

What Stands in the Way of Access to Healthcare for Every Patient?

mlincoln214

Jul 6, 20211 min read

The Rare Life, Part II

mlincoln214

Jul 6, 20211 min read

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