MS Society Grande Prairie

Many government programs are created to address injury rather than chronic disease. My healthcare team had trouble helping me access them because so many of the requirements are irrelevant to people who live with MS or another chronic disease. I imagine this creates more back and forth between insurance providers and doctors and in turn increases the burden on an already-taxed health system, particularly the chronic disease specialists. I also worry about how many people are... wrongly denied access to these programs or simply get tied up in the process longer than necessary. Nicole Nicole was diagnosed with MS in 2012. While she’s lucky to have a generous employer with an extended sick leave policy, not everyone is so fortunate. Many Canadians rely on public programs like the Employment Insurance (EI) sickness benefit when they encounter personal health challenges that impact their ability to work. Unfortunately, for too many Canadians the inadequate length of time provided under the EI sickness benefit framework and other gaps in our social support systems means that they can’t use the program in the way it was intended, to help keep them working as long as they are able. The #TakeActionForMS campaign calls on the federal government to address these gaps in our support system which have always existed but were brought into stark focus by the COVID-19 pandemic. It’s time for our federal government to #TakeActionForMS by extending the EI sickness benefit period up to at least 26 weeks. Join the campaign and #TakeActionForMS today: https://bit.ly/3o3lBHt See more

Today, we kick off our #MSConnect conference as keynote speaker, Dr. Jack Antel, McGill University, and Dr. Pamela Valentine, President and CEO, MS Society of Canada, lead the welcome session Building on progress in MS research - a multi-discipline effort. This week, you can connect, discuss, and learn about current MS research with the MS community people living with and affected by MS, health professionals, and researchers. Topics will include: neurorehabilitation and MS, cognition, nutrition, fatigue, and more. There’s still time to register. Register now for the 6:30pm ET/3:30pm PT start: https://bit.ly/3flaGp2.

Help unlock the future of medical cannabis treatment for multiple sclerosis. The University of Alberta is seeking participants for a research study exploring ca...nnabis use in people with multiple sclerosis. U of A researchers need people with MS to share their experiences and attitudes toward medical cannabis, whether they have used it or not. Participation requires filling out an anonymous online survey that should take only 10 minutes to complete. For more information, check out our research portal and complete the survey by December 31: bit.ly/35zkCYQ

If you could describe MS fatigue in one sentence, how would you explain it? Approximately 90% of people living with MS experience fatigue. MS fatigue can have a negative impact on work, family life, mental and physical health and social and recreational activities. On Friday, November 27th from 11 AM 12 PM ET, join Dr. Marcia Finlayson for an informative panel discussion on fatigue management as a part of our virtual MS Connect conference. Fatigue management is gaining ...more attention in the MS research community and a wider variety of approaches are being evaluated and tested for effectiveness. My panel discussion will address what we know about MS fatigue and the new directions being explored to help fatigue management. Sleep has a lot to do with fatigue, but we don’t study sleep much in this disease. I’ll be discussing how the interest in sleep is beginning to grow. - Dr. Marcia Finlayson, Queen’s University Register for Fatigue: Research Session and Q&A and the rest of our MS Connect sessions here: https://bit.ly/32frvwr. See more

Q: How has MS affected your dating life? A: Dating is already difficult, but with MS, it’s become a daunting reality. I’ve found myself asking questions like w...hen should I tell them about my MS? or how soon is too soon? You never know how the other person will react. In my opinion, telling them earlier is better. I want to respect their time, so they should know before things get too serious. With or without MS, there is always a fear of being rejected. But if I told someone about my diagnosis and they responded negatively, I know that they aren’t the person for me. Observing the reactions almost serve as a filter, helping weed out the people who I feel might not grasp compassion or understand my situation. The person I date should be okay with accommodating my needs when I need to take care of myself. I've become a lot more guarded when it comes to meeting new people, but I'm slowly learning to embrace the vulnerability. With many impacted by MS during the formative years of their adult lives, millennials are not alone in the fight against MS. In 2020, millennials with MS are diving into the workforce, starting families, and advancing their education all during the biggest global crisis of the last century. In our latest blog series ‘Millennials and MS’, we sit down with young adults across Canada to discuss topics such as self-care, social media, mental health, and more to hear what they have to say about life with MS. This week, we sat down with Trish Yeung, a 30-year old woman living with MS, who has turned to mindfulness and meditation to support her through her MS journey. Read Trish's story: bit.ly/2UAiHNs

