So far Jami has been the sole poster to our blog, but no more! For those of you who have been following this thing, you know about our leg issue. Seems everyone is having a leg problem at our place lately, including me. For the record, I wasn't all that disappointed that my bruise (or lack thereof) was all that colorful, it was more like I was surprised. Wally did pop me a good one that day, and all I could do was gimp around a bit, although I wanted to give as good as I got. By then, Wally was all the way across to our arena (or the spot where an arena will go, when we finally get one built), and, since he didn't intentionally kick me (I hope), I had no right to get mad it him. He was just being a horse, and as far as I know, that is what he does best.
So I have meandered away from my current leg issue (although it is fading rapidly). As most of you probably already know, I was diagnosed with MS almost 10 years ago (has it been that long?). Well, last Friday my immune system worked with my central nervous system to help remind me that I still have the stupid disease, because I tend to forget.
About 4
ish Friday, I noticed an all too familiar numb feeling creep into my left hand and foot (and eventually my left leg). This is something that I have expected to happen eventually, so I was not too surprised. This is what happened back in March 1999, but then I didn't know what was happening, so I did nothing for about a month. By then, the entire right side of my body was wither partially or fully "numb", and starting to get very weak. I was weak enough that I limped when I walked, as well as staggered about like a drunken sailor on the slippery deck of a ship in a nasty storm.
Ok, maybe not that bad, but it was not good. By the time I finally saw someone, my first MS attack was started, finished and crawling back into its hole (which, apparently, is located on my brain, I got pictures to prove it). If it was not for a sharp nurse in a clinic on the
CWU campus, who by just asking me to walk about 10 feet knew something bad was going on, I would not have been sent to the hospital in
Ellensburg, carted to the hospital at
UW, and finally (3 months later) diagnosed with MS. Keep in mind that everything that had happened to me that was MS related had happened on my right side, but, like I said, I was expecting that something would eventually happen on the other side,
although I was prepared to wait as long as it did.
To make a long story short (too late), I had the worst MS attack I have had since it all started last century. However, this was not even half as bad as the first time. I have had no problems at all with my vision or speech, which some of you might remember were both very affected by that first attack. Also, the only weakness I have experienced has been due to the steroids that I have been on the for last couple days. That was the big mistake I made that first time, not getting help for a month. I waited just through the weekend to be sure I knew exactly what was going on before I called someone, but I know
exactly who to call, what to say and ask, and , most importantly, what was happening. I started a three day course of
Methylprednisolone Monday about 2 hours after I called the MS clinic (which, luckily, is only about a 10-15 minute drive from where I work). I expected to start the steroid treatment on Tuesday, so it was a nice surprise to find out that I could get started to fast. The steroids are not meant to stop an attack, I don't think much can stop it. What the steroids do is accelerate the healing process, which is exactly what they have done.
I have had two of three treatments (third one is this afternoon), and my "numbness" is down by, I would guess, 80% or more. I use quotes for numb and numbness, because it is only partial. I lost most of the feeling in my left side
extremities. I could not at all sense hot and cold, but I would feel pressure. That allowed me to be able to walk and use my hand to utilize tools and pick up things, but if they were hot or cold, I would not have been able to tell. I could tell if something was extremely hot or cold. It wasn't much, but I could sense a strange tingle that told me to stop touching the hot/cold thing. As an example, I canned some beets this weekend. Normally, right after you take the jar out of the pressure cooker, it is too hot to pick up. I was able to pick up a hot jar and hold it for a couple seconds before getting that tingle, but as soon as I realized that the tingle meant (skin damage about to occur) I put down the jar. So I knew I had to be very careful for a while when using sharp things or when cooking. All I have is one small nick from a knife I was using to cut up an apple for lunch on Monday. No other damage has
occurred. Jami wanted me to include a
picture of the nifty IV thing in my hand, which will be gone after today. Not sure why she wanted me to include it, but here it is:

I wrote all this to explain to you, the avid reader, that you should not worry too much about what has happened. It is what happens when someone has this disease. I an extremely lucky that I did not get saddled with the nasty form of the disease, primary-progressive MS. I will soon be back to my ?normal? self, and by the time I see some of you next Thursday, it will be impossible to tell that anything happened.
On a final note, the pictures you see of me below messing with my bees were taken after the attack, but before any treatment. As you can see, I never lost the ability to function normally, I just had to put up with the hassle of an odd feeling one half of my body.