• About Us
  • Education
  • Programs
  • Get Involved
  • Events
    • TradeUp Challenge
    • Purple Day
  • News
  • Shop
  • Contact
  • About Us
  • Education
  • Programs
  • Get Involved
  • Events
    • All Events
    • TradeUp Challenge
    • Purple Day
  • News
  • Shop
  • Contact
  • Donate

  • About Us
  • Education
  • Programs
  • Get Involved
  • Events
    • TradeUp Challenge
    • Purple Day
  • News
  • Shop
  • Contact
  • About Us
  • Education
  • Programs
  • Get Involved
  • Events
    • All Events
    • TradeUp Challenge
    • Purple Day
  • News
  • Shop
  • Contact
  • Donate

  • About Us
  • Education
  • Programs
  • Get Involved
  • Events
    • TradeUp Challenge
    • Purple Day
  • News
  • Shop
  • Contact
  • About Us
  • Education
  • Programs
  • Get Involved
  • Events
    • All Events
    • TradeUp Challenge
    • Purple Day
  • News
  • Shop
  • Contact
  • Donate
Home / Apparel / Kids

Kids

No products were found matching your selection.

Recent Posts

  • Improving Online Accessibility for Individuals with Photosensitive Epilepsy
  • Healing Harmonies: Exploring Music’s Potential in Epilepsy Therapy

Recent Comments

No comments to show.

epilepsycalgary

We provide support services to people with Epilepsy that do not exist elsewhere in Calgary and Southern AB.

Family Day is a chance to recognize the people who Family Day is a chance to recognize the people who support, encourage, and stand beside us in meaningful ways. At the Epilepsy Association of Calgary, we are grateful for the families, caregivers, and communities that continue to uplift those living with epilepsy. Their support makes a real difference.

Our offices will be closed on Family Day, February 16, 2026, so our staff can spend time with their own families. We will reopen on the following business day and continue to provide information, programs, and support to the epilepsy community.

If you need information about our services, please visit our website or contact us at programs@epilepsycalgary.com and we will respond when we return.
Did you know? St. Valentine is the Patron Saint o Did you know?

St. Valentine is the Patron Saint of Epilepsy. 

A story that appears several times in different books of the New Testament has Jesus Christ exorcise a demon from a figure frequently interpreted today to have had epilepsy--though there was little understanding and no diagnosis at the time. Over time dozens of saints became associated with healing the ill who may have been epileptic. In the Medieval period, a St. Valentine is venerated who is often represented in art with someone who would today be seen as epileptic, the epileptic usually lying at his feet. (ref. Dr. C. Churchill)

Today, Valentine’s Day reminds us of the importance of genuine care and connection. At the Epilepsy Association of Calgary, we support individuals and families who live with epilepsy, and we recognize the strength it takes to navigate this condition every day.

Use today as an opportunity to appreciate the people who stand beside us. Love can look like listening, learning, and offering steady support. For many in our community, it also looks like advocating for understanding and reducing stigma.
If you or someone you know is living with epilepsy, our team is here to provide information, programs, and support throughout the year. You are not alone, and your experiences matter. To learn more or connect with us, please contact programs@epilepsycalgary.com. 
Happy Valentines Day everyone.
Take the pledge and help spread epilepsy awareness Take the pledge and help spread epilepsy awareness and education in your community. 

Purple Day - National Day for epilepsy awareness is coming up March 26.

#ilae #epilepsyawareness #internationalepilepsyday #spreadtheword #takethepledge #globalimpact #purpleday #epilepsycalgary
The 2026 Winter Olympics begin today in Milan–Cort The 2026 Winter Olympics begin today in Milan–Cortina, Italy, marking the official start of 16 days of international competition across 116 events.

As the world turns its attention to these Games, we are reflecting on the qualities that define both Olympic athletes and people living with epilepsy: focus, determination, and the ability to persevere through challenges.

At the Epilepsy Association of Calgary, we recognize that many in our community demonstrate these strengths every day. While athletes prepare for competition, individuals and families affected by epilepsy continue navigating their own demanding realities, often quietly and without public recognition.

During this Olympic season, we aim to amplify awareness, reinforce community support, and remind Calgarians that no one managing epilepsy should have to do so on their own. If you would like to learn more about our programs or connect with our team, reach out anytime at programs@epilepsycalgary.com.
February is here, the shortest (and often coldest! February is here, the shortest (and often coldest!) month of the year.
We hope 2026 is off to a warm and positive start for you and your loved ones.

Our February 2026 program calendar is now available, giving you a full look at what’s coming up this month.

If you missed registration for our January group programs, not to worry — PACES, UPLIFT, and ACT for Caregivers will all be offered in April.

If you would like to register or learn more about these programs, please reach out to us at:
programs@epilepsycalgary.com
Follow on Instagram
  • About Us
  • Education
  • Programs
  • Get Involved
  • Events
  • News

CONTACT US

#120 – 2836 Railway St SE
Calgary, AB T2H 2V6
403-230-2764
[email protected]

  • Follow
  • Follow
  • Follow
  • Follow
Charitable Registration Number: 11890 0778 RT0001 | Copyright © 2024 Epilepsy Association of Calgary
×

Tips For Disclosing Epilepsy To An Employer

1) Be honest, straightforward and factual. Disclose epilepsy if it affects the job; don’t worry about disclosing it if it does not affect job abilities or the safety of yourself or other employees.

