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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05/10/2020

💜💜💜💜💜💜💜Repost from @iiproductions1

Happy Mother’s Day. Appreciate all the nurses for being on the front line. The single is for you. LINK IN BIO!! @ajiscooler @aj_satterfield @wlsjrprod #independent #independentfilm #nursesweek #singlemom #iiproductions #floydsoul #newmusic #heat #loveyourself #lovequotes

05/09/2020

This is some more footage from the single coming out for epilepsy. Hope you enjoy💜💜💜#epilepsywarrior #epilepsyawareness #epilepsy #epilepsyfighter💜 #epilepsyproblems #epilepsysucks #epilepsysupport #epileptic

05/08/2020

Everyone knows me as a music artist but not as a person who lives with epilepsy. So I decided that I would put the two together so people the harsh truth about epilepsy.



💜💜💜 Repost from @epilepsystrong•Who else feels like this? #epilepsyawareness #epilepsywarrior #epilepsysucks #epilepsysu...
05/01/2020

💜💜💜 Repost from @epilepsystrong

Who else feels like this? #epilepsyawareness #epilepsywarrior #epilepsysucks #epilepsysupport

💜💜💜 Repost from @epilepsystrong•Who else feels like this? #epilepsyawareness #epilepsywarrior #epilepsysucks #epilepsysu...
05/01/2020

💜💜💜 Repost from @epilepsystrong

Who else feels like this? #epilepsyawareness #epilepsywarrior #epilepsysucks #epilepsysupport

Always 💜💜💜💜 Repost from @socal.epilepsy•PLAIN. AND. SIMPLE!--I have to rant for a second, because I’m about to lose it w...
04/29/2020

Always 💜💜💜💜 Repost from @socal.epilepsy

PLAIN. AND. SIMPLE!
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I have to rant for a second, because I’m about to lose it with my friend (who doesn’t have an Instagram so 😈) and his stubbornness with taking care of his epilepsy.
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I’m not a doctor, never have claimed to be; I’m not him; he doesn’t have my epilepsy and vice versa, but STILL...
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⚠️YOU NEED TO MAKE YOUR EPILEPSY YOUR FIRST PRIORITY⚠️
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Read that again🗣
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People want SO badly to “feel” like the “norm” that they’re willing to push their epilepsy, that is LIFE-THREATENING, to the super back burner, way in the back of their mind, buried in a friggen sarcophagus under the ground, and not even think ONCE, let alone TWICE about it to feel like they “fit in”
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I GET IT! Trust me, I do. But this is one of the 👉🏼STUPIDEST👈🏼 things you can do, besides refusing to adhere to your doctors’ advice.
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Is going to work a few hours after you’ve had a seizure REALLY worth the lack of rest you’re giving your brain? HELL NO! HELL NO, it’s not! Is it worth putting yourself at risk riding a bike around the streets because you feel like you need to transport yourself like everyone else does? NO! NO IT IS FRIGGEN NOT!
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Do you want to make it worse? Do you want to seriously injure yourself or others? Do you want to be put out on your ass even LONGER than you already are because you didn’t listen to advice? DIDN’T THINK SO!
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Don’t be stupid, be kind, take care of yourself, look out for others, mind your brain and body, and manage your epilepsy, that’s all I ask! That’s all you should ask of yourself too!
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Being mindful is FREE!
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#epilepsy #epilepsi #epilepsie #epilepsia #epilepsyawareness #cureepilepsy #f**kepilepsy #epilepsysucks #endepilepsy #mindfulness #mentalhealth #mentalhealthawareness #mentalhealthmatters #epilepsywarrior #epilepsyfighter #epilepsyadvocate #seizures #seizuressuck #sudep #endsudep #sudepawareness #chronicillness #invisibleillness #disabled #disability #disabilityawareness

💜💜💜💪🏽 Repost from @awaywithepilepsy•Happy #PurpleDay2020! Here are some good ideas for spreading awareness and acceptanc...
04/26/2020

