Alzheimer Society of Canada

Yesterday, Canadians across the country came together for our National Day of Action during Alzheimer’s Awareness Month, united by a simple but powerful message: no one should face dementia alone. From sharing photos and wearing Forget-Me-Not pins to speaking up and challenging stigma, people across the country showed what collective action and community can look like. This important conversation was also amplified nationally through our appearance on Global News (bit.ly/4t808iy), helping bring greater awareness to the realities of dementia and the importance of support. We’re deeply grateful to everyone who took part and helped remind people that the Alzheimer Society is always here — for individuals living with dementia, for caregivers, and for families. Thank you for standing with us, and for helping ensure we #ForgetNoOne 💙

Your voice can help shape the rights of people living with dementia, around the world. A global consultation is now open to inform upcoming United Nations discussions on a Convention on the Rights of Older Persons. This is a critical opportunity to ensure the experiences and priorities of people living with dementia—and those who support them—are reflected in what comes next. We encourage you to take part and help strengthen the Canadian voice in this work. Takes 15–20 minutes Deadline: April 15, 2026 On the final page, select “Alzheimer Canada” Take the survey: s.surveyplanet.com/510g29xj Learn more: ageknowble.com/pdf/humanright… Together, we can help advance dignity, inclusion and human rights for all.

Did you know that by 2050, an estimated 1.7 million Canadians will be living with dementia — and roughly 60 % of them are projected to be women? In this insightful Dementia Talks! Canada discussion, experts explore how gender influences dementia risk and symptoms. Age has long been understood as a major factor in dementia, but research is showing there’s more to the story — including how biological and health differences can shape risk, symptom patterns, and care needs. This clip offers clear, evidence-based insight into why women’s brain health deserves attention from research, health systems, and communities across Canada. Watch, learn, and share to help strengthen understanding of brain health — and why equitable research and care matters for all. 💙 Full video available at bit.ly/4kEPbBp

Some cultural moments leave a lasting impact on how dementia is understood. As enter Oscars weekend, we're looking back on Julianne Moore winning an Academy Award for her stunning performance in Still Alice. Still Alice brought dementia into the public conversation in a powerful way, challenging assumptions about who dementia affects and what living with dementia looks like. It helped move understanding beyond stereotypes and encouraged more open dialogue about brain health. At ASC, we know that awareness matters. Thoughtful storytelling and public conversations play an important role in reducing stigma and creating space for understanding, compassion, and earlier engagement with brain health. Read more: bit.ly/4soEfur #Dementia #Oscars #Oscars2026 #Alzheimers #JulianneMoore

On International Women’s Day, we pause to recognize women’s brain health — and the many forces that shape it over a lifetime. From changing biology to daily responsibilities and long-term stress, women’s experiences leave an imprint on brain health. Acknowledging these realities helps guide research, care and support with greater empathy and understanding. When women are supported, care ripples outward — strengthening families, communities and the future we share. #WomenInCanada #DementiaImpact #MoreUnderstanding #SupportCare #InternationalWomensDay

Women’s brains are highly adaptable across the lifespan — shaped by hormones, pregnancy, menopause and caregiving.” - Dr. Liisa Galea Much of what we now know comes from women’s brain health researchers like Dr. Liisa Galea, a senior scientist and professor whose work explores on how women’s brains change across a lifetime and why those changes matter for dementia risk, care and support. Because of generous donors like you, the Alzheimer Society can offer education, caregiver counselling, ongoing support and community-based programs that reflect women’s realities, helping women living with dementia, and the women who so often care for them, feel less alone. Brighten the future of dementia. Donate today at bit.ly/4sgb50o #InternationalWomensDay #WomensBrainHealth #ForgetNoOne #DementiaAwareness #AlzheimerSociety ---- « Le cerveau des femmes doit constamment s’adapter – aux hormones, à la grossesse, à la ménopause, à la parentalité et à la proche aidance. » – Liisa Galea, Ph. D. Les connaissances actuelles sur le sujet viennent principalement de spécialistes en santé cérébrale des femmes – notamment Liisa Galea, une professeure et scientifique d’expérience qui étudie l’évolution du cerveau féminin et son incidence sur les risques de troubles neurocognitifs, ainsi que sur les soins et le soutien aux personnes touchées. Grâce à la générosité de gens comme vous, la Société Alzheimer propose de l’information, de l’accompagnement, du soutien continu et des programmes communautaires adaptés aux femmes vivant avec un trouble neurocognitif et à celles qui en prennent soin au quotidien, afin qu’elles se sentent moins seules. Illuminez leur avenir. Donnez aujourd’hui bit.ly/4udyWQj #JournéeInternationaleDesFemmes #SantéCérébraleDesFemmes #NOublionsPersonne #SensibilisationAuxTNC #SociétéAlzheimer

