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Thank you Epilepsy.com for bringing a new way of sharing our story to the public. As previous posters have stated, it's all to often that journal articles are written by Academics for Academics. This is a great resource that will hopefully educate the public and new sufferers of Epilepsy about the various treatment options and how they may or may not benefit a specific individual.
I will spread the word to others!
Please, check out my site where I attempt to chronicle my journey; www.xaviersjourney.com
I wish I could find a doctor who would listen and care. My seizures made me unable too work but the meds make me feel like crap,so I just have to stay home and feel unproductive.
As a longtime NYC advertising copywriter who's been dealing with epilepsy in a multitude of forms for over 35 years, I must take off my proverbial hat and give a bow to all folks involved with the on-line publication of Epilepsy: Insights & Strategies. I'd gotten a bit tired over the years of reading articles written by third persons, if you will, most of them containing merely dictionary definitions of a neurological malfunction that over 55-million people 'round this world of ours must deal with. Not to mention the social, financial, legal, career sides of it. The articles herein are done in a style I'd hoped to see offered to me over a cup of coffee (yes, doctor, decaf) shared with a friend in a New York sidewalk cafe. Just what have so many of us been avoiding when it comes to communication about our epilepsy? Oh, probably the ill looks we just figure will greet us if we admit it. This publication ought to grow in size, so much so that someday soon it'll be on the newsstand! In the meantime, I'm warming up my keyboard and will pop something in the mail very soon!
In 1985, I had an AVM repaired and I have had seizures since that time. I have been taking anti-seizure meds but no one told me I have never been told I had Epilepsy until last year.(a new doctor) I need to know...Just because someone has a chronic problem of seizures, usually under control with meds...DO I HAVE EPILEPSY?
As a website, we cannot make a diagnosis of epilepsy in an individual. In general, the diagnosis of epilepsy is made when a person has two or more seizures, without an immediately preceding event to bring them on.
This first issue of "Epilepsy: Insights & Strategies" is a landmark event: the first eJournal by and for people with epilepsy. Dr. Fisher, Editor of www.epilepsy.com , considered this an unmet need, that is now fulfilled. Epilepsy Therapy Project is proud to bring you this program as one of the many ways we try to bring information to the community.
I resonate with the purpose of the eJournal, and Dr. Fisher's explanation that it is about people with epilepsy who know the issues. This is what I have been preaching to doctors for years: quality of life is in the eye of the beholder (the patients). That concept recently changed to the term "Patient Reported Outcomes" to encompass the multiple domains of what people experience in LIVING with a chronic disorder.
All too often, busy doctors overlook these issues, thinking they are not pertinent to clinical practice (MD knows best) or simply not having time to address individual personal concerns during brief visits. That's why I am so excited about the eJournal!
I am a man who will be retiring in the not too distant future. I have Epilepsy throughout my life, but have had some sucess with medications. As it turned out I am sucessful and know all about growing up with the disease, loosing jobs over it, etc. My goal in retiremant, is to help other Epileptics live through the disease, teach them to cope with issues and learn how to live their with PMA. PMA is not a medication, but a state of mind. "POSITIVE MENTAL ATTITUDE". I am looking for some guidance as to how I can assist in helping some of the younger folk, deal with the illness.
My 20 year old son has epilpesy. He was seizure free for about 5 years but has has 2 siezures in the last 2 months. Any light and encouragement you can share with him would be wonderful. He is depressed and angry. He has had epilepsy since he was about one year old. How does one cope with such a difficult disease?
Add your comments
Thank you Epilepsy.com for bringing a new way of sharing our story to the public. As previous posters have stated, it's all to often that journal articles are written by Academics for Academics. This is a great resource that will hopefully educate the public and new sufferers of Epilepsy about the various treatment options and how they may or may not benefit a specific individual.
I will spread the word to others!
Please, check out my site where I attempt to chronicle my journey; www.xaviersjourney.com
Thanks,
Xavier Snipes
I wish I could find a doctor who would listen and care. My seizures made me unable too work but the meds make me feel like crap,so I just have to stay home and feel unproductive.
As a longtime NYC advertising copywriter who's been dealing with epilepsy in a multitude of forms for over 35 years, I must take off my proverbial hat and give a bow to all folks involved with the on-line publication of Epilepsy: Insights & Strategies. I'd gotten a bit tired over the years of reading articles written by third persons, if you will, most of them containing merely dictionary definitions of a neurological malfunction that over 55-million people 'round this world of ours must deal with. Not to mention the social, financial, legal, career sides of it. The articles herein are done in a style I'd hoped to see offered to me over a cup of coffee (yes, doctor, decaf) shared with a friend in a New York sidewalk cafe. Just what have so many of us been avoiding when it comes to communication about our epilepsy? Oh, probably the ill looks we just figure will greet us if we admit it. This publication ought to grow in size, so much so that someday soon it'll be on the newsstand! In the meantime, I'm warming up my keyboard and will pop something in the mail very soon!
In 1985, I had an AVM repaired and I have had seizures since that time. I have been taking anti-seizure meds but no one told me I have never been told I had Epilepsy until last year.(a new doctor) I need to know...Just because someone has a chronic problem of seizures, usually under control with meds...DO I HAVE EPILEPSY?
Thank you.
As a website, we cannot make a diagnosis of epilepsy in an individual. In general, the diagnosis of epilepsy is made when a person has two or more seizures, without an immediately preceding event to bring them on.
You can find more information about this here on our website starting at http://www.epilepsy.com/101/ep101_epilepsy.
:o) Karen
epilepsy.com webmaster
This first issue of "Epilepsy: Insights & Strategies" is a landmark event: the first eJournal by and for people with epilepsy. Dr. Fisher, Editor of www.epilepsy.com , considered this an unmet need, that is now fulfilled. Epilepsy Therapy Project is proud to bring you this program as one of the many ways we try to bring information to the community.
I resonate with the purpose of the eJournal, and Dr. Fisher's explanation that it is about people with epilepsy who know the issues. This is what I have been preaching to doctors for years: quality of life is in the eye of the beholder (the patients). That concept recently changed to the term "Patient Reported Outcomes" to encompass the multiple domains of what people experience in LIVING with a chronic disorder.
All too often, busy doctors overlook these issues, thinking they are not pertinent to clinical practice (MD knows best) or simply not having time to address individual personal concerns during brief visits. That's why I am so excited about the eJournal!
Joyce Cramer, President, Epilepsy Therapy Project
Joyce,
I am a man who will be retiring in the not too distant future. I have Epilepsy throughout my life, but have had some sucess with medications. As it turned out I am sucessful and know all about growing up with the disease, loosing jobs over it, etc. My goal in retiremant, is to help other Epileptics live through the disease, teach them to cope with issues and learn how to live their with PMA. PMA is not a medication, but a state of mind. "POSITIVE MENTAL ATTITUDE". I am looking for some guidance as to how I can assist in helping some of the younger folk, deal with the illness.
Thanks
My 20 year old son has epilpesy. He was seizure free for about 5 years but has has 2 siezures in the last 2 months. Any light and encouragement you can share with him would be wonderful. He is depressed and angry. He has had epilepsy since he was about one year old. How does one cope with such a difficult disease?