Quality Of Life? | MyEpilepsyTeam

Connect with others who understand.

sign up Log in
Resources
About MyEpilepsyTeam
Powered By
Real members of MyEpilepsyTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
Quality Of Life?
A MyEpilepsyTeam Member asked a question 💭

Do any of you feel you have a quality of life or no? For those that do, what do you do or have in your life that gives you that? For those that feel they do not have a quality of life, how do you cope?

posted July 8, 2019
View reactions
A MyEpilepsyTeam Member

I feel both depending on the day.. But mostly feel it could always be worse but I also feel like its ok to have days where I get stuck in a dark hole... but I always come back to light! My grown children and husband give me strength because I feel accountable to them and learning that I’m valuable eventhough I have an illness that keeps me more dependent on others but sooo grateful for the good in my life.

posted July 9, 2019
A MyEpilepsyTeam Member

I have a good quality of my life. I control what I decide. I’m independent and can do many things the average person can do. I have great support from family and friends. I have my own wife and Kids. I love to help others understand Epilepsy whether it be to a stranger, friends, families, and everyone on this site.

My life is worth it . Im always learning Epilepsy tidbits of info myself . I control my life not Epilepsy.

posted July 9, 2019
A MyEpilepsyTeam Member

I don’t have the quality of life that I’d like and that I feel like other people have. I take my good days and enjoy them and thank God for them. I remember to remind myself that there are others who are much worse off than I. I hope this helps 😊.

posted July 9, 2019
A MyEpilepsyTeam Member

MarinaDevries: Don't talk like that. Everything is temporary. When things are good, enjoy them because it's temporary and when things are crappy (which we all know a lot about) know that it will pass. You have friends here so we want you to stay!

posted July 8, 2019
A MyEpilepsyTeam Member

I'm sorry Marina!! Please talk to your Dr. Maybe your meds could be changed to help you feel better?

posted July 8, 2019

Related content

View All
Vns Therapy
A MyEpilepsyTeam Member asked a question 💭
Help Identifying Seizure Type
A MyEpilepsyTeam Member asked a question 💭
What Type Of Seizures Does The Vns Implant Helpful For?
A MyEpilepsyTeam Member asked a question 💭
Continue with Facebook
Continue with Google
Lock Icon Your privacy is our priority. By continuing, you accept our Terms of use, and our Health Data and Privacy policies.
Already a Member? Log in