March 6, 2023 News by Marisa Wexler, MS ACTRIMS 2023: Can Do MS brings education, connection, activation Can Do MS has three missions for people with multiple sclerosis (MS) and their care partners ā providing education about life with the disease, building connections among people, and activating them to be proactive about managing their condition. “Those are the three pillars that our programs are built…
July 7, 2022 Columns by Benjamin Hofmeister The MS Paradox Results in Many Conflicting Feelings āThanks, I hate it.ā Odd way to begin a column, I know. I suppose Iād better explain myself. That phrase regularly appears in memes and other pop culture media as an expression of dislike for an image or tweet. No one seems to know where or from whom it…
December 28, 2021 News by Margarida Maia, PhD Donations to MS Society of Canada Triple in Value Through Dec. 31 Donations to the Multiple Sclerosis Society of Canada through the end of this year will be double matched, meaning each donation will go three times as far in supporting Canadians with multiple sclerosis (MS) and in advancing research into the disease. All donations received until midnight on Dec.
August 20, 2021 Columns by Jamie Hughes Celebrity or Not, You Matter to the MS Community Christina Applegate, star of classic ’90s films like āDonāt Tell Mom the Babysitterās Deadā and TV shows like āMarried with Children,ā announced last week that she had been diagnosed with multiple sclerosis at age 49. She didnāt share much beyond that, only that itās been āa tough roadā since…
August 3, 2021 Columns by Jessie Ace The Beginning of the End: A Reminder to #StayENabled Itās with a heavy heart that I write this.Ā I donāt want to, but I have to do what’s right. This will be my last column. Lately, things have been crazy busy for me, with a mix of expected events, such as moving to a new home, and a few unexpected…
October 20, 2020 Columns by Jessie Ace Finding Support in an Online Community Finding an understanding community makes such a difference to people diagnosed with multiple sclerosis (MS).Ā Our partners, families, children, and friends do their best to listen and empathize, but at the end of the day, they can only empathize so much. Unless they have an illness…
June 6, 2019 Columns by Jennifer (Jenn) Powell Consortium for a Cure: Witnessing Hope Our emotional selves are unique to each of us. The catalysts that elicit tears and fears vary. We feel emotions rise and await their eruption. Contrarily, they can catch us off guard. Sometimes a seemingly benign stimulus can invoke strong feelings. I should know better than to assume that anything…
February 18, 2019 Columns by Debi Wilson Being Kind to Others with MS Can Help Our Own Well-being Sometimes I feel that some in the multiple sclerosis (MS) community do not show kindness to each other. Perhaps they canāt relate to others’ MS realities because their symptoms are dissimilar or they have a different disease type. I have witnessed interactions between people with MS in which one…
January 6, 2016 News by Patricia Silva, PhD Multiple Sclerosis Association of America Appoints New President and CEO The Multiple Sclerosis Association of America (MSAA), a national nonprofit organization and leading resource for the multiple sclerosis (MS) community, recently announced thatĀ Gina Ross MurdochĀ has been namedĀ the association’s new president and CEO. Ms. Murdoch is nowĀ the MSAAās leader in areas comprising strategic progress, programmatic growth, and business development strategies.