2) Use your best judgement in educating employers. Some employers are knowledgeable about epilepsy, but many are not. Be prepared to give employers information about epilepsy, or let them know where they can find out more.

3) Be aware of any special accommodations you will need to do the job.

4) Be brief – don’t dwell on epilepsy. Try not to build it into a major point of discussion.

5) Be knowledgeable about your epilepsy. Inform employers about your level of seizure control, medications, auras, first aid, recovery and seizure precipitants.

6) Be enthusiastic and assertive in emphasizing your skills, abilities, ideas and assets.

7) Talk with assurance.

8) Know your rights as a person with a disability.

9) Be positive, honest and specific.

10) Relate your disclosure comments to the job and your performance. Be realistic about how epilepsy may affect your work. If possible, relate positive work experience and performance.

11) Inform the employer if your physician has made any job restrictions, or recommendations on what type of work to avoid.

12) At the end of the interview, ask if there is anything else they need to know.

×

NO

But your decision will probably be a little more complicated than that. It will depend on factors like the type of seizures you have, their frequency, the type of work you do and your need for assistance. If your seizures or your medication could affect your ability or the safety of you and your coworkers, then we agree with the Canadian Human Rights Commission: it’s probably best to tell.

Unless you feel like a seizure could occur at any time, you don’t have to inform them on your first day of work or in your interview. There are probably better things to talk about (avoid the weather, though – that’s pretty boring). Whether you tell one or two people like your boss, or all your coworkers is up to you. If you have told your coworkers about your condition and what to do if a seizure does happen, you’ll probably be in better shape if a seizure does happen. But that’s totally up to you.

We know as well as you do that the understanding of epilepsy varies a great deal from person to person. Fortunately you’ve got some options in terms of support for helping people in your workplace properly understand you and your condition:

Contact the Canadian or Provincial Human Rights Commission in your area for further information about your rights and obligations as an employee/employer in employing someone with a condition such as epilepsy.

The Epilepsy Association of Calgary can provide in-person or printed material to any work-place if desired, and this can make all the difference. When people are prepared to assist with a seizure, there is usually less fear.

×

YES

But your decision will probably be a little more complicated than that. It will depend on factors like the type of seizures you have, their frequency, the type of work you do and your need for assistance. If your seizures or your medication could affect your ability or the safety of you and your coworkers, then we agree with the Canadian Human Rights Commission: it’s probably best to tell.

Unless you feel like a seizure could occur at any time, you don’t have to inform them on your first day of work or in your interview. There are probably better things to talk about (avoid the weather, though – that’s pretty boring). Whether you tell one or two people like your boss, or all your coworkers is up to you. If you have told your coworkers about your condition and what to do if a seizure does happen, you’ll probably be in better shape if a seizure does happen. But that’s totally up to you.

We know as well as you do that the understanding of epilepsy varies a great deal from person to person. Fortunately you’ve got some options in terms of support for helping people in your workplace properly understand you and your condition:

Contact the Canadian or Provincial Human Rights Commission in your area for further information about your rights and obligations as an employee/employer in employing someone with a condition such as epilepsy.

The Epilepsy Association of Calgary can provide in-person or printed material to any work-place if desired, and this can make all the difference. When people are prepared to assist with a seizure, there is usually less fear.

×

Project Uplift

Modules Include: Noticing Thoughts | Checking and Changing Thoughts | Coping and Relaxing | Attention and Mindfulness | The Present as a Calm Place | Thoughts as Changeable, Thoughts as Not Fixed | Focus on Pleasure and the Importance of Rewards | Preventing Lapses and Giving Thanks

Key Features: Education about epilepsy and mood, depression and anxiety, and mindfulness | Training and practice using specific strategies to cope with negative thoughts | Personalized goal-setting and support to help you identify when and how to implement the skills learned into your everyday life | Qualified facilitator teams to include a trained epilepsy mental health professional and a trained peer with epilepsy | A virtual group program via Zoom
×

PACES in Epilepsy

Modules Include: Epilepsy and Medical Issues | Managing Stress and the Blues | Compensating for Cognitive Challenges | Getting the Most Out of Community Living | Managing my Epilepsy Care | Effective Communication About my Epilepsy | My Health and Wellbeing

Key Features: Education about seizures types and available treatments, the influence of epilepsy on mood, stress, and thinking, and strategies for healthy lifestyle and active community engagement | Training and practice using specific strategies to cope with stress and the blues | Personalized goal-setting and support to help you articulate and pursue life changes that are important to you | Qualified facilitator teams to include a trained epilepsy mental health professional and a trained peer with epilepsy | A virtual group program via Zoom

×

Information Session Request

This field is for validation purposes and should be left unchanged.
×

Camp Fireworks

This field is for validation purposes and should be left unchanged.