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Jade had her first seizure when she was 9 years old. She described it as a bad dream. After some similar events, her family doctor comfortably suspected epilepsy and sent her on her way for a diagnosis by a neurologist. Jade’s journey to a final diagnosis has been a long road. Initially, she was told she has epilepsy, no particular type. It warms our hearts to know that it was through home monitoring at Seer last year that Jade achieved a diagnosis of focal epilepsy. A weight lifted off her chest — empowering her to speak about her condition with more confidence and awareness. Jade has found comfort in talking about her epilepsy more openly. In fact, she only spoke about it for the first time at an epilepsy event last year. ‘It doesn’t have to be a lonely thing’ — Jade hopes everyone can find the courage to talk about their epilepsy because it’s not something anyone should process alone. Thank you for sharing your story, Jade. Moments by Seer is an interview series seeking to spread awareness about epilepsy. Through honest and heartfelt conversations, these interviews explore how epilepsy impacts and affects people differently. Join us in spreading awareness and share Jade's story with your network. If you need advice or support related to epilepsy, reach out to an epilepsy organisation: @epilepsyact @epilepsyactionaustralia @epilepsyaustralia @epilepsycentre @epilepsyfoundationaus @epilepsyqld @epilepsytasmania @epilepsywa
Jade had her first seizure when she was 9 years old. She described it as a bad dream. After some similar events, her family doctor comfortably suspected epilepsy and sent her on her way for a diagnosis by a neurologist. Jade’s journey to a final diagnosis has been a long road. Initially, she was told she has epilepsy, no particular type. It warms our hearts to know that it was through home monitoring at Seer last year that Jade achieved a diagnosis of focal epilepsy. A weight lifted off her chest — empowering her to speak about her condition with more confidence and awareness. Jade has found comfort in talking about her epilepsy more openly. In fact, she only spoke about it for the first time at an epilepsy event last year. ‘It doesn’t have to be a lonely thing’ — Jade hopes everyone can find the courage to talk about their epilepsy because it’s not something anyone should process alone. Thank you for sharing your story, Jade. Moments by Seer is an interview series seeking to spread awareness about epilepsy. Through honest and heartfelt conversations, these interviews explore how epilepsy impacts and affects people differently. Join us in spreading awareness and share Jade's story with your network. If you need advice or support related to epilepsy, reach out to an epilepsy organisation: @epilepsyact @epilepsyactionaustralia @epilepsyaustralia @epilepsycentre @epilepsyfoundationaus @epilepsyqld @epilepsytasmania @epilepsywa
‘Not knowing when it’s going to happen. That’s the problem.’ For Kent, epilepsy has affected his life in more ways than one — From work, to daily chores, to seeing his family. Epilepsy isn’t just a diagnosis you get one day, for many it’s a disruper to everyday life. At age 38, Kent began to experience seizures. It was through video-EEG monitoring in 2015, that Kent was officially diagnosed with generalised epilepsy. Kent is 70 years old now and the seizures haven’t stopped. In the face of uncertainty we have the opportunity to get stronger and more resilient — and that’s Kent! Despite the challenges living with epilepsy, Kent has fully immersed himself in support groups across the US and Australia, and is actively involved in ongoing research. He is an advocate for awareness and a driver for change. Moments by Seer is an interview series seeking to spread awareness about epilepsy. Through honest and heartfelt conversations, these interviews explore how epilepsy impacts and affects people differently. Join us in spreading awareness and share Kent's story with your network. Stay tuned for another 'Moments by Seer’. If you need advice or support related to epilepsy, reach out to an epilepsy organisation: @epilepsyact @epilepsyactionaustralia @epilepsyaustralia @epilepsycentre @epilepsyfoundationaus @epilepsyqld @epilepsytasmania @epilepsywa #MomentsBySeer #EndTheStigma #EpilepsyAwareness #SeerMedical #Epilepsy #EpilepsyAustralia #EpilepsyAwareness #EpilepsyWarrior #EEG #ECG #EpilepsyFoundation #EpilepsyAction #WearableTech #MedTechSolutions #MedicalTechnology #EpilepsyJourney #PediatricEpilepsy #EpilepsyStrong #EpilepsyAdvocate #EpilepsyAwarenessMatters #EpilepsyMonitoring #Wellbeing #HolisticHealth #Neurologist #Seizures #SeizureStrong
