PostedMay 21, 2021 · 3 minute read
Kevin Dooley founded Cure IBM in 2017 to raise awareness of inclusion body myositis (IBM) and encourage research for an effective treatment and cure.
By Taylor Kane
Cure IBM is a testament to the fact that small organizations can make a big difference in research.
IBM is a rare muscle-wasting disease that typically occurs in mid to later life. The progression of the disease is usually very slow, with patients becoming unable to walk 15 years after symptoms first occur. Some lose the ability to use their arms and legs, and swallow.
While the cause of IBM is unknown, Cure IBM has made strides in supporting research for the condition, having garnered over $250,000 of funding for research and involving itself in a research project regarding hand function in patients with IBM. Cure IBM has made this investment in research possible by founding two IBM research funds and participating in the 2019 and 2020 Million Dollar Bike Ride events organized by Orphan Disease Center of the University of Pennsylvania. They will also be participating in the Million Dollar Bike Ride in 2022!
Still, as founder Kevin Dooley explains, “The inclusion body myositis community has large unmet needs.”
”IBM is the most common acquired muscle disease in people over the age of 50, but most people, including doctors, have never heard of it.”
This is why the organization’s two main goals are to fund another research grant and to raise awareness of IBM by sharing information with medical professionals and the general public.
Kevin emphasizes the many misconceptions surrounding IBM, such as that it is simply a disease that causes older people to become unable to walk. He explains that the disease is much more severe than meets the eye: “People lose the use of their hands, and may not be able to dress themselves, hold a glass of water, or feed themselves.”
“Many people with IBM find swallowing difficult or impossible, and some need to have a feeding tube,” he describes. “Choking is a constant threat for many, and some die from aspiration pneumonia after food or liquids goes down into their lungs.”
Thankfully, Kevin, himself, is still able to walk and loves the outdoors and hiking. Before he decided to become a doctor, he studied nature and was skilled at identifying plants. He notes that he is able to remain confident despite the progression of his condition having met people with advanced IBM “who have inspired [him] by showing [him] that it is possible to have a happy, productive life in spite of their disabilities.”
To Kevin, research is key; hence his enthusiastic praise for AllStripes and Cure IBM’s partnership to grow the AllStripes IBM research program.
“AllStripes excites me because of its innovative approach to helping rare disease communities. Rather than focusing on an individual drug or therapy for IBM, AllStripes is laying the foundation to support the efforts of many pharmaceutical companies and researchers.”
Kevin further explains that the easy, organized and secure access to medical records is certain to serve patients with IBM. Most importantly, Kevin believes AllStripes “enables patients to help themselves.”
If you are a patient, or family member of a patient, with IBM and are interested in contributing medical history to advance research, learn more at allstripes.com/ibm.