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Tiki Barber: Epilepsy in the Family

Posted: Thursday, December 13, 2007 10:05 AM by Dan Fleschner
Filed Under: ,

This morning, Meredith moderated a panel on epilepsy with Dr. Nancy Snyderman, Susan Axelrod, the founder of the epilepsy advocacy group CURE, and Tiki Barber. WATCH VIDEO

Tiki and his twin brother, Ronde, suffered from seizures as children, and Tiki's older son, A.J., has had about 10 seizures, generally brought on by high fevers.

Before the segment, we talked about his family's history of seizures and what parents can learn from his experience:

DF: How old were you when you had your first seizure?

Tiki Barber: I think I was one when we -- talking about me and my brother -- had our first seizures. I don't know if it's genetic or coincidence, but we would always have them at the same time. So my mom was always extremely stressed about it.

Back then, they didn't have a lot of ways to treat it other than to pump kids full of phenolbarbitol. If you've ever seen a kid on phenolbarbitol, it's like he's a walking zombie. So they've come a long way.

We eventually grew out of it, after we were six or so. I have no lasting effects from it, but having seen my kid go through it, it's not easy.

DF: So you have no recollection of going through it as a kid?

Tiki: None. But my mom used to say that she'd thrown us in the pool when she sensed us getting to a certain point. And I remember always being at the pool when we were younger. That I remember, but I don't remember going through an episode.

DF: Before your older son, A.J., had his first episode, had you talked about the possibility of him having one with your wife?

Tiki: I think Ginny knew that I had had them. But it wasn't anything in my consciousness, because my son was past where I had started having them. Then one day, we were laying in bed together, and I could feel him getting hot, because it was making me hot.

So I moved him to another room, and 30 seconds later, he went into a seizure. I picked him up and ran downstairs. Luckily, we were only a block away from New York Presbyterian, so we took him there. He came out of it quickly, but it shocks you to see it.

DF: Has he had any since then?

Tiki: He's had probably 10, and by definition, he's epileptic. But it's only by definition. He doesn't have some of these lasting conditions that epileptic people have: memory loss, cognitive issues with development, etc. His condition is febrile, meaning in the presence of fever or when he's about to spike a fever; when he goes from normal to 102 in 10 minutes. He's predisposed to having a seizure, as I was predisposed to it.

Anyone who gets a very high fever can have a seizure, but some people are predisposed to it. I was, my father was, my brother was, my son is. But we grew out of it, and we're hoping that A.J. will grow out of it.

DF: Have you talked to him about any of this?

Tiki: We've talked about it, but he doesn't remember. He knows he was sick, but he doesn't know what happened. The only time we got scared was when I was actually playing in Philadelphia. It was the first game of the season, four years ago. He just fell over. It wasn't a convulsing seizure, and he got up after 10 seconds. But he was just in a daze.

Ginny knew something was wrong, so she took him to the hospital. Thirty minutes later, he went into a tonic seizure when his temperature spiked. That one scared us, because there was no fever when he had his first seizure. But it clued us in to the fact that we can tell when he's gonna have an episode.

We were in Hawaii for the Pro Bowl at a players' luau, and he just started to zone out. So we ran upstairs, put him in the bathtub with lukewarm water, and luckily we were able to control it by controlling his temperature, giving him motrin and tylenol. We always have to be aware, because you never know when it's going to happen.

Like I said, it's not dangerous, but you don't want your kid sitting around having a seizure.

DF: Now that you're talking about this more publicly, what do you want parents to take away from your story?

Tiki: I think parents need to be aware, because any kid can have a seizure. A lot of parents will see their kid have a high temperature, and they'll think, "Oh, it's just a temperature." But you never know when you're predisposed to having this disorder, so you have to keep an eye out.

But also, there's a stigma that comes with this word "epilepsy." I don't want to say that it's normal, because it's not normal, but it's just like any other condition. It needs to be researched, there needs to a cure for it, there needs to be awareness about it.

If someone had a seizure right now, would you know what to do? Most people wouldn't. It affects a lot of people.

