Epilepsy Association of Utah

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Seize: The Story – Taylor Ferguson

Monday, September 1, 2014

 
Seize:  The Story – Taylor Ferguson
 
 
Nobody
knew I was having seizures, not even my parents. I just thought I was having
blackouts as I would call them, until I went to my guitar lesson and had one of
my “blackouts”.  My guitar
teacher worked with epileptics so she knew I had just had a seizure.  I remember peeking around the corner and
wondering why my guitar teacher was at my house, what they were talking about
and why my mom was crying?  We then took
a visit to a doctor’s office…it was true, I had epilepsy, but at the age of
nine I had never heard of epilepsy before, so I just thought it was like the
flu and would go away.  The day I
realized it wouldn’t go away I cried myself to sleep.

School was
hard!  I lost almost all of my friends
because they thought I was “contagious” and when I explained to (my
at the time best friend) that I wasn’t she just said “okay” and
walked away.  See if you were friends
with me you couldn’t be popular.  It took
me awhile to really realize what happened with my best friend; at the time
everything was crashing in on me.  I got
made fun of all the time; it was so bad my mom put me in home hospital.  When I was having a lot of seizures I would
be home with a tutor but when they would get under control I would go back to
normal school.  I then went to a charter
school in eighth grade just so I could get away from all the kids that knew
about my epilepsy and would make fun of me. 
When I was sixteen I had brain surgery and had a piece of the brain
removed to try and stop my seizures, so I was out of school my sophomore year.
I then went back to school my junior year of high school.  But with only the people from my elementary
knowing me, well you would think high school kids would be more mature, no some
of them still made their stabs at me I was just not as affected by it and knew
how to stand up for myself.

About two
years after my brain surgery I was going to get my driver’s license, the day
before I was going to take the driver’s test I had another seizure.    My
parent’s and I started looking into other options. We then decided to have a
VNS (Vagus Nerve Stimulator) implanted. 
We decided to have the VNS surgery (which is a device like a pace maker
that is hooked to the vagus nerve and sends shock waves through my brain every
3 minutes for 30 seconds to try to stop or lessen the severity of my seizures
or after affects), about six months to a year later the VNS stopped working and
I gave up all hope.  Nothing had worked and
there was nothing left to do; pills didn’t work and there was no surgery left.

I never
thought that I would get married because of my epilepsy but when I was twenty
one I found the greatest guy in the world, who loved me for me and didn’t care
that I had epilepsy like a lot of the other guys out there.  So he proposed and I said “yes” and
we were married about six months later. A little while later I got pregnant and
I had an ectopic pregnancy (where the baby is growing in the Fallopian tube),
but two years later I got pregnant again and had a daughter in May 2014.

Granted I
have been talking about my epilepsy, so it hasn’t been the best of memories. My
life hasn’t been all bad.  I have an
amazing family, daughter, husband, and friends, have had awesome vacations to
Bear Lake, Pinedale, Disney World/Florida, Disney Land, Island Park and many
more.  I have had a great life with many
bad experiences but I wouldn’t take them back for anything because they have
made me who I am today. 

I hope this
helps someone out there in some way!

Taylor A. Zobell Ferguson

Epilepsy Association of Utah & Hope 4 Children With Epilepsy – Federal Call to Action

For Immediate Release 

Epilepsy Association of Utah &
Hope 4 Children With Epilepsy
Federal Call to Action
SALT LAKE CITY, Utah – Tuesday,
August 26, 2014
One year ago today, the
Epilepsy Association of Utah became the first epilepsy organization in the
United States to take a stance in support of expanding treatment options to
include high-CBD/low-THC cannabis extracts. Since that time, dozens of organizations have
followed suit, leading to the passage of HB105 “Charlee’s Law” in Utah and
similar bills across the nation.
The Epilepsy Association of Utah and Hope 4 Children with Epilepsy
have withheld public support of federal legislation until today. We have now
chosen to openly support federal bill H.R. 5226: Charlotte’s Web Medical Hemp
Act of 2014, sponsored by Rep. Scott Perry (R – PA), and will work toward its
passage. The bill proposes to exclude industrial hemp and cannabidiol (CBD)
from the definition of marijuana, granting those suffering with epilepsy access
to the treatment according to the laws of their own states. Industrial hemp is
defined as cannabis with THC content below .3%.
“A federal change in policy regarding cannabis is essential,’ said
Annette Maughan, President and CEO of the Epilepsy Association of Utah, “My son
can be treated with cannabis openly in Utah, but he can’t go to Disneyland with
his family? All because his oil is grown in the United States? The incongruity
of that is staggering.”

