by Kevin Dooley, MD | Apr 11, 2018 | News and Information
Positive Attitude Patrick Warner is an optimistic person, and that didn’t change when he was diagnosed with a rare, untreatable muscle disease, inclusion body myositis (IBM). Life is an adventure, and Patrick is going to enjoy it. As his muscles gradually deteriorate,...
by Kevin Dooley, MD | Apr 7, 2018 | News and Information
Introduction Living independently with a muscle disease like inclusion body myositis (IBM) can be a daunting, but Patrick Warner has accepted the challenge. He views it as a puzzle that needs to be solved. Faced with a disability that involves both his hands and his...
by Kevin Dooley, MD | Feb 25, 2018 | News and Information
What is Rare Disease Day 2018? Rare Disease Day 2018 takes place on February 28. Since its start in Europe in 2008, Rare Disease Day has been an annual event that has grown to involve people all over the world. This is a day to celebrate all of us who live with a rare...
by Kevin Dooley, MD | Jan 1, 2018 | News and Information
His muscles are being destroyed by a disease called inclusion body myositis (IBM), but Martin Jarry is resilient. After recovering from the shock of his diagnosis, he began to fight back, working to increase public awareness of myositis and to bring hope to other...
by Kevin Dooley, MD | Dec 8, 2017 | News and Information
From the soil of Easter Island to the clinics of Paris, the journey of rapamycin to its current position as a potential treatment for sporadic inclusion body myositis is a fascinating story of scientific discovery. A recent clinical trial provided encouraging results,...
by Kevin Dooley, MD | Nov 15, 2017 | News and Information
The purpose of the Cure IBM Blog is to share news and information about the muscle disease, inclusion body myositis (IBM). Articles will discuss research findings, clinical trials, medical information, meetings and events, motivational stories, caregiving, and...