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Comments

Thank you so much for being willing to talk about this.  We need more people to understand epilepsy.  As a mother of a child with epilepsy, thank you.
Dr. Snyderman-

I was very interested in the discussion of epileptic conditions. Being epileptic myself, I have had little information (other than from my Dr.) about the "disease". But your patients all seem to be child-onset in nature. I had my first "recorded" seizure when I was driving my car at the age of 49. Is there any adult-onset epilepsy that may explain my "late-bloomer" situation? (It is very ironic, but I am a type-1, child-onset diabetic, diagnosed when I was 15.)Where can I obtain more information? Also, say "hi" to Matt for me (we met in 1984 in RI).
I have a son who didnt have any seizures until he turned 19,we been through many doctors and they cant seem to find any signs of what is causing it. He was told it was all in his mind , but I am  there when he has his seizures and these are not made up,recently he was taking a shower and he felt like something was wrong he tried to get out of the shower,but didnt have time,Me and his father broke opened the door he was in a full blown seizure,I know this isnt in his mind,he loses memory ,he passes out Ijust feel like I am at the in of my rope. If there is anything any one knows please share it with me.
You should be sure to remind people that at no time should you leave a person in seizure attack alone in or near water due to drowning possibility.  And drowning can happen in very little water.

Seizures come in all types.  I've had gran mal and am now in complex partial seizure types.  Drugs for seizures are expensive and some are almost as dazing as the seizures themselves.  

It was eluded to, but not stressed enough, that epileptics are not retarded.  This happens to brilliant people as well as any other level of intelligence.  College graduates with wonderful careers can be affected, some slightly.  

Life with complex partials, from my viewpoint as a sufferer, is limiting.  I no longer drive, am scared to be in public with my grandchildren for fear of losing them, and wonder if one day I'll find myself lost.  My husband has delt with this for years and it's only getting worse.  

Some of the drugs are horrible.  Tegretol gave me drug induced Lupus; depakote made me nervous, sick and upset; another drug caused me to lose the ability to add, spell and keep from crying.  It's always an experiment for epileptics to find the right treatment, if ever.

Young people, epilepsy is not a reason to stop living.  It's just a thing we must deal with, making us stronger.  Keep struggling.  One day you may be the person to find the cure or treatment that really works.
I was so glad to hear your report on Epilepsy this morning.  I too have a child who had a seizure disorder that she outgrew.  My youngest daughter had her first seizure January 1st 1999, she was 22 months old and I am very happy and lucky to say that she outgrew this disorder two years later.  

My daughter had 7 seizures within this period of time.  We went through all the testing, CT Scan, EEGs, and MRI.  My daughter’s seizures were considered “Seizures with Illness”.   They were not true Febrile seizures, because her temperature was never high, only 100 degrees.  Both my husband and I had seizures as children so unfortunately our children were predisposed.  Our older daughter never had a seizure though.  I consider us to be very lucky, because there is so many parents out there whose children have not outgrown their Seizures.

I have researched Epilepsy for my own personal knowledge and I am a donor and advocate for the Epilepsy Foundation.  I hope to help to take the stigma away from Epilepsy.  Knowledge is power and the more we spread the word the better understanding everyone will have.

