Saturday, January 18, 2014
Wal-Mart Name Tag From the Early 1990s
This is a Wal-Mart name tag that employees wore in the early 1990s. Wal-Mart called their workers associates, which I think they still do today. This was before they removed the dash from their name.
Downtown South Bend, Indiana 1929
REX RISHER, long a prominent name in law enforcement circles, provided this photograph of downtown South Bend, Indiana as it looked from the air in 1929. About one third way down the photo from the top at the extreme left is City Hall. At the extreme right at about the same level is the Sherland Building.
The plane was owned by the Saint Joseph Valley Aviation Club of which Risher was a member and was based at the South Bend Municipal Airport, located at Brick and Fir Roads north of State Road 23.
Risher served in the uniforms of city and state police, later was deputy U.S. Marshal.
Saturday, March 31, 2012
My Wife's Epilepsy and Her Video
For years my wife has suffered with several things. Two of which are depression and fatigue, which the doctors tested for all sorts of different things with no luck.
The depression they treated with medication for a while, which just made things worse. The medication made her emotionally numb and drugged all day long. Consequently the kids often just ran wild around the house exploring and also trying to get attention.
The fatigue they did all sorts of research on, but found nothing. They tested thyroid and gallbladder and any number of different organs and they all checked out as normal. They did a sleep test and said everything was fine, except maybe a little twitching in the leg, which after everything else I am thinking they didn't pay attention correctly to what the symptom was. She have had several ultrasounds of various organs and parts of the body. She has had a few MRIs to look at different areas of the brain. She has chest x-rays, EKGs, stress tests, many blood tests. Most everything was "normal".
Several times they checked her heart do to weakness in the body or chest pains.
We were thinking maybe it was Fibromyalgia at one point.
She has also had memory loss and for lack of a better term ditsiness. Both of which we just blew off as being blonde or whatever and didn't think much of it, other than it was frustrating at times. It turned out that these symptoms were probably related too.
Finally after years one doctor sent us to a neurologist. They did an EEG on her and still just barely saw anything, but for the most part it was normal. By her symptoms and what he slightly saw on the EEG he figured she was having seizures and diagnosed her with epilepsy. They did an MRI and could not find the lesion that would cause the seizures.
As she has thought about it she thinks there are two possibilities as to what caused it. She recalled that when she was a child she was being pulled behind a vehicle in the snow on a tube or a sled with her uncle. They rolled off the sled in order to avoid hitting a puddle and her head went into a tree. She recalls being out of it for a few days after that, but seemed to recover fine.
The other incident was as a passenger in the front seat of a car, years after the tree incident, the driver hit the breaks hard and she recalls hitting her head on the dash board or windshield.
It has been very frustrating trying to find the right diagnosis and subsequently the right treatment. It has also been hard for her to not be able to function like she wants to, being tired and sore all the time.
Most of her seizures have been at night or in ways that we didn't recognize as seizures. Lately we have noticed things before bed time happening and it has been very frustrating and scary for her to not be in control of her body.
Before we knew what was happening she would sometimes start laughing for no reason and we would ask her what was so funny and she didn't know and then she would cry, also for no apparent reason. She would also at time space out for a few seconds and we would have to repeat things to her.
Now she does that a little more frequently and it is a bit more noticeable. She also will sometimes twitch her right hand or arm, but lately once in a while both sides jerk. They are quick jerks and then a pause and then a quick jerk or some other symptom. Sometimes she will stretch her head forward and make a pucker face. Sometimes her eyes will roll back in her head for a moment. This sort of thing will go on for an hour or so at times. Not a constant seizure, but several small quick ones.
Once she was eating something and she couldn't chew, nor could she respond to our asking what was wrong. Not because she was choking or anything, but just because she was seized up. We would be talking to her and she was aware of what we were saying, but could not respond. Tears would just begin to stream down her face.
Her triggers seem to be fatigue, evening time, and light. Like clock work around 7 at night things start up with her feeling seizures coming on.
To combat the trigger of light she has gotten some big sunglasses and a brimmed hat. She found that being in stores for very long would trigger a seizure later in the day. The same things with lighting in our home and at church and also with looking at a TV or computer monitor.
