One of the biggest challenges for Shawn is how to be parent. He tries
his best to be an effective parent but unfortunately the brain injury poses
obstacles that we have yet figured out how to overcome. He has the hardest job
of trying to figure out what role he is suppose to have. It is physically
impossible for him to be the disciplinarian and also physically impossible for
him to be the playful parent. I sometimes feel like he just observes and
watches from the outside. I try desperately for him to be involved and figure
out his role but it is not always the easiest thing to do. One side of it,
we have older children who remember Shawn before the accident and have always
struggled with how life and Shawn have changed.
Then we have our youngest who only knows his dad the way he is now. It
was so strange when we were talking about the past one day and our youngest
turned to his dad and said " daddy, you used to walk?”. It never dawned on us that this was something
so strange for him to overhear. I love the fact that he is loving and
accepting to anyone with a disability because seeing someone in a wheelchair is
just so normal for him. It truly is a testament to how our children can adapt
and just seem to know how to best accommodate Shawn. It really made me
proud and happy when I saw our youngest ask his dad to play a board game.
He went and got the game and set everything up on Shawn's right side,
knowing it was the only side he can use and therefore reach with. No one
told him to do that, he just knew and it was a great feel good parenting moment
for us both. Even with the great moments there are still other moments
that I know are so difficult for Shawn and something that he works on as part
of his therapy. Shawn's brain injury tends to put things in black and
white and we all know with small a child that doesn’t always work. Shawn
is working weekly with his speech therapist to deal better with more abstract
situations and not so much the absolutes. Quite often he will get in an
argument with our youngest about tiny little details that are not that
important but for him he has a hard time just "letting it go".
That again is the brain injury so it will be an ongoing part of his speech
therapy and just working on strategies when dealing with the kids. About
5 years ago, Shawn's speech therapist mentioned to Shawn that maybe he could
start asking our son what colour his shirt was, to help with him learning his
colours. Well every day for 5 years, Shawn has asked him what colour his
shirt is. You can imagine what kind of reaction he gets when he asks a
now 6 year old what colour his shirt is, everyday for the last 5 years lol.
I have tried multiple times to get him to stop asking that and come up
with something else and he said that he does it so he learns his colours.
I told him he is 6, he knows his colours! It is just something that
is basically stuck with him and we are desperately trying to stop that
question!! As annoying as it is, I know he means well and now we are
trying new ways for him to engage in conversation without the constant
questions. It sounds simple but it is surprisingly difficult for him to
come up with new questions and conversation topics. It is a constant
challenge to try and parent together but well worth every frustrating question
because it is how he feels he is having a part as a father. However, it
is also very sad for me knowing that our youngest will never know the dad that
Shawn would have been if life had dealt us different cards. It makes me wonder
who is more fortunate the kids that remember who Shawn was/is with the
incredible wit and sense of humour and playfulness with his kids or the child
that will never know that entire side of his father so therefore can’t miss it.
No comments:
Post a Comment