In our house we celebrate the anniversary of our daughter’s last seizure.  She knows and can remember some of her hospital and ambulance experiences.  She can now spread the word to make others aware of the truth not the stigma.
Watching the segment on Epilepsy this morning brought back many terrifying memories for me. The segment was presented from the point of view of children having epilepsy, it probably should have included the perspective of being a child with a parent who has epilepsy. I spent many hours of my childhood wondering if I was going to come home from school and find my mother dead at the bottom of the stairs or having swallowed her tongue, the house burned down,or my baby brother or sister dead because she had dropped then during a seizure, not to mention the social stigma that was attached to it. Our child hood was totally traumatic and terrifying.She suffered from two types of uncontrollable seizures and back then they were called grand and petite malls.Just wanted to share another aspect of Epilepsy that is often considered.
Thank you so much for talking about your child's epilepsy.  My child has suffered from uncontrolled seizures for 12-years now and we feel so hopeless.  To add insult to injury, we have no idea why she has seizures.  Thank you for your willingness to raise awareness about this disorder that can be so devastating.  
Hi! I have been epileptic since I was approx. 10 yrs old. Although I didn't know this later, I had spinal meningitis and almost died. The closest small town hospital(40 min away)told my dad there was NOTHING they could do for me so he drove to the next closest city, 100mi. away. I went thru various medicine at first, that changed thru my Puberty years. I have absent seizures or  petit mal seizures. I blank out for a cpl sec or a min. The docs said I may grow out of them but never did. I guess since I quit breathing, I have to be thankful it was not worse. My life has had it's ups and downs as I was teased in junior high/hs as being retarded. I have some cognitive functions where studying was a challenge for me. Possibly due to meds also. I am now almost 38 yrs old, but still have seizures(possibly due to my health, daily stress, perimenopause). Until recently I really have not met many epileptics until I subscribed to an online blog. I have a yearly review by my docs to drive in my state. Thanks for doing this segment as it isn't as known as other conditions/diseases. Nicole
I was very disappointed with your feature on Epilepsy, I am a 47 year old woman who suffers with complex partial seizures since age 14 due to a head injury. This type of seizure is life long; you won’t grow out of it, yes medication keeps it controlled, but life changing none the less. People in my category need to be informed of all the new methods available to them. The location of brain damaged or central point of activity, not critical to life, can be removed becoming seizure free. So please don’t do a story for one “type” of epileptic, do one for all. My life was drastically changed in 1974, for the worse, due to the lack of knowledge not only from society but doctors as well. UCLA Neurology clinic is a great starting point for such information, giving other teens the opportunity at a “normal” life.
I have a eight year old son with a form of epilepsy that he will out grow around his middle school years.They say his type looks like ADHD and alot of boys mainly go untreated for this unless they have a visable seizure. We have stopped all meds due to the effects it has on his personality.He started having sezuires at the age of two and half.I am so glad someone is talking about this who might be able to get some action on finding a cure or a way of making better meds.
For Tammy:  My son had his first and only seizure after falling in the shower when he was 16.  The neuro told us he has juvenile myoclonic epilepsy (JME) which is characterized by jerking motions (which caused him to fall in the shower) and onset is ages 12-30, with teen years most predominant.  He takes Depakote ER which has controlled his condition to date.  The Epilepsy Foundation of America (EFA) and Epilepsy.com websites both have good information and message boards that may be helpful.  Good luck.  
Thank You sooooooo much for the info on epilepsy this morning. I am 43 and have been having seizures since the age of 15--one of the worst things about epilepsy is the not knowing why. After MANY doctors and tests I went to The NC Baptist Hospital in Winston Salem NC (Bowman Gray School of Medicine) and with the help of the GREATEST DOCTORS IN THE WORLD-  I have gone from having 300-400 seizures a week to about 1 every 8 months!!!! I had surgery and I went from taking 14 pills a day to 2!!! I have my life back--thanks to the Epilepsy Monitoring Center and the great doctors!!!!  
For Tammy,  my seizures first started when I was 31 and only diagnosed with scar tissue from birth/before birth injury.  Never any seizures until then but gran mal.  Some doctors tend to make you feel they think we are "nuts".  Get another doctor.

For Michael, I had complex partial seizure which was discovered after a wreck at about your age as well.  These can come on for no reason or can be the next step in epilepsy.  Check for these types of seizures to better understand what's happening to you.  I always wondered what I did during these seizures until I recently underwent monitoring.  Got a dvd of one of my seizures and now know that I don't exhibit many "tells" and don't appear crazy.  Was very reassuring to me.  

Keep the faith.
I'm 52 I had eilpesy since Iwas 17.  Still have great life.  Just go for it.   There are great doctors out there.   Seattle Washinton.  Thanks. great piece on your show.
I was so glad to see this issue appear on the Today Show as my granddaughter (whom we have raised since she was 4yr) was diagnosed with petite mal. She is now 12yr and very athletic. She recently experienced a grand mal seizure while playing soccer and 2 wks later another while running laps at school. Would like more info. on this issue when possible.  Schools really need to receive necessary information also.
Thank you for airing this segment. As an adult with epilepsy I know how misunderstood the condition (not disease) is. Please let people know you can not catch epilepsy. A good source of information on treatments, research and finding a Dr. who is an expert in treating epilepsy is the Epilepsy Foudation. There are local chapters that sponsor informational seminars for epileptics and caregivers. In LA each year the foundation sponsors the "Brain Storming conference" which brings experts from around the country to speak about diagnosis, new treatments and ongoing research. I am sure similar meetings are held around the nation. Check out efa.org
As an employee of the Epilepsy Foundation of New Jersey it was so wonderful to see the spotlight on epilepsy today. Unfortunately, epilepsy is rarely given the attention needed in the media, and as a result there are is often a negative stigma in public opinion.

Thanks to this morning's segment, I hope that we were able to dispell some of these myths. In particular, Tiki Barber's willingness to discuss how he and his family are leading full and productive lives with epilepsy will empower young people and let them know they can achieve their dreams.

It is important for parents and individuals with epilepsy to know that organizations such as the Epilepsy Foundation of New Jersey exist and are providing many programs and educational opportunities, often free of charge.  For more information about services in NJ please visit www.efnj.com or call 1-800-336-5843.  

