Brainstorming Epilepsy Festival

Brainstorming Epilepsy Festival This is a celebration for ongoing Battle of epilepsy. Epilepsy does not have to stop you from enjoying your life and finding success in all that you do.
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This is crazy.🧐💜 Repost from @epilepsyaction•Recent figures from the Office for National Statistics demonstrated just ho...
02/19/2020

This is crazy.🧐💜 Repost from @epilepsyaction

Recent figures from the Office for National Statistics demonstrated just how difficult it can be for someone with epilepsy to find and stay in work.⠀

In addition to this, research by the @tradesunioncongress has highlighted that people with epilepsy are paid on average 11.8% less than their peers.⠀

Follow the link in our bio to read more about these figures and about the change we want to see.⠀

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#epilepsy #epilepsyawarness #epilepsysupport #epilepsysucks #seizures #seizuressuck #seizurefree #seizurefreedom #epilepsylife #epilepsyproblems #epilepsypositivity #epilepsypositivity💜

02/15/2020

I’m feeling way better. With every battle we get stronger. We have a lot of surprises for you. Stay tuned....

I love this💜 Repost from @epileptic_warrior•Repost @seizetheday.e Absolutely LOVE this! 💜•••#epilepsy #epilepsysucks #ep...
02/15/2020

I love this💜 Repost from @epileptic_warrior

Repost @seizetheday.e
Absolutely LOVE this! 💜



#epilepsy #epilepsysucks #epilepsystrong #epilepsyfighter #epilepsyawareness #warrior #epilepsywarrior #epilepsylife #epilepsysupport #epilepsyadvocate #epilepticwarrior #epileptic #seizures #seizuressuck #seizuredisorder #seizurestrong #chronicillness #fighter #lifewithepilepsy #epilepsyproblems #seizuredisorder #epilepsystrength #epilepsystrong #spreadawarness #seizurestrong #purplequeen #epilepsylife #epilepsyissues #epilepticwarrior101

Please understand yourself and your health! Repost from @findepilepsysupport•Not all seizures look the same!! I’ve been ...
02/14/2020

Please understand yourself and your health! Repost from @findepilepsysupport

Not all seizures look the same!! I’ve been having seizures for three years and didn’t know it until last month. What type of seizures do you have?
#epilepsyawareness #epilepsywarrior #epilepsy #epilepsysupport #educateyourself #epilepsypositivity

02/12/2020

You can have a wonderful life with epilepsy! Believe it 💜💜💜 Repost from @camilacoelho

I HAVE EPILEPSY, and I am grateful for my life every single day! In honor of #EpilepsyDay I decided to finally open my heart about living with this condition, after keeping it to myself since I was 9. There are over 50 million people globally living with epilepsy, most of whom live a normal life, so we must break the stigma by talking about it. If you have epilepsy, please know you’re not alone and that YOU CAN BE whoever you want to be in this life! Don’t be ashamed (as I was during my teenage years ) and don’t let it stop you from going after your dreams. I would love to hear your stories!!! 💜🙏🏻
Thank you @cbsthismorning and @drtaranarula for believing in me and helping tell my story. (A link to the interview is on my IG stories - I was very emotional as it is still new for me to talk about it, but I’m so happy to open my heart to all of you)! #epilepsyawareness ————- EU TENHO EPILEPSIA, e sou grato por minha vida todos os dias! Em honra ao Dia da Epilepsia, decidi finalmente abrir meu coração sobre minha condição, depois de manter pra mim mesma desde que eu tinha 9 anos. São mais de 50 milhões de pessoas vivendo com epilepsia, a maioria vivem uma vida normal, então devemos quebrar este estigma e falar sobre o assunto! Se você tem epilepsia, saiba que não está sozinho e que você pode ser tudo que desejas nesta vida! Não tenha vergonha, medo e insegurança (como eu tive na adolescência) e não deixe que isso te impeça de ir atrás dos seus sonhos. É libertador finalemnre falar sobre o assunto e Ouvir a história de vocês será muito especial pra mim!
Obrigado @cbsthismorning por acreditar em mim e me ajudar a contar a minha história. (Tem link no stories com o vídeo da CBS - mas vou fazer um vídeo contanto tudo em detalhes)! Estava muito emotiva, ainda é muito novo pra mim falar abertamente sobre o assunto, mas ao mesmo tempo é libertador, e estou muito feliz em abrir meu coração!

