Coping With Epilepsy Austin Biofeedback and EEG Neurofeedback Center
10% off neurofeedback training for CWE members - Austin, TX
Neurofeedback Partner - Free Advertisement
 

Go Back   Epilepsy Forum > Peer Support > The Kitchen


Reply
 
LinkBack Thread Tools
  #1  
Old 07-08-2010, 03:04 PM
PhylisFeinerJohnson's Avatar
CWE Benefactor
 
Join Date: Sep 2009
Location: West Chester, Pennsylvania
Posts: 870
Thanks: 69
Thanked 243 Times in 154 Posts

How does having epilepsy affect you?


In one study, participants anticipated that their self-perceptions and self-esteem would be more positive if they didn’t have epilepsy.

Self-perception turned out to be one of the most important predictors of successful social relationships in people with epilepsy — even more important than seizure frequency, severity, or other medical factors!

What is most important to you?
__________________
www.epilepsytalk.com
Add Post to del.icio.usNetscape this post!Stumble this Post!
Reply With Quote
  #2  
Old 07-08-2010, 05:56 PM
Endless's Avatar
Super Moderator / Even Keel
 
Join Date: Feb 2010
Location: U.S.
Posts: 4,287
Thanks: 753
Thanked 1,048 Times in 853 Posts
Send a message via AIM to Endless
I'm not sure I understand the question?

What's most important to me in general is to be able to function, seizure free. I want to be able to think, take care of my life on my own, not suffer from seizures, not suffer from brain damage, and not be doped up or changed up by meds. Maybe that's asking for a lot, but that's what's most important to me.
Add Post to del.icio.usNetscape this post!Stumble this Post!
Reply With Quote
  #3  
Old 07-08-2010, 05:57 PM
Bernard's Avatar
Your Host
 
Join Date: Mar 2005
Location: Friendswood, TX
Posts: 5,794
Thanks: 189
Thanked 705 Times in 309 Posts
Originally Posted by PhylisFeinerJohnson View Post:
... What is most important to you?

Sorry... I couldn't resist...

On a slightly more serious note:

On self esteem and perspective
__________________
New to CWE? I suggest reading the proactive prescription and epilepsy 101 threads. Also check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback. More great stuff can be found in the list of the best forum threads.

Would you like to help support this forum?
Add Post to del.icio.usNetscape this post!Stumble this Post!
Reply With Quote
  #4  
Old 07-08-2010, 08:41 PM
valeriedl's Avatar
Venerable Voice of CWE
 
Join Date: Feb 2010
Location: Pittsburgh, Pennsylvania
Posts: 1,002
Thanks: 130
Thanked 169 Times in 146 Posts
I really haven't lost any self esteem because of the eplispey. The way I look at it is that I get happy when I find that I can now do things that I may not have been able to do a few years back.

My family wouldn't let me out of their sight when we would go places because I could have a seziure at any time. I still could have one at any time, but then I was having maybe 5 a week, where as now I might have 3 a month. I feel like I have a little more freedom now.

At first my memory was horrible, I was lucky if I could remember things that may have happened only a few days ago. Now my memory is much better, but things that might have happened months ago start slipping away. I find myself remembering things that have happened in the last few years, not much but some stays. I get excited about this.

I keep a diary of things that go on so I can remember them and little notes of what happened that I want to make sure that I don't forget. Sometimes when I'll go back and read it I'll remember the event and sometimes I won't.

Almost everything from about 10 years before I got epliepsy was gone. I love to talk with friends and find out all the goofy things that I'd done. I sit there and laugh with them.

I've always been a positive person in general, it takes alot to get me down. I have much less seizures now than when I first was diagnosed with epilepsy 7 years ago. I've never really been depressed about any of it. I know that my family was. I don't know if it was just because of the fact that I didn't know what was happening to me or what.
Add Post to del.icio.usNetscape this post!Stumble this Post!
Reply With Quote
  #5  
Old 07-09-2010, 06:37 AM
huskymom's Avatar
Esteemed Pillar of the Community
 
Join Date: Apr 2010
Location: South Bend, Indiana
Posts: 735
Thanks: 14
Thanked 152 Times in 125 Posts
The most important thing to me is that I manage to wake up alive each morning

Also, LOVED the Conan video! No wonder that film is one you can watch over and over again and just enjoy laughing
Add Post to del.icio.usNetscape this post!Stumble this Post!
Reply With Quote
  #6  
Old 07-09-2010, 08:06 AM
BuckeyeFan's Avatar
Super Moderator / Grandpa
 
Join Date: Feb 2008
Location: Ohio - Buckeye country
Posts: 1,885
Thanks: 12
Thanked 99 Times in 60 Posts
Mine is better than it used to be. My worst times have been when it seriously interfered with my work. Not bragging, but I am fairly intelligent and when my side affects like inability to concentrate get bad, I know they are hurting me in my career. At least I have rather tolerant bosses who recognize my value even if my work is sometimes delayed.

On a relationship/family level I feel pretty good about myself.
__________________
Character is doing the right thing when no one is looking.
Add Post to del.icio.usNetscape this post!Stumble this Post!
Reply With Quote
  #7  
Old 07-09-2010, 08:57 AM
Weaving the Community Fabric
 
Join Date: Jul 2009
Location: South Carolina
Posts: 258
Thanks: 27
Thanked 30 Times in 27 Posts
You guys are so much more well-adjusted than I am. I have flare-ups of frustration that I cannot go shopping by myself. I feel like at least somebody everywhere I am on a regular basis should know that I have seizures because, though it is rare, I want someone to know that the last thing I want is to be hauled off in an ambulance - I hate that. And, after having spent a couple of years being rather isolated from large groups due to losing my job on account of my seizures, when I returned to school I discovered to my surprise that I had developed a lovely anxiety-reaction to speaking in public, quite a turn-around from someone who deliberately took debate classes and worked in public service. I didn't see that coming. So, yeah, epilepsy, has interacted with my self-esteem and not for the better, but most people have some sort of problem that is unique to them that they have to deal with, whether it is obvious or not.
Add Post to del.icio.usNetscape this post!Stumble this Post!
Reply With Quote
Reply

Tags
epilepsy, esteem, perception, social

Thread Tools

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Trackbacks are On
Pingbacks are On
Refbacks are On


Similar Threads
Thread Thread Starter Forum Replies Last Post
Can certain smells affect your threshold with epilepsy? Edward183 The Kitchen 20 01-05-2011 06:47 PM
medicine that doesn't have weight gain as a side affect elicia The Kitchen 11 01-26-2010 07:09 AM
How does your epilepsy affect your relationships? C0nn0rCh0sen The Kitchen 15 12-27-2009 10:45 AM
Ultrasounds affect brain development Bernard The Library 1 07-20-2008 12:18 AM


All times are GMT -5. The time now is 10:51 AM.


Powered by vBulletin® - Copyright ©2000 - 2012, Jelsoft Enterprises Ltd.
Content Relevant URLs by vBSEO ©2009, Crawlability, Inc.
Copyright 2005 © Measuring Up. ALL rights reserved.