She feels self conscious wearing sunglasses everywhere in doors, especially big ones, but they seem to be helping. She frequently gets comments from people that find it difficult to talk to her through sunglasses or or ask if she had her eyes dilated that day or that she must be all ready for summer or that she looks all Hollywood. I myself thought they reminded me of glasses I have seen Yoko Ono wearing before.
Possibly related to the light issue is that she finds that using a colored overlay when reading a book helps her. It appears from research we have done that each person is different on what color overlay works best for them. We are finding that the overlays may be helping our kids reading and each one of them needs a different color.
She has tried several medications. Most of them, if she took them morning and night would keep her knocked out all day, so she just takes her medication at night now. Others would give her intense anxiety. Others would drop her blood pressure and temperature. After some of those she had another MRI to check to see if the thermostat in the brain was damaged, but everything was "normal". She has always run a little cold and had blood pressure on the low side within the normal spectrum, but the meds dropped her into danger zones in both temperature and blood pressure.
She is current taking generic Keppra. Sometimes it works fantastic and she sleeps through the night with no seizures. Most nights she wakes up around three or four in the morning and can't fall back to sleep. Perhaps she has had a seizure. She is generally exhausted the next day.
Sometime when she wakes up in the middle of the night she has an intense craving for milk. We heard one source say that milk is not good for epileptics. We are not sure what to make of the cravings. Maybe her body is needing more Calcium or Vitamin D or something in milk, even if she shouldn't have the other stuff that is in milk that might cause epilepsy complications.
She has found a community at http://www.epilepsyfoundation.org/ where she has been gathering information and also feeling support for others having common experiences. She has also enjoyed being a strength to others who have been feeling down because of going through it themselves or because of having a child that has epilepsy.
She has generally been shy about sharing personal things on the internet, other than the casual Facebook use, so I was surprised recently when she suggested that she might want to put a video up on YouTube about her experience with Epilepsy. I have included the video below.
We have found through this process that we have to do most of the research ourselves and present a plan to the doctors on what we want to do. We found that for the years that we tried to find out what the problem was. At times we resigned that no one knew and we stopped going to doctors to pursue it and then things would get worse and we would start again. Sometimes during the process the doctors would forget where we had been and start over with us. I think one of the first things we went in for was headaches and when we presented to the doctor we had been going to for a while a possible diagnosis, she told my wife it couldn't be that because she would be having headaches if it was that. That was very frustrating to have been walking down this road with a doctor and have it made clear to us that no one was researching the problem except the five minutes were speaking to them when we came in and the only thing they were working on was the symptom we had brought to them that day and not the ones we had previously come in with that had no gone away.
It is best to keep a record of which medications you have been on and what dosage and why you were taking off of them (side effects and what not). We have had times where the doctor did not know what medications we had taken previously even though they had prescribed them. We also found that some medication that had been prescribed during the day that were unacceptable, were worth trying as a nighttime medication. Without documenting what the side effects were we wouldn't know if we should suggest going back to it.
We have found that due to the memory problem that can be associated with Epilepsy and with Epilepsy medication my wife has to try various things to remind herself of what is going on during the day and even when to take her medication. We have different medication containers for day and night and for each day of the week, so she can visually see that she has already taken them. Even with that occasionally she gets the blue container mixed up with the orange or whatever colors we are using and also sometimes get days of the week messed up.
Recently I saw someone post on Facebook about people being sensitive to chewing or other noises and that someone has given it a name, Misophonia. The headline stated that it can cause rage. I thought the wording was very inflammatory, which I think is the trick publishers use to drive views these days. Nonetheless, for years my wife has tended to get irritable and somewhat irrational when someone is eating an apple in the same room as her or chewing gum or various other noises. I am wondering if it is related to the Epilepsy. It seems to get worse when she is on the verge of having a seizure. At those times she is very sensitive to noise or having her chair bumped or any sort of disturbance.
Update 17 Jan 2012
We are now finding that what was once diagnosed as Epilepsy is now likely
The depression they treated with medication for a while, which just made things worse. The medication made her emotionally numb and drugged all day long. Consequently the kids often just ran wild around the house exploring and also trying to get attention.