Couldn’t have put it better💜 Repost from @fibromyalgia_inspirational•#epilepsy #epilepsyawareness #epilepsywarrior #epil...
02/07/2020

Couldn’t have put it better💜 Repost from @fibromyalgia_inspirational


#epilepsy #epilepsyawareness #epilepsywarrior #epilepsysucks #epilepsyfighter #epilepsysupport #mentalhealthmatters #healthyliving

I believe all of us are stronger than epilepsy. Don’t you? Repost from @life_with_epilepsy•Facts! I believe everyone is ...
02/02/2020

I believe all of us are stronger than epilepsy. Don’t you? Repost from @life_with_epilepsy

Facts! I believe everyone is stronger than they think they are! They just have to try and over come the mental block 💜💪🏼 Stay strong my friends!! #epilepsy #epilepsywarrior #epilepsysucks #epilepsysupport #epilepsystrong #epilepsyquote #epilepsyqueen #epilepsystrength #epilepsystrong #life_with_epilepsy #purpleawareness #purplestrong #purpleribbon #seizuredisorder #seizuressuck #lifewithseizures #seizureawareness #seizurestrong #staystrong #helpspreadawareness #makeadifference #cureepilepsy #endepilepsy

Cherish your life💜💜 Repost from @seizetheday.e•God bless his family. 😞💜 | #epilepsyawareness #epilepsy #epilepsywarrior ...
01/31/2020

Cherish your life💜💜 Repost from @seizetheday.e

God bless his family. 😞💜 | #epilepsyawareness #epilepsy #epilepsywarrior #epilepsylife #epilepsyfighter #epilepsyadvocate #epilepsystrong #invisableillness #survivor #purpleribbon #awareness #chronicepilepsy

#nofilter 💜💜 Repost from @fibromyalgia_inspirational•#epilepsyawareness #epilepsywarrior #epilepsy #fibromyalgia #mental...
01/28/2020

#nofilter 💜💜 Repost from @fibromyalgia_inspirational


#epilepsyawareness #epilepsywarrior #epilepsy #fibromyalgia #mentalhealth #epilepsyawareness #epilepsyfighter #epilepsysupport #chronicillnesswarrior

Opinions? Repost from @absence_seizures_sucks•💜#epilepsywarrior #epilepsyeducation #epilepsypositivity #endepilepsy #epi...
01/26/2020

Opinions? Repost from @absence_seizures_sucks

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#epilepsywarrior #epilepsyeducation #epilepsypositivity #endepilepsy #epilepsysurgery #epilepsystrong #epilepsymom #epilepsyfighter #epilepsyjourney #epilepsyadvocate #epilepsyawarenessday #epilepsyfoundation #epilepsyawarness #epilepsyfamily #epilepsy #epilepsyaction #epilepsyaware #epilepsyproblems #epilepsyday #epilepsyawarenessmonth #epilepsywarriors #epilepsyawareness#epilepsysupport

01/25/2020

Be on the lookout for some special events that are Organization is a part of. 💜💜🏁

Same thing, different states. 💜💜💜#epilepsywarrior #epilepsyawareness #epilepsy #epilepsysucks #epilepsyfighter #epilepsy...
01/25/2020

Same thing, different states. 💜💜💜#epilepsywarrior #epilepsyawareness #epilepsy #epilepsysucks #epilepsyfighter #epilepsysupport #epileptic

#nocaptionneeded 💜💜💜 Repost from @colourblind_zebra•Invisible disabilities are no less valid than visible ones 🌷..Having...
01/22/2020

