Concussion: Six Months On

Posted: November 29, 2011 in Uncategorized
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As this blog has documented in detail my struggles with concussion, I thought it would be a good idea to give you an update on what the after effects have been. You tend to read a lot about the symptoms of concussions, but once a player/person has gotten over the symptoms it is presumed that you carry on as normal.

 

Please do bear in mind that concussions vary from individual to individual and what I have experienced might not be applicable to some.

 

It has now been over six months since the concussion and I am symptom free from the actual concussion, but there have been several things that have not been the same. If you hear people who have suffered from concussions say that they have good and bad days, it is true. I have days when I feel normal and days when I still have to lock myself in a dark room due to intense migraine like headaches that have become more frequent since the concussion. When the headaches come they are pretty bad. It feels like someone is yanking at the inside of my eyeballs and I literally cannot move my head or I feel nauseous. There isn’t a set thing that I’ve noticed what would set it off, but sometimes it can be certain smells or even things like flashing lights.

 

The flashing lights is another thing that I can’t deal with. If I’m in a nightclub (rarely) I can’t be in for a long time as the lights they have really get to me and make me feel dizzy and that’s before I would’ve drank anything. The worse are strobe lights, if there is a strobe light that’s going off, I feel like I’m going to be sick. Other lights, what you normally see in clubs or at parties, give me a headache and ultimately ruin my night. Then again, I wasn’t that big on the club scene anyways so I’m perfectly happy to sit down at a bar or a pub.

 

The strobe light issue doesn’t have to be in clubs or on nights out. It’s also in films or TV when there are flashing lights or scenes that flash back and forth. Like in the movie Black Swan, the night club scene really made me turn away. Also I have trouble watching shows like the X-Factor (apart from the terrible singing and the mundane judges) due to the light show/screens they use.

 

The third biggest thing that I have noticed are short term memory problems. I still have a trouble remembering things that I have done or what I’ve been asked to do. A good example of this is from a few weeks ago when I left training and I could not remember where I had parked my car. I was wandering around the parking garage with a couple of teammates not being able to remember what level I had parked my car or where on the level I had parked it.

 

Then there is head banging or sudden jolts of the head i.e. if I sneeze. The head banging to music has stopped as I can visibly feel my brain move around in my head and it is an uncomfortable feeling. Similarly if I have a cold/flu and I sneeze and my head jerks because of it, it feels doubly bad.

 

So despite being over the main issues of the concussions it has had a profound effect on my life and the things that I do. Most of the time I don’t think about the concussion, but I still get reminders that I have suffered a blow that has altered things. Despite this, I still love to play and I am thankful that I am able to carry on playing, but most of all, I’m grateful that I can lead a normal life most of the time.

Comments
  1. Brianna says:

    I am glad to hear that you are playing again. Its been two years since I was diagnosed with post concussion syndrom, after a series of blows to the head. while I am not a hockey player I am a horse back rider and I do understand the passion and drive of an athelte. I have not been on a horse for two years! while this state makes me ache and I am discouraged by doctors, family and friends not to ever consider it again, I do know that I will ride again no matter what it takes. For now I am unable to do so, and hold onto the fact that it is better to live even if its in this state of constant illness and pain. I came very close to loosing my life and the only thing that saved me was a helmit. I am thankful for my life, and I find it very interesting to hear stories of others who have been in a similar situation as me. I just want to say always where a helmit! you never know when it will save your life. 🙂

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