Saturday, September 03, 2005

 

Devastating

My wife and I have been watching the coverage of the devastation in the Alabama, Mississippi, and Louisiana area and have been just overwhelmed by the devistation and suffering of the people in those areas. As I sit here at my computer in my cool, dry home with food in the fridge and a car with gas in it, I feel extremely blessed.

I called Ron & Linda Juneau to check in on our friends in the airgun community that live in the Louisiana area. Ron & Linda didn't have any damage to their properly other than some tree limbs that came down. They were without power for a few days but they now have it restored. They also said that everyone in their club were doiong ok too. That was some good news.

I lived in the Melbourne Florida area for 13 years and was there when Andrew went through south Florida and rode out Opal and let me tell you, what I went through was nothing like this. I have been watching the governmental officials and most say the best way for the average American to help is to give to the Red Cross. My wife and I have decided to give and I hope that you will thoughtfully consider doing the same. Even if you can't give much, $5, $10, or $20 would certainly help. The safest way to give is to use the Red Cross website so that you can be sure that it goes to where it is needed. There are some scammers out there claiming to be collecting for the Red Cross but keep the money for themselves, so be careful where you give. Also, many of the New Orleans people are being helped in the Baton Rouge area. Linda said that many of the churches in the area are opening their doors to those affected by the storm and flood. She said that if anyone wanted to send money directly to the affected area they could send it to them and she would take it to some of the organizations in Baton Rouge helping those in need. If you would like more info on giving directly to those in Baton Rouge, please email me.

Monday, August 29, 2005

 

Doctors Visit

I was diagnosed about 4 years ago with a Mitral Valve Prolapse. The Mitral Valve is located between the upper left chamber and lower left chamber of the heart. It is made of two flaps of tissue that normally open and close in a rhythmic way to allow blood to flow in one direction--from the atrium (upper chamber) to the ventricle (lower chamber). The left ventricle is responsible for much of the heart's pumping and propels oxygen-rich blood into the arteries. The arteries then carry the blood throughout the body. When the mitral valve doesn't open and close properly, the flaps may "billow" backward slightly into the upper chamber during the heart's contraction. This is called mitral valve prolapse (MVP). As a result of MVP, a clicking sound can often be heard by the doctor listening to the heart sounds with a stethoscope. MVP tends to run in families, so those with blood relatives with MVP have a greater chance of also having the condition. MVP itself isn't life threatening and doesn't get worse over time so there aren't any real health threats associated with it, unless a heart murmur develops. Thankfully, I don't have a murmur.

The real problem with MVP is an associated syndrome that has a wide variety of affects on the body. The syndrome is called Mitral Valve Prolapse Syndrome or Dysautonomia (pronounced dis-auto-no-me-a). Some people with MVP don’t show any symptoms of the MVPS/D, unfortunately I am not one of them. When I was first diagnosed with MVP, I wasn’t told about the associated syndrome and just recently learned of it. This is very common since many doctors don’t know about the syndrome or don’t believe it really is associated with MVP.

Mitral Valve Prolapse Syndrome or Dysautonomia or MVPS/D affects the autonomic nervous system which controls a lot of the common bodily functions. MVPS/D can cause sleeplessness, fatigue, irritability, depression, anxiety, back pain, tension headaches, irregular heartbeats, racing heartbeat, extra heartbeats, and numbness in feet and hands. Over the past years I have exhibited many of these problems, particularly the sleeplessness and fatigue.

One interesting fact is that people with MVPS/D typically have about 80-85% of the normal blood volume as other people and are subject to dehydration and the ill affects of that. Also, the Autonomic Nervous System (ANS) is much more sensitive and tends to over react to caffeine and refined sugar. In my own life I noticed that when I would drink a cup of coffee I would feel good for about a half hour and then I would feel like I needed to lie down and sleep. Also, if I ate or drank anything with a lot of sugar (like ice cream) I would get a terrible headache. The ANS also likes a consistent routine, skipping meals can cause weird reactions.

I bought a couple of books on the MVPS/D subject and went last Friday to the Mitral Valve Prolapse Center of Alabama clinic in Birmingham Alabama. I found out most of this information after the Nationals last week, which is really too bad since looking back at that match, I did a lot of things wrong that adversely affected my performance. I also look back to several other big matches and can see how my efforts in setting up the match or preparations before the match were actually detrimental to my ability to shoot well (you just knew that all this would come around to shooting sometime!). At the 2002 and 2004 Nationals I helped setup the courses and did other prep work without proper hydration and limited food intake which ended up causing fatigue and weak muscular control for the next couple of days. Over the last couple of years I also started drinking sweet tea (a real staple in the south) and Frappuccinos which really had a drastic affect on my ability to hold still and shoot well.

The only real cure for this problem is regular aerobic exercise, eating right, drinking lots of water, taking supplements, and elimination of caffeine and refined sugar from the diet. I am implementing these things in my life but it will be something I have to better manage as I compete in the future so that it won’t have such an adverse affect on my shooting. However, it does give me an excellent excuse for future field target matches!

To learn more about MVP and MVPS/D, visit the Mitral Valve Prolapse Center of Alabama website at http://www.mvprolapse.com/.



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