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By Dr. Eva Jackson Every MS diagnosis begins with a different story. For me, the diagnosis brought an unexpected sense of relief. After seven long years of searching for answers, I...
“I am so grateful for this community and the wonderful people here. It has been life-changing for me to have so much support, be able to help others, and to find great resources. B...
There is a beautiful, humbling irony in the rhythm of my life. When I was in my 20s, Bike MS — a cycling series to raise money for multiple sclerosis (MS) research and support that...
By Stacie Prada When looking for things to do in the summer months, I think of my favorite experiences and memories. Some were big, pricey events with lots of planning, and some co...
Note: This column describes the author’s own experiences with phototherapy. Not everyone will have the same response. Consult your doctor before starting or stopping any therapy. R...
MSAA features the work of many talented artists affected by multiple sclerosis as part of our annual MSAA Art Showcase. Each month we share these artists’ inspiring stories and bea...
Living with a chronic illness means mastering a complicated dance. For individuals navigating multiple sclerosis (MS), that dance includes an uninvited partner who constantly chang...
By Angel Blair When it comes to relationships, it’s important to surround yourself with people you feel comfortable with and enjoy being in the company of. The great part about thi...
By Dan and Jennifer Digmann To us, community is more than a group of people who happen to live in the same town, attend the same church, share an interest, or know our story. Commu...
Physician and MS patient Annie Brewster, MD, explains how living with multiple sclerosis transformed her approach to medicine. She emphasizes listening, empathy, and storytelling a...
By Stacie Prada When I think of my community, I first think of where I live, my friends and neighbors who will show up for me, and those I’m compelled to show up for. In times of c...
By Angel Blair It’s that time of year again— the peak of the summer months is upon us. For those living with MS affected by the heat, staying cool becomes top priority. And for ind...
Multiple sclerosis (MS) support groups allow those with the condition to share their experiences and feelings with each other. Most organizations that provide information about MS,...
The post Getting to Know You Survey appeared first on Multiple Sclerosis News Today.
By Nicole Robinson Summer looks a little different when you are living with multiple sclerosis. The heat, the fatigue, the unpredictability of symptoms – it all factors into how I...
I’m drowning. Well, not literally. I’ve never even come close to actually drowning — not even with last year’s pneumonia and the occasional aspiration of liquids. I’m just using it...
By Susanna C. Editor’s Note: The story in this week’s blog post comes from a 2013 issue of New Beginnings in magazine form. La Leche League News, a bimonthly LLLI publication for m...
It’s funny how multiple sclerosis (MS) has a way of silencing me. Since my diagnosis in 2016, I’ve felt as if something else has been speaking, moving, and living through me. Altho...
Contrary to popular belief, I did not attend this year’s Consortium of Multiple Sclerosis Centers (CMSC) annual meeting just for the buffets and to loot the vendors. I was there ma...
By Dr. Eva Jackson Have you ever wanted to free yourself from your daily routine, but an elaborate vacation was not within your budget? Maybe your family and friends do not have th...
Fadekemi Adeleye is an Assistant Psychologist in the BartsMS Team, working in research and running the remote assessment programme. Her journey to Barts started with studying psych...
Recently, after I shared some of the harder parts of caring for my husband, Rhead, a stranger left a comment on a recent column implying that I was simply monetizing his multiple s...
The most dreaded part of my year has arrived yet again: MRI time. Since I was diagnosed with multiple sclerosis (MS) in 2016, I have undergone at least one MRI every year to monito...
MSAA features the work of many talented artists affected by multiple sclerosis as part of our annual MSAA Art Showcase. Each month we share these artists’ inspiring stories and bea...
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