Dementia is one of the most pressing health and social challenges facing our country. Brain health is shaped across a lifetime: by biology, lived experience, access to care and the systems around us. This month, we’re looking at brain health through the lens of women, who are disproportionately impacted by dementia, both in diagnosis and in caregiving. Because awareness alone isn’t enough. We need investment in research. We need stronger public policy. We need community-based programs. And we need collective action to reduce risk and ensure no one is left without support. The Alzheimer Society of Canada — as part of a federation serving communities nationwide — is advancing brain health, supporting people living with dementia and driving meaningful change. Because brain health is lifelong and no one should face dementia alone. Learn more about our advocacy work at: alzheimer.ca/en/get-involve… #BrainHealthAwarenessMonth #WomensBrainHealth #DementiaInCanada #PublicHealthLeadership #AlzheimerSociety

We are proud to share that the @IGWealthMgmt Walk for Alzheimer’s has been named one of the Top 30 peer-to-peer fundraising programs in Canada for 2025, ranking #8 overall and #4 among walk programs. This recognition reflects the collective effort of volunteers, fundraisers, donors, sponsors, and staff across the country, and the continued partnership and support of IG Wealth Management. Together, we raised over $7.2M to support people living with dementia and their care partners. peertopeerforum.com/canadian-top-t… ---- Nous sommes fiers de partager que la Marche pour l’Alzheimer IG Gestion de patrimoine a été reconnue parmi les 30 meilleurs programmes de collecte de fonds de pair à pair au Canada en 2025, se classant au 8e rang au classement général et au 4e rang parmi les événements de marche. Cette reconnaissance reflète l’effort collectif des bénévoles, des collecteurs et collectrices de fonds, des donateurs et donatrices, du personnel, ainsi que le partenariat et le soutien continus de IG Gestion de patrimoine. Ensemble, nous avons amassé plus de 7,2 M$ pour soutenir les personnes vivant avec la maladie et leurs proches aidants. 🔗 peertopeerforum.com/canadian-top-t…

The @AlzCanada has developed the Diversity and Dementia course for health-care providers and policymakers who would like to learn about dementia care and support within ethno-racialized populations. Access the free course at alzheimer.ca/learn.

Canada’s Drug Agency has issued a draft recommendation against public reimbursement for lecanemab, a new disease-modifying therapy for early-stage Alzheimer’s disease that received conditional approval from Health Canada last fall. "People living with early-stage Alzheimer's disease and their care partners have consistently told us that slowing disease progression and preserving autonomy matter deeply," said Christina Scicluna, CEO, Alzheimer Society of Canada. "While evidence-based review processes are essential given the limited treatment options available, this decision reinforces the need for more equitable access to treatments for those who need it most." This decision will be open for public feedback until March 5th before a final recommendation will be determined. Read our full response to the draft recommendation on our website, where you can also find the CDA link for public feedback, and learn more about Lecanemab: alzheimer.ca/en/about-us/na…

