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Epilepsy Ontario
Registrace 18. 11. 2013
2016 Statement on Purple Day - Global Day of Epilepsy Awareness
Credits to MPP Yurek and his office for the video coverage.
zhlédnutí: 254
Video
Absence Seizure
zhlédnutí 18KPřed 8 lety
A joint project of Epilepsy Ontario and Epilepsy Toronto with funding provided by Ontario Trillium Foundation. This video if available for public use if unaltered and for non-commercial purposes only.
Focal Dyscognitive
zhlédnutí 2,5KPřed 8 lety
A joint project of Epilepsy Ontario and Epilepsy Toronto with funding provided by Ontario Trillium Foundation. This video if available for public use if unaltered and for non-commercial purposes only.
Tonic Clonic Seizure
zhlédnutí 28KPřed 8 lety
A joint project of Epilepsy Ontario and Epilepsy Toronto with funding provided by Ontario Trillium Foundation. This video if available for public use if unaltered and for non-commercial purposes only.
Seizure Success with Electronic Seizure Diaries
zhlédnutí 140Před 9 lety
Epilepsy Ontario presents Seizure success with electronic seizure diaries as a part of their webinar series.
Women, Hormones and Epilepsy - September 18, 2014
zhlédnutí 1,5KPřed 9 lety
Epilepsy Ontario presents the third webinar in its series.
Understanding Epilepsy Treatments - April 24, 2014
zhlédnutí 2,2KPřed 10 lety
Epilepsy Ontario presents the second webinar in its series. There are a variety of treatments available for people who are living with epilepsy. Join us in this webinar to learn from experts about the different options people can choose from to help treat their seizures. Guest Speakers: Dr. Richard McLachlan, Professor of Neurology at Western University in London, ON Maria Zak, Nurse Practition...
Help Us Support Those Living With Epilepsy
zhlédnutí 332Před 10 lety
With a $25 donation, your name will be painted on the Epilepsy Awareness Rally Car which will be seen by thousands around the world during the Targa Newfoundland Race. From Sept. 14 to 19 the Epilepsy Awareness Car will be driving/racing some 2000 KM across Newfoundland. All donations will go directly to Epilepsy Ontario and will go toward providing awareness, support services, advocacy, educat...
Epilepsy and Memory: Coping Strategies - May 22, 2014
zhlédnutí 2,6KPřed 10 lety
Epilepsy Ontario presents the third webinar of the series. Memory problems are well-recognized in some people with epilepsy. Whether it is as a result of seizures or medication, they can pose a significant problem in daily living. Join in to hear a leading expert speak about why memory loss may occur, as well as learn a variety of coping strategies . Guest Speaker: Dr. Brent Hayman-Abello, C. P...
Intro to Epilepsy - March 2014
zhlédnutí 869Před 10 lety
Epilepsy Ontario presents the first webinar of the series - Intro to Epilepsy.
A Friend's Story
zhlédnutí 197Před 10 lety
Ben Howlett's friend Lia Turner has epilepsy. But he says he accepts her for who she is. Ben shares his story in this interview clip. Visit www.epilepsystories.com. #letsgetsocial
Lia and Echo
zhlédnutí 268Před 10 lety
Lia Turner shares a special bond with her horse Echo. Even when Lia has had seizures while riding, Echo remains calm, almost protective. The two share an incredible bond and friendship. Visit: www.epilepsystories.com for more stories. #LetsGetSocial
FamilyTies
zhlédnutí 215Před 10 lety
Rudy and Agatha Platiel have watched their granddaughter Lia Turner grow up with epilepsy since she was 9 years old. They share their experience on having a grandchild with epilepsy and about Lia's determination in life. Visit: www.epilepsystories.com for more stories. #LetsGetSocial
A Proud Coach
zhlédnutí 202Před 10 lety
Claire Gillies is Lia Turner's riding instructor. Although she doesn't treat Lia differently than her other riders, Claire shares that she was particularly proud watching Lia achieve her dreams at a special competition. Visit: www.epilepsystories.com for more stories. #LetsGetSocial
Lia Turner's Story
zhlédnutí 1,6KPřed 10 lety
Lia Turner has had epilepsy since she was nine years old. But she doesn't let that define her. Watch this powerful story of Lia's determination and courage to continue with the things she loves to do in life, and her special bond with her family and her beloved horse Echo. Lia's story is just one story you will find when you visit: www.epilepsystories.com. Please share this video with others. #...
