Admittedly, my posting has been very sporadic of late (oh, who am I kidding, for the last 3 years...) It has been almost 6 years since my stroke (it will be 6 years on December 8, but I am getting waaay ahead of myself), and it seems that some of the side-effects are becoming a little more apparent to others. My wife has had some people comment to her that I seemed to be having problems swallowing during church awhile ago; others have noticed that I look really tired and I have had some tell me that they have noticed that I am having problems with my left leg being weak from time to time. I fell getting out of bed about 6 months ago and wound up with some pretty bad hip pain. When I went to physical therapy, they noticed that ever since my stroke I have changed the way I walk; when I had to relearn how to walk, I would "kick my left leg out" so that my right leg would not cross over. Over the next 5 years it became second nature to walk with my left leg constantly kicking out. The result is that it effectively makes me walk as if my left leg is shorter. What the physical therapist wants me to do is to force that left leg to come back in line when I walk; that should alleviate the hip pain. In essence, I have to re-learn how to re-learn how to walk. (I had noticed that for a few years people would ask my why I was limping...I did not realize I was limping, but that was the result of my left leg kicking out...) I said all that for this purpose: I think my side-effects are become more noticeable to those around me. I have known ever since my stroke that my deficiencies will one day become more evident. My neurologist told me that those symptoms (left leg weakness, left arm weakness, increased headaches, etc.) are not necessarily new problems; they have always been there but my brain compensates for those deficiencies and makes them seem to be absent. When I over-work my brain, it loses its ability to compensate and those deficiencies become evident. I know that many people will not understand what I am about to say, but those who have dealt with the after effects of a stroke might: this sucks!
For the last few weeks I have been experiencing some pretty terrible headaches; not the kind that you can relieve by rubbing your temples or taking Tylenol, but headaches that radiate from the back of my head. It seems as though I have tried several things to relieve them: taking naps, lying down on heating pads, taking Tylenol, turning the lights of, etc. but nothing seems to help. Now, I don't have them all the time, only a few days a week and I can tell that they are more from muscle tightness than anything else. I have been instructed to go the ER if they flare up again, because of my past history of headaches before my stroke, but most likely it is due to the muscles that were cut in the back of my head for the Craniotomy. I would say that most days I do not struggle with headaches at all; but, the days I do have headaches they are a doozy. I don't have blurred vision with them or sensitivity to light or sound; it just hurts. As I look back over the past 3+ years I realize
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