#nocaptionneeded 💜💜💜 Repost from @colourblind_zebra

Invisible disabilities are no less valid than visible ones 🌷
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Having an invisible disability means that going out into the world can often be daunting
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There's always a worry that someone may not take you seriously and you could end up getting hurt because of it or that you'll be confronted about needing to use disabled parking or toilets
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For many with chronic health issues, their level of needing support may change. For instance, they may need to use a wheelchair when going long distances, but they may be okay walking a short distance from their front door to their car
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We also need to remember that disability isn't always physical or it can be a mixture of both physical and mental. Please also remember that we shouldn't be treating anyone differently because of this
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Do you have an invisible disability? How does it affect your day-to-day life? 🌈
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ID: An illustration of a sentence that reads "invisible disabilities are no less valid than visible ones". Some of the words are in bold rainbow capitals. Beside this sentence are two purple wheelchairs
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#invisibledisability #invisibleillness #youdontlooksick #butyoudontlooksick #chronicillness #chronicallyill #cfsme #potssyndrome #dysautonomia #ehlersdanlossyndrome #ehlersdanlos #lupusflare #lupusfighter #lymewarrior #lymedisease #chronicpainawareness #crps #fibromyalgia #fibroflare #type1strong #type1diabetes #disabilityrights #disabilityinclusion #chronicfatiguesyndrome #chiarimalformation #multiplesclerosis #epilepsywarrior #epilepsysupport

💜💜💜💜🙏🏁 Repost from @epilepsylifestyleblog•“During this journey and experience of getting brain surgery I met someone ver...
01/20/2020

💜💜💜💜🙏🏁 Repost from @epilepsylifestyleblog

“During this journey and experience of getting brain surgery I met someone very important, someone who became a great friend but also knows what it's like to live with epilepsy. He knows how tough it is 💜 thank you so much for being there by my side through this experience getting brain surgery. 💜💜”
#epilepsywarriors #throwbackthursday
#epilepsy #epilepsyawareness #epilepsyfighter #epilepsysupport #epilepsypositivity

01/19/2020

This is so amazing 💜💜 Repost from @loveintheleadclt

Gracie is working on her dissociation alert task. When her owner experiences dissociation due to small focal seizures (auras), Gracie will alert her owner by nudging her leg/knee with her nose. ⠀

As you can see in the video, when I start to mimic dissociation, Gracie begins to nudge my leg with her nose. I then mark that behavior and reward. Gracie has also started to use her paw if the nose nudge isn’t enough to get my focus back. Such a smart girl!!! ⠀

#loveinthelead #servicedog #dogtraining #seizureresponse #epilepsy #psychiatricservicedog #servicedogtraining #alerttask #dogswithajob #dogswithpurpose #labrador #obedience #positivereinforcement #clickertraining #helpingothers #lovemyjob #charlottenc #Charlotte #queencity #northcarolina #epilepsy #epilepsyawareness #epilepsyfighter #epilepsysupport @loveintheleadclt 🙏

This is an interesting statement! Repost from @endepilepsygla•Some types of epilepsy run in families and are both inheri...
01/17/2020

This is an interesting statement! Repost from @endepilepsygla

Some types of epilepsy run in families and are both inherited and genetic. However, not all epilepsies that are due to genetic causes are inherited. In new website content from our genetics editorial team, find out about the chances of inheriting epilepsy, definitions of basic genetic terms, whether there are epilepsy-related genes, what research is being done, and how to participate.

Read the new page on epilepsy and genes: bit.ly/35GUecD

Sign up now for our webinar on epilepsy and genetics on January 22 at 5 p.m. PT: bit.ly/2R2r02A
#epilepsy #endsudep #epilepsyawareness #epilepsyfighter #epilepsywarrior

Here we go again 🙄. Er’s suck.#epilepsy #epilepsywarrior #epilepsysucks #epilepsyfighter #epilepsyawareness #epilepsysup...
01/11/2020

Here we go again 🙄. Er’s suck.
#epilepsy #epilepsywarrior #epilepsysucks #epilepsyfighter #epilepsyawareness #epilepsysupport #epilepsypositivity

I always preach this. 💜💜💜💜💜 Repost from @epilepsylifestyle using @_repostplus•#epilepsy #epilepsywarrior #epilepsyfighte...
01/09/2020

I always preach this. 💜💜💜💜💜 Repost from @epilepsylifestyle using @_repostplus


#epilepsy #epilepsywarrior #epilepsyfighter #epilepsyawareness #epilepsysucks #epilepsyproblems #epilepsyadvocate

The on and on list 💜💜 Repost from @beccalc_journey2018 using @_repostplus•So true just wish people would have a better u...
01/07/2020

The on and on list 💜💜 Repost from @beccalc_journey2018 using @_repostplus

So true just wish people would have a better understanding and don’t pick on us. God made us different each fighter is strong in our own way
#epilepsy #epilepsyawareness #epilepsywarrior #epilepsysupport #epilepsypositivity #epilepsysucks

01/04/2020

Happy 2020! Let’s make it a goal to spread more awareness this year.

