awareness

Multiple sclerosis awareness is for people with MS, too

The Cambridge Dictionary defines awareness as “knowledge that something exists, or understanding of a situation or subject at the present time based on information or experience.” That definition perfectly matches the stages of my personal awareness of multiple sclerosis (MS). I don’t recall hearing much, if anything, about…

New bilingual graphic aims to raise awareness of early MS symptoms

A bilingual graphic educational message, dubbed VISIBL-MS, has been developed by researchers at the University of Connecticut (UConn) to raise awareness about the early symptoms of multiple sclerosisĀ (MS). The graphic ā€” bearing the word ā€œVISIBLYā€ in English and ā€œVISIBLEā€ in Spanish ā€” uses the letters in each phrase…

MS awareness events are an opportunity to build understanding

We’ve all heard comments from people who aren’t educated about multiple sclerosis (MS). Some that I’ve heard include “My friend had that and is fine now,” “Eating better will fix you,” and “Try a parasite cleanse.” I have to chuckle at these statements.Ā  With March not far away,…

One Month of MS Awareness Isn’t Enough

I’m changing my mind about MS Awareness Month ā€” at least a little ā€” thanks to “31 Days of MS.” Whether it’s an awareness month or a week, or whether it’s for MS or disabilities in general, I’ve never been a big fan of these types of initiatives. But this…

Autoimmune Patients Want Clearer COVID-19 Vaccine Info

Patients with autoimmune diseases, including multiple sclerosis (MS), are uncertain about how to protect themselves against COVID-19, especially with regards to booster shots of the vaccine. According to a national survey by the nonprofit Alliance for Patient Access, these patients are confused due to conflicting information from the…

MS Advocacy Gives Me Strength and Purpose

I want to help in any way I possibly can. My lonely confusion in the early days after being diagnosed with aggressive relapsing-remitting multiple sclerosis was mentally and physically paralyzing. However, this column isnā€™t about how ā€œHurricane MSā€ battered my body. Instead, it’s about why I chose to…

MS Society to Hold Black MS Experience Summit

The National Multiple Sclerosis Society will host the second edition of its Black MS Experience Summit, a virtual event to help forge connections among those who understand the experience of living with multiple sclerosis (MS) as a Black person. Register hereĀ to join the interactive, two-day…

World MS Day, May 30, Goes On … But Online

Despite the COVID-19Ā pandemic, there are many ways to participate inĀ World MS Day 2020Ā on May 30, set aside to raise awareness about the neurodegenerative disorder that affects more than 2.3 million people globally. Organized by the MS International Federation (MSIF), the event brings together the global…

Sex and Intimacy Is Focus of MSAA Webinar

Sex and intimacy are good for people with multiple sclerosis (MS), just as they are for anyone without the disease. And while fear of talking with a partner about possible sexual challenges created by MS is perfectly normal, there is help available to deal with potential problems. Thatā€™s according…

Visibly Me, Visible MS

Multiple Sclerosis Awareness Month has arrived, lasting throughout the month of March. All things orange and popular hashtags flood social media sites. Awareness months like this have great value, though some may disagree. Awareness months become vessels to engage and encourage individuals and communities to get involved.

Thinking About Selma Blair and Her MS

By now you may have heard that actress Selma Blair has revealed that she has multiple sclerosis (MS). That took a lot of guts. Those of us who share her diagnosis might learn a few things from what she’s shared and how she’s shared it. Blair may be…