Showing posts with label epilepsy research. Show all posts
Showing posts with label epilepsy research. Show all posts

Sunday, January 29, 2012

In The News

Margot
Lisbeth
Calvin
Excerpt from the article The Scourge of Epilepsy
Brunswick Times Record, Friday, January 27, 2012
Margot
By Madeline Curtis, age 14, Margot’s sister
I wish there was a cure. The pills are supposed to
work, and maybe they do—on other people. But they don’t work on Margot. The diet
didn’t work, either. The fancy diet, the one that led to so much stress in our
house, didn’t work. The seizures just keep coming back, and my little sister,
eight years old, has to endure them. I wish there was a cure so that Margot, who
can’t even speak or walk, wouldn’t have to struggle so much. I wish there was a
cure, because I’m tired of all the new medicines that show up in the cabinet
above the sink. I wish there was a cure, because I hate the helplessness I feel,
watching her limbs freeze and her eyes roll up into her head. I wish there was a
cure, because I want all of the people who carry the burden of epilepsy to feel
relief.
* * * * * * * * * *
Lisbeth
By Martha Miller, Lisbeth’s mom

Write about lost love, my professor says.
All I can think of is Lisbeth, and how I lost the little girl she was that day in
sparkling summer. She'd been ill and was feeling better, then awoke that morning
saying, “Mommy I don't feel good.” I laid her on the couch and gave her some
Tylenol. Twenty minutes later it happened: she was grey, her eyes rolled back,
the whites of them now yellow, moist, a faint clicking in her throat. Her body
was stiff, jittery. I yelled to my husband Garry to come. “Call 911,” he said,
and somehow I did. Waiting on the front steps for the ambulance the word
EPILEPSY kept playing in my head. The ambulance arrived and the men carried her
out. Garry rode with her. I followed in our car praying, “Oh God, please, this
is not how I want her to grow up." In the emergency room Lisbeth laid on the
stretcher. They'd cut her pink summer shorts in half, shoved tubes down her
throat. Garry leaned over her tiny body, her perfect pink six year old body, her
blue eyes, now shut. What (the Hell) was happening? I wanted to turn and run
away. Garry saw it in my face and said gently, “C'mon Mart.” I walked to the cot
where she lay, and I began to sing to her. I sang all the lullabies I'd sung to
her when she was a baby. I knew what my job was now.
* * * * * * * * * *
Calvin
By Christy Shake, Calvin’s mom
Our nightmare started when Calvin was eighteen months old. He had
spiked a fever, so we gave him some acetaminophen and called our local hospital.
The doctor assured us that we had nothing to worry about even though I’d told
him Calvin had serious neurological deficits. Within mere minutes of hanging up
the phone Calvin suddenly cracked like a whip into an arch stiff as a steel rod.
His eyes bulged and his lips pursed as if drawn up with thread. My husband
Michael gathered him up, instinctively—worriedly—rocking him back and forth as
if to jostle the seizure out while I white-knuckle-called for an ambulance. “My
son is having a seizure,” I blurted, “he’s not breathing—he’s turning blue!” The
walls began closing in on me. Sounds morphed and muffled. Everything around me
looked hazy—blurred—as if in a cloud, except for my boy who remained in sharp
focus. Cradled in Michael’s arms, now jerking rhythmically—violently—Calvin
turned ashen like a corpse and his eyes rolled back into his head. Time stood
still as in a dream. I wasn’t sure if Calvin was alive even though his
convulsions persisted—I couldn’t find a pulse.My next memory is of the
cold hard edges in the ambulance, the sterile, sickeningly gray vinyl benches.
My tiny child lay in the center of a sheeted white gurney—his eyes now vacant
and still—staring up in a catatonic gaze at the bluish light in the ceiling. I
feared he might remain that way forever because of the seizure, or worse—die.
Little did I know then that some kids do.
* * * * * * * * * *
Margot, Lisbeth and Calvin are just three of as
many as three million Americans, and their families, who suffer from epilepsy,
and who likely will not be released from their misery until a cure is
discovered.During this brief campaign please, show your compassion and
donate to CURE epilepsy research at:

Tuesday, January 17, 2012

Lisbeth's Story on Calvin's Story

Brunswick, Maine writer Christy Shake and her son, Calvin.