A true statement in our life’s Repost from @chro.nicallyfabulous using @_repostplus•I must be superwoman 🦸🏻‍♀️ #chronicf...
01/04/2020

A true statement in our life’s Repost from @chro.nicallyfabulous using @_repostplus

I must be superwoman 🦸🏻‍♀️ #chronicfatiguesyndrome#chronicillnesswarrior#chronicfatigue#chronicwarrior#chronicillnessmemes#chronicillnessawareness#chronicpainawareness#chronicillnessawareness#chronicdisease#chronicpainlife#chronicallyawesome#chronickidneydisease#chronicillnesslife#chronicpainsurvivor#chronicpainmanagement#chronicillnessfighter#chronicpainrelief#chronicmigraines#chronicallyfabulous#chronicpainsucks#chronicbackpain#chroniclymedisease#chronicpaindisorder#chronicillnesscommunity#chronicpain#chronicillness

Happy 2020🎉🎆🏁 Repost from @epilepsynow using @_repostplus•Happy New Year's Everyone!A new year is a fresh start. It may ...
01/03/2020

Happy 2020🎉🎆🏁 Repost from @epilepsynow using @_repostplus

Happy New Year's Everyone!

A new year is a fresh start. It may be cheesy but I like to make new year resolutions every year.

Even when I don't stick to what I planned (let's be honest most resolutions end before the end of the year lol) Thinking about your goals and making a plan really helps you see what is truly important to you and can help you set multiple goals throughout the year.

This year my resolution is getting healthier. I've neglected my body and it's starting to affect my energy. Starting today I am reevaluating my routines and habits. Im already started and excited to see where it takes me.

Have you set any new year resolutions❓
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#epilepsynow #happynewyear #seizurefree #newyearresolutions #makingaplan #goals #behealthy
#epilepsyawareness #epilepsy #seizures #seizureawareness #epilepsywarrior #epilepsyfighter #epilepsia #epilepsysupport #epilepsypositivity #epilepsyadvocate #epilepsymemes #epilepsylife #epilepsyfamily #togetherwearestronger #epilepsyfacts #invisibleillnessawareness #chronicillnessawareness #autismawareness #community #purplewarrior #epilepsysociety #beatepilepsy #cureepilepsy

This statement is very true to me. Repost from @socal.epilepsy using @_repostplus•They might understand where we’re comi...
01/02/2020

This statement is very true to me. Repost from @socal.epilepsy using @_repostplus

They might understand where we’re coming from and be able to give us the support we need, but until they’re diagnosed, they won’t fully understand all of it, and that’s not their fault. All we can do is educate them and be thankful for them doing their best💜
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#epilepsy #epilepsi #epilepsie #epilepsia #epilepsyawareness #endepilepsy #cureepilepsy #epilepsysucks #f**kepilepsy #epilepsywarrior #epilepsyfighter #epilepsyadvocate #seizures #seizuressuck #sudep #sudepawareness #endsudep #chronicillness #invisibleillness #disability #disabilityawareness #disney #frozen #olaf

12/31/2019

Happy New Year and have a seizure free 2020

Happy New Year 🎈🎊 Repost from @jenniejacques1 using @_repostplus•For any person experiencing chronic pain - inspired by ...
12/31/2019

Happy New Year 🎈🎊 Repost from @jenniejacques1 using @_repostplus

For any person experiencing chronic pain - inspired by #epilepsyawarenessmonth #epilepsy #healthiswealth
#epilepsyawareness

12/30/2019

All we can do is epilepsy warriors is be brave!! Repost from @epilepsymemes using @_repostplus

