No friend of the coal miner

By Just Transition Fund - Grist, June 21, 2022

While working at a West Virginia mine, Gary Hairston dashed up a set of stairs to get out of the rain, but he only made it halfway. Doubled over and breathless, he didn’t yet know how completely his life had changed.

Hairston was eventually diagnosed with coal worker’s pneumoconiosis (CWP), commonly called black lung disease—a progressive and incurable condition caused by inhaling coal and silica dust, which causes scarring and impairs lung function.

Living with the impacts of black lung disease for the past twenty years—having to sit on the side-lines instead of playing basketball with his grandson—Hairston knows first-hand how devastating the disease can be. As the president of the National Black Lung Association, Hairston now works to help other miners secure benefits and healthcare from an increasingly vulnerable safety net.

The federal Black Lung Program was enacted in 1969, and since 1977, the Black Lung Disability Trust Fund has provided benefits when liable companies can’t be determined, or if a company goes bankrupt—an increasingly common occurrence in coal country. But in 2021, Congress failed to extend the excise tax on coal, which provides the fund’s sole source of income—jeopardizing the fund’s long term viability, and the support it offers for thousands of former miners afflicted with black lung disease. 

Read the rest of the article here.

Disclaimer: The views expressed here are not the official position of the IWW (or even the IWW’s EUC) and do not necessarily represent the views of anyone but the author.