We welcome the addition of other federal bills regarding the rescheduling of
cannabis and reserve the right to evaluate each on the merits of its potential
impact. The federal stance that cannabis holds no medicinal value places it on
Schedule 1 of the DEA’s list of controlled substances:

“Schedule I
drugs, substances, or chemicals are defined as drugs with no currently accepted
medical use and a high potential for abuse. “

With the published reports of success in treating epilepsy, among other
conditions (http://hope4childrenwithepilepsy.com/research-links/), the claim of
“no medical use” is no longer valid; therefore, cannabis should be rescheduled.
Because cannabis is currently listed on Schedule 1, research and compassionate
use are very difficult to accomplish, even with the involvement of medical
specialists and research institutions. This needs to change.
We call upon all federal legislators to join us in this very
critical and urgent cause by supporting and/or co-sponsoring H.R. 5226:
Charlotte’s Web Medical Hemp Act of 2014. Likewise, we urge our state
legislators, as well as all citizens of Utah and the United States, to let
their voices be heard in support of those suffering with intractable epilepsy
in our country.
The language for H.R. 5226: Charlotte’s Web Medical Hemp Act of
2014 can be found at https://www.govtrack.us/congress/bills/113/hr5226/text.
#####
ABOUT THE
EPILEPSY ASSOCIATION OF UTAH
Founded in 1973, the Epilepsy Association of Utah is a
501(c)(3) charity dedicated to enhancing the quality of life for all
individuals living with epilepsy and seizure disorders. One in 26 people will
develop epilepsy at some time in their lives, leading to over 100,000 people with
epilepsy in Utah alone. Epilepsy is the fourth most common neurological
disorder in the US, after migraine, stroke, and Alzheimer’s disease. The
Epilepsy Association of Utah offers a public education program, statewide
support groups, personal and professional advocacy, college scholarships, art
exhibits, educational conferences, summer camp and more.
ABOUT HOPE 4
CHILDREN WITH EPILEPSY
We are parents of children with severe forms of epilepsy. The
seizures take a toll on our children’s overall health, ability to function, and
quality of life, leaving them with increased risk for sudden death. We
desperately
need new treatment options. We lobby to make high-CBD/low-THC
cannabis extract available in Utah, and across the United States, to those who
suffer with intractable epilepsy. The extract is not smoked and does not cause
a “high”, but it can save the lives of children.
Press Contact: Jennifer May
Phone:                    801-400-0046
Email:                      jennifer.h.may@gmail.com
Website:               www.epilepsyut.org
Website:               www.hope4childrenwithepilepsy.com

Seize: The Story – Jenny Rebecca Lester

My name is Jenny and I am turning 4 this month!  I love to dance and play school with my Aunt.
My mom noticed that I would stare off into space and would fall down for no reason.  She made an appointment with my pediatrician.  My doctor thought it sounded like I was having seizures so he referred me to a neurologist.  The neurologist ordered an EEG nothing wrong.  He decided we needed to have an MRI of my brain.  We found a sore on my brain that I have had since I was born.  I started taking Keppra and my seizures went away for 7 months.  We increased my medicine and I have been fine the past 5 months.  I have become very hyper and keep my parents and grandparents very busy!  My doctor is very proud of how well I balance.  I already know my colors, abc’s and some of my numbers.

Press Release: Epilepsy Association of Utah Announces “Seizure Smart” Education Conference

For Immediate Release

Epilepsy Association of Utah Announces 
“Seizure Smart” Education Conference
SALT LAKE CITY – Monday, May 19, 2014 
The Epilepsy Association of Utah (EAU) announces its annual “Get Seizure Smart!” Epilepsy Education Conference, presenting the latest in epilepsy science and treatment options, as well as tools and resources for those affected by epilepsy. The “Seizure Smart” conference will be held Saturday, June 7, 2014 from 8 a.m. to 4 p.m. at Little America Hotel, 500 South Main Street, Salt Lake City. Individuals with epilepsy, families of those affected, medical personnel, educators, and first responders, as well as the general public, are invited to attend.

Dr. Ian Miller, pediatric neurologist at Miami Children’s Hospital, international expert in treating Dravet syndrome and member of the Dravet Syndrome Foundation’s Professional Advisory Board, will be the keynote speaker and special guest. He is scheduled to discuss the discovery of genetics in epilepsy and the push for research into CBD-based treatment options.

The conference will feature breakout sessions with renowned experts presenting on topics including the complexities of epilepsy, genetics of epilepsy, latest treatment options, alternative therapies, coping and advocacy, managing behaviors and sibling behaviors, mental health, trusts and living wills and patient resources. Several organizations and vendors will be in attendance with tables providing helpful information, a few of which include the Division of Services for People with Disabilities, Hope 4 Children With Epilepsy, Utah Kids, Utah Parent Center, Autism Council of Utah and Brain Balance Centers.

