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Old 05-15-2015, 07:09 PM
musicman musicman is offline
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Join Date: May 2015
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8 yr Member
musicman musicman is offline
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Join Date: May 2015
Posts: 3
8 yr Member
Default Totally relate to this thread!!

Quote:
Originally Posted by Canadoc View Post
Hi everyone,
This is the first time posting a "thread" as well as the first time I've ever been part of an on-line forum, let alone any forum for that matter. I'm a family physician in Canada, and like most Canadians, enjoy playing hockey. Unfortunately, in 2006, I suffered a concussion during a hockey game which resulted in a prolonged recovery. After about a year, I was finally able to tolerate and enjoy sports again without inducing a headache. As you can imagine, I was forbidden by my wife to lace up my skates again (no argument).

In retrospect, I now realize I made 2 errors in recovery (wish I knew then what I know now). First, I quickly returned to work without much cognitive rest and pushed my way through long clinic hours. Second, I lifted a heavy article on day 2 post mTBI which quickly brought significant and instant head pain.

What has now become a permanent disability is an inability to strain or lift articles more than ~10 lbs without feeling a discomfort in my head. This discomfort eventually becomes pain if I persist with the strain or lift. The more intense the pain, the longer it takes to dissipate. With new head trauma (such as loghtly bumping my head on a shelf, running in my squash opponent....ie sudden deceleration), this intolerance to strain is magnified for a few weeks. Eventually it settles back to a baseline but never goes away. Essentially I am extremely sensitive to any increase in intra-cranial pressure(ICP) (physical strain--->increase venous pressure--->increase ICP. The problem is that it is now taking less force to temporarily magnify this phenomenon. I've recently had a second MRI specifically to rule out a head trauma induced Chiari-type CSF obstruction. Thankfully everything was normal. I've consulted local "concussion specialists" who can only come up with theories of meningeal hypersensitivity post injury with the consideration for medication dampen the pain during effort (which I'm reluctant to do).

The other phenomenon that now follows any head bump (and I mean just a bump), is a decline in cognitive stamina that slowly improves over 2-3 weeks. It's difficult to cancel patients who have been waiting so long to see you. So, against better judgement, I often will push myself cognitively through a days work. I now can appreciate that these changes (following repeat minor injuries) are both structural (at a cellular level) but also biochemichal (increased neuron vulnerabilty and cell dysfunction). What puzzles me is why the worsening trend over time.

Once I'm 3-4 weeks past a "head bump", I feel cognitively great again. I'm able to enjoy aerobic sports that don't increase venous pressure much or for long. In other words, I have no problems tolerating an increase in arterial pressure when I'm "well" (I can ride my bike but just can't lift it!).

I wonder if anyone else has been experiencing similar post-concussive symptoms and whether investigations have shed any light.
So I can completely identify with every post! I've been suffering with PCS since January of this year and it has completely turned my life upside down!! Canadoc have you made any more progress since this original thread? As in treatments etc... I'm particularly interested b/c your symptoms are so similar to mine and you also work in the medical field. I can say with out a doubt that Hyperbaric oxygen therapy has been the ONLY thing that has made any significant difference in my recovery. And I mean almost immediately, however I cracked my head on the hatchback of my van as I was unloading equipment for work and have regressed pretty significantly!! The minor bumps are maddening!! I went to hug an elderly lady at church and she came in a little too quick and that small bump just set me back even further. I was at a social function today telling people please dont hug me as Ive re-injured my head. Even thought about wearing a neck brace just so people would be more careful when they approach (we hug eachother down here in the South). I'm struggling with the fact that I might not be able to exercise the way I used to. (talk about anxiety and depression) At this point, I can't excercise at all, however I was making progress in the early part of my hyperbaric treatment which is now so much more frustrating since I am now back to balance problems, muscle weakness, brain fog, vision problems, cognitive issues, etc... Was considering Atlas orthogonal, but I've also read about that making things worse. Anybody with some experience with that type of therapy for PCS?
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