If you are not located in New Jersey, you can contact the National Epilepsy Foundation at www.efa.org.
I was glad to see epilepsy addressed. I would like to see more of a story on the absence or partial seizures.
My son is now 9 and was diagnosed when he was 3years old...it was very scary he just started rolling his eyes  and stuttering....we immediately took him to the dr.... 50-100 seizures was a daily routine,after a trail of medications/depakote caused tremors, lamictal made him dizzy, topamax caused total loss of speech, finally Celontin worked and he has been seizure free for 3 years....he only has about a 10-15% chance to outgrow the seizure....
We need to bring this disease out into the open, families like myself need support for what we go through on a daily basis Thank you
Thank You  for talking about Epilespy.
 I have had Grand Mal seizures since I was 18. I am now 53 and still have seizures. I have found I have I have to stay away from stress, and certain movies have set off my seizures.
 As I get  older I am more involved with my local Epilepsy  Foundation in my area. By website or by mail.
 In my opinion hearing a calm voice that I know talking  to me, and of course getting  things out of my way and keeping me safe from harm.
  I was a teen from the sixties when  my mother a nurse would put a spoon  over my tongue, and later a tongue depressure. I am glad those days are over.
  Please keep finding why we have seizures, because even though I have auras that that tell me I'm going to have Grand Mal seizures at my age. They will always scare evweryone around me unless I get lucky and have someone near me who knows what to do about seizures, eveyone around will call 911.Which is a blessing, but embaressing at times when I know I just have to let the sizure run  it's course, but always helpful if someone can time  how long a seizure is so they can tell the Emts or fire deptartment. who ever arrives first at the scene.
  This is all that has that has happen to me.Nueologist that you like are good to have also.
 

   
 
Tiki and NBC group,

Thank you for the segment on Epelipsy this morning.  I connected with everything you were saying because my daughter Ashley was diagnosed with Petit Mal seizures at age 4.  Like Tiki and his family the doctors hope that your child will grow out of them but unfortunately she has not and also deals with complex partial seizures. What I would pray that someone would talk about is the emotional issues that these children go through once they hit the teen years.  Ashley is now 16.  Though she has grown up with this and has been a trooper undergoing years of tests and procedures alond with the Vegus Nerve stimulator surgery to control the seizures; there is nothing more heart wrenching than to see your child wanting to go through some of the normal teen stages when their peers are taking those steps. I have seen the disappointment in her eyes this past year knowing that she will not be able to do everything she would like to (like driving)and how will her future be affected as an adult. Side affects of medications have caused weight gain and other medical issues have come from that.  This time in any young persons life is so critical to keep them on the right path.  Our faith and Ashley's faith in God has kept her from falling through the cracks of anger and bitterness and for that I am thankful.
I do believe that their are many teens with Epelipsy or other disorders that are dealing with the same issues as Ashley.  I wish there was a peer group with a medical facilitator where these teens could gather on a monthly basis to vent their emotions, concerns, fears. To be around others their age who understand them.  Communication is the key and this concept could only bring positive results. I really hope that NBC will do a future segment on advocating the need for our teens who deal with these disorders.

Thank You.
Thank You, finally someone is reporting on Epilepsy. I am a 48 year old woman who has had epilepsy since I was 6 yrs old. I have grand mal seizures but they are under control. When I was 35 yrs old I was having more seizures, and it was what I think brougt on because of my periods. I would track my seizures and about 3 days before my period or 3days into my period I would have a seizure. I found that I was not eating as well and under stress and emotional that my glucose and insuline were off then the combonation of my hormornes kicking in I would have a seziure. After 10 months of having seziures I went to a new Doctor and she put me on Progescream to help with my seizures.

I am also on Tegrotal and Mysoline along with Progescream.  I am under control now, but would like to know will I grow out of my seizures?

I would love to know more about people who had epilepsy as a child and still have it today.  Or is there hope that we will grow out of it like Tiki and other lucky people that have had seizres.
Thank you SO much for your segment on epilepsy.  We are working hard every day to end the stigmas attached to seizures.  Tiki, it means so much to all of us to have someone like you speak on behalf of your son.
In Minnesota we've started a program called "Shining Stars" to recognize all kids with epilepsy.  Our hope is that they know that they are not alone and that epilepsy is something they have - and not who they are. There are more than 200 kids in our program that recognizes and celebrates kids with seizures.
Thank you again for bringing much needed attention to this important topic!

