I'll be honest (side note, why do pastor's always feel compelled to start a personal story with "I'll be honest", how often are we not? Anyway, I digress), I have not made a habit of taking my blood pressure as often as I should, but I started again, recently, and to my horror my blood pressure was pretty consistently 150-160/80-90 at night. Normally it is pretty good in the morning, because I take my blood pressure medicine in the moring. I messaged my doctor and he reminded me that my blood pressure will fluctuate during the day, depending on activity, stress level, time of day, how tired I am, etc. I understand all that, but I get worried because the one thing Dr. Piper stressed above all else is make sure my blood pressue is under control, because I only have one vetebral artery left and I don't want that one to blow! I don't think I need to be on different blood pressue medicine, as these seem to work, in general. My question is, for those who have had a stroke and now have blood pressue issues, do you have a "rescue" medicine (much like an asthmatic has a "resuce inhaler") in case your blood pressue spikes? Just wondering.
Oh, by the way, Life is a gift, treasure it!
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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