The Doctor at my pharmacy said "You need to go to the hospital, the generic anti epileptic drug you're taking is not safe" (there's a shortage of Sandoz Carbamazepine). I went to the hospital to say I've been falling down and feeling really messed up, eyes rolling around, no control at all. There's a shortage of the one I need, and the hospital nurses kicked me out after waiting over 10 hours, The only people that were on my side and truly understood what I was going through, were the security guards. The nurses threaten me to call the police because I was getting upset, they wanted me to sit in the pouring rain on the side walk waiting for my ride home. The security let me sit at the bench at the entrance of the hospital. They understood that I was not a threat to anyone other then myself. The security were the hero of my day. What is going on with our health care?
I would say that this video is somewhat disingenuous. It said that emergency assistance is NOT required. Well, like most seizures that’s true, but if it’s the first time it happens you should call an ambulance. If the staring spell lasts for 5 minutes or more you should call an ambulance. Finally, if the person has another seizure soon after the initial one you should call an ambulance.
I've had epilepsy since 1979 and if there was one thing I could change about myself, it would be to have a better memory. It would make life so much easier.
very helpful thanks
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Tired doesnt explain it. It's like you were hit by a truck and it backed up and ran you over again. Then all you can do is sleep
Hello
7 th
I’m sending the link to this vid to my colleagues, had a seizure at work and no one knew what to do.
Tbh I have no idea how I got here and why I’m watching this but it could come in handy one day 🤷🏾♀️
Bites cookies 🍪🍪
Great job!
I have absence seizures. I was diagnosed at the age of 5 but have been seizure free since the age of thirteen and so was taken of meds which caused massive weight gain a hand tremor and memory loss. The point is meds are good up until a point an then it becomes a pill no pun intended. my triggers are flashing lights, specifically the transition from the out doors to inside a classroom getting too hot and recently sleep deprivation. The effects of my epileptic seizures is that i have Aspie like tendencies due to my epilepsy which i know is difficult to understand to put it in simple terms as a result of my seizures my brain compensated and rewired itself and so i have all of the symptoms of Aspergers but lack any sort of understanding math which for most Aspergers people they are gifted with math abilities. After my father died, it seems I have had a relapse if that is possible. i still have my absence seizure but it is not enough to put me on meds . i have been getting driving lesson and have my usual 10 seizures in the drivers seat. i take omega 3 cod liver oil liquid form as i can not swallow pills. ( also helps decrease the too -small -to -medicate -seizures) i think i said that my seizures came back i wanted to clarify the EEG showed misfiring not seizure activity per say.
I stare in space for that long i stare and be normal again i started when i was 6
great video :) very helpful
Thank you this can save lifes. I'm showing this to my teacher
48:19
Yes!! This is me at work! Infront of customers. Its the worst!!
I had no idea what purple day was until today.
Great presentation, very helpful.Many thanks.
Very well presented! Very informative!Many thanks for your work and research on epilepsy.
Very good summary for epilepsy Treatment.Thanks to all participating on epilepsy research to find a cure.
Hey thanks for all for all of this great information. I've had epilepsy for 30 years and memory issues are the worst side effect. Having to ask your friends and coworkers what you've been doing for the last few days is the worst feeling. Many thanks from Colorado.
I am the same 😭
I would really like to see and hear the very beginning of the webinar. I want to understand exactly what types I am having trouble with. This helps me to know which techniques to try to learn to cope. I appreciate your info. It is the most thorough I have found. Best. Thanks.
Lia your story is absolutely heartwarming and remarkable. We thank you for having such courage and strength to create this inspirational video! We will be sharing this to our Facebook page for our followers to have the opportunity to see!
Hello! I am so happy to have other organizations fighting for the same cause take notice of my story. It is out here to encourage others to share their story and take action in gaining acceptance, educating others, and destigmatizing this disability. Thank you so much for sharing!!