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Improving Online Accessibility for Individuals with Photosensitive Epilepsy

Improving Online Accessibility for Individuals with Photosensitive Epilepsy

by Isabella Edlinger | Nov 21, 2024 | Uncategorized

One of the better known epilepsy accessibility frameworks today is the warning displayed before media content that features heavy flashing lights. In Improving Online Accessibility for Individuals with Photosensitive Epilepsy (2022), South asks: what do we do about...
Healing Harmonies: Exploring Music’s Potential in Epilepsy Therapy

Healing Harmonies: Exploring Music’s Potential in Epilepsy Therapy

by Isabella Edlinger | Nov 20, 2024 | Uncategorized

Music as Healing: Could it Work for Epilepsy? Across Indigenous cultures, music (and cultural arts as a whole) plays a significant role in healing (France, 2020). Music is understood as an expression of the spirit and in turn as a form of medicine; the vibrations of...

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

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epilepsycalgary

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

Our group programs are back! Project UPLIFT and P Our group programs are back!  Project UPLIFT and PACES in set to begin at the end of January.  We are now recruiting interested participants! 

To learn more about these programs, determine the right fit for you or get your name on the list please email programs@epilepsycalgary.com

#epilepsyeducation #mentalhealth #epilepsysupport #community #pacesinepilepsy #projectuplift #calgaryepilepsyassociation
Do you know that we have a quarterly newsletter? K Do you know that we have a quarterly newsletter? Keep on top of the latest information from EAC --> research, fundraising, programs, advocacy and more! 

Check your inboxes!  Winter 2025 was delivered December 2. 

Not there? Read past issues and SUBSCRIBE today: News - epilepsycalgary.com 

#brainbuzz #epilepsyeducation #epilepsyresearch #calgaryepilepsyassociation
We’re just days away from our 70th Anniversary c We’re just days away from our 70th Anniversary celebration.  Drop-in to share stories and memories of the last 70 years of learning, awareness and friendship. 
Please be sure to RSVP to https://tinyurl.com/EAC70TH so we know you’re coming.
We’re celebrating 70 years of community support We’re celebrating 70 years of community support by inviting 70 friends to become monthly donors. Will you be one of them?

Your gift — even $5 a month — can spark meaningful change. Together, small contributions create life-changing support for those who need it most.

💜 BONUS: FREE PURPLE T-SHIRT TO NEXT 20 NEW MONTHLY DONORS.  Join us today and help build a future where everyone impacted by epilepsy can thrive.
The year may be coming to an end, but we’re stil The year may be coming to an end, but we’re still going. 

Join us for our highlight event – 70th Anniversary and Holiday Drop-in Open House on December 5! 

Save your spot for January registered programs.  Or catch the last Community Education Session of 2025.

Please note our office will be closing at noon on December 24 until January 2.

#holidays #epilepsycalgary #epilepsyeducation
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Charitable Registration Number: 11890 0778 RT0001 | Copyright © 2024 Epilepsy Association of Calgary
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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.

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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
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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

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Camp Fireworks

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