💜💜💜💪🏽 Repost from @awaywithepilepsy

Happy #PurpleDay2020! Here are some good ideas for spreading awareness and acceptance in this time of social distancing: *make/share epilepsy related posts on social media
*change your profile pictures to something purple for the day
*make a donation to your local or favorite epilepsy foundation
*hold a live stream where you state facts about epilepsy
*send virtual gift cards to friends and family with an epilepsy fact attached in the note. Tell them to pay it forward to someone else in the name of purple day!
*make painted rocks depicting something epilepsy related (brains, lightning, etc) and leave them at local parks for people to look at
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#awaywithepilepsy #epilepsy #epilepsyawareness #epileptic #epilepsysucks #seizuressuck #seizures #purpleforepilepsy #purpleformegan #epilepsyadvocate #teenadvocate #epilepsyblogger #invisibleillness #invisibledisability #chronicillness #spoonie

This is a new line of CBD. I think it’s worth giving it a try💜💜💜#epilepsyawareness #epilepsy #epilepsywarrior #epilepsyf...
04/20/2020

This is a new line of CBD. I think it’s worth giving it a try💜💜💜#epilepsyawareness #epilepsy #epilepsywarrior #epilepsyfighter #epilepsysupport

I love this statement! @epilepsynow Repost from @epilepsynow•I am a person. I have a name. I have dreams, goals, struggl...
04/19/2020

I love this statement! @epilepsynow Repost from @epilepsynow

I am a person. I have a name. I have dreams, goals, struggles, and accomplishments and they are not all related to having epilepsy.

Epilepsy is something I have but it isn't who I am.
It is important to remember that, especially when times are hard.

You are more then epilepsy.

So keep fighting for not only your health, but every other beautiful part that makes you who you are.

Have you ever felt consumed by your epilepsy❓
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#epilepsynow #epilepsydoesnthaveme #youareimportant #iamnotmydisease #epilepsywarrior #epilepsysupport #1in26 #epilepsy #inspitationalquotes #epilepsypositivity #warriormindset #selflove #purpleribbon #epilepsyfamily #epilepsystrength #purplemovement #beatepilepsy #epilepsyfighter #epilepsysurvivor
#fightepilepsy #epilepsyawareness #epilepsysociety #seizures #invisibledisability #chronicillnesswarrior #epilepsyadvocate #epileptic #seizureawareness #livingwithepilepsy #cureepilepsy

💜💜 couldn’t have said it better! Repost from @epilepsyfact•Just a simple message for you. Stay strong ❤️————————————————...
04/16/2020

💜💜 couldn’t have said it better! Repost from @epilepsyfact

Just a simple message for you. Stay strong ❤️———————————————————#epilepsyaction
#epilepsyeducation
#epilepsylivesmatter
#epilepsystinks
#walktoendepilepsy
#athletesvsepilepsy
#epilepsycommunity
#epilepsymemes
#epilepsyawarenessday
#epilepsystrength
#epilepsysurvivors
#epilepsysociety
#cureepilepsy
#f**kepilepsy
#epilepsywarriors
#epilepsymom
#epilepsyproblems
#epilepsystrong
#epilepsyadvocate
#epilepsyfoundation
#epilepsyday
#epilepsylife
#epilepsyawarenessmonth
#epilepsypositivity
#epilepsysupport
#epilepsyfighter
#epilepsysucks
#epilepsywarrior
#epilepsyawareness
#epilepsy

💜💜💜💜 Repost from @epilepsy_warr•#epilepsy #cbd #epilepsyawareness #epilepsywarrior #chronicillness #ptsd #love #cerebral...
04/03/2020

💜💜💜💜 Repost from @epilepsy_warr

#epilepsy #cbd #epilepsyawareness #epilepsywarrior #chronicillness #ptsd #love #cerebralpalsy #depression #seizure #cancer #anxiety #adhd #seizures #neurology #cannabiscommunity #vegan #cbdoil #epilepsyawarenessday #hemp #seizurefree #speechdelay #cannabis #epileptic #hempoil #inflammation #bhfyp

I can vouch for this one!💜🙏😳 Repost from @handimor•I 277 minutter har Mille været i toniske kramper siden 1 januar - I Å...
04/01/2020

I can vouch for this one!💜🙏😳 Repost from @handimor

I 277 minutter har Mille været i toniske kramper siden 1 januar - I ÅR!

