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2025 Awareness Week

Awareness Week isn’t for those with fibromyalgia, it’s for those who don’t have fibromyalgia, to help them understand what life is like for those of us who do have fibromyalgia

Awareness Week 2025 with Hands holding a purple fibromyalgia awareness ribbon.

2025 Awareness Week

Awareness Week isn’t for those with fibromyalgia, it’s for those who don’t have fibromyalgia, to help them understand what life is like for those of us who do have fibromyalgia. Awareness Week highlights the chronic pain, the overwhelming fatigue, and brain fog that affect our daily functioning, work, and quality of life.

Raising awareness helps employers recognize the effort it takes to  just to show up for work, helps our family and friends understand that appearing “okay” doesn’t mean we aren’t in pain, and explains why socializing can be exhausting.

Awareness Week also informs doctors, researchers, and policymakers about the prevalence of fibromyalgia and the need for support, research, and funding.
By speaking out and rai

Day # 1 - Trudy

Trudy Flynn, Chair of the Fibromyalgia Association Canada (FAC), introduces Fibromyalgia Awareness Week and the “Fresh Start September” theme, focused on self-care and self-management. Throughout the week, FAC Board Members will share how they cope with fibromyalgia, alongside announcements, a peer support session (mindfulness and Qigong), and a roundtable with healthcare professionals.

Trudy shares her personal strategies for managing fibromyalgia, emphasizing the importance of consistent sleep routines, regular (but paced) exercise, and maintaining a positive mindset. She highlights the impact of diet and avoiding allergens, as well as the need for relaxation and stress management to prevent flares. Activities like music, podcasts, and gardening help her relax, though she stresses pacing to avoid overexertion.

Overall, her message encourages individuals to find what works best for them, prioritize self-care, and adapt activities to support their well-being.

Day 2 - Sherry

Sherry, Vice Chair of the Fibromyalgia Association Canada (FAC), shares how she manages fibromyalgia by adapting her self-care to two phases: flare-ups and “doing okay” days. She emphasizes that even on better days, she experiences baseline pain and focuses on preventing flares.
During flares, her key strategies include planning ahead, avoiding overloading herself, saying no to activities, using a self-care kit (like migraine supports, comfort items, and rest), and—most importantly—asking for help and communicating her needs.
On better days, she continues to prioritize planning, setting boundaries (like limiting in-person commitments), pacing tasks, and breaking activities into manageable steps. She also incorporates short, gentle exercise sessions, which help reduce pain over time.
Overall, her approach highlights the importance of pacing, flexibility, self-compassion, and building routines that support both physical and emotional well-being.

Day # 3 - Mary

Mary, a board member of the Fibromyalgia Association Canada, shares that coping with fibromyalgia has required significant life adjustments and acceptance. She focuses on aligning her daily activities with her limitations, emphasizing self-care and planning ahead to reduce strain.

Key strategies include setting realistic expectations (“good enough” instead of perfection), managing sensory overload, pacing activities, and resting when needed. She also uses mobility aids and supports like a shower chair, cane, or walker when necessary.

Overall, her approach centers on acceptance, listening to her body, and adapting her lifestyle to maintain balance and well-being.

Day 4 - Lina

Lina, a board member of Fibromyalgia Association Canada, shares a holistic approach to managing fibromyalgia, focusing on physical, mental, and spiritual well-being.

Physically, Lina adapts her activity levels based on the season and how she feels each day, incorporating gentle stretching, simple exercises, and daily activities like gardening.

Mentally, she manages stress and anxiety by staying connected with others and engaging in uplifting activities, especially spending time in nature.

Spiritually, she finds the greatest support through her faith, community, and time in nature, which bring her peace, purpose, and joy.

Overall, her approach emphasizes flexibility, self-awareness, and nurturing all aspects of well-being.

Day # 5 - Janice

Janice Sumpton from London, Ontario, shares her experience living with fibromyalgia since 2005. Receiving a diagnosis allowed her to learn about the condition, empowering her to manage symptoms and educate others, including medical staff.

She emphasizes the importance of self-education, sharing knowledge, and seeking reliable information. Janice has adapted her lifestyle by giving up physically demanding activities while discovering new coping strategies, like knitting for relaxation and creative distraction, spending time in nature, and maintaining a consistent sleep-wake routine.

Her approach highlights staying curious, exploring enjoyable activities, pacing oneself, and resting as needed to manage daily life with fibromyalgia.

Day 6 - Natasha

Natasha Flynn, a board member of  Fibromyalgia Association Canada, shares her strategies for living with fibromyalgia. Her primary coping method is gentle, paced exercise, such as walking, interval running, swimming, using a sliding elliptical, and light weights, adjusted daily based on how she feels. She emphasizes pacing, recognizing limits, and restarting each day with a fresh mindset.

Natasha also highlights the importance of mindset: staying positive, accepting that some days will be harder, and using music or TV to make activity easier.

Social pacing and consistent effort help prevent flares and maintain energy.

Overall, she focuses on adapting activities, staying active within her limits, and maintaining a positive outlook to manage fibromyalgia and enjoy life.

Day # 7 - Website announcement

Trudy, Chair of the Fibromyalgia Association Canada (FAC), and Sherry, Vice-Chair and web developer, used Fibromyalgia Awareness Week to announce the launch of FAC’s new website at fibrocanada.ca.

Sherry highlighted key features: a refreshed homepage, easy navigation, a translation option (French), search functionality, a menu with organized resources, upcoming events, and members-only content like peer support sessions.

The website includes educational resources for the public and healthcare professionals, updated fact sheets, research summaries, and a FAQ section.

Trudy and Sherry also explained how Canadians can join FAC for free, access member benefits, and volunteer on committees with an onboarding process.

Trudy and Sherry emphasized exploring the site, the new flare kit (upcoming update), and the wealth of resources available. They concluded by congratulating the web development team and teased that a second major announcement would be coming soon.

Day 8 - Charity Status and Wrap up

Trudy, Chair of the Fibromyalgia Association Canada (FAC), marked the close of Fibromyalgia Awareness Week by emphasizing that the week’s purpose is to educate the public, employers, families, and policymakers about the daily challenges of living with fibromyalgia—chronic pain, fatigue, brain fog, and social limitations.

Raising awareness helps improve understanding, care, and advocacy.

She highlighted FAC’s achievements: the launch of the refreshed, user-friendly website (fibrocanada.ca) and FAC’s new charity status, allowing the organization to issue tax receipts to donors, expand outreach, and strengthen support for Canadians living with fibromyalgia.

Trudy also announced upcoming community events:
Sept 16: First peer support/mindfulness session with Lynne Hearte Qigong instructor).
Sept 23: Roundtable with Andrea Furlan (physiatrist), Tyler Dillman (physiotherapist), and Eleanor McGroaty (psychologist) on fibromyalgia self-management.
Oct 1: Fibro chat on self-management with Lynn Cooper and Trudy.
Oct 8: Presentation on insomnia and non-medication sleep strategies with David Gardner (Dalhousie University).

Trudy encouraged members to sign up via the new website, thanked the community for their engagement, and reinforced that FAC is building a strong, supportive community for people living with fibromyalgia.

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