The Hardest Conversation

This is long so please bare with me!

Seeing all the posts about Cameron Boyce conjured up a lot of emotions, maybe because I knew Meg would be seeing it too and now she’d be exposed to some of the ugly truths that were out there and associated with epilepsy. It made me reflect a lot on our own journey and how things have evolved and changed as she’s gotten older.

When I opened my phone and read the news I froze. It hit me like a punch in the gut! My heart began to ache as it often does when I see these tragedies in some of the groups I’m in and when I think about how some of the foundations like Danny Did and Chelsea Hutchinson came to be.

I wondered how Meg would react to the news? When she was little it was easier to shield her and keep everything happy and positive, but now she’s almost 17, the information is out there, and she was going to see it!

We live in a social media culture where a smorgasbord of information is available at our fingertips. The internet is unedited, its raw and it can be pretty harsh. News like Cameron Boyce’s death is often splashed all over the internet in mass amounts without any thought for who might be reading it. People make assumptions without facts and lose filters they’d normally have in person. Emotions run high and it can be overwhelming.

I’m not speaking sanctimoniously, it’s been a learning moment for me too, I’ll admit I’ve participated in this culture. We see a post and are quick to post our fears not thinking who might be on the receiving end. At the same time the good parts of social media aren’t lost on me as I know the power and global reach of social media when it comes to raising awareness. A double edged sword I guess?!

When Meg was little we advocated hard, I was fiercely protective and unapologetic for it. We were in and out of hospitals, and I wanted to protect her in any and every way I could. I wanted to learn everything and put all that information out there, because in my mind the more people knew about epilepsy the safer she was. I took a lot of flack from moms who said a lot of hurtful things and gave very critical, unsolicited advice. I was often written off as hypersensitive or as a “helicopter mom” that one was used a lot! The truth is, most of the time, I really just needed friends. It can be a difficult journey and as parents we beat ourselves up plenty, wondering if we’ve made the right decision on the meds, the procedures, the doctors, the hospitals, the care, etc… If you really want to help someone be a friend, be inclusive and don’t judge, but I digress!

We made some unbelievably supportive friends online (one of the most positive parts of social media for us) and we even got to meet a few of them when we ventured to D.C. to participate in the National walk for Epilepsy, but as Meg got older and as kids became assholes (like they do in middle and high school) Meg decided she wanted to be a bit more private and I respected her wishes.

When we told Meg about Cameron she thought it was a hoax, but we told her his family had confirmed and we saw her mind start to churn. She’s been a huge fan of Cameron since he was on Jessie and most recently as Carlos in Descendants. We knew throughout the day she would be bombarded with all the posts and comments. She was going to have questions!

“Mom he died from a seizure!”

I thought carefully about how to respond.

I explained that a seizure doesn’t always mean epilepsy. There are many addictions and other disorders that can result in seizures and told her we shouldn’t assume anything.

A few days later it was confirmed that Cameron did, in fact, have epilepsy. We talked about how there are many different types of epilepsy, the importance of taking meds and safety. We discussed how we wish we’d known Cameron was epileptic and I explained that while some people choose to use their fame as a platform to raise awareness others like their privacy.

We continued to have little chats here and there, but as the articles seemed to quiet so did Meg’s questions and up until today she seemed okay with it all!

Today was hard!

Meg saw a post from one of Cameron’s co-stars in Descendants. Apparently Descendants 3 comes out tomorrow and the co-star has posted a tribute.

“Mom Cameron had epilepsy and he died from a seizure…” she paused and rubbed her face. I could tell she wanted to ask me something, but was struggling.

“It’s okay baby you can tell me what your thinking.”

“I just don’t know how to say it!”

I knew what she wanted to say, I had been dreading this moment.

I took a deep breath and said you’re wondering because Cameron had epilepsy and he died from a seizure if the the same could happen to you?

She looked at me like I’d lifted a huge weight off of her and hugged me really tight!

“He was 20 mom!”

I’ve always been honest with her and as hard as I knew it was going to be I had to finally tell her about SUDEP (sudden unexplained death in epilepsy). I explained that it was rare and just because this had happened to Cameron didn’t mean it would happen to her. We don’t know everything that led up to Cameron’s death, if he’d missed his meds, if he’d been drinking, etc… we talked again about the the different types of epilepsy, the importance of taking meds and keeping your doctor informed of changes. I told her how all disorders have risks from diabetes to heart disorders. Her eyes welled up…

“There are days I don’t mind being epileptic and there are days I hate it, today I hate it!”

My throat tightened!

“I know! I wish so much I could take it from you, but this is one thing I can’t fix baby I’m so sorry!”

I could feel my eyes starting to well up too.

We both hugged each other and cried. In that moment I just wanted to take it all away, all her pain and all her fear. I don’t know if I handled it well? How do you handle such a hard question? So I did the only thing I could in that moment…

“Oh my goodness, Meg your crying and I’m crying and it’s raining, we’re a hot mess!”

She threw her head back and laughed glad, I think, that I’d injected a little humor into the conversation. She looked at her watch.

“Why are you looking at your watch?”

Meg smiled at me through her tears.

“I was just thinking it would be funny if daddy walked in right now!”

“Oh my gosh, right!”

We hugged some more and Meg grabbed her phone. I was glad we were able to laugh a little and she seemed content with everything we’d talked about.

“I love you Mommy!”

“I love you too!”

We snuggled and watched some videos together and while it had been a difficult moment my heart swelled with pride at how well she handled everything.

Let’s Talk About It…

It’s November! You know what that means… It’s time to talk about it!

