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Athanasios Gaitatzis, Anthony L. Johnson, David W. Chadwick, Simon D. Shorvon, Josemir W. Epilepsy carries a risk of premature mortality, but little is known about life expectancy in people with the condition. A cohort of patients with definite epilepsy has been followed for nearly 15 years and there have been deaths. These data have been used to estimate life expectancy of people in this cohort by employing a parametric survival model based on the Weibull distribution. Life expectancy in people with epilepsy was estimated as a function of age at, and time from, diagnosis according to two broad aetiological groups. These estimates were then compared with life expectancy in people of the same age and sex in the general population. Reductions in life expectancy are highest at the time of diagnosis and diminish with time.

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Talk to your child’s doctor about what activities your child can do and encourage your child to participate. As your child grows, help him become more independent. Seizures occur most frequently during the first few years of life , during a time when the brain is going through its most dramatic growth and changes.

Seizures threatened to sideline him until he had two brain surgeries. dating soon after Parker started suffering from violent seizures for the.

Learn about our expanded patient care options for your health care needs. These patients — returning war veterans, mothers in child-custody battles and over-extended professionals alike — have what doctors are calling psychogenic non-epileptic seizures PNES. Their display of uncontrollable movements, far-off stares or convulsions, Johns Hopkins researchers say, are not the result of the abnormal electrical discharges in the brain that characterize epilepsy, but instead appear to be stress-related behaviors that mimic and are misdiagnosed as the neurological disorder.

The researchers also say the diagnoses appear to be on the rise, at least by what they have seen in recent months. In some cases, those afflicted have become paralyzed or blind because of emotional trauma. People at risk for pseudo-seizures are typically highly suggestible, the Hopkins scientists say, which is why physicians often have tried not to publicize or draw attention to the condition. However, they seem to lack effective coping mechanisms necessary to deal with those stresses and feel more distressed by them.

Clearly, not every overwhelmed person develops seizure symptoms, they note, nor is it known how many people experience pseudo-seizures. For the study, published online in the journal Seizure , the researchers evaluated 40 patients with PNES, 20 people with epilepsy and 40 healthy control volunteers, all of whom were asked to report the frequency of various stressful life events both positive and negative over the previous five years. The research subjects then appraised the distress these events induced.

Each group reported roughly the same number of stressful events, but the PNES group reported much higher distress levels than the other two groups.

First Seizure

I met Daniel properly for the first time on the 4 th May He had read a lot of my blogs before we even started talking, so he knew all about my condition. He knew my younger brother, Joe, who had also mentioned a few things here and there, so I never had to break it to him that I live with this unpredictable condition of Epilepsy.

Here are the things you should know when dating someone with epilepsy: Be epilepsy aware -People with epilepsy may not feel comfortable.

As a result, patients and their doctors have a difficult time deciding whether a person who has one seizure should take medication in hopes of preventing another incident, researchers say. Now, a new guideline announced here today April 20 at the American Academy of Neurology annual meeting may offer some advice for this gray area. Currently, most patients and doctors end up waiting, without treatment, to see if a second seizure occurs , said Dr.

That’s because, if left untreated, about 50 to 75 percent of patients will never have another seizure. The new seizure guideline may change this practice of waiting, said French, who was senior author on the new recommendation. The guideline offers doctors suggestions, based on certain results seen on EEG or MRI tests, about which patients would likely benefit from starting medication right away. And therefore they can put that into their risk-benefits assessment.

That risk, French explained, is a balance between the chance of having a second seizure, which could be deadly depending on where and when it happens, versus taking medication that might not be necessary. And that medication could have side effects. The new seizure guideline, issued by the American Academy of Neurology and the American Epilepsy Society, is published in the April 21 issue of the journal Neurology.

Seizures can take on many forms. Among the more visible is the tonic-clonic or grand mal seizure , in which a person loses consciousness, clenches up and then has convulsions for upward of several minutes. But more often, seizures can result in short loss of consciousness, or a blank stare and upward rotation of the eyes, with no clenching or convulsions. In the United States, epilepsy is defined as having two or more seizures that are “unprovoked,” meaning they are not due to other underlying triggers, such as a high fever or low blood sugar.

Relationships and sex

Share your best tips you’ve picked up throughout your life, and learn from others! ULPT: Dating someone with epilepsy and having a fight? This happened to my then friends mom. I had a fight with her and later that night she had a seziure from her medication being mixed with her alcohol ism.

Imagine looking at your husband and saying, “I’m sorry, I have no idea who you are.” Yes, that happened. We’d been married almost fiv.

C ompared with the general population, patients with newly diagnosed symptomatic epilepsy have reduced life expectancy, according to an investigation published in the November issue of Epilepsia. Patients with newly diagnosed idiopathic or cryptogenic epilepsy, however, have a normal or prolonged life expectancy. The year of diagnosis and the type of epilepsy appear to influence life expectancy.

Many studies have suggested increased mortality among patients with epilepsy. Two previous investigations have reported the more specific measure of life expectancy in epilepsy, but both had methodologic weaknesses and were prone to substantial bias, said Claudia A. Granbichler and colleagues examined data for all patients visiting the epilepsy outpatient clinic of Innsbruck Medical University in Austria to calculate their life expectancy.

