The definition of multiple sclerosis (MS) itself describes one of the challenges of this chronic illness.
A good relationship between persons living with multiple sclerosis (MS) and their healthcare providers (HCPs) leads to better health outcomes.
People living with MS are used to being told unfavorable healthcare news. From the time of diagnosis, we are prepared for bad test results to appear.
For persons living with a chronic illness, such as multiple sclerosis (MS), the relationship with a primary physician is only one of many.
Finding a sport to watch that includes people who look like me, a Duchenne muscular dystrophy (DMD) patient, is difficult.
Multiple sclerosis (MS) made me a member of a club I never wanted to join, and I am going to share my advice with new members.
When I found out I had multiple sclerosis (MS), I was in shock. It took some time for my diagnosis to sink in.
It is lonely when you have a rare disease. To know that there are people out there supporting patients, like me, is comforting.
Lassitude interferes with many multiple sclerosis patients to the point that they are unable to work and are forced to leave their jobs.