Når Mille er i en tonisk krampe, vender hun det hvide ud af øjnene, hele hendes krop bliver stiv og hendes læber bliver blå, fordi hun ikke får nok ilt.
I de lange kramper bliver Milles hjerneceller brændt af og hendes krop forbruger enorme mængder af energi.

Mille har kæmpet mod epilepsien siden januar 2014💔

#epilepsi #epilepsy #epilepsyawareness #epilepsywarrior #fightlikeagirl #seizures #oneminute #1minut #tonicseizures #følgesygdom #rettsyndrome #rettsyndromeawareness #awareness #thisisepilepsy #sygdom #purpleday #purpledayforepilepsy #fokuspåepilepsi #lilla #purple #illness #fokus

Can’t wait for this! I’ll keep you posted on times and dates. We can all make a difference.💜💜💜#epilepsy #epilepsyawarene...
03/30/2020

Can’t wait for this! I’ll keep you posted on times and dates. We can all make a difference.💜💜💜#epilepsy #epilepsyawareness #epilepsywarrior #epilepsyfighter💜 #epilepsyadvocate #epilepsysupport

03/27/2020

Purple day 🏁🏁🏁💜💜💜

What do you think? Repost from @cannabismymedicine•There’s many that are watching others and waiting to try the plant an...
03/27/2020

What do you think? Repost from @cannabismymedicine

There’s many that are watching others and waiting to try the plant and it’s extracts. Others deny it due to the stigmas created by prohibition and more - Using caution is wise but forgoing nature’s abilities could delay healing that can’t be found within western medicine #healingjourney #cannabismymedicine #cannabiscommunity #fueledbythc #alternativemedicine #wellnessjourney #cancersurvivor #cancersucks #cbdmovement #marijuanamovement #mmj #autism #epilepsy #plantmedicine
#natureheals #cannabissociety #autismawareness #lupus #lymedisease #arthritis #painmanagement #addiction #recoveryispossible #recovery #recoveryjourney #peoplematter #Communityovercompetition #healthyalternatives #healingenergy

💜💜💜 Repost from @epilepsynow•In society, when people think of a brave person, they often think of a confident warrior, a...
03/23/2020

💜💜💜 Repost from @epilepsynow

In society, when people think of a brave person, they often think of a confident warrior, a fearless leader, or an independent adventurer. Someone with might and power!

In the real world, fairytales and stigmas aside, most bravery goes unnoticed by others. You may even fail to see it yourself.

I've heard from others "you're really brave to (insert action here)" and I smile and say thank you as I think about how terrified I am.

I've also heard "don't be so afraid of it, you need to be brave!". And I just wonder how they expect me to just turn off being afraid!

Fear is a part of life. The trick is, you have to learn how to fight that fear. Don't let it consume you.

Use your support system, learn about your fear, and take it one step at a time. That is what makes you brave.

You can be brave and scared at the same time.

What does brave mean to you❓
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#epilepsynow #inspirationalquotes #beargrylls #positivequotes #bravery #bebrave #truestrength #fightfear #overcome #overcomingobstacles #invisibleillness #chronicillness #chronicillnessquotes #mentalhealth #mentalhealthquotes #epilepsy #epilepsyawareness #epilepsywarrior #epilepsyfighter #epilepsia #epilepsysupport #epilepsypositivity #warriormindset #mentalhealthawareness #purpleribbon #epilepsyfamily #epilepsystrength #purplemovement #beatepilepsy #epilepsysurvivor

#nocaptionneeded Repost from @epilepsy.waarriors•Epilepsy Warriors 💜🙏#epilepsyawareness #cerebralpalsy #autism #Epilepsy...
03/21/2020

#nocaptionneeded Repost from @epilepsy.waarriors

Epilepsy Warriors 💜🙏
#epilepsyawareness #cerebralpalsy #autism #Epilepsy #epilepsywarrior #CameronBoyce #disability #cbd #anxiety #fibromyalgia #spoonie #chronicillness #cancer #depression #ENDSUDEP #adhd #SUDEPInstitute #SUDEP #health #epilepsypositivity #spoonielife #seizures #greatdane #medicine #puppy #greatdanesofinstagram #love #spooniecommunity #chronicpain

