Articles

Right now most of you are rejoicing that summer is over, because it finally means getting some relief from the symptoms that come along with being overheated. However, I seem to...

So this is something I noticed in 2013 when I first traveled to Ireland. Ireland was experiencing an extended winter, so it was an average of 32 degrees outside. It...

Whether you are newly diagnosed or have been living with multiple sclerosis for many years, MSAA understands that each person's journey with MS is unique. We also know it can...

Explaining what it’s like to live with multiple sclerosis (MS) can often be difficult…and frustrating. We recently asked our community what they wanted others to know about MS. Here's what...

When people talk about Multiple Sclerosis, they often talk about the difficulties of getting people to believe them or understand them when it comes to describing a certain symptom. Is...

I have spent so many years in school that at this point, it’s just best not to think about it too much. I can’t help it! I love learning new...

Even before my Multiple Sclerosis years, I was told this all the time as I have always dealt with serious depression. “You just got to try to stay positive”. “Stay...

PML and the JC virus have been in the headlines a lot lately following the death of a person taking Tecfidera. Today, I want to focus on PML, the JC virus, and...

The Multiple Sclerosis Association of America (MSAA) is excited to announce the launch of a new website section dedicated exclusively to helping the MS community better understand and utilize health...

The immune system is a fascinating and complex thing! In fact, scientists still have a lot to learn about the immune system and autoimmune diseases. But we do know it...

A newly diagnosed person was asking about fatigue and I went looking for information to share.  In the process, I learned a few new things about MS fatigue, but first...

I not long ago talked about MS-related fatigue and lassitude; I mentioned how taking Nuvigil (Armodafinil) seems to be my personal solution to my fatigue/lassitude. What I may not have...

I have a theory that education leads to empowerment, and empowerment leads to people being good advocates for themselves and improved health overall. It can be hard for healthcare providers...

Let’s face it, dealing with the changes to life that multiple sclerosis brings is hard enough but when the day comes that you may start having trouble with mobility those...

Of late, the MS has been giving me a pretty good a** whuppin'. It's getting harder for me to stumble around my apartment, and I'm pretty close to making the...

I think that there is a lot of contradiction on this specific topic/symptom when it comes to MS. For a long time, it was believed that those with MS did...

As a co-moderator of an active private MS Facebook group, I lend my voice by posting articles on the latest research, and sharing articles that I write, about living with...

Some days, I have to remind myself that I’m a young girl in her mid-20s. Some days, my body makes me feel like I’m much older than I really am...

Starting in December 2013, when winter launched itself in SE Michigan with single digit temps and hat-high piles of snow, my mother and I locked horns in a power struggle...

A shocking 67% of people with multiple sclerosis know what it is like to live with chronic pain. There are many different causes of MS pain such as muscle spasms, MS “hugs”,migraines...