I have the great honor of being featured today on Christy Shake's noble blog, Calvin's Story. Christy writes:


My son Calvin was born six weeks early with significant neurological problems of unknown origin. When he turned two he was diagnosed with epilepsy, which eclipsed all other adversity we had yet encountered. No drug or dietary treatment has completely controlled his seizures and they continue to pummel our little boy. The seizures and drugs have stifled his development and there seems to be no end in sight to this nightmare. The only hope is a cure. On behalf of Calvin and the three million Americans who suffer from epilepsy please help bring us one step closer to that dream.

Sunday, January 9, 2011

Butterfly




Lisbeth had dinner with us last night at her favorite restaurant, China Rose. Lis has gone through so many changes lately, the most visible being pronounced weight loss. Medications had caused weight gain and bloating the past few years, not a good side effect. When Lisbeth was very young, she was emaciated. So we'd lost track of the real Lis as far as size. We think that now she is where she is supposed to be, around a size 6. Lisbeth had a loss of appetite while on Keppra, so that, combined with taking her off Vimpat last spring (one of the drugs that caused weight gain) resulted in dramatic weight loss. Now we want to be certain that she doesn't lose too much weight! She is eating better since off the Keppra, so we have fingers crossed that she's hit a plateau.
Lisbeth's psychological state is improving as well. Her helpers report that she's like a new person off Keppra - more positive, relaxed, and energetic, even though she's having seizures again. She told one of her helpers that the old voice in her head that was saying "getting dead" is going away. She said, "It's going in the trash. Now there is the new sweet voice." (Lisbeth continues to blow us away with her insights...)

Things can still change on a dime - last night Lisbeth was fine for the first half of dinner then suddenly reared up out of her chair panic stricken - saying she needed to go home with us right that minute. We tried to gently re-direct her, but she remained agitated, and started to feel like she was going to have a seizure. We used her magnet, and finally had to administer her PRN lorazepam. We went back to her house, and it took a couple of hours to calm her down and settle her in for the night. I called her house this morning, and her helper reported that she is clear again and in good spirits. The up and down and back and forth of it. This is how it is. It will never be perfect, but all things considered, for now, it's a whole lot better.

Wednesday, April 28, 2010

The Kid Hospital, Part II

Once Lisbeth recovered from the first surgery, she had daily visitors. High Tea with Sister Kaitlyn...

High Tea with Jessica Lindgren, who was in the hospital for long term monitoring...

Lunch with Gramma and Grampa Simmon (Lis-ism for Simmons)...

Cousin Elizabeth stopped in on her way to a dance recital...



Sister Kaitlyn and Brother Eben...

Making funny faces...

Brother Alec and Brother Andy. Lisbeth's illness has been a strengthening experience for my other children, but also a very, very difficult way to grow up. There need to more resources for families with children with special needs regarding the challenges for the siblings...

Place of refuge in the middle of the city...

...where tears were shed and many prayers voiced aloud to these magnificent old beech trees...

Visits from other kids in The Kid Hospital...

...who enjoyed making art with Lisbeth...

Paper plate ladies and rubber glove critters...

More airplane glue...

New headdress...

A sweet poem from Gramma Simmon...
At this point the doctors were gradually taking Lisbeth off her meds to stimulate seizure activity. With the implanted electrodes, they would now be able to get an EEG with far more detailed information than a topical EEG can yield.
More pics tomorrow...

Monday, February 1, 2010

February = Love

Lisbeth Miller loves Little Milkweed...
...and Little Milkweed loves Lisbeth Miller!
Lisbeth's lovely Valens (Lis-ism for Valentines)...
...with the heart cuts! (another Lis-ism...)

Available now in Lisbeth's Etsy shop!
I love Lisbeth's new shirts!


C'mon over to Brain Storm Studio and do a little shopping for someone you love for Valen's Day! A portion of all Lissie's sales goes to support epilepsy research. Gotta love that!