Recharged and Rewired - a Column by Brittany Foster

Brittany is the HR associate for BioNews (the publisher of this site) and a columnist for Pulmonary Hypertension News. Brittany is from the smallest state in the U.S., Rhode Island. She manages multiple chronic conditions including pulmonary hypertension and congenital heart disease. Some of her illnesses are visible, but most are invisible. She hopes that her column, “Recharged and Rewired,” will show those reading that having a body that’s wired a little differently doesn’t keep her from being the best version of herself every day. Brittany is happy to work in the HR department at BioNews because she is passionate about advocating for herself and others who may be going through physical and emotional challenges of living with a rare disease.

‘When Will I Learn?’ A Poem

“When Will I Learn?” is a poem I wrote to express my feelings about my own denial over my medical condition. In it, I write about what I have gone through medically as a result of my own denial. Toward the end, I move to what “I am starting…

Body Image and Chronic Illness is an Inside-Out Issue

Many people in the chronic illness community will talk about how their illness affects their mental health. They talk about grief, depression, health, anxiety, chronic pain, and post-traumatic stress disorder. What is not talked about as openly is the effect of chronic illness on our body image. I…

Fear Change, or Adapt to Change

“Change. We don’t like it. We fear it, but we can’t stop it from coming. We either adapt to change or we get left behind.” – Meredith Grey, Grey’s Anatomy When I started oxygen, I had to get used to staring at myself with a cannula…

Top 10 Ridiculous Comments I’ve Received in the ER

I have learned the hard way that some of my chronic illnesses should NOT be managed in an emergency room. Some circumstances, however, warrant immediate medical attention. It has been difficult to figure out what exactly is an emergency and what is “normal” for a life with chronic hypoxia,…


A Conversation With Rare Disease Advocates