Traumatic Brain Injury and Post Concussion Syndrome For traumatic brain injury (TBI) and post concussion syndrome (PCS).


advertisement
Reply
 
Thread Tools Display Modes
Old 08-20-2012, 05:25 PM #1
Mark in Idaho Mark in Idaho is offline
Legendary
 
Join Date: Feb 2009
Location: Somewhere near here
Posts: 11,417
15 yr Member
Mark in Idaho Mark in Idaho is offline
Legendary
 
Join Date: Feb 2009
Location: Somewhere near here
Posts: 11,417
15 yr Member
Default Family communication and other family dynamics

I realized that one thing that has greatly improved my life has been changes in how issues are handled at home.

My serious PCS struggles started in January 2001. My cognitive and memory struggles have not changed in the 11 years since. But, my daily life has improved greatly.

What has changed is my attitude and the growth in work-around skills and the attitude and communication with family members. Something that made a big difference was when my wife finally read and tried to understand my NeuroPsych Assessment report.

With the knowledge she gained, she became a support system rather than a conflict system. She would try to calmly pull me aside when she could tell I was about to lose control or struggling with anxiety/over-stimulation. She also stopped expecting me to do things that she thought were obvious. We began using a white board on the refrigerator to help keep order around the house.

With poor memory, I would forget to finish tasks or not even start them. Instead of her getting upset, she would just write it on the white board. Communication with someone with PCS / memory problems needs to be carefully considered. Family especially needs to adjust to reduce the stress and conflict from poor communication.

I hope others have learned some of the adjustment that can be made with friends and family and sometimes even co-workers to make life better.

If others could post their experiences, I'm sure many could be helped.
__________________
Mark in Idaho

"Be still and know that I am God" Psalm 46:10
Mark in Idaho is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Astrid2803 (08-20-2012), SpaceCadet (08-20-2012)

advertisement
Old 08-21-2012, 01:48 PM #2
bigdoug bigdoug is offline
Junior Member
 
Join Date: Aug 2012
Location: west michigan
Posts: 6
10 yr Member
bigdoug bigdoug is offline
Junior Member
 
Join Date: Aug 2012
Location: west michigan
Posts: 6
10 yr Member
Default

Quote:
Originally Posted by Mark in Idaho View Post
I realized that one thing that has greatly improved my life has been changes in how issues are handled at home.

My serious PCS struggles started in January 2001. My cognitive and memory struggles have not changed in the 11 years since. But, my daily life has improved greatly.

What has changed is my attitude and the growth in work-around skills and the attitude and communication with family members. Something that made a big difference was when my wife finally read and tried to understand my NeuroPsych Assessment report.

With the knowledge she gained, she became a support system rather than a conflict system. She would try to calmly pull me aside when she could tell I was about to lose control or struggling with anxiety/over-stimulation. She also stopped expecting me to do things that she thought were obvious. We began using a white board on the refrigerator to help keep order around the house.

With poor memory, I would forget to finish tasks or not even start them. Instead of her getting upset, she would just write it on the white board. Communication with someone with PCS / memory problems needs to be carefully considered. Family especially needs to adjust to reduce the stress and conflict from poor communication.

I hope others have learned some of the adjustment that can be made with friends and family and sometimes even co-workers to make life better.

If others could post their experiences, I'm sure many could be helped.
mark , my name is doug , i went down with a brain aneurysm two years ago , im 1/2 the person i was before that morning , but the one thing that did not change was the love and support from my wife , she is the true north on my compass of recovery , she has been by my side for all 7 surgeries and each nite in the hospital , she watched me being flow away in a medical helicopter to take me to the other side of the state to the university of michigan , then drove her truck the three hrs to be by my side , not once has she complained about a thing , i can no longer drive so she does that for me , i struggle with memory so she leaves notes for me on what to do and when to do it , she is my rock and i believe id never have gotten threw all this with out her / family does matter and when you have a wife a kids that are willing to give up there daily rutine to help you get threw yours , its god sent, i pray every day and thank the lord for my wonderfull wife and my four daughters
bigdoug is offline   Reply With QuoteReply With Quote
Reply


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


Similar Threads
Thread Thread Starter Forum Replies Last Post
Family Dynamics AfterMyNap Multiple Sclerosis 9 11-26-2007 06:06 PM


All times are GMT -5. The time now is 10:08 PM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.