When life changes, love finds a way. When one partner is living with dementia, a couple’s relationship can change in deeply personal ways. Communication, roles, and daily routines may shift, and partners may grieve what once felt familiar. At the same time, emotional closeness, affection, and shared moments can still hold meaning. With understanding, patience, and support, couples can adapt together — finding new ways to express love, maintain connection, and honour their relationship through change. The Alzheimer Society of Canada offers guidance to help couples navigate these transitions with compassion and respect throughout the dementia journey. Read more: bit.ly/4krMGCi

The Alzheimer Society is your first step in finding the right information, support and education. We are excited to share that we have developed Diversity and Dementia, a new course that explores how social and systemic inequities disproportionately affect dementia care and support for ethno-racialized communities in Canada. It highlights strategies to better support these communities. Access the course for free at alzheimer.ca/learn. ---- La Société Alzheimer est votre premier contact vers les renseignements, le soutien et l’éducation dont vous avez besoin. Nous avons le plaisir d’annoncer que nous avons élaboré un nouveau cours, Diversité et troubles neurocognitifs, qui porte sur les conséquences disproportionnées des inégalités sociales et systémiques sur les soins et le soutien offerts aux personnes touchées par les troubles neurocognitifs dans les communautés ethnoracisées du Canada. Il propose également des stratégies pour mieux soutenir ces communautés. Suivez gratuitement le cours à alzheimer.ca/apprendre.

As dementia progresses, change can reach beyond routines and roles: touching friendships, relationships and the wider circle of connection. Caregivers may struggle to know what to say or how to help. People living with dementia may begin to feel isolated over time. With encouragement and support, people can keep inviting others in and remember they are not alone. At the Alzheimer Society, we show up in those critical moments — offering understanding, guidance and connection. Make a difference today. Donate to help ensure this support remains available at bit.ly/3M3PCIM ----- Les troubles neurocognitifs ne changent pas que les routines et les rôles dans le foyer; ils peuvent aussi transformer les amitiés et les relations hors du noyau familial. Les proches aidant·es ne savent pas quoi dire ni comment agir ou aider, et les personnes touchées finissent souvent par se sentir seules. Avec de l’encouragement et du soutien, elles peuvent toutefois continuer à aller vers les autres et se rappeler qu’elles ne sont pas seules. La Société Alzheimer les accompagne dans ces moments critiques en offrant compréhension, accompagnement et soutien. Contribuez dès aujourd’hui. Cliquez au bit.ly/4r6iTld pour faire un don et ainsi favoriser l’accessibilité du soutien pour les troubles neurocognitifs.

When life changes, love finds a way. When a family member is living with dementia, children and teens are affected too — even if they don’t always have the words to express how they feel. They may notice changes in behaviour, routines, or family dynamics, and experience confusion, worry, or sadness as life begins to look different. With honest, age-appropriate information and reassurance, young people can better understand what’s happening and feel supported — knowing that love and connection remain, even as circumstances change. The Alzheimer Society of Canada offers resources to help children and teens learn about dementia, share their feelings, and know they are not alone. Learn more: bit.ly/4krMGCi

“We’re equals. She inspires me in everything.” — Walter Gowing For Walter and Lillian, love has always been about partnership: creating, exploring, and living life side by side. Today, that partnership continues through care, compassion, and unwavering support as they face dementia together. Because when life changes, love finds a way.

Health-care providers, policymakers, and those involved in dementia care and planning play a vital role in ensuring equitable access to dementia care and support. To further this commitment, the Alzheimer Society of Canada has launched a new course designed to explore the impact of social and systemic inequities in dementia care for ethno-racialized communities in Canada. It includes strategies to better support these communities through more inclusive, culturally safe practices. Access the Diversity and Dementia course for free at alzheimer.ca/learn ---- Les prestataires de soins, les décideur·euses et les personnes assurant et planifiant les soins aux personnes vivant avec un trouble neurocognitif jouent un rôle vital pour garantir un accès équitable aux soins et au soutien. Pour appuyer leurs efforts, la Société Alzheimer du Canada lance un nouveau cours qui porte sur les conséquences des inégalités sociales et systémiques sur les soins offerts aux personnes touchées par les troubles neurocognitifs dans les communautés ethnoracisées du Canada. Le cours propose également des stratégies d’adoption de pratiques plus inclusives et adaptées aux cultures, qui soutiendront mieux ces communautés. Suivez gratuitement le cours Diversité et troubles neurocognitifs à alzheimer.ca/apprendre.

