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This document is a sponsorship form for a golf tournament held in honor of Braxton Ried, seeking underwriting sponsorships for various event necessities.
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How to fill out play fore dravet
How to fill out Play FORE Dravet
01
Gather necessary information about the individual with Dravet syndrome.
02
Obtain a copy of the Play FORE Dravet application form.
03
Fill out personal details such as name, contact information, and relationship to the individual with Dravet syndrome.
04
Provide medical information related to the diagnosis and treatment of Dravet syndrome.
05
Include any relevant supporting documents, such as medical records or letters from healthcare professionals.
06
Review the completed application for accuracy and completeness.
07
Submit the application via the designated method (online, mail, etc.).
Who needs Play FORE Dravet?
01
Individuals diagnosed with Dravet syndrome.
02
Families or guardians of individuals with Dravet syndrome.
03
Healthcare professionals looking for resources to support patients with Dravet syndrome.
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What is the cause of Dravet's syndrome?
CAUSES. About 80% patients with Dravet syndrome have a mutation in their SCN1A gene. This gene provides instructions for making part of a sodium channel found mainly in the brain cells. The channel is involved in transmitting signals from one nerve cell to another.
Is Dravet syndrome like autism?
Unlike some other traits shared with autism, patients with Dravet syndrome are often overly social, although some may prefer interactions with adults versus peers. There are also reports of depression or anxiety, especially as children approach teen and adult years.
What does Dravet syndrome look like?
Symptoms of Dravet syndrome Tonic-clonic seizures affect the whole brain and start with a sudden loss of consciousness, followed by body stiffening (tonic phase) then jerking movements all over the body. Other children have hemi-clonic seizures that cause jerking on one half of the body.
What is the rarest seizure?
Dravet syndrome is a rare, catastrophic, lifelong form of epilepsy that begins in the first year of life with frequent and/or prolonged seizures. Previously known as Severe Myoclonic Epilepsy of Infancy (SMEI) 80% of people have a mutation in their SCN1A gene.
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What is Play FORE Dravet?
Play FORE Dravet is an initiative or organization aimed at raising awareness and funds for Dravet syndrome, a severe form of epilepsy that begins in infancy.
Who is required to file Play FORE Dravet?
Typically, individuals or organizations participating in fundraising activities related to Play FORE Dravet may be required to file relevant documentation, depending on local laws and regulations.
How to fill out Play FORE Dravet?
To fill out Play FORE Dravet, participants should follow the specific guidelines provided by the organization, which may include entering personal information, event details, and fundraising goals.
What is the purpose of Play FORE Dravet?
The purpose of Play FORE Dravet is to support research, raise awareness, and provide resources for families affected by Dravet syndrome.
What information must be reported on Play FORE Dravet?
Information that must be reported may include participant names, fundraising totals, event details, and any related financial disclosures as required by law.
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