Skip to main content

I guess I should back up...

My wife first suspected I was having the stroke on December 9th pretty early. At first she didn't know what to think because I was just stumbling around. I don't remember much of that morning, but my wife says that I was hitting my head against the wall trying to get to the bathroom and such. That was when she called the local hospital 911 because it was only 4 a.m. and she did not want to wait until 8 a.m. when all the Dr. offices opened. She wound up calling the nurse at Mercy 911 and she said that I should go to the local emergency room to get treatment ASAP.

I can only guess that I was having symptoms of the stoke 3 or 4 weeks before my actual stroke because I wa having sudden intense headaches. Looking back, I can see that was a sign of a stroke, but I attributed it to using a new bathroom cleaner. Now the Drs. think I had a "perfect storm" sort of speak that all came together. I had borderline high blood pressure, I was taking over the counter cold midication that raised my blood pressure, I was taking herbal remedies which only raised my already high bl00d pressure, and I had a massage the morning of the 8th of December. None of those things are dangerous independently, but together they think it was what caused my stroke.

The Drs. are also trying to figure out what would casue a 38 year old man in pretty good shape (I was going to the Rec. Center everyday and had lowere my Cholesterol by 68 points in a year) to have a stroke. They think it may be a genetic problem that casued weakness in the muscle that surrounds the blood vessel that allowed blood to leak into the brain. That, combined with all the aforementioned things, may have caused the stroke. They are not certain, but that is what the think.

The rest of the next 2 weeks are just a blur to me. My wife says that I was actually at 2 hospitals in Des Moines, but I can only remember waking up at CCU in Iowa Methodist. My wife says that abotu 30 - 50 people from my church were there on during my surgery and for the first few days. I don't remember them, but I will take her word for it. She also said that my brain swelling was so severe before the surgery that my kids had to come in and spend a few minutes to tell me goodbye if I didn't make it through the surgery. My associate Pastor, Ethan Book, was in my room or at the hospital constantly throughout my hospital stay. He was tremendous to me and my wife during this difficult time for me.

I also had visitors from the first church I pastored in Stratford, Iowa. I don't remember what they said, I just remember them being there.

Laura (my wife) said that my surgery lasted 4 or 41/2 hours. They Drs. had to repair the muscle and the vein and then suction out the bleedign and then they put a shunt in to relieve the pressure that was building in my head. Dr. piper said to my wife to expect 6 months of intense therapy. But I have fooled the Drs. and today is my 5 week anniversary of my surgery. I have been bck to work for about a week and Laura has been back to work for a week too. God is good.

Comments

Popular posts from this blog

Does it get any worse than a stroke? Yes

On December 8, 2008, my life changed forever. I had a double sided cerebellar stroke with 2 brain stem compressions. It was not until December 10, 40 hours after my stroke, that surgery was finally done to relieve the pressure. Dr. Piper, the neuro-surgeon from Iowa Methodist hospital in Des Moines, told my wife that surgery was nothing more than an attempt to save my life, but that it would not erase the deficiencies as a result of the stroke. Although she admits that she did not really understand what Dr. Piper had just said, my wife, Laura, agreed to the surgery and the care team performed a decrompessive craniotomy, to hopefully relieve the pressure and allow my brain to function somewhat normally. For those who have followed my blog for the last 14+ years, the surgery was successful, I returned to the church and I now live a relatively normal life, although I do have some pretty severe, though not always visible, defieciencies. I really thought that life could not get any worse th

Sometimes I forget...and sometimes I just have a problem putting words together

It has been almost 15 years since my stroke, so you would think that, by now, I would be readily prepared for everything that life can throw my way; but, I often forget what it's like to have a simple head cold after my stroke. Now, understand, I am not suggesting that other people don't feel bad when they have a cold; it is just that it is different for a stroke survivor. Maybe some of the other stroke survivors feel the same way: many times when I get a head cold with the congestion, suffy nose, fever, etc., it begins to feel like I'm having a stroke again. For those who don't know what this is like, let me try to explain. I get up at night, whether to go to the bathroom or some other reason, and I feel completely disoriented for a few seconds. Not like I'm groggy, but that I feel the room is spinning, I can't tell which direction I am going, I forget where the bathroom is for an instant, things like that. On the first day of this last cold, I was going down

Sometimes my new life stinks...

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