‘Not knowing when it’s going to happen. That’s the problem.’ For Kent, epilepsy has affected his life in more ways than one — From work, to daily chores, to seeing his family. Epilepsy isn’t just a diagnosis you get one day, for many it’s a disruper to everyday life. At age 38, Kent began to experience seizures. It was through video-EEG monitoring in 2015, that Kent was officially diagnosed with generalised epilepsy. Kent is 70 years old now and the seizures haven’t stopped. In the face of uncertainty we have the opportunity to get stronger and more resilient — and that’s Kent! Despite the challenges living with epilepsy, Kent has fully immersed himself in support groups across the US and Australia, and is actively involved in ongoing research. He is an advocate for awareness and a driver for change. Moments by Seer is an interview series seeking to spread awareness about epilepsy. Through honest and heartfelt conversations, these interviews explore how epilepsy impacts and affects people differently. Join us in spreading awareness and share Kent's story with your network. Stay tuned for another 'Moments by Seer’. If you need advice or support related to epilepsy, reach out to an epilepsy organisation: @epilepsyact @epilepsyactionaustralia @epilepsyaustralia @epilepsycentre @epilepsyfoundationaus @epilepsyqld @epilepsytasmania @epilepsywa #MomentsBySeer #EndTheStigma #EpilepsyAwareness #SeerMedical #Epilepsy #EpilepsyAustralia #EpilepsyAwareness #EpilepsyWarrior #EEG #ECG #EpilepsyFoundation #EpilepsyAction #WearableTech #MedTechSolutions #MedicalTechnology #EpilepsyJourney #PediatricEpilepsy #EpilepsyStrong #EpilepsyAdvocate #EpilepsyAwarenessMatters #EpilepsyMonitoring #Wellbeing #HolisticHealth #Neurologist #Seizures #SeizureStrong
Paula was diagnosed with epilepsy at aged 34, over two decades after her first seizure at age 8. The healthcare industry refers to this as 'delayed diagnosis', it is a story that is all too common. Paula lives with absence seizures — a seizure type that can easily be mistaken for daydreaming. “It was an embarrassment in lots of ways because I would drift off into a seizure and then I would come back again and think, “Oh my gosh, what was I talking about?” Both delayed diagnosis and misdiagnosis of epilepsy puts people at extreme risk. Paula’s story really emphasises the need to spread awareness and increase compassion about the multiple challenges experienced by people living with epilepsy. Moments by Seer is an interview series seeking to spread awareness about epilepsy. Through honest and heartfelt conversations, these interviews explore how epilepsy impacts and affects people differently. Join us in spreading awareness and share Paula's story with your network. Stay tuned for another 'Moments by Seer’. If you need advice or support related to epilepsy, reach out to an epilepsy organisation: @epilepsyact @epilepsyactionaustralia @epilepsyaustralia @epilepsycentre @epilepsyfoundationaus @epilepsyqld @epilepsytasmania @epilepsywa #MomentsBySeer #EndTheStigma #EpilepsyAwareness #SeerMedical #Epilepsy #EpilepsyAustralia #EpilepsyAwareness #EpilepsyWarrior #EEG #ECG #EpilepsyFoundation #EpilepsyAction #WearableTech #MedTechSolutions #MedicalTechnology #EpilepsyJourney #PediatricEpilepsy #EpilepsyStrong #EpilepsyAdvocate #EpilepsyAwarenessMatters #EpilepsyMonitoring #Wellbeing #HolisticHealth #Neurologist #Seizures #SeizureStrong
Paula was diagnosed with epilepsy at aged 34, over two decades after her first seizure at age 8. The healthcare industry refers to this as 'delayed diagnosis', it is a story that is all too common. Paula lives with absence seizures — a seizure type that can easily be mistaken for daydreaming. “It was an embarrassment in lots of ways because I would drift off into a seizure and then I would come back again and think, “Oh my gosh, what was I talking about?” Both delayed diagnosis and misdiagnosis of epilepsy puts people at extreme risk. Paula’s story really emphasises the need to spread awareness and increase compassion about the multiple challenges experienced by people living with epilepsy. Moments by Seer is an interview series seeking to spread awareness about epilepsy. Through honest and heartfelt conversations, these interviews explore how epilepsy impacts and affects people differently. Join us in spreading awareness and share Paula's story with your network. Stay tuned for another 'Moments by Seer’. If you need advice or support related to epilepsy, reach out to an epilepsy organisation: @epilepsyact @epilepsyactionaustralia @epilepsyaustralia @epilepsycentre @epilepsyfoundationaus @epilepsyqld @epilepsytasmania @epilepsywa #MomentsBySeer #EndTheStigma #EpilepsyAwareness #SeerMedical #Epilepsy #EpilepsyAustralia #EpilepsyAwareness #EpilepsyWarrior #EEG #ECG #EpilepsyFoundation #EpilepsyAction #WearableTech #MedTechSolutions #MedicalTechnology #EpilepsyJourney #PediatricEpilepsy #EpilepsyStrong #EpilepsyAdvocate #EpilepsyAwarenessMatters #EpilepsyMonitoring #Wellbeing #HolisticHealth #Neurologist #Seizures #SeizureStrong
Since 2017 Seer Medical has built a trusting community of referring doctors. The impact of these relationships has meant over 10,000 people have received world class epilepsy diagnostics outside of the hospital system. Seer Medical has over 20 clinics across the nation, both in metro and remote areas, meaning greater access and reduced waitlists for those needing epilepsy diagnostics.
Since 2017 Seer Medical has built a trusting community of referring doctors. The impact of these relationships has meant over 10,000 people have received world class epilepsy diagnostics outside of the hospital system. Seer Medical has over 20 clinics across the nation, both in metro and remote areas, meaning greater access and reduced waitlists for those needing epilepsy diagnostics.
Screengrab of Dr Ewan Nurse giving his presentation.
Blog

Melbourne Epilepsy Meeting 2021

Posted on March 26, 2021September 6, 2022 by Christina

Last week, the University of Melbourne hosted the Melbourne Epilepsy Conference. Seer’s Data Science Lead, Dr Ewan Nurse shares his top 3 highlights from the event.

Watch below

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