I guess it was the fact that today marks the 2-month anniversary of my surgery. Everyone, except my wife, is acting like nothing has really changed. I know, I know, I should be grateful that I am not in a state that everyone is reminded of my stroke. From a purely knowing, logical standpoint I know that. It is just the fact that, as of right now, life as I knew it on December 8th has ceased to exist and that affects no one except me and my wife. She has to get up everyday (that I am on it) AT 6:00 to give me shots of Lovenox. She has to fill my pill minder every day. I cannot do the things that I used to be able to do. Life, as I knew it, is changed. I know it has only been 2 months, but at the same time it is a miracle of God that I am walking around, it has only been 2 months for me to get used to my new life. That is not much time. Anyway, probably I won't write much else (I hope) about my struggles adapting. I just wanted to vent a little.
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
Comments
Post a Comment