We are honoured & humbled to receive the generous donation of $3560 from Christina's Lights and the Paul Family. Their story has brought together the Grimsby community and far beyond in memory of their beloved daughter Christina who continues to touch the lives of many. Thank you

The MS Society of Canada recognizes that depression can be a symptom of MS. On #BellLetsTalk Day, we want to remind you that it's okay to ask for help. Our MS Navigators are here to direct you to resources for support. Contact us at 1-844-859-6789 or [email protected].

Thousands of Canadians with MS struggle to manage their mental health in the face of an unpredictable disease. On #BellLetsTalk Day, we want you to know that you’re not alone. Our MS Navigators can help you find support for your mental health concerns. Contact 1-844-859-6789.

Yesterday we visited an elementary school to chat about MS. When the children were asked what symptoms they think people living with MS experience, their answers were: frustration, sadness, & fear. These crucial experiences are not often focused on, but are so real. #BellLetsTalk

Participants needed for study on robotic rehab training for multiple sclerosis | brocku.ca/brock-news/202… #brocku

"MS can rob you of a lot of things, but it can't take away true love. My fiancé Adam is not with me because he has to be, he's with me because he wants to be - with or without MS." - Estelle, diagnosed in 2019 Read more about their story here: bit.ly/37sAbzg

This is what happens when a community comes together to support Canadians living with MS. Adam Goldberg, who lives with MS, asked his followers for birthday wishes & donations to #MSWalk. With the support of his community, he has raised more than $2400! Thank you for your support!

"As a woman, I feel we should emphasize the importance of sexual health and well-being for all women living with this disease. This means more research on women’s health and MS.” Read more about women and MS in our latest blog post: bit.ly/2vDSAfD

Women are 3x more likely to be diagnosed with MS than men. Today we are proud to celebrate the empowerment of women around the world with over 700 men and women in Niagara at #IWD2020. Visit our website to read more about MS and women’s health mssociety.ca

We’re delighted to announce the launch of the MS Society Young Adult Committee and to welcome our 2020/21 committee members! Young Canadians affected by MS are looking to change the narrative for young people affected by the disease. Reply to give them a warm welcome!

Join us at your local Mandarin restaurant on March 25th for 50% off your buffet meal! All you have to do is register for the MS Walk before March 25th! Register at mswalks.ca or call us for more information. See you on March 25th & May 3rd! eatmandarin

What does COVID-19 mean for people living with MS? For information, visit: mssociety.ca/resources/news…, or contact our MS Navigators at 1-844-859-6789 or [email protected]. You can also read the MSIF’s global COVID-19 advice for people with MS: mssociety.ca/library/docume…

What does COVID-19 mean for people living with MS? Visit mssociety.ca or contact our MS Navigators at 1-844-859-6789 or [email protected]. Slow the spread of #COVID19 and practice social distancing.

An important message from Pam Valentine, President and CEO of the MS Society:

Anyone else missing social interaction right about now? We miss our MS community! Drop a selfie below - we want to see your faces 👇

Due to the unpredictable nature of the disease, managing one's MS during #COVID19 can be stressful and challenging. Read the National MS Society's checklist of tips and resources to help you manage your MS through this uncertain time: bit.ly/2UpzcLS #MSCOVID19

It's #WorldHealthDay! Take a minute to say #ThanksHealthHeroes! pscp.tv/w/cVsbFjI2MTAy…

On #WorldHealthDay, let's support those who are at the forefront of this pandemic. Thank you to our frontline healthcare workers including Christa, a long-term care nurse whose son lives with MS, along with other nurses, doctors, support staff, cleaning staff, and more.

On #NationalCaregiverDay, the MS Society, Alzheimer Society of Canada, and Parkinson Canada bring you an all-new podcast, showcasing insightful stories of people caring for a loved one living with a debilitating disease. Listen to April’s story: bit.ly/2UOXAql

Do not hesitate to call or email us at any time if we can support you. Call 905-937-7772 or email [email protected]