They included 1, adults who presented between January 1, , and December 31, , in their analysis. Patient data were recorded and updated continuously over time. They defined symptomatic epilepsy as the result of a known or suspected CNS disorder. Epilepsies not preceded by another disorder were considered idiopathic. The authors defined epilepsies of unknown cause as cryptogenic.

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I remember the very first time that someone spoke the words, “Everything will be okay! Fire engulfed my stomach. When a family member spoke this to me, I knew they meant well, however, I wanted to curl into a ball and cry until I had no strength left in me. The way it looked, it didn’t look okay in that very moment.

I didn’t hold anything against them.

For people living with the long-term effects of brain injury, the idea of dating can be a daunting and challenging prospect. He heard me collapse and go into seizure.” “Sometimes you don’t want advice; you just need someone to listen.”.

Here young people talk about their experiences of dating, relationships and sex, and how having epilepsy affected these areas of life. Dating Young people’s experiences of dating and relationships were very positive on the whole. Most we spoke with said that having epilepsy hadn’t had a negative impact on their experiences of dating or going out with people. Quite a few people said that, since their diagnosis, they had become more cautious or careful about who they ask out or develop a relationship with.

Many preferred to get to know people as friends first, before getting involved more seriously. This way, people didn’t need to feel awkward about when and how to tell a new boyfriend or girlfriend about epilepsy because they were already aware of it. A few people said they felt less confident about dating now than before their diagnosis. Some also talked about how, because of frequent seizures and lack of social networks, it was difficult to meet new people.

One woman said epilepsy had knocked her confidence so much she didn’t want to ask anyone out because she feared being rejected. Many people felt that, if their boyfriend or girlfriend couldn’t cope with their epilepsy, then they wouldn’t be the right person for them anyway. One man said that epilepsy was a part of his life so any girlfriend would just have to ‘take it or leave it’.

“My Boyfriend Has Epilepsy and I Can’t Handle It”

PAT: So I don’t need you to introduce yourself. That’s usually the thing we do, but we’re not telling people who you are. That’s — yeah, that’s my name. Not suspicious at all.

A relationship made stronger. I think because I was diagnosed with epilepsy before I had even thought about dating someone, it wasn’t so hard.

Going on a first date can be nerve-wracking under the best of circumstances; epilepsy just adds another twist. One question people often worry about is how soon they should tell their date that they have epilepsy. Being able to ask questions and share feelings on any topic, including epilepsy, will only make a relationship stronger. Although it may seem tempting to tell the other person over the phone, in an email or by text, instead of in person, any serious conversation like this is probably best done face-to-face.

The more comfortable you are with the other person, the better the conversation will go. Everyone worries about it to some degree. Some people worry so much that they never ask anyone out at all. Unfortunately, this does happen from time to time.

Epilepsy Resource Center

Grand mal seizures, or generalized tonic-clonic seizures, are seizures that involve muscle contractions, muscle rigidity, and loss of consciousness. These seizures result from abnormal electrical activity in the brain. Grand mal seizures affect the entire body, and may happen just once or multiple times as in the case of epilepsy.

friends can—sports, dating, hanging out, working, Epilepsy may be part of your life, but it doesn’t define someone with a genetic susceptibility for epilepsy.

Bertha C. Ekeh, Udeme E. Background and Aim. Epilepsy remains a stigmatized disease especially in Sub-Saharan Africa. Lack of information and illiteracy has been blamed as the cause of the stigmatization. This stigmatization stems from the fact that the traditional African belief views epilepsy as a spiritual disease. We studied the knowledge, attitude, and perception towards epilepsy amongst medical students comparing the knowledge of the clinical students with that of the basic medical preclinical students.

Grand Mal Seizures

Due to the popularity of social media, we have seen decreasing engagement on our forums and chat. Please know we want to keep talking to you about epilepsy, seizures, and what you need. We want to stay connected with you. I also have epilepsy. As a guy it is more difficult to discuss epilepsy.

We married about a year after his second seizure. At that time, his seizures became more frequent and started presenting problems for him. He was not able to.

Improving life after brain injury Need to talk? For people living with the long-term effects of brain injury, the idea of dating can be a daunting and challenging prospect. Brain injury survivor Kathryn found dating and intimacy very challenging following her haemorrhage but explains that with time, and after many emotional highs and lows, she again felt able to meet people.

He heard me collapse and go into seizure. After a number of operations, Kathryn slowly began to recover. However, she was left with a host of issues including partial vision, speech and walking problems, cognitive impairment, acute fatigue, anxiety and low-self esteem. But a week after I returned home from hospital, he walked out on me completely and I never saw him again.

This rejection hit Kathryn hard and she felt very isolated as she tried to come to terms with the effects of her brain injury. I started to believe I would be alone for the rest of my life. To help make the date as easy as possible, Kathryn put in place some simple steps. We had something to eat and a drink before watching the world go by for a short time in a nearby park.