The MS Society’s Young Adult Committee, a voice for young people affected by MS to help enact change, asks you to be a part of the movement: #TakeActionForMS! As young adults, work is an important part of our lives. We want to contribute to our communities, but we need help to remain part of the workforce. As a person with multiple sclerosis, the episodic nature of our disease can affect our career path. The Employment Insurance sickness benefit framework, in its current state, does not work for everyone, including many people with MS. Send an email to your Member of Parliament asking to extend the EI sickness benefit period from 15 to at least 26 weeks! Send your email now https://bit.ly/34XfD3Q. Let's act together! Let's be the movement! Let's #TakeActionForMS!

In the 70s, Canadian workers gained access to 15 weeks of paid leave under the newly-created Employment Insurance (EI) sickness benefit. Fifty years later, the benefit remains virtually unchanged. The EI sickness benefit allows Canadians who are impacted by a personal health issue to adjust their work status and access financial support while focusing on their medical needs. Once an employee has worked 600 hours in the previous year, they are eligible to access the sickness b...enefit, which dispenses 55 per cent of insured wages for a maximum of 15 weeks. Once the 15 weeks are up, an employee must requalify by logging another 600 hours of work. As it stands, 15 weeks is too short a time-frame for many people with chronic conditions like MS to adequately recover given existing coverage gaps, and overall, Canada’s EI sickness benefit lags behind supports found in other countries. The #TakeActionForMS campaign is calling on the federal government to extend the EI sickness benefit to at least 26 weeks. We’re advocating for crucial changes to help ensure people who live with MS and want to continue working are able to do so. Take five minutes to email your Member of Parliament asking them to #TakeActionForMS today. Join the campaign: https://bit.ly/38Oj6nV. See more

International Day of Persons with Disabilities is virtual this year. The guest speaker Patrycia is an individual who lives with MS and will share her story. The zoom link https://zoom.us/j/94298733964

When it comes to my MS, what works for me is being open and honest about my mental health. When you’re battling a chronic disease and feel like your life as yo...u know it is being taken away, to say you’re emotionally affected is an understatement. Research has shown the link between living with MS and depression, and that’s why it’s critical for me to have strong coping skills and a loving support system. Researching lifestyle modifications and applying it to my own life enables me to take control of my health, which otherwise would be out of my hands. - Amanda, MS Society Young Adult Committee member As young adults try to manage MS, along with other aspects of life, prioritizing the importance of informed lifestyle decisions that can alleviate the impact of MS and minimize its progression is critical. On Friday, November 27 from 4:30-5:30 pm ET, join the MS Society’s Young Adult Committee in welcoming an expert panel of speakers who will provide an overview of relevant research in lifestyle modification and tips on how to apply them. Topics will include: exercise and physical activity, mental health, diet and nutrition, and research, and the panel presentation will be followed by a Q&A session. Register for the session here: https://bit.ly/388cyQF. Following the panel, there will be a Young Adult Social Engagement Session, where you can connect with other young adults from across Canada, talk about the information presented in the panel, and discuss what’s important to young adults affected by MS.

Did you know that women are three times more likely to be diagnosed with MS than men? It’s time for a change. By attending #WAMS you help build awareness and r...aise much needed funds to support people affected by MS. Show your support and purchase tickets for the Gala on November 20 and get access to the weekly Speaker Series leading upto the Gala: wamsgala.ca