Showing posts with label Connecticut Epilepsy Advocate. Show all posts
Showing posts with label Connecticut Epilepsy Advocate. Show all posts

Walk raises epilepsy awareness



Walk raises epilepsy awareness

Published: Thursday September 23, 2010 by Carole Walker, Correspondent

Robert Fiore of Milford, president and founder of Connecticut Epilepsy Advocate, said that even though the first known description of epilepsy, from Hippocrates' "On the Sacred Disease," dates to 350 B.C., many people today, more than 2,000 years later, do not understand the condition and so the stigma remains.

Hippocrates wrote, "Persons habituated to the disease know beforehand when they are about to be seized and flee from men; if their own house be at hand, they run home, but if not, to a deserted place, where as few persons as possible will [see] them, and they immediately cover themselves from shame of the [affliction]."

Connecticut Epilepsy Advocate, a nonprofit organization, was created by Fiore in November 2009 in large part to educate people about the condition, provide support and resources, and help erase the stigma often associated with epilepsy.

The first annual "Walking Miles for Epilepsy" occurred Wednesday, Sept. 15, with Fiore beginning his solo walk on U.S. Route 1 at the Housatonic River, and ending 10 miles later at the University of New Haven.

Fiore said, "The whole idea was to let people know about the organization and let them know we are here."

To that end, Fiore submitted postings to public access channels, and posted the information on the Connecticut Epilepsy Advocate Web site, ct-ea.org Fiore hopes to make this an annual event and involve more people, whether they want to walk 500 feet or five miles for epilepsy.

To date, Connecticut Epilepsy Advocate is continuing to receive donations for the walk, and all proceeds will go to Yale New Haven Hospital's epilepsy program.

According to Connecticut Epilepsy Advocate, epilepsy is a neurological condition that from time to time produces brief disturbances in the normal electrical functions of the brain. Epilepsy affects more than 50 million people in the world, more than three million in the United States, and approximately 60,000 in Connecticut.

Fiore, diagnosed with epilepsy at nine months old, has had hundreds of epileptic seizures throughout his life.

"It is difficult for many people who suffer from epilepsy to live a normal life," he said. "After I'd regain consciousness following a seizure, I'd be out for the rest of the day because of all the excruciating head pain and the toll it would take on me.

"In some cases", Fiore continued, "it's hard for a person to get a job or have a relationship. It's tough on young people because kids will see kids with epilepsy have a seizure and often they won't want to touch them or have anything to do with them."

Fiore has been free of seizures for the past three years through a combination of prescription medicine and a temporal lobectomy, a surgical procedure in which a cut is made to the place in the left temporal lobe that triggers seizures.

In addition to the annual Walking Miles for Epilepsy event and hosting the Web site ct-ea.org Connecticut Epilepsy Advocate has a Facebook page that provides information and support to its 1,170 friends, and it has plans for future events and fund-raisers.

Fiore said, "We at Connecticut Epilepsy Advocate are going to do everything we can to erase the stigma of epilepsy by helping to inform people about epilepsy, and provide support in any way we can."

The Connecticut Epilepsy Advocate, Robert Fiore, Walking Miles for Epilepsy

By: Maggie Griffin

The Connecticut Epilepsy Advocate, Robert Fiore, the President and Founder will be starting the 1st annual Walking Miles For Epilepsy on September 15th. It will begin 8:00AM at the Washington Bridge in the Devon section of Milford and along U.S. Rte 1 to The University of New Haven.

With Fiore leading the walk, he is raising the bar in awareness through his work, research and dedication to those who have Epilepsy. Daily Fiore receives emails from professional to personal stories of those with Epilepsy.

Epilepsy is a common chronic neurological disorder characterized by recurrent unprovoked seizures. Seizures are excessive or synchronous neuronal activity in the brain. Epilepsy is usually controlled, but cannot be cured with medication, although surgery may be considered in difficult cases. However, over 30% of people with epilepsy do not have seizure control even with the best available medications.

With Robert Fiore, a mission he is dedicated to, Epilepsy awareness and resource information has, and continues to, reach levels where bringing the awareness help those who have epilepsy. Robert has traveled a long journey as one with epilepsy. Since he began his mission to bring awareness, he has captured the eyes and ears of others in a large fashion of attention. He has been seen in articles in several sources.

Please take a moment and watch the video about Epilepsy below to understand the impact one with Epilepsy faces along with the strength and examples they set for others with Epilepsy. With Robert Fiore being there to provide resource information and support, millions across the globe will know they are not alone.

November is Epilepsy Awareness Month. On September 15th, 2010, Robert Fiore is putting is Best Foot Forward Walking Miles for Epilepsy. Visit:www.CT-EA.org, where you can find information and resource links about Epilepsy along with writing your personal experience to Robert Fiore, Connecticut’s Epilepsy Advocate.

The Connecticut Epilepsy Advocate is proud to announce its: First Annual "Walking Miles for Epilepsy"

The Connecticut Epilepsy Advocate is proud to announce its:

First Annual

"Walking Miles for Epilepsy"

Wednesday, September 15, 2010.

Robert Fiore, the President and Founder will be starting 8:00AM at the Washington Bridge in the Devon section of Milford and walk along U.S. Route 1 to The University of New Haven.