Vicki Kopplin
Epilepsy Foundation of Minnesota
www.efmn.org
My son has a epilepsy since he was 5years old he is  
8years of age.  We had try 6 different epilepsy medication. We also try Methylprednisolone. Medication is not helping with control of seizure yet! He haslots
of learning disability and cognativites. Next year we are thinking to put him on diet call Ketogenic diet.  I would like to know if any body has try and how it helps. If MSNBC today show would have more information or bring more information about The ketogenic Diet on tv. Thank you very much.
Mom

This sement really hit home for me. When my son was 15 months old he had his 1st febrial seizure. It was the SCARIEST moment of my life - even to this day. At the time I knew nothing about this, but my nephew who is only 2 months older than my son, was beginning seizures. After several visits to the doctor (for my nephew)his situation unfortunately turned out to be epilepsy. My son only ended up having 2 more seizures and grew out of them. I am convinced though that my sons seizures had something to do with the MMR shot he received 2 days prior to his 1st seizure. I always have, but today reminded me again, how fortunate I am that my son out grew this and is all in all a healthy 12 year old boy! My nephew though (and I feel somewhat guilty) is another story, even though he is able to go to school, he is just not like other kids his age and has been on numerous medications. I too am hoping there will be a cure or treatment, that really works, in the NEAR Future.
Thank you so much for this segment.  I am the mother of a four year old boy who started having seizures at the age of two.  We are still trying to find the right treatment for him. The other children's stories are very similar to my son's.  It makes me ask myself what I should be doing to raise awareness and help all of our kids.
This is for Rebecca Fernandez:

My daughter is also 16, and has been having grand mal seizures since she was about 2 years old. I just wanted you to know that I completely empathize with what you are going through! This is such a painful time for our family, as my daughter is not able to drive or do things that other teens are doing, and it's difficult to see her go through it. It would be helpful for us to find a support group for her. It's much better now than when she started having seizures -- with the internet, we are able to connect with more people who are affected by epilepsy. We used to feel very isolated, and while there is still some isolation now that she's a teenager, it's better than it was 14 years ago!
My son's struggle with epilepsy is so similar to the first boy's story that I felt I the father was speaking for us.  It makes me ask myself what more I can do to raise awareness and help all of our kids.  Thank you for helping to raise awareness.
very good topic I was diagnoised a few week ago
as having seizures.
  Your report on epilepsy Thursday morning was very interesting and informative, especially considering Tiki Barber's personal experiences with the disorder.
In my case, I had epilepsy for more than three decades as the result of encephalitis when I was an infant. The years with epilepsy were challenging, to say the least, when considering the seizures and the medications. Every day was a mystery considering that we never knew what might happen.
 However, I am one of the lucky ones, since epilepsy was removed from my life on Dec. 6, 1994, when doctors at Scripps in La Jolla, Calif. performed right-side lobectomy brain surgery (I was nearly 44 at the time of the surgery). I had four seizures the day before the surgery and haven't had another since, so I am undoubtedly one of the luckiest people in the world.
 Most important, though, is that epilepsy needs to be discussed so that people are (a) aware there is help out there and (b) understand that they are not alone in their struggles. Your staff and Tiki Barber did a wonderful job of presenting the story while also showing that there is hope in dealing with epilepsy, which can be both frustrating and frightening.
 In my particular case, I learned about the surgery while watching a KVBC TV-3 news report in 1993 in Las Vegas. Truthfully, that report probably saved my life and your report this morning could very well do the same for many thousands of people suffering either directly or indirectly with epilepsy.
  Because of my own past experiences with epilepsy, it pains me to see people struggling with the disorder. Hopefully, stories such as the one on the Today Show will help provide guidance to those in need.
 Keep up the good work!
 

