The Epilepsy Shield Project

The Epilepsy Shield Project The goal of this project is to spread awareness of and information about Epilepsy through
my artwork.

All pictures and post on this page can be freely shared and all my awareness paintings can be seen on the project's site www.TheEpilepsyShieldProject.com The goal of this project is to spread awareness of and information about epilepsy with use of my artwork. Sorry, I know that the colors of the paintings are too bright for some people with photosensitive epilepsy. The goal is to use the colorful

imagery to attract the attention of other people. People do not read shirts and other items with one color writing nearly as often as shirts with bright colors that catch the eye, creating awareness. Each painting series has a different theme for the paintings and the subject of the paintings range from very educational to just funny. The pictures and post from the page can be freely shared to help spread awareness and they are available on T-Shirts and other items under the “Shop Now” button at the top of the page.

I received my Epilepsy Warriors T-shirt yesterday and it is great. If you would like one they are available in the Print...
05/16/2026

I received my Epilepsy Warriors T-shirt yesterday and it is great. If you would like one they are available in the Printful store under the Epilepsy Recognition series, the 7th one down on the left side.

They are also available in black and the premium shirts also have purple.

The link to the store is under the Shop Now button at the top of the page.

Painting  #8 EPILEPSY WARRIORS of the Epilepsy Recognition Series.Here is a painting for us to share showing the public ...
05/07/2026

Painting #8 EPILEPSY WARRIORS of the Epilepsy Recognition Series.
Here is a painting for us to share showing the public just how many of us are out there. According to the Epilepsy Foundation there are 65 million people living with epilepsy around the world, but they have been using that number for over a decade now, so it must be higher than that because during that time the count in the US alone has gone up by at least 400,000.

Instead of saying “one of millions” I did a play off ONE IN A MILLION by saying “one in millions” and I did not want two OFs that close together “ONE OF MILLIONS OF EPILEPSY WARRIORS.”
with the larger warrior to represent the person sharing it and the small warriors in the background to represent the rest of us. I used shading on the shields to make them look angled to deflect a swords strike of to one side or the other deflecting the force and the blade. The ribbons also show a darker shade on the right side because of the angled surface. For the title line I made the lettering look like metal letters with beveled edges riveted on to go with the metal armor theme.

I think this painting will get lots of interesting comments on the shares and with it on the T-shirts I think it will get lots of comments from strangers, spreading awareness out in public.
I think we should create a more accurate count of people living around the world with epilepsy. If you can get a reliable figure of the number of people in your country fighting it then please put it into a comment, so I can start working on the new count. I know the latest count for the United States is 3.44 million, so I am starting the count there.

Painting  #7 EPILEPSY’S STIGMA of the Ending the Stigma series.We are people with a medical condition who society should...
11/13/2025

Painting #7 EPILEPSY’S STIGMA of the Ending the Stigma series.

We are people with a medical condition who society should not reject for it. When one of us has a seizure in public especially a Tonic Clonic, people still believe the myths instead of the facts. I only put faces on the people making comments to get them to stand out from the crowd and help put emotions with the comments.

Some still believe it is a form of possession which is why I put the Grand Mal comment. The Mal names were dropped because they came from a time when everyone thought epilepsy was a form of possession, translated from French to English it is “Evil” making Grand Mal mean Great Evil and Petite Mal mean Small Evil which you can see if you go to Google Translate and do the translation yourself.

Some just think it is funny to see someone in any dire situation thing the person is not as important as they are.

Then there are the people who think they should post everything on social media to get as many likes as possible without thinking about our rights and dignity. They do not have the right to share videos of us without our permission, but they do it anyway.

The last one I put is the first thing most people will think when they see a person having a Tonic Clonic seizure which is they’re a drug addict overdosing.

11/10/2025

WARNING to all Chevy Equinox drivers OR any other vehicles that have timing chains instead of belts. Which I learned the extremely expensive way! 😦

The Chevy Equinox uses a timing chain that needs to stay lubricated using oil to do so. Some sites say it uses oil fed tensioners for the chain, but either way it uses more oil than cars with a timing belt. Because of this design the oil needs to be changed every 5,000 miles or every 6 months, whichever comes first.

Our 2016 Equinox with only 89,000 miles on it apparently went too long between oil changes before we knew about the issue allowing timing chain to jump some teeth on the gears destroying the engine. This is what the report from the mechanic that checked it said.

Attempted to start vehicle, the vehicle does not have compression and spins freely. Checked oil, oil level OK, oil has exhaust smell and is dark. Removed valve cover and found almost all exhaust rockers broken, lifters damaged, cam damaged. Cams spin with engine starter, vehicle jumped timing or stretched chain and valves met with pistons. Engine replacement required.

These engines are known for stretched chains and jumped chains due to high oil consumption and infrequent oil changes; engine has large amount of sludge build up. Nothing was found that is not a common failure for these engines.

