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I Host A Virtual Support Group For Adults But I Would Like To Start On For Teenagers. Do You Think Teens Would Be Interested?
@A MyEpilepsyTeam Member
You said the cord around the throat sounds familiar. I just saw where your son has asthma. That sounds familiar. After birth I acquired asthma and pneumonia.
@A MyEpilepsyTeam Member
I am now 41 years old and my first seizure was noticed when I was 10 years old. So that makes it 31 years of seizures. I once had the Vagus Nerve Stimulator but it didn’t help. Now I have the Neurostimulator (RNS) but still have seizures. My mom has told me that I wasn’t breathing at birth so I wasn’t expected to live.
I have noticed with my son, headaches, not eating, stress, and not sleeping. also he has asthma so if his lungs get infected or if he get boils infection causes fever and could possibly cause a seizure.Im on a hunt also because he just started having them 4 years ago after he had a spinal tap.
@A MyEpilepsyTeam Member
I have had seizures ever since I was 10 years old. During childhood I had many friends but when we reached our teens everybody else could drive so I was left out of everything. So I think teens would enjoy to meet up with others who suffer in the same way. I’m now over 40 years old and I still have seizures.
this sounds familiar . the cord around the throat. so how old are you and how long have you noticed the seizures?
Have Got A Teenage Girl With Malonic Teenage Epilepsy And Is Suffering With Anxiety Won't Go Out Has Any One Got Any Advice Please
Is There Something You Once Had Been Doing Say A Hobby, Sport And Leisure Activity And Such Etc, But Like To Get Back To, More Below
How Many People Here On This Site Have Met Face To Face Here? And If We Could All Meet Everyone Here In A Reunion Let's Say, Would You?
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