Archive for the ‘Epilepsy Awareness Month’ Category

I’m going to hit the highlights of the last several months so this one goes allll the way back to mid November when P.E.A.C.E. presented the Passionate for Purple Gala.

I won 2 tickets to attend this swanky fundraiser for my favorite local organization. I saw that the Little Rock Family magazine’s Facebook fan page was hosting a giveaway for a random commenter. I was the 5th person to comment that my child had epilepsy. Apparently, the random number generator came up with 5 and they were looking for a person who mentioned their child. So, the 5th person to mention their child with epilepsy was me!! Lucky ol’ me!!!!

I found an awesome black dress, just my size, at a local consignment store. $35 for a $300+ BCBG dress! I found some amazingly perfect purple pumps (like my alliteration?) at Target for $25 and spent a few bucks on some jewelry. The piece that really set off my outfit was my purple zebra print half jacket or whatever something like that is called. Whatever it was totally pulled my thrown together in a couple days, super inexpensive outfit together. I had my cousin Marilee from Payton Place Salon do my hair and I total felt amazing with my hair done just right and my dress…

Nick and I had an amazing time. We met some really incredible people at the event, saw some young runway models give a fashion show, ate some yummy food from the Peabody (where it was hosted) and listened to Mr. Happy play music! We didn’t dance. Mr. KillJoy does the GOP Shuffle and refuses to dance in public. I also, won something I bid on at the silent auction! I bid on a $100 gift card to Payton Place, where Marilee works. I bid $50 so I was pretty happy about that one.

(This photo was taken by a local reporter for In Sync magazine or something like that. We were in print! People kept saying they saw us in the magazine!!)

After the event was over, a couple we met asked us to meet them in the bar to listen to some jazz music. I think we stayed out there until after 1am. It was the best night we have had in a long, long time. Consequently, it was the first night we had ever spent away from Luke. Now, I don’t mean that to sound like it was the best night because we were away from him! Because that’s not the case!

We spent the night at the Peabody. I was looking forward to getting some sleep but Nick was so anxious to see Luke he woke me up early! He says he was starving but we all know he was ready to get home to see his baby Luke! Mama, .. well, mama could’ve slept like 15 more hours and been ok getting home to Lukie later. 🙂 It’s just how those things go.


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Tina Alexander approached me earlier this week to ask if we would allow Luke to be featured this month on the P.E.A.C.E. website. How exciting! 😀

Writing the whole story was hard. I’ve already written – the long story – once and that pretty much sucked the life out of me. I tried to tell the story without getting too dramatic and emotional though I did a little Im sure. Heck! I’m a chick! What can I say?

Anyways… mosey on over to P.E.A.C.E.’s site and read the little special piece (<– click) I wrote on Luke. And, check out the photos Nick chose too.



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New Story Link Here

*Oct 29 - 00:05*

“School nurses mistakenly gave the swine flu vaccine to two students who didn’t sign up for it – including a Brooklyn girl with epilepsy who wound up in the hospital.

“I was outraged,” Naomi Troy, 26, told the Daily News after her 6-year-old daughter, Nikiyah Torres-Pierre, had a possible allergic reaction to the shot.

Officials at Public School 335 in Crown Heights called an ambulance to take Nikiyah to SUNY Downstate Medical Center when she fell ill following the arm jab.

“My stomach was hurting, and I was itching,” Nikiyah said after she was released from the hospital.

The snafu and a similar mixup at a Staten Island school came in the first days of the city’s in-school H1N1 vaccination program.

City officials have stressed the vaccine is safe and urged parents to sign up for it – though less than half have sent in permission slips.

Troy was waiting for advice from her family doctor on whether Nikiyah should get the shot since she takes medicine to control her epilepsy.

When the nurse called for a student Thursday morning, Nikiyah’s teacher misunderstood and sent the wrong student, Troy said.

The error was compounded when the nurse didn’t check Nikiyah’s name before sticking her in the shoulder, the mother said.

“The school made a horrible mistake,” she added. “They never asked for her name. They have no paperwork….How do you make a mistake like this?”

After the mistake was discovered, officials summoned Troy to the school, she said.

Troy said the nurse – a Department of Health employee – tried to get her to sign a consent form, after the fact.

“I was insulted. I was really angry. ‘You just incriminated yourself even more,'” Troy recalled thinking.

“If they’d taken proper precautions in the school this never would have happened.”

A student at PS 65 in Staten Island also received the vaccine without parental permission on Wednesday, but officials gave no further details.

Officials for the nurses union declined to comment. The Health Department said the incidents were under investigation.

