Does Anyone Feel Like You’re A Burden? My Life Has Changed So Much. Some Family Don’t Understand What It’s Like To Be How I Feel At Times. | MyEpilepsyTeam

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Does Anyone Feel Like You’re A Burden? My Life Has Changed So Much. Some Family Don’t Understand What It’s Like To Be How I Feel At Times.
A MyEpilepsyTeam Member asked a question 💭
posted January 20
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A MyEpilepsyTeam Member

Keppra 1000mg 3X daily
Lyrica 20mg 2X daily
Siezure free since January 2019.THANK GOD!
I live alone with my Siezure Alert Response Service Dog Josie. I am thankful to be independent and strong. My daughters both live close by and will help when needed. They are very busy with their businesses and teenagers so I take Tri County Transportation to MDs haircut grocery vet...Monday through Friday. Have to watch church on TV. Gets lonely and wish I could do more, but GOD knows I have limitations on to much stimulating excitement, lights,much rest needed! I give it to GOD and HE LOVES ME!
BLESSED TO BE WALKING TALKING PRAISING GOD. No one expected me to live after Traumatic Brain Injury 7-2012. Careflighted to Pensacola where world known neurologist surgeon and his team where waiting for me. GOD has more plans for me! STAY STRONG MY WARRIOR FRIENDS
ENJOY EACH MOMENT 😊👣🐾🐾

posted January 22
A MyEpilepsyTeam Member

I think all of us appreciate the kindness and respect of family and friends. We need folks who are helpful and willing to help when they can. Sadly, many friends and family have little understanding and no empathy. Those folks have questionable ethics and values. That's THEIR deficit; not yours.

posted January 21
A MyEpilepsyTeam Member

Lena we are like family here. I feel guilty because when I’m well i can get so busy that I forget to check in on rveryone or post an update. I have to learn to slow down. Being part of this community helps me care for myself emotionally and that’s just as important as taking care of myself physically.

posted March 15
A MyEpilepsyTeam Member

Good morning Devin YOU are not alone. Most of us on this site have had the same problems with work and even our loving family
No one knows Epilepsy and the many complications we suffer, until they themselves have Epilepsy! No one takes the time to research complex neurological disease. You must do the research and be your own best advocate! Many kind friends on this site will help you! Do you have a great neurologist? What is your diagnosis and treatment? There are so many different types of siezures. We learn from experience. I suggest keeping a journal of your siezures and all medical records. Keep journals of your work interactions! American's With Disabilities will help you with your rights to work and adaptations employers must make available to you to continue to work. It takes time to get all the resources. Keep trying! Ask questions! Pat yourself on the back! You are amazing! Keep believing in yourself! Write me or any member of your team we will help you with anything we can! I have Temporal Lobe Epilepsy after a traumatic brain injury 7-2012. I was referred to Mayo Clinic Epilepsy Monitoring Unit Jacksonville FL in 2018.Now gramal siezure free since January 2019.THANK GOD! Most major University Medical Centers have Epilepsy Monitoring Units.
I had a full week of constant monitoring of EEG 24-7 EEG MONITORING! Every department checked me out! RX changes and diet changes has helped me understand myself and accepting myself.
GOD BLESS AND HELP YOU!
GOOD LUCK! Keep believing in yourself and keep trying! It's not easy but you have found a great place to help you find resolutions!😊👣🐾🐾

posted January 24
A MyEpilepsyTeam Member

I have been seizures free for 2 months thank God.

posted January 21

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