As dementia changes daily life, communication may change too. A person with dementia may repeat a question. Conversations may feel harder to follow. But connection often shows up in other ways — a shared look that says, “I’m here.” Having trusted support during these moments can ease uncertainty and help families feel grounded as they adapt. The Alzheimer Society helps make connection possible when communication might not be. Help keep dementia support within reach. Make a one-time or monthly gift today at bit.ly/3M3PCIM ----- Quand les troubles neurocognitifs redessinent le quotidien, la façon de communiquer se transforme aussi. Les questions commencent à se répéter, les conversations deviennent plus dures à suivre. Dans ces moments, le lien se manifeste souvent autrement, par exemple par un regard partagé qui dit simplement : « Je suis là ». La transition peut être déstabilisante, et les familles qui la vivent bénéficient grandement d’un soutien fiable. La Société Alzheimer aide à maintenir la connexion, même lorsque la communication est difficile. Favorisez l’accessibilité du soutien pour les troubles neurocognitifs. Faites un don ponctuel ou mensuel dès aujourd’hui en cliquant sur le lien dans notre bio ou en vous rendant au bit.ly/4r6iTld.

This Valentine’s Day, we’re celebrating the power of community — and the role you play in it. Your generosity helps create a network of care where people living with dementia, their families, and caregivers can find understanding, connection, and support at every stage of the journey. Because of you, individuals are met with compassion, families are reminded they are not alone, and communities grow stronger through shared care and kindness. Thank you for being part of the Alzheimer Society of Canada community and for showing, in so many meaningful ways, that love truly makes a difference.

When life begins to change because of dementia, people learn new ways of showing care. Love takes on new forms. Changes often arrive quietly: a routine that no longer looks the same, a role that shifts, a conversation that takes more time. These small moments can slowly reshape daily life. That’s why the Alzheimer Society is here. From early signs, to understanding a diagnosis and through the progression of dementia. With trusted support, change doesn’t have to feel overwhelming. Your gift helps ensure support is there: and that when life changes, love finds a way. Donate today to help people affected by dementia across Canada at bit.ly/3M3PCIM --- Quand les troubles neurocognitifs s’installent, la vie change, et avec elle, la manière d’exprimer l’attention… et l’amour. Sans crier gare, la routine se transforme, les rôles se redéfinissent, les échanges demandent plus de temps. Tous ces petits moments finissent par transformer le quotidien. La Société Alzheimer est là pour vous aider. C’est sa raison d’être : offrir un accompagnement, depuis les premiers signes jusqu’aux stades avancés en passant par le diagnostic. Avec un soutien adéquat, le changement peut se faire en douceur. Votre générosité permet d’offrir ce soutien et de montrer que même quand tout change, l’amour persiste. Tendons la main aux personnes touchées par les troubles neurocognitifs au Canada : donnez dès aujourd’hui au bit.ly/4r6iTld

When life changes, love finds a way. Anger can surface for many people affected by dementia — often rooted in stress, exhaustion, shifting roles, or the uncertainty that comes with change. These emotions are a normal response to a challenging situation, and recognizing them is an important step toward coping. With understanding, patience, and the right support, families can find healthier ways to respond — protecting both their own well-being and their relationships with those they care for. The Alzheimer Society of Canada provides trusted information and resources to help individuals and families manage difficult emotions with respect, empathy, and care. Read more at: alzheimer.ca/en/help-inform…

Walter Gowing shows us what love in action looks like. As his wife Lillian lives with dementia, Walter remains by her side every day: offering support, companionship, and unwavering devotion. He also extends that care to others, volunteering in Memory Care and giving back to the Alzheimer Society of Canada to help families facing similar journeys. Because love doesn’t disappear when life changes — it finds new ways to show up.