Hello everyone,

I know this has been done a couple times now. However, I find it more and more difficult to get my parents to understand what it's like. Hell, sometimes I don't even know how exactly I feel. I've tried explaining situations that make my head hurt or when they talk too fast, I've tried explaining how stressful it is for me.

Right now I'm on highschool summer break. Currently I work 3 hours a week at a loud grocery store. I'm doing an English course to catch up for the course I had to drop last year. It's one hell of a toll on me. School ended last wed, started this course thursday. 5 lessons to complete every two weeks. Minimum probably 3 hrs a day or more on lessons and I'm exhausted. Lately I've been getting complaints that I didnt think to do the dishes or that I don't do anything all day.

How can I explain it? I've given my parents the tbi guide (father didnt read it, mom read a few pages and never looked at it again), I've tried explaining the fatigue, but they do not seem to believe me because they are "more tired because they worked all day."

Anyways, long story short, Is there a good way to explain that I'm doing more than enough as it is? Or a way to get them to understand the fatigue I feel every day?

Thanks Everyone!

Kayley, maybe show them this article (I see you're in Ontario):

http://www.theglobeandmail.com/life/...rticle4363998/

“We want people to rest cognitively and physically after a concussion,” added Dr. Tator, founder of ThinkFirst Canada. “We feel you get the best recovery if you follow a graduated program, after a concussion.”

Hi Kayley,

This sounds like a difficult situation and I am very sorry you have to deal with it. Given what you've said here, it sounds to me like your folks are not interested in understanding your situation right now. If you've given them the TBI survival guide and they're not even willing to look at it or take it seriously, that suggests to me that there isn't much you can say to change that. It's not that you haven't explained things the right way; it's that they have decided that they aren't going to listen to you.

Perhaps they would take your situation more seriously if they heard from a professional. Do you know if any of your doctors would be willing to explain the situation to your folks? Do you have any upcoming appointments that your folks could sit in on?

I'm sorry I can't think of anything better to offer. Like I said, it sounds to me like a tough situation.

As far as the fatigue goes, one thing I suggested on another post is to ask people what they feel like when they have the flu. Ask your folks how much energy they have when they're very sick, and tell them that's pretty much what you feel like all the time. It's worth a shot.

Yes, my mother has been to 4 or 5 neurologist appointments. My father has been to one. Part of it is that my father wouldn't get paid for time taken off, but my mother can take a holiday. That flu suggestion is good, I will try it! Thanks!

"Lost & Found: What brain injury survivors want you to know."

Here's an excellent 1-page article for you and your family.
I'd recommend: print and tape it to the refrigerator.
This weblink has been posted by others several times. Check those posts related to that thread.
I wish you well and good luck.

http://m.brainline.org/#content/content.php?id=5498

And here's another good one! "Spend a Day on Planet TBI"
http://www.mindyourheadcoop.org/blog/?p=1075

So sorry you are going through this at that age. I see many others your age at my various therapies and wish their parents understood better how incredibily hard daily living is with a brain injury.

I'm slightly older than you, (was in the middle of grad school/working full time, seriously relationship, time for big girl decisions about houses and cars and such), and then my world fell apart after a car accident.

I have tried throughout my recovery to get old collegues, my boyfriend (who really tries so hard to get it), my parents, my teenage brother, etc. This article, although related to lupus, helped my family finally get it! I hope it helps you.

Even though the woman has lupus, I feel like the cognitive and physical fatigue we battle daily is very similar. The point she makes in the article is applicable to us as well.

http://www.butyoudontlooksick.com/ar...e-miserandino/

my best to you and your recovery