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[trx_sc_title title_style=”accent” title_align=”center” title_color=”#5c1a9f” link_style=”default” scheme=”taylen_custom” title=”Welcome to the ||Taylen Lauren Horton Foundation!” subtitle=”Let’s Help Together”]
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[trx_sc_button type=”default” new_window=”” icon_position=”left” hide_on_wide=”” hide_on_desktop=”” hide_on_notebook=”” hide_on_tablet=”” hide_on_mobile=”” title=”Read Taylen’s Story” link=”/about/”]
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[trx_sc_title title_style=”default” title_tag=”h1″ title_align=”center” link_style=”default” title=”Help Taylen strike out cancer!” subtitle=”Let’s Help Together”]
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[trx_sc_title title_style=”accent” title_tag=”h4″ link_style=”default” title=”Taylen’s Story” description=”Taylen, born a bright-eyed bundle of joy to William and Jenece Horton, didn’t experience any issues in the few months of life. That is until her parents noticed at about three months old, that their baby girl was having some difficulty with her arm. Taylen’s arm started to jerk unexpectedly and the infant clinched her fist tightly, which was troubling enough for her parents to take notice.”]
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This fundraiser is for Taylen and to help so many other children affected by Dravet Syndrome to help them offset medical expenses.

Dravet syndrome, previously known as severe myoclonic epilepsy of infancy (SMEI), is a type of epilepsy with seizures that are often triggered by hot temperatures or fever. It is treated with anticonvulsant medications. It often begins around six months of age.

Taylen was diagnosed with Dravet Syndrome at the age of one after a painful year for her parents trying to figure out what was wrong and an abundance of tests, misdiagnoses and ill health’.

Dravet syndrome has been characterized by prolonged febrile and non-febrile seizures within the first year of a child’s life. This disease progresses to other seizure types like myoclonic and partial seizures, psychomotor delay, and ataxia. It is characterized by cognitive impairment, behavioral disorders, and motor deficits.

It affects around one in 20,000 people worldwide.

With her strong will and EVERYONE’S prayers and support, we all believe we can help Taylen and so many more children affected by Dravet Syndrome. It’s time we come together and help Taylen and her family in this time of need!! Please help in any way you can!

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[trx_sc_title title_style=”accent” title_tag=”h4″ link_style=”default” title=”Getting to Know Taylen”]
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[trx_sc_title title_style=”accent” title_tag=”h4″ link_style=”default” title=”Taylen’s Story”]

This fundraiser is for Taylen and to help so many other children affected by Dravet Syndrome to help them offset medical expenses.

Dravet syndrome, previously known as severe myoclonic epilepsy of infancy (SMEI), is a type of epilepsy with seizures that are often triggered by hot temperatures or fever. It is treated with anticonvulsant medications. It often begins around six months of age.

Taylen was diagnosed with Dravet Syndrome at the age of one after a painful year for her parents trying to figure out what was wrong and an abundance of tests, misdiagnoses and ill health’.

Dravet syndrome has been characterized by prolonged febrile and non-febrile seizures within the first year of a child’s life. This disease progresses to other seizure types like myoclonic and partial seizures, psychomotor delay, and ataxia. It is characterized by cognitive impairment, behavioral disorders, and motor deficits.

It affects around one in 20,000 people worldwide.

With her strong will and EVERYONE’S prayers and support, we all believe we can help Taylen and so many more children affected by Dravet Syndrome. It’s time we come together and help Taylen and her family in this time of need!! Please help in any way you can!

[trx_sc_socials icons=”%5B%7B%22link%22%3A%22http%3A%2F%2Fwww.facebook.com%2Fsharer.php%3Fu%3D%7Bhttp%3A%2F%2F198.57.200.253/~jeneceh%2Fjulias-story%2F%7D%22%2C%22icon%22%3A%22icon-facebook%22%7D%2C%7B%22link%22%3A%22https%3A%2F%2Ftwitter.com%2Fintent%2Ftweet%3Ftext%3D%7BJulia’s%20Story%7D%26url%3D%7Bhttp%3A%2F%2F198.57.200.253/~jeneceh%2Fjulias-story%2F%7D%22%2C%22icon%22%3A%22icon-twitter%22%7D%2C%7B%22link%22%3A%22https%3A%2F%2Fplus.google.com%2Fshare%3Furl%3D%7Bhttp%3A%2F%2F198.57.200.253/~jeneceh%2Fjulias-story%2F%7D%22%2C%22icon%22%3A%22icon-gplus%22%7D%5D” title_style=”default” title_tag=”h6″ title_align=”left” link_style=”default” hide_on_wide=”” hide_on_desktop=”” hide_on_notebook=”” hide_on_tablet=”” hide_on_mobile=”” title=”Share the Story”]
[trx_sc_title title_style=”accent” title_tag=”h4″ title_align=”left” link_style=”default” title=”Taylen’s Updates”]
[trx_sc_blogger type=”excerpt” hide_excerpt=”” no_links=”” cat=”2″ show_filters=”” orderby=”post_date” order=”desc” slider=”” title_style=”default” title_align=”left” link_style=”default” count=”2″ columns=”1″]
[trx_sc_title title_style=”default” title_tag=”h5″ title_align=”left” link_style=”default” title=”Subscribe for Updates About Taylen”]

[trx_sc_title title_style=”default” title_tag=”h5″ title_align=”left” link_style=”default” title=”Subscribe for Updates About Taylen”]

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[trx_sc_title title_style=”default” title_tag=”h2″ link_style=”default” title=”Help Me Find a Cure”][trx_sc_title title_style=”default” title_align=”right” link_style=”default” subtitle=”- Taylen”]
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[trx_sc_title title_style=”default” title_tag=”h1″ link_style=”default” title=”Help Me Find a Cure”][trx_sc_title title_style=”default” title_align=”right” link_style=”default” subtitle=”- Taylen Lauren Horton”]
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[trx_sc_title title_style=”default” title_tag=”h1″ title_align=”right” link_style=”default” title=”Help Me Find a Cure”][trx_sc_title title_style=”default” title_align=”center” link_style=”default” subtitle=”- Julia Hunter”]
[trx_sc_title title_style=”accent” title_tag=”h4″ title_align=”left” link_style=”default” title=”Make a Donation. Any Amount is Appreciated!”]

This fundraiser is for Taylen and to help so many other children affected by Dravet Syndrome to help them offset medical expenses.

Dravet syndrome, previously known as severe myoclonic epilepsy of infancy (SMEI), is a type of epilepsy with seizures that are often triggered by hot temperatures or fever. It is treated with anticonvulsant medications. It often begins around six months of age.

Taylen was diagnosed with Dravet Syndrome at the age of one after a painful year for her parents trying to figure out what was wrong and an abundance of tests, misdiagnoses and ill health’.

Dravet syndrome has been characterized by prolonged febrile and non-febrile seizures within the first year of a child’s life. This disease progresses to other seizure types like myoclonic and partial seizures, psychomotor delay, and ataxia. It is characterized by cognitive impairment, behavioral disorders, and motor deficits.

It affects around one in 20,000 people worldwide.

With her strong will and EVERYONE’S prayers and support, we all believe we can help Taylen and so many more children affected by Dravet Syndrome. It’s time we come together and help Taylen and her family in this time of need!! Please help in any way you can!

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[trx_sc_title title_style=”accent” title_tag=”h4″ title_align=”center” link_style=”default” title=”Thanks to All of You Who are Supporting Me”]
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