I am 40yrs old and was diagnosed with epilepsy at the age of 5yrs. It has been said that I have outgrow it twice now in 35yrs. I am currently having siezures, I guess I just want people to know that if they are ever diagnosed with epilepsy they will have to continue being on the lookout for seizures. Even when you are off the medication you need to watch your diet, sleep and alcohol usage. I also would like it if you did a more complete segment on epilepsy showing the different types as well as the medical  advancements that have been made through the years. When I was first diagnosed the only test they had was the EEG now there is the CAT Scan and the MRI. I would not say the advancements have been fast coming but at least they are there and epilepsy has become better know in the last 35yrs.
Please Read.
8 months ago I had a my beautiful grandson and life was good. For about 2 weeks! He started having siezures, arms, legs, head would all shake. First they would last 5 second, but they would happen alot. My daughter knew something was not right. Gosh he was only 2 weeks old. WE took him to the hospital where he was having them every ten minutes. after that he has been in and out of the hospital alot. They have done spinal taps, eegs, genetic testing, ekgs, metabolic testing, and lots of blood testing. He now has 5 different type of siezures. grand mall, silent siezures, internal siezures, sceaming siezure, some type of sleep siezure. this child of 8 month old is on high dose of phabaritol and kepper with some type of med you place in his behind in an enmergentance and then rush to the hospital. Right now he is just starting to roll over and grab toys. He doesnt hold his head up for long before he gets tired and you need to support him again. He is a wonderful baby, never crys and has a killer smile even after all he is going through. He was at U of M at first but we were told to take him to J.H.H. We have and he now is being seen by the head of peds nero. depatment. Still looking for answers.
I suffered with epilepsy from 1960, I was 14, until 1994.  In 1993 while working overseas I had a major seizure.  My employer, Citibank, flew me to Singapore where I was diagnosed, and for the first time told I had an operable condition.  Up until this time I had only been given medication and more medication.  I returned to the States and after a 10 hour right temporal lobectomy, I was cured.  I have since used my position and international background to speak with patients considering and/or preparing for the operation.  Should there be anyone that is considering surgery and would like someone with whom to speak, I am always ready.
NBC & Tiki,