I love that more and more people are starting to band together 🏁🙏@myserectworldofseizures thank you so much for being in...
03/17/2020

I love that more and more people are starting to band together 🏁🙏@myserectworldofseizures thank you so much for being in the fight!
#epilepsy #epilepsyawareness #epilepsywarrior #epilepsysucks #epilepsyfighter

03/12/2020

Thank you guys so much💜. I feel like you guys are my extended family. Let’s crush 2020. #epilepsyawareness #epilepsywarrior #epilepsy #epilepsysucks #epilepsyfighter #epilepsypositivity #epilepsyadvocate

Stay positive! You’re worth much more than you know. Repost from @anxietyhealer•Follow @AnxietyHealer ✨ for more ❤️📸 Via...
03/07/2020

Stay positive! You’re worth much more than you know. Repost from @anxietyhealer

Follow @AnxietyHealer ✨ for more ❤️
📸 Via @stacieswift 💖
#epilepsyawareness #epilepsywarrior #epilepsy #epilepsysucks #epilepsysupport #anxietyproblems #epilepsyfighter

03/06/2020

💜💜💜💜#epilepsyawareness #epilepsywarrior #nocaptionneeded #epilepsy #thechallenge #hope #liveyourbestlife Repost from @getdownforepilepsy

Get Down is about epilepsy research add all as epilepsy awareness. Learn more via the app or at rebrand.ly/gDown

🙏🙏🙏 Repost from @epileptic_warrior•Pray 👏🙏 May 2020 be my year!•••#epilepsy #epilepsysucks #epilepsystrong #epilepsyfigh...
03/06/2020

🙏🙏🙏 Repost from @epileptic_warrior

Pray 👏🙏 May 2020 be my year!



#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

03/04/2020

Good morning guys. I wish I could tell you what special events I have planned for this year but, if you stay tuned you’ll find out. I Hope everyone has a seizure free day today.

This is crazy but I be feeling this way though💜 Repost from @socal.epilepsy•I’m gonna post an amazing, positive story af...
03/04/2020

This is crazy but I be feeling this way though💜 Repost from @socal.epilepsy

I’m gonna post an amazing, positive story after this, but I need to get this out for my personal mental health.
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I’m bummed. I’m pissed. I’m frustrated. I’m sad. I’m just overall UGH about having a seizure. I know it was a small one; I know it was time-stamped and caught by my doctors; I know I didn’t feel it; and I know it was the first not induced one in over a year, but it’s still getting to me.
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I hate the false sense of security meds can give you sometimes. I love that they work and give you a better shot at functioning and controlling seizures for some, but it is such a donkey kick to the face when they fail suddenly.
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I’m not naive and thought I was going to automatically be fixed coming out of surgery or I’d find a magical prescription that would work - I definitely didn’t expect that. Sadly, I know I never will be or find that, and it’ll be hard to get to the 100% seizure free route, but it doesn’t mean I’m not gonna try, obviously.
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I know I say tomorrow’s another chance to be seizure free, and it is of course, but it doesn’t mean it doesn’t take the wind out of you or put a huge cloud over your mental state. So even though I say it, I know it’s hard to put yourself in that mindset and just move forward like it’s in the past.
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So I guess, all in all, what I’m trying to say is F**K EPILEPSY and the toll it takes on us. If only people REALLY REALLY knew all that goes into it.
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#epilepsy #epilepsie #epilepsi #epilepsia #epilepsyawareness #cureepilepsy #f**kepilepsy #epilepsysucks #endepilepsy #epilepsyproblems #epilepsylife #epilepsywarrior #epilepsyadvocate #epilepsyfighter #sudep #sudepawareness #endsudep #seizures #seizuressuck #mentalhealth #mentalhealthmatters #mentalhealthawareness #chronicillness #invisibleillness #depression #disabled #disabilityawareness #disability