We have been taking it to Meineke for oil changes and the check oil light did not come on and there were no warning sounds that is supposed to have been heard if the chain is “stretching” which makes no sense, a chain stretching! It drove fine over to the body shop where we were having some work done and one time when they drove it into the shop it stopped and clearly jumped timing. The mechanic at the dealership said they would have just heard a short loud sound because it happens so fast and a new engine is going to cost us $10,500. The problem was more common on the early 2012-2014 models, but it can happen to any model. It seems like Chevy should have fixed this problem by now even if they just make the oil light come on sooner.

Happy Epilepsy Awareness Month!
11/01/2025

Happy Epilepsy Awareness Month!

Painting  #7 “LIGHT HEADED” of the Motivational Series.This is a humorous painting for those of us who have had brain su...
10/30/2025

Painting #7 “LIGHT HEADED” of the Motivational Series.
This is a humorous painting for those of us who have had brain surgery. Since I had my surgery, I have been telling people that because they removed part of my brain, I am always light headed. 😊

Even if the titanium plate and screws they put in to cover the hole they cut through my skull did weigh more than the piece of skull and brain tissue they removed, which I don’t think it did it is still a funny thing to say. I separated the words and put quotes around them to make it clear that it is not talking about being dizzy like lightheaded would be.

Painting  #6 WHAT’S YOUR PROOF of the MOTIVATIONAL series.  I have seen lots on memes like this saying excuse instead of...
10/14/2025

Painting #6 WHAT’S YOUR PROOF of the MOTIVATIONAL series.

I have seen lots on memes like this saying excuse instead of proof, which I do not think is good for us because asking someone for their “excuse” in connection to our proof of having a brain implies that they do not have one and are stupid and it also implies that epilepsy is our excuse for being stupid, which we are not!

Think about how you would take it if someone told you that something you do not have is proof that they have a brain? Most people would take that as if they were saying that you do not have a brain implying that you are stupid. Then they ask you what your excuse is that would make you think that what they have that you do not is their excuse for being stupid.

Painting  #1 EPILEPSY SPECIALIST of the EPILEPSY TREATMENTS series.THIS IS NOT meant to demean Neurologists, becoming an...
09/25/2025

Painting #1 EPILEPSY SPECIALIST of the EPILEPSY TREATMENTS series.
THIS IS NOT meant to demean Neurologists, becoming any type of doctor is an amazing achievement and I know there are plenty of great neurologists out there. It is to show members of our community the difference between going to a doctor how knows something about epilepsy and one who took extra training to specialize in Epilepsy, treats only patients with epilepsy and has dedicated their careers to getting people seizure free. You can do a search of “Epileptologists near me” or “Epilepsy Centers near me” to find the closest one in your area. Mine is over 30 miles away and it is well worth the drive!

I am not saying that an epileptologist will be able to get everyone seizure free, every case of epilepsy is different and I understand that people in smaller towns or poorer countries well not have access to an epileptologist, but it is important for anyone who does have one available in their area to find one to receive the much better treatment they provide!

I got the idea for this painting after someone said the picture should be a picture of a neurologist with his ears plugged not listing to us.

I personally went to neurologists for 14 years with them only trying different medicines and combinations of medicines while still having breakthrough seizures. Before I learned about the group of epileptologists at the IU Neuroscience Center in Indianapolis. Once I got there, they started doing test to see where my seizures to see where my seizures were coming from including a SEEG “Intracranial VEEG” in 2014 where they drilled through my skull and put electrodes into and onto my brain directly. After that test they knew my they were coming from my right temporal lobe, and I was able to have the right temporal lobectomy. While still on medicines I have been completely seizure free since the surgery, but I was able to lower my Lamictal dosage from 800mg down to 500mg per day.

I had my time seeing two neurologists end abruptly when their ego got hurt, after another doctor said they did something wrong. Once my family doctor did blood work and said the anti-seizure medicine level was too high and when I called the neurologist’s office to see what he thought the receptionist told me he said, “If they think it is too high then they can control it!”

Then a neurologist put me on a different medicine at a high dose, dropping me off the medicines I was taking. Starting off at such a high dose got me to the point of being so dizzy that I was crawling and fell over. I called him and said I could not take it and asked if I should go back to the Lamictal and Dilantin I was taking before. He said I should start taking the Lamictal again, but not the Dilantin. What I did not know at the time was that the Dilantin was helping keep the Lamictal from building up too much in my system. After taking just it, for a couple of weeks I ended up in the hospital. When another neurologist he works with came in and talked to me and said that my Lamictal level did get way too high because of not having the Dilantin to help clear some of it out. When I had a follow up with the neurologist and told him that the issue was because of the medicine and not epilepsy related he said “Chris, you have to realize that you have epilepsy and stop blaming the medicines.” As soon as I walked out of his office I went straight to the receptionist and asked form a copy of all my records and never went back. The next doctor I went to see was an epileptologist and within one year I was seizure free.

09/04/2025

AMAZINGLY, THE LAST PAINTING I POSTED "MUSCULAR EFFECTS" WAS THE 200th EPILEPSY AWARENESS PAINTING
I'VE COMPLETED FOR THE EPILEPSY SHIELD PROJECT!
Chris Arceneaux

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Baton Rouge, LA

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