Talk about what? 

Talk about Epilepsy of course!

Our daughter Meghan has Epilepsy so it’s important to us to spread the word about Epilepsy! 

We want to educate YOU! 

Did you know there are 65 million people worldwide that suffer from epilepsy or a seizure disorder of some kind?

Over 3 million of those people live in the United States and 300,000 of them are children under the age of 15!

Those are pretty astonishing numbers! 

Let me put it another way:

The number of people living with epilepsy or a seizure disorder is GREATER than the number of people living with Multiple Sclerosis, cerebral Palsy, Muscular Dystrophy, and Parkinson’s Disease combined!

You know what else is crazy…

One third of those 3 million people  live with uncontrolled seizures, because right now there isn’t a treatment available to them that works and for 6 out of 1o of those people the cause of their seizures is unknown.

So what do I want you to know about epilepsy?

I want you to know:

  • Epilepsy is a medical condition that is not contagious, but talking about it should be!
  • A person having seizures is not possessed by the devil!  A seizure is an electrical misfiring in the brain and can cause many symptoms, from convulsions and loss of consciousness to some that are not always recognized as seizures by the person experiencing them or by health care professionals: blank staring, lip smacking, or jerking movements of arms and legs. ~Epilepsy Foundation~
  • NEVER put something in a person’s mouth when they are having a seizure! Contrary to popular belief a person can’t swallow their tongue.  You are more likely to get hurt or hurt the person having the seizure, by trying to force their mouth open.

*Video courtesy of The Talk About It Foundation

  • Treat a person who has seizures no differently than how you’d treat any other friend or family member!
  • If you ever have a seizure find yourself an epileptologist you feel comfortable with and talk about your options.  You may only need a small amount of medicine to control your seizures! However there are other treatments available like VNS and even surgery.

Most important TALK ABOUT IT!  Don’t be afraid to ask questions or go online, there are lots of really great places to get information:

So are you gonna help me get the word out?

Cool!

Here are some tweetable facts courtesy of Ken Lowenberg of The Talk About It Foundation.  Use the hashtags #EpilepsyAwareness

#Epilepsy  #TalkAboutIt

If someone is having a seizure, NEVER put anything in their mouth! #Epilepsyawareness

If someone is having a seizure, NEVER hold them down or restrain them in any way! #epilepsyawareness

#Epilepsy is NOT Contagious but talking about it should be. #epilepsyawareness

#Epilepsy is NOT a mental illness. #epilepsyawareness

65 MILLION people around the world live with #epilepsy.#epilepsyawareness

NEARLY 3 MILLION people in the United States have #epilepsy. #epilepsyawareness

BETWEEN 4 AND 10 OUT OF 1,000 people on earth live with active seizures at any one time.#epilepsyawareness

There are 200,000 new cases of #epilepsy in the United States. #epilepsyawareness

ONE-THIRD of people with #epilepsy live with uncontrollable seizures because no available treatment works for them. #epilepsyawareness

For 6 OUT OF 10 people living with #epilepsy, the cause of their seizures is unknown. #epilepsyawareness

50,000 people die from epilepsy-related causes in the United States every year. #epilepsyawareness

90 PERCENT of people with #epilepsy live in developing nations. #epilepsyawareness

9 OUT OF 10 people with #epilepsy living in Africa do not receive proper treatment. #epilepsyawareness

Orlando Magic Supports Epilepsy

I’ve always wanted to go to a basketball game and our family is getting the opportunity to go see the Orlando Magic in November thanks to the Epilepsy Association of Central Florida! I’m really excited because not only will we see our first game, but the Orlando Magic will be mentioning Epilepsy during the halftime show and allowing a group of us to make signs before the game! What a great way to spread awareness!

Our tickets finally arrived in the mail today!

Ever since I opened the envelope I’ve had this song stuck in my head!

Meg is so excited and we can’t wait to go!

The Epilepsy Association of Central Florida is dedicated to improving the quality of life for children and adults with epilepsy and seizure disorders throughout Central Florida. Not only does EACF provide services for those with epilepsy and seizure disorders, but we also offer many programs and opportunities for your office/community/church group to learn more about epilepsy. ~Epilepsy Association of Central Florida~

Epilepsy… Talk About It Y’all!

I will keep this post at the top of my blog and the link open for the entire month of November!

Be sure to scroll down to see newer posts and lets

Talk About It!

It’s November which means its National Epilepsy Awareness Month and time to

Talk About It!

 Did you know that over 3 million Americans and 50 million people around the world live with some form of Epilepsy?!

My daughter Meg is one of them!

So… 

We will be spending the month of November talking about Epilepsy and dispelling some of the ridiculous myths associated with it!

For instance…

Did you know some people think if you have Epilepsy you can’t play sports or be active?

FALSE

Tell that to Chanda Gun a goalie on the women’s Hockey team during the 2006 Winter Olympics or to Bobby Jones one of the most admired defenders to ever wear an NBA uniform! 

People with Epilepsy CAN play sports and have fun, they just have to be seizure smart about it and make sure their friends, coaches and fellow team mates are educated.

While epilepsy has had its challenges for my daughter, it has never stopped her from playing a sport and certainly doesn’t stop her from having fun!

Maybe you or someone you know lives with Epilepsy?

 Come on y’all let’s get people talking about it! 

Share your story, dispel a myth or just tell people to Talk About It on your blog and then come back and link up by clicking on the little froggy fellow below! 

I will keep this post at the top of my blog and the link open for the entire month of November!

Be sure to scroll down to see newer posts and lets

Talk About It!