The fatigue they did all sorts of research on, but found nothing. They tested thyroid and gallbladder and any number of different organs and they all checked out as normal. They did a sleep test and said everything was fine, except maybe a little twitching in the leg, which after everything else I am thinking they didn't pay attention correctly to what the symptom was. She have had several ultrasounds of various organs and parts of the body. She has had a few MRIs to look at different areas of the brain. She has chest x-rays, EKGs, stress tests, many blood tests. Most everything was "normal".
Several times they checked her heart do to weakness in the body or chest pains.
We were thinking maybe it was Fibromyalgia at one point.
She has also had memory loss and for lack of a better term ditsiness. Both of which we just blew off as being blonde or whatever and didn't think much of it, other than it was frustrating at times. It turned out that these symptoms were probably related too.
Finally after years one doctor sent us to a neurologist. They did an EEG on her and still just barely saw anything, but for the most part it was normal. By her symptoms and what he slightly saw on the EEG he figured she was having seizures and diagnosed her with epilepsy. They did an MRI and could not find the lesion that would cause the seizures.
As she has thought about it she thinks there are two possibilities as to what caused it. She recalled that when she was a child she was being pulled behind a vehicle in the snow on a tube or a sled with her uncle. They rolled off the sled in order to avoid hitting a puddle and her head went into a tree. She recalls being out of it for a few days after that, but seemed to recover fine.
The other incident was as a passenger in the front seat of a car, years after the tree incident, the driver hit the breaks hard and she recalls hitting her head on the dash board or windshield.
It has been very frustrating trying to find the right diagnosis and subsequently the right treatment. It has also been hard for her to not be able to function like she wants to, being tired and sore all the time.
Most of her seizures have been at night or in ways that we didn't recognize as seizures. Lately we have noticed things before bed time happening and it has been very frustrating and scary for her to not be in control of her body.
Before we knew what was happening she would sometimes start laughing for no reason and we would ask her what was so funny and she didn't know and then she would cry, also for no apparent reason. She would also at time space out for a few seconds and we would have to repeat things to her.
Now she does that a little more frequently and it is a bit more noticeable. She also will sometimes twitch her right hand or arm, but lately once in a while both sides jerk. They are quick jerks and then a pause and then a quick jerk or some other symptom. Sometimes she will stretch her head forward and make a pucker face. Sometimes her eyes will roll back in her head for a moment. This sort of thing will go on for an hour or so at times. Not a constant seizure, but several small quick ones.
Once she was eating something and she couldn't chew, nor could she respond to our asking what was wrong. Not because she was choking or anything, but just because she was seized up. We would be talking to her and she was aware of what we were saying, but could not respond. Tears would just begin to stream down her face.
Her triggers seem to be fatigue, evening time, and light. Like clock work around 7 at night things start up with her feeling seizures coming on.
To combat the trigger of light she has gotten some big sunglasses and a brimmed hat. She found that being in stores for very long would trigger a seizure later in the day. The same things with lighting in our home and at church and also with looking at a TV or computer monitor.
She feels self conscious wearing sunglasses everywhere in doors, especially big ones, but they seem to be helping. She frequently gets comments from people that find it difficult to talk to her through sunglasses or or ask if she had her eyes dilated that day or that she must be all ready for summer or that she looks all Hollywood. I myself thought they reminded me of glasses I have seen Yoko Ono wearing before.
Possibly related to the light issue is that she finds that using a colored overlay when reading a book helps her. It appears from research we have done that each person is different on what color overlay works best for them. We are finding that the overlays may be helping our kids reading and each one of them needs a different color.
She has tried several medications. Most of them, if she took them morning and night would keep her knocked out all day, so she just takes her medication at night now. Others would give her intense anxiety. Others would drop her blood pressure and temperature. After some of those she had another MRI to check to see if the thermostat in the brain was damaged, but everything was "normal". She has always run a little cold and had blood pressure on the low side within the normal spectrum, but the meds dropped her into danger zones in both temperature and blood pressure.
She is current taking generic Keppra. Sometimes it works fantastic and she sleeps through the night with no seizures. Most nights she wakes up around three or four in the morning and can't fall back to sleep. Perhaps she has had a seizure. She is generally exhausted the next day.