With the recent passage of HB105 “Charlee’s Law” allowing for the possession of high-CBD/low-THC cannabis oil for the treatment of intractable epilepsy in adults and children, the EAU will present the specifics of the new Hemp Extract Registration Program and the safe and effective use of the therapy. Jennifer May, co-founder of Hope 4 Children With Epilepsy, the EAU’s parent advocacy group who lobbied in favor of the bill, will be walking patients through the details of the law and the processes required to gain access to approved extracts for treatment. As the leading provider of high-CBD/low-THC cannabis oil, Realm of Caring’s own Heather Jackson will present information about the oil as a treatment for intractable epilepsy. Realm of Caring is a non-profit organization in Colorado who oversees the cultivation of the Charlotte’s Web plant and its processing and distribution as Alepsia, a non-psychoactive extract infused in oil.

“Our goal with the Seizure Smart Epilepsy Conference is to provide those affected by epilepsy with the tools needed to educate themselves, as well as those around them, and obtain the best treatments possible, whether they be mainstream or alternative,” said April Sintz, EAU Conference Chairperson and H4CE leadership member. “We want to empower people by giving them choices and resources that are available to all of us here in the state of Utah,” Sintz stated.

Cost for the conference is $30 for the public ($15 for EAU members) if registered in advance; an additional $10 charge will apply for those registering at the door. A light breakfast, a catered lunch, and a “loot bag” will be provided for each attendee. Registration is open on the EAU website at http://epilepsyut.org/conference2014.html.

##### 
ABOUT THE EPILEPSY ASSOCIATION OF UTAH 
Founded in 1973, the Epilepsy Association of Utah is a 501(c)(3) charity dedicated to enhancing the quality of life for all individuals living with epilepsy and seizure disorders. One in 26 people will develop epilepsy at some time in their lives, totaling over 100,000 people in Utah alone. Epilepsy is the fourth most common neurological disorder in the US, after migraine, stroke and Alzheimer’s. The Epilepsy Association of Utah offers a public education program, statewide support groups, personal and professional advocacy, college scholarships, art exhibits, educational conferences, summer camp and more. Visit http://epilepsyut.org for additional information. 

Media Contact: Jennifer Hardy May 
Email: info@epilepsyut.org 
Website: www.epilepsyut.org 

Seize: The Story – Austin Beardall

My son Austin, who had been a totally normal baby up to this point, had his first seizure at four months old. What appeared at first to be a hyper-moro reflex turned into him having more than 12 episodes of his whole body jerking and his eyes open and staring in 12 hours, lead us to believe he was really having seizures. The following day an EEG was performed and indeed he was having seizures. We began mediation that for the next two months seemed to control his seizures and then the seizure pattern changed and he began having more of a tonic/clonic-generalized seizure. Most of Austin’s seizures happen when he is going to sleep, during sleep and upon waking up in the morning. Because of this he cannot sleep alone or he would try to get to someone and hurt himself, therefore he has to sleep with a member of our family at all times.

Since four months of age Austin has never been completely controlled and has been on approximately 10 different medications, including ACTH injections daily at nine months old for 30 days, even with all of these we have not been able to help him be completely seizure free. Many of these medications are given together in hopes of control. Currently, Austin takes three different seizure medications and recently had to weaning off of one due to the side effects that caused a severe tremor in his hands, much like that of a Parkinson’s patient, this tremor was preventing him from performing normal tasks such as feeding himself and getting dressed. Austin has had up to as many as 10-15 seizures in a day and currently is having anywhere from 1-8 per day. His seizures typically last around 30sec. to 3 minutes, causing total body shaking, eyes opening staring or eye fluttering, gurgling noises, and sometimes he tries to climb out of bed.

In 2001, Austin had a Vagus Nerve Stimulator (VNS) placed. The purpose of the VNS is to stimulate the brain counteracting the electrical impulses that the brain is giving off causing seizures and hoping to stop the seizure from either happening at all or decreasing the severity of the seizure. For Austin the VNS is on a setting called rapid cycle, which means that it is stimulating his brain for 25 seconds than off for 5 seconds than on again continually. The VNS also has the capability to increase the amplitude of the stimulation and stay on for one full minute if a seizure is seen by family, we do this by swiping across his chest with a high powered magnet where the VNS is located. Because, the VNS is ran by a battery it only lasts about 4-5 years requiring a replacement of the battery pack.

So far, Austin has had three surgeries just for his VNS since it was placed in 2001. Austin started showing development delays around the age of two and has continued to have delays throughout his life. He has speech, fine motor, and academic delays; he has been classified as Intellectually Disabled. He is 20 years old and academically functions at about a 4-5 year old and socially about a 12-14 year old. He also has a diagnosis of ADHD and Anxiety, both requiring medications. He also needs medications to help him sleep at night.

Even through all of this Austin is a fun, loving, energetic young man that is loved by all! His favorite thing to do is play his Xbox and he can play just about any game you give him. Austin also participates in special needs sports league and love to play baseball, basketball and soccer. He has lots of friends and it seems like anytime we are out he finds someone he knows. We are so proud of all the accomplishments he has had in his life and look forward to many more!

Keri Beardall