IF I WAS DOING WELL I WOULDN’T BE IN THE HOSPITAL WOULD I 😅😅😂😂 nah but fr I know ppl are just trying to be nice ❤️❤️😉
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#epilepsy #chronicillness #epilepsyawareness #disabilityawareness #disability #meme #epilepsymemes #epilepsypositivity #epilepsyadvocate #recovery #livingwithepilepsy #seizures #epilepticseizure #funnysh*t #EEG #neurology #hospital #medication #epilepsyproblems #epilepsia #epilepsie #instadaily #christmas

Does it really work? Repost from @socal.epilepsy using @_repostplus•Whose memory sucks?! Mine is pretty damn awful, espe...
12/28/2019

Does it really work? Repost from @socal.epilepsy using @_repostplus

Whose memory sucks?! Mine is pretty damn awful, especially my short-term memory, and it’s frustrating as hell! I’m sure I irritate people with my goldfish-like attention span, but meh 🤷🏻‍♀️ not my fault.
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However, I’ve asked my doctors for advice on how I can improve it. If you’re like me and sick of feeling like you’re standing there, mouth agape, trying to remember simple tasks, you might want to take some of these tips into consideration!
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If you have your own tips, what do you do?
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#epilepsy #epilepsi #epilepsia #epilepsie #epilepsyawareness #endepilepsy #cureepilepsy #f**kepilepsy #epilepsysucks #seizures #seizuressuck #sudep #sudepawareness #endsudep #memoryloss #neurology #memory #chronicillness #invisibleillness #disability #disabilityawareness #mentalhealth #mentalhealthawareness

💜💜💜💜💜💜 Repost from @ig_epilepsylife using @_repostplus•#epilepsyawareness #epilepsywarrior #epilepsie #epilepsia #epilep...
12/27/2019

💜💜💜💜💜💜 Repost from @ig_epilepsylife using @_repostplus

#epilepsyawareness #epilepsywarrior #epilepsie #epilepsia #epilepsyfighter #epilepsi #epilepsysupport #epileptic #epilepsyfoundation #epilepsypositivity #epilepsyfamily #epilepsymemes #epilepsylife #epilepsysociety #epilepsyfacts #epilepsystrength #epilepsy #epilepsysucks #endepilepsy #canineepilepsy

Merry Christmas 🎄. I just had to repost this. From👇🏿 Repost from @epilepsylifestyleblog using @_repostplus•I want to tak...
12/23/2019

Merry Christmas 🎄. I just had to repost this. From👇🏿 Repost from @epilepsylifestyleblog using @_repostplus

I want to take today & thank all those epilepsy warriors out there. Whether you’ve been fighting for a year or 20, it’s people like you that make a difference in this world. You show strength when times get rough, faith when things seem to not go your way, but every day you inspire someone. Keep fighting 💜
#epilepsy #epilepsyawareness #epilepsywarrior #merrychristmas🎄 #epilepsyfighter

When is the truest statement I’ve ever heard. Repost from @planetneurodivergent using @_repostplus•It sounds trite but i...
12/22/2019

When is the truest statement I’ve ever heard. Repost from @planetneurodivergent using @_repostplus

It sounds trite but if we were all the same, life would be rather dull.
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Embracing neurodiversity doesn’t mean we believe our brains are perfect, it just means we embrace ourselves and work with what we’ve got. Because we are all beautiful in our own unique way.👌😊
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@sharing.diversity ❤️ this 🙏.
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#singyoursong #neurodiversity #neurodiverse #unique #neurodivergent #diversity #selflove #actuallyautistic #autismawareness #aspie #adhd #bipolar #dyslexia #dyspraxia #dysgraphia #dyscalculia #autism #sensoryprocessingdisorder #stuttering #tourettes #epilepsy #schizophrenia #endthestigma #planetneurodivergent #differentnotless #learningdisabilities

12/21/2019

I have something special in mind for 2020?