This year's donations will be used for the The Yale Epilepsy Program. Please make checks payable and sent to:

Connecticut Epilepsy Advocate, Inc.
20 Salem Walk
Milford, CT 06460-7132

The Yale Epilepsy Program provides promising options for many adult and pediatric patients with epilepsy. Internationally known for clinical excellence and innovative research, this program was one of the nation's first and has evolved into one of the most active and advanced in the world.

For more information please visit our web site: www.ct-ea.org

The Connecticut Epilepsy Advocate, Inc. is a 501 (c) (3) Non-Profit Organization. Because we are Connecticut's latest independent organization whose goal is to make people "Aware About Epilepsy" we will handle a very broad-based realm of responsibility. We are planning to start various events and fundraisers throughout the state. For each event we are hoping for the largest amount of press coverage possible in Connecticut.

Respectfully submitted,

Robert A. Fiore,

President and Founder

Connecticut Epilepsy Advocate


…Progress Through Awareness

www.ct-ea.org

Maggie's Corner: The Face behind Connecticut Epilepsy Advocate Robert Fiore

Maggie's Corner: The Face behind Connecticut Epilepsy Advocate Robert Fiore

The Face behind Connecticut Epilepsy Advocate Robert Fiore




For over 4 years, Robert Fiore has dedicated to bring awareness in Connecticut on behalf of those with Epilepsy. Bringing Epilepsy awareness to a higher level, Robert’s web site was officially launch in November of 2009, this web site is www.ct-ea.org. This web site has been growing since and is updated weekly. Robert encourages people world-wide to submit their experience to post on this web site. "It is amazing what can be learned through sharing real experiences from people who have Epilepsy, even those who are related to family members with epilepsy or have friends with epilepsy",said Robert.

Robert, now 55 years old, is a role model to those who have epilepsy. Since he was 9 months old, he was diagnosed with epilepsy, leaving his life’s mission to help others with epilepsy as well as their family and friends. The web site, along with the Facebook page called, Connecticut Epilepsy Advocate, brings awareness and attention along with links to valuable information to gain access to resources for help and assistance. Robert Fiore is registered with the State of Connecticut as The Connecticut Epilepsy Advocate, Inc. The organization’s purpose will keep the provisions and requirements of Section 501 (C) (3) of the Internal Revenue Code, as amended in 1986, as amended.

Why is Robert dedicated to bring awareness about epilepsy? Because having epilepsy, Robert knows, along with others, the importance of bringing the awareness of Epilepsy to the Public. He is available at all times, bringing support to individuals with epilepsy and their family along friends. “I will gladly speak to anyone who has epilepsy or who has a family member or friend with epilepsy, helping them anyway I can. If there is something I do not know, and trust me I do not know it all, I will do my best to find someone for them to provide the information they need”, said Robert.

Robert has many sources from information, links, and transportation, along with personal stories, support groups, events, glossary of terms and more on his web site. The Connecticut Epilepsy Advocate was formed as an alternative organization to make more people aware about epilepsy. Robert has set goals to focus on the many facts of epilepsy not currently explored to their fullest. Those facts are: testing, medications, N.I.H funding, support groups, senior scientist, junior scientist, HOPE mentoring, research dollars.

Felicia North, who met Robert a few years ago, stated it is excellent to find another web site source of information as Robert’s web site is not connected to the Foundation’s site. Louise Harris considers Robert as one of the key peoples in the state in bringing the awareness about epilepsy as her daughter has epilepsy as well. Louise Harris founded the support group for epilepsy in Stamford, Connecticut.
Here is a fact – an average of over 3 million people in the United States has the epilepsy disorder. I feel it needs as much funding and attention as with other diseases with similar numbers.

As Robert Fiore’s dedicated mission to help others, I stress more people need to become aware of epilepsy. I admire what Robert is doing to bring this awareness out in the open to raise more awareness as I told him that I have relatives and friends with epilepsy as well.

The mission, the cause and the courage is what defines Robert Fiore. Robert strongly emphasizes; “The objective of the Connecticut Epilepsy, Inc., is to assist individuals afflicted with epilepsy and their family or friends. We help the unique needs encountered by those with epilepsy, sharing experiences of all aspects of daily living, providing information about where to find services and support.” Robert includes; “there are support groups in Connecticut located in Milford, Bethel, Middletown and the newest location in Stamford, Connecticut.”

Robert has traveled a long journey as one with epilepsy. Since he began his mission to bring awareness, he has captured the eyes and ears of others in a large fashion of attention. He has been seen in articles in several sources. To archive these articles, you can review them as follows: written by reporter Pam McLoughlin in The New Haven Register on November 9th of 2008 and again on November 10th 2009, another written by reporter Devon Lash in The Advocate on June 13, 2009. You can view on youtube.com under the key phrase “Robert Fiore Epilepsy” to view the videos when Robert appeared on April 12th and 13th, 2008 advocating on Cablevision’s 12 on Health along with his first interview about epilepsy on Fox 61 in November 2007.

It is an honor for me to interview and speak to Robert Fiore, reporting the word of awareness about Robert in his mission, an awareness to bring more awareness about Epilepsy to more people in CT and world-wide. To include announcing who is the face behind Connecticut Epilepsy Advocate, Robert Fiore.

“It is important that more people become aware about Epilepsy everyday along with November being Epilepsy Awareness Month”, said Robert Fiore. Robert can be emailed at ctepilepsy@optonline.net