Thankyou for taking the time out to discuss epilepsy nationally!!  I am 44 years old and had an auto accident on December 1st.  I began to have a siezure, my foot pressed on the gas and I crashed through a yield sign and finally into a telephone pole.  My 11 year old son was in the car with me.  I have not had a seizure since I was 9 (35 years ago).  Now it has come back.  I am currently on medication and undergoing numerous tests! I have no recollection of the accident and now the even scarier part is finding out the results of the tests.  An unknown reason could be better than some other findings.  Time will tell.  Thanks again, a huge Tiki fan!
My son is struggling with epilpsey He has Grand Mals they are wso frightening even more when he doesnt want to take the meds He had two seizures at his work and he really loves the job he is hoping they wont fire him He wants to have the brain surgery but his dr says to risky
A tremendous "Thank you" for a wonderful segment on epilepsy. We desperately need more coverage and information to share with the public. My daughter was diagnosed 2 years ago with epilepsy at the age of 20. She suffers with grand mal seizures. She has had to try many different medications and recently had the VNS placed to help control her seizures. She is currently in college, which is wonderful considering the amount of medication she has to take. Each day is a victory when there is no seizures! But the anxiety that constantly effects her and the family is huge! She suffered from petit mal seizures as a young child, whereas she would "drift off" We never new that she was actually suffering from epilepsy! Her Dr.'s missed it as well. Many children are misdiagnosed with ADHD and not properly diagnosed as with my daughter. I hope with your attention to this widespread disease it will trigger more awareness and more research to help the ones suffering with this and their families. Thank you again for recognizing and featuring this segment that is so rarely discussed
I had a sister who had grande maul seizures.  The first one was when she was two months old.  That was in the summer of 1969 when there wasn't alot of information on epilepsy.  We lived in a rural area were we didn't have the privileges of specialist.  Once a year a doctor would come up to the upper penninsula of Michigan and would see several of these children with this medical condition.  My sister was put on several medications, some experimental-none ceased her seizures.  The medication would help decrease the seizures for a while and if we were lucky a new aniti-seizure medication would come out and that would work for a while.  After many years of being on anti-zeisure medications, it started to take a toll on my sister at the age of 33 my sister had a seizure and passed away. It was just to much for her body to handle any longer.  It's been 5 years since my sister has passed and I can't beging to tell you how greatful  I that someone is finally looking at the cause of epilepsly and not just the treatment.  Hopefully that there will be a cure for this life affectting disease.
It"s about time Epilepsy  is being discussed nationwide,thanks to the Today Show.We need much more money being invested by our government,like they do for cancer, aids, and other diseases,to find a cure for this sometimes debilitating disease.Although medication can be helpful to some,there are others, that have to take multi medications,with horrendous side effects,and even then ,there are for some, breakthrough seizures.Its almost equivilant to putting a bandaid on a bullet hole. Temporarily it will help,but in the long run, the hole is         still there.Just like with seizures,the medication is the bandaid,but the disease is still there.I have a 20 year old son with autism( high funtoning) that started having seizures when he was 16,snd although he has not had any for over a year,he still has to be on medication ,and so the bandaid is in place,but instead of relying on a temporary solution,we need to have a permanant solution.I thankyou Tiki Barber,Meredith Viera,and Nancy Snyderman,for doing this show,and to continue doing more shows,and updates,as to what is being done to find a cure.Recently Supreme court Justice Roberts,had suffered a seizure,and I only wished that he would have publicly discussed it,because he is such a powerful person,which would have brought more attention and awareness to this disease,and in turn ,opening the eyes of many powerful people who can make a difference ,in our government,to push for more funding ,to find a cure.
I'd be willing to bet that the Today Show had no idea how much this really affects Americans, not to mention other countries.  So many individuals with the seizures but also their families.  For those of us no longer able to drive (and I feel the pain for the teenagers) it is painful to put this burden on our families both financially and time consuming.  Just once I'd love to run out to pick up something I need at the moment I need it or to drive out to the country by myself.  It's funny but of everything I've been through, the lose of individual freedom is the hardest.  Suburban living means pleasant areas to live but no public transportation available at the drop of the hat.  But, the day I realized I was (still inside the building) somewhere not intended, with my toddler granddaughter is when I started to really be frightened by this condition.  I temper all my decisions concerning my grandchildren because of this condition.  To think that something could have happened to her is so very, very scary.  That's one reason I've considered brain surgery.  Now I just have to wait for the results to see if I fit the doctors' criteria.
Thank you so much for discussing this.  My son had his first febrile when he was one and has had 7 since.  Plus he also has a history of myoclonics and currently has absence (petit mal) seizures.  When he has the absence... which he has multiple times a day, it is hard for anyone who isnt familiar with epilepsy to recognize.  He just zones out, it kinda looks like daydreaming.  As a result of the seizure and the medications he take to try to control them he struggles in school.
There are more people diagnosed with epilepsy than breast cancer annually yet you never hear about them because they are living with it in silence for fear of ridicule and being treated differently.
It is great that you had this kind of story to enlighten so many people.  I had been treated for epilepsy for about 35 years.  My last seizure was about 21 years ago.  They really have come a long way with medicines for it.  I have two children and each of them had seizures, one brought on by his fever and the other only had one.  They have not had any more since, so we hope they have outgrown them.
Thanks so much for letting this information out.
Thank you so much for the subject today on seizures.
My son Jon who is now 29 experienced the fevbrile
seizures for most of his young life.  HE had his first
one at age 10 months.  After getting the rescue squad
he was immediately rushed to the hospital and immediately put on phobarbian whic he had to stay on until the age of 9.  I saw the mood changes and how
his mental and physical developement were hindered. I
still believe that this has had a long time effect on
his mental growth.  I was just really glad that this condition was made public, I felt that I was the only
parent living with this dreadful situation.  I have
often wondered if there was any research being done
on this condition.  Please, let me know if our situation can be of help during any study.
I wan t to thank you for your segment on seisures.  I would like to see this topic expanded to the onset of seizure disorders in adult.  My son married in March of 2005 and his wife woke up to him having a seizure in bed.  That was the first of 6 he would have during that day.  After testing, he was sent home with a theraputic dose of anti-seizure medicine.  Five days later his wife went to the store for groceries and he had a grand mall.  When his wife returned home, he had inhaled his own vomit.  After 4 days in ICU, with inhalation pneumonia and more tests, we learned that our son had a Venious Angioma growing in his right frontal lobe of his neocortex.  This type of disorder we have been told onsets between the ages of 20 - 40 years and is inopperable.  It is considered a birth defect.  As the mom, I always wonder if I could have in someway prevented this.
There is so much information needing to get out to the public on this subject.  I would like to know of support groups for those who suffer with Epilepsy and for their families as well.
I'm so impressed to see that finally someone is taking a interest in getting the word out about seizures and epilepsy.  My 16 year old son has had idiopathic seizures for over 9 years.  And he will be one of the many that probably will never drive.  It's very important that american's learn to support the people and families that Epilepsy strike.

So thank you for the timely story today
I was really impressed with your epilepsy segment this morning. Kudos to Tiki Barber for talking about his family's personal experience.

Also, well done and thank you to the woman representing Cure. They sound like a great organization, and I hope to hear more from them in the future. Their video was nothing short of inspiring. It's great to see that someone is putting a human face on epilepsy without diminishing the terrible effects the disease can have on children and their families. Also, what a great job they've done to change the dialogue. We need to fund research and find a cure!

Great job!
What a fabulous segment.  I have a 3-year-old son with uncontrolled patrial-complex seizures.  It means so much to hear people get E out in the open!  You have raised so much awareness and given many people hope.  Thank you.  

A side note - The Epilepsy Foundation of Minnesota is doing an education week in our town the week of April 7th.  If you would like to see this wonderful group in action out in the community, come see us!