True or false?💜💜 Repost from @epilepsymemegirl using @_repostplus•Thought of the day.***#epilepsy #epilepsyawareness #ep...
12/21/2019

True or false?💜💜 Repost from @epilepsymemegirl using @_repostplus

Thought of the day.
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#epilepsy #epilepsyawareness #epilepsywarrior #epilepsia #epilepsie #disney #meme #memes #macro #macros #reddit #smm #epileptic #health #healthy #sleep #naptime #dj #music #nightclub #strobelights #epilepsysucks #epileptic #epilepticseizures #epilepsymemes

One step in the right direction.💜💜 Repost from @the.brain.dietitian using @_repostplus•Give me a 🙌🏻 if you have tried CB...
12/19/2019

One step in the right direction.💜💜 Repost from @the.brain.dietitian using @_repostplus

Give me a 🙌🏻 if you have tried CBD! ⁣

In 2018, the FDA approved the use of CBD as a method of therapy for individuals with certain seizure-related conditions (1). Other than epilepsy, there are no other conditions that have strong evidence to support CBD as a treatment method.⁣

CBD is not well understood because of the limited amount of research on the subject. There have been no long term or clinically controlled trials on its efficacy and it might not be as therapeutic as the media leads on.⁣ ⁣
With that said, there have also been no safety issues or concerns regarding the use of CBD. If you choose to use CBD, make sure you’re buying from a company that is transparent about how they source and process their CBD. ⁣ ⁣
I also recommend trying full spectrum since the cannabinoids have a synergistic effect. My favorite brand is Charolette’s web! What are your personal experiences with CBD?⁣ ⁣
We will get more into the research on CBD and neurological diseases later this week!⁣

Johnson, J. (2018, July 27). CBD oil: Uses, health benefits, and risks. Retrieved from https://www.medicalnewstoday.com/articles/317221.php#benefits.⁣
#epilepsy #epilepsyawareness #epilepsywarrior #epilepsyfighter #cbdoil #epilepsysupport

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Even though you have epilepsy please take the time to enjoy life.
A NEW EPILEPSY FESTIVAL WEBSITE IS ABOUT TO BE PUBLISHED! HOPE EVERYONE IS EXCITED BECAUSE WE ARE! Here's a "sneak peak" into whats coming with the brand new Epilepsy Festival website... 🤯 Founder of Epilepsy Festival - Stacii Floyd - recently reached out the our foundation (Epilepsy Connections Affiliated - or ECA as we're more commonly known - "www.epcona.org") and became a registered Connection with our international foundation. We were thrilled to hear from him and are very proud for the opportunity to support his amazing work in the field of Epilepsy and raising Awareness about the condition. Our foundation offers free online services to charities and website design is (just one) of those services. I have been working personally with Stacii on the new Epilepsy Festival website to be launched via ECA's free hosting platform - so both the design services and website itself are being done for 100% NO COST under our foundation's mandates. Firstly - I would like to thank Stacii Floyd for his amazing and pro-active work in getting this website up-and-running so quickly. Although ECA can offer these services, we can't just "create a website out of thin air" and rely heavily on the CEO / Founder of each organisation to provide content, and be active in the design process to create a personal, interactive website that suits their audience and needs. Stacii has been so amazingly pro-active, intelligent, and insightful in this aspect... it has made the website process fast and easy, plus he has been an absolute pleasure to work with. But more to the point - here is a "sneak peak" i to what is coming soon... - A brand new website with multiple features and full foundation description of services and current / prior work. - Fully integrated connections to all of Epilepsy Festivals current social media platforms such as Facebook, YouTube, Instagram, Twitter and more... - Easy contact features, not just basic links to email - but automated contact systems across all platforms (email, social media and more) so you can contact Epilepsy Festival at the click of a button. - An "Awareness Page" with easy to use blog systems so you can go and find all of Epilepsy Festivals most popular work, be it articles or video posts. Plus links to ALL OTHER CONTENT from the organisation. So if it's been done by Epilepsy Festival... you'll be able to find it no matter which platform it was posted on. Now... we don't want to give too much away at this point (and there is a LOT more to come lol) - but basically the new Epilepsy Festival website will centralise all the fantastic work that's been done by Stacii Floyd and his organisation (no matter which platform it was posted on) so you can find it easily - and share it with others on any other social media platform you like! It will also mean no matter how you choose to contact the Epilepsy Festival foundation (be it via the website, email, various social media platforms etc...) you can be 100% sure it's going to the right place. I am sure Stacii Floyd will be running his own updates about the upcoming website launch but we will also be running promotional updates via the ECA foundation - and will be encouraging everyone to get excited about the upcoming website! From: Paul Lang - ECA CEO & Founder
Consistency and Awareness is the key.
I see epilepsy as the world of unknown.