#nocaptionneeded Repost from @illinoisepilespysupport•#illinoisepilepsysupport #epilepsyawareness #epilepsysupport #brai...
03/02/2020

#nocaptionneeded Repost from @illinoisepilespysupport

#illinoisepilepsysupport #epilepsyawareness #epilepsysupport #braininjuryawareness #epilepsyfighter #notallinjuriesarevisible #epilepsystrong #epilepsymom #epilepsylife #epilepsyeducation

Quote of the day💜💜 Repost from @epilepsynow•One of the worst things about having an invisible illness is feeling the nee...
02/29/2020

Quote of the day💜💜 Repost from @epilepsynow

One of the worst things about having an invisible illness is feeling the need to prove that it is real.

What's worse is when people know it's real, but don't think it's important.

This happens within the epilepsy community as well. "You shouldn't complain, at least you didn't pee your pants". "You need to cheer up, yours aren't as frequent as mine". "You should be grateful, mine are worse". Saying things like this is hurtful and untrue.

It isn't a competition! No one should have to prove their pain! You don't know the battle others are fighting.

We need to support eachother. We need to show others that it is safe to speak about their challenges without the fear of being judged.

Everyone deserves acceptance and support.

Have you ever felt like you had to "prove" that your challenges are real❓
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#epilepsynow #epilepsy #invisibleillness #chronicillness #supporteachother #acceptance #epilepsysurvivor #epilepsyawareness #epilepsywarrior #epilepsyfighter #epilepsia #epilepsysupport #epilepsypositivity #epilepsyadvocate #epileptic #epilepsyproblems #epilepsyeducation #epilepsysociety #1in26 #mentalhealthawareness #depressionawareness #bekind #seizures #seizureawareness #seizure #discrimination #raiseawareness #dontbeabully #givelove #lovenothate

The statement of the day💜💜 Repost from @dysautoaware•• It’s not in your head •Dysautonomia/ chronic illness patients oft...
02/27/2020

The statement of the day💜💜 Repost from @dysautoaware

• It’s not in your head •

Dysautonomia/ chronic illness patients often get told that they are overexaggerating and symptoms are all in their head.

If your symptoms are not immediately obvious at first and you continue daily as best as you can, why should people not believe you? What more do they want to see to verify their perception of what is ‘chronically ill’? Time to end the stigma 🙅🏻‍♀️ .

#fibromyalgia #lymedisease #dysautoaware #chronicillnessawareness #ehlersdanlossyndrome #epsteinbarrvirus #spooniecommunity #hashimotosdisease #chronicillnessblogger #hypermobility #chronicallyill #autoimmunewarrior #spooniestrong #coeliac
#spoonie #invisibleillness #butyoudontlooksick #chronicdisease #endometriosis #chronicpain #chronicillnessblogger #autoimmunedisease #spooniesisters #dysautonomia #crohnswarrior #arthritis #lupusawareness #chronicfatiguesyndrome #epilepsywarrior

💜💜💪🏽✅ Love! Repost from @epilepsynow•You can't always control what life throws at you. What you can control is how you r...
02/24/2020

💜💜💪🏽✅ Love! Repost from @epilepsynow

You can't always control what life throws at you. What you can control is how you react.

With epilepsy, there are a lot of things you just can't control physically. At times it can feel like complete chaos!

But no matter how rough things get, as long as you are still breathing, there is something to be thankful for.

So when you are faced with challenges try to focus on what you CAN control, and what you ALREADY have that makes you happy. Once you can do that, everything changes.

It is amazing the things you will find.

What is something in your life that you are thankful for❓
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#epilepsynow #positivequotes #keepfighting #silverlining #epilepsyquote #truehappiness #epilepsywarrior #1in26 #epilepsy #inspitationalquotes #positiveoutlook #seethegood #epilepsyinspiration #epilepsypositivity #warriormindset #purpleribbon #epilepsyfamily #epilepsystrength #purplemovement #beatepilepsy #epilepsysurvivor #epilepsytruth #epilepsyawareness #epilepsysociety #seizures #invisibledisability #chronicillnesswarrior #epilepsydisorder #epileptic #livingwithepilepsy

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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.