 I was so happy to see coverage on Epilepsy. I had one convulsion when I was 8 months old, and that was it until I turned 11 and that's when the seizures started. I had complex partial seizures for over 25 years before going through all the testing to see if I was a canidate for surgery.

My neurologist sent me to the Universtiy of Va in Chaarlotesville Va for ten days of testing. Doctors found scar tissue on the right side of my brain.

I was a canidate for the surgery and had the surgery in June of 2002. I have remained seizure FREE for five years now. It feels so good to have my Freedom back!  and to be able to drive again is such a blessing.

I have been blessed with three beauitful daughters all of which are healthy and do not have epilepsy. I do hope to see another segment on epilepsy not just for children but also adults. it can be so lonely when you think you have to suffer in silence because no one understands the condition.

I am a H.O.P.E. mentor for the epilepsy foundation in my area. Thanks again for the great job!

Cindy
My son was diagnosed with seizure disorder when he was 12.  They tell me his resistance was low due to flu symptoms and he suffered a grand mal seizure while traveling.  He is now 24 yrs. old, He takes Depakote 3 time a day to control.  He hasn't had a seizure due to medincine in quite a while.  Although when he misses his doses, he will have a breakthrough seizure.  We were also told he would grown out of them.  I am waiting for the Lord to just heal him totally.  I will say each time he has one they are less dramatic than the one before.  He has had less than 10 in twelve years.
I have a 40 year old brother that has had seizures since he was about a year old.  He started with just noraml seizures that did not last but a couple of minutes and just about one every two or three years.  Then, in May of 2005 he had a seizure that lasted 8 hours and had to be put on a vintalator for a day.  He then started having drop down seizures that would affect his everyday life.  Then, finally he had another seizure in October 2005 that literally almost killed him, it lasted 8 hours and he was on life support in ICU for about 5 days.  He now has a seizure about every 6 weeks with drop down seizures in between.  I am not telling this to scare anyone but most symptoms of epilepsy seem to be when a person is a child and not as dramatic but I want everyone to be aware that they can get progressivly worse.  The one thing that has seemed to help in his situation is the Vega Nerve Stimulator that was implanted near his heart in November, 2005.  It seems to bring him out of his seizures so they do not last as long.  I found this very weird that this story aired because he was at my house Saturday night and had a seizure. He is fine and it was not bad but it is nice to know there are other families out there like ours.  This disease has affected my family for almost 40 years and still affects us everyday.  My brother is an amazing man that just takes this in stride and goes on.  He never complains that he can't drive or that he is limited on his activity.  He is the most positive person you will ever meet in spite of his hand he has been dealt.  He is amazing and I wish everyone could have his big heart and live life to the fullest like he tries to do.
What an absolutely fantastic piece for the Today Show to host!  Thank you to that show and NBC for dedicating airtime to such an important and overlooked cause.  Epilepsy effects so many families around the world, and yet so little focus is put on finding a cure, this program was a breath of fresh air.  Without attention being paid to this disease (such as that given by Tiki Barber and the Today Show) and the crucial work being done by organizations like CURE to not only understand, but also successfully treat and prevent the disease, we will be hard pressed to make forward progress.
I was so struck by the video shown about the fathers of children with epilepsy that I decided to look on the internet a little and see where it came from.  I didn’t realize that CURE had produced that video, along with many others.  In fact, the organization has a fantastic website with information about epilepsy, lots of resources, and ways to become involved in finding a cure, in addition to some of the most touching and gripping videos I have ever viewed. They are simply brilliant, well produced with powerful stories of hope and perseverance in the face of tremendous odds.  What I liked most was this organization’s constant dedication to the belief that with the proper resources and energy, a cure for epilepsy is possible.  I encourage everyone to visit www.cureepilepsy.org   I promise it will be well worth your time.
Susan Axelrod, CURE and all those who are working to find solutions, answers and understanding for epilepsy should be highly commended for their dedication.  The Today show should commit more time to such individuals and organization because our society needs to be reminded of the hardships so many of us face.  But more than the hardship, it should be a reminder that with our combined efforts and energies, real solutions are possible.  Thank you to CURE and Susan for bringing us that awareness and hope.
Thank you so much for covering this topic on your show.  Many people do not understand this disorder or do not want to. My daughter was 6 years old when she had her first grand mal seizure.  she is now 11 years old and we were told that she would outgrow them instead as she got older they have gotten worse.  We thank GOD for everyday that she goes seizure free. And thank you to the people who research this disorder.


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