“The Health Department does not expect any future adverse medical effects for these children, but we are working to determine how this misstep occurred,” said spokeswoman Jessica Scaperotti.

“We will develop additional safeguards to prevent similar instances in the future.”

She added that the vaccine is safe for kids suffering from epilepsy.

Roughly 1,800 students have received the vaccine in the first phase of the school blitz.”

Luke had his first set of shots at 6 wks old. 2 days later he began having seizures. Ironic? Medical professionals say it’s unrelated. Luke got a seasonal flu shot this year and 2 days later began having seizures. Hmm, now it got the doctors to thinking….

The neurologist told us not to vaccinate for H1N1 and to continue to hold off on any other vaccinations as well until we have establish FIRM seizure control.



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  • Since seizures are so prevalent, knowing proper first aid is paramount.

Proper Seizure First Aid…


Stay calm, be reassuring and don’t hold the person having a seizure down.

  • Protect the person from injury by removing nearby harmful objects.
  • Put a cushion, pillow or soft item under their head to prevent head injury.
  • Loosen tight neckwear (tie, scarf).
  • Place them in the recovery position (on their side) as soon as the seizure has ended.
  • Look for a bracelet ID or an identity card.
  • Stay with the person until the seizure is over and they have recovered.
  • Call 911 and get medical assistance if:
    • The seizure lasts more than 5 minutes.
    • They do not have an ID stating that they have epilepsy.
    • They are not waking up after the seizure or are having difficulty breathing.
    • They are pregnant.
    • They have injured themselves due to the seizure


    Luke has rescue medicine that we are instructed to administer if a seizure lasts longer than 3 minutes. We have a 5mg ‘pen’ of Diastat. For us we follow the above guidelines and we begin immediately timing the seizure because we’re time nazi’s and want to administer Diastat as soon as possible if he goes past three minutes. However, since we’ve gotten this Rx we’ve never had to use it, thank the Lord.


    We turn Luke on his side in the recovery position as he is seizing (vs after which is what is recommended above) because he seems to produce a lot of saliva that he potentially choke on. Usually, one of us holds him on his side gently in our arms. He’s still tiny enough to do that.


    We always talk to Luke through the seizure to reassure him we’re there, love him, and will help him. I have no idea if he can understand that. Probably not, but it makes me feel better. It forces me to remain calm which is so hard for a mama to do while he baby lies there helpless.


    We always call each other if we’re not together when Luke has a seizure. Usually Nick calls ACH neuro on call to find out what we should do. They normally have us alter his meds until we can be seen.


    Ultimately, the best thing would be for no one to ever have a seizure. Unfortunately, that’s not the case. Millions of people around the world suffer from all kinds of seizures. So, if you happen you be witness to person having a seizure please remember these simple first aid guidelines



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“Epilepsy affects over 3 million Americans of all ages – more than multiple sclerosis, cerebral palsy, muscular dystrophy, and Parkinson’s disease combined. Almost 500 new cases of epilepsy are diagnosed every day in the United States. Epilepsy affects 50,000,000 people worldwide. ”

“Historically, epilepsy research has been under-funded. Federal dollars spent on research pale in comparison to those spent on other diseases, many of which affect fewer people than epilepsy.”


-CLICK photo above to view larger-



Why is epilepsy not talked about?

“Historically, epilepsy has been neglected, feared, and misunderstood. A veil of secrecy surrounding the disease has resulted in myths, superstitions, and a general lack of knowledge. This has impeded scientific progress toward finding answers to one of the oldest-known and most prevalent neurological diseases, leaving treatment and research efforts in the dark ages.”



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I have decided to dedicate this month to helping raise awareness about Epilepsy to my friends and family and anyone else I can reach this month. Epilepsy is more prevalent than people realize.

– 300,000 people have a first convulsion each year.

– 120,000 of them are under the age of 18.

– Between 75,000 and 100,000 of them are children under the age of 5 who have experienced a febrile (fever-caused) seizure.


– Epilepsy and seizures affect almost 3 million Americans of all ages, at an estimated annual cost of $15.5 billion in direct and indirect costs.

– Approximately 200,000 new cases of seizures and epilepsy occur each year.

– Ten percent of the American population will experience a seizure in their lifetime.

– Three percent will develop epilepsy by age 75.


Luke’s seizure disorder has given our family a purpose.. we desperately, along with many many other families just like ours, want to see a cure for epilepsy someday. The more we can raise awareness the more funding can be aimed at researching the cure.

Epilepsy awareness month ribbon

Let’s fight this so “that not another moment is lost to seizures”


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