Sometime when she wakes up in the middle of the night she has an intense craving for milk. We heard one source say that milk is not good for epileptics. We are not sure what to make of the cravings. Maybe her body is needing more Calcium or Vitamin D or something in milk, even if she shouldn't have the other stuff that is in milk that might cause epilepsy complications.
She has found a community at http://www.epilepsyfoundation.org/ where she has been gathering information and also feeling support for others having common experiences. She has also enjoyed being a strength to others who have been feeling down because of going through it themselves or because of having a child that has epilepsy.
She has generally been shy about sharing personal things on the internet, other than the casual Facebook use, so I was surprised recently when she suggested that she might want to put a video up on YouTube about her experience with Epilepsy. I have included the video below.
We have found through this process that we have to do most of the research ourselves and present a plan to the doctors on what we want to do. We found that for the years that we tried to find out what the problem was. At times we resigned that no one knew and we stopped going to doctors to pursue it and then things would get worse and we would start again. Sometimes during the process the doctors would forget where we had been and start over with us. I think one of the first things we went in for was headaches and when we presented to the doctor we had been going to for a while a possible diagnosis, she told my wife it couldn't be that because she would be having headaches if it was that. That was very frustrating to have been walking down this road with a doctor and have it made clear to us that no one was researching the problem except the five minutes were speaking to them when we came in and the only thing they were working on was the symptom we had brought to them that day and not the ones we had previously come in with that had no gone away.
It is best to keep a record of which medications you have been on and what dosage and why you were taking off of them (side effects and what not). We have had times where the doctor did not know what medications we had taken previously even though they had prescribed them. We also found that some medication that had been prescribed during the day that were unacceptable, were worth trying as a nighttime medication. Without documenting what the side effects were we wouldn't know if we should suggest going back to it.
We have found that due to the memory problem that can be associated with Epilepsy and with Epilepsy medication my wife has to try various things to remind herself of what is going on during the day and even when to take her medication. We have different medication containers for day and night and for each day of the week, so she can visually see that she has already taken them. Even with that occasionally she gets the blue container mixed up with the orange or whatever colors we are using and also sometimes get days of the week messed up.
Recently I saw someone post on Facebook about people being sensitive to chewing or other noises and that someone has given it a name, Misophonia. The headline stated that it can cause rage. I thought the wording was very inflammatory, which I think is the trick publishers use to drive views these days. Nonetheless, for years my wife has tended to get irritable and somewhat irrational when someone is eating an apple in the same room as her or chewing gum or various other noises. I am wondering if it is related to the Epilepsy. It seems to get worse when she is on the verge of having a seizure. At those times she is very sensitive to noise or having her chair bumped or any sort of disturbance.
Update 17 Jan 2012
We are now finding that what was once diagnosed as Epilepsy is now likely
Retrolisthesis in her neck, which produced some Neurological symptoms, but just because it is rubbing on her spinal cord.
Labels:
Depression,
Epilepsy,
Fatigue,
Keppra,
Medication,
Memory Loss,
Seizures
Friday, March 30, 2012
How To Play the Card Game Dutch Blitz
When I was a kid, growing up in Amish country in Indiana, there was a packaged card game called Dutch Blitz that had colored and numbered cards with pictures of little Amish buggies on them. We played it a lot at what our town called Summer Fun.
Summer Fun was where the town has older kids and adults monitor kids playing games while on summer break. I seem to recall the kids came and went freely. The adults appeared to pretty much just be there to get games out, organize groups, and keep the peace. I think there were also some crafts and stuff the adults did with the kids.
I didn't want to buy a special deck of cards and I had tons of face cards around, so I just used them. You could use any deck of cards that has multiple suits and has at least 10 cards in each suit. I will explain the game using face cards.
The Premise of the Game
The game is kind of like Skip Bo and multi-player Solitaire rolled into one game. The object is to play as many of your cards as possible and get rid of your Dutch Blitz pile as fast as possible by playing them ace through ten of the same suit on common piles in the middle that everyone plays on. Once one person has gotten rid of their Dutch Blitz pile, then everyone counts up the number of cards they have played to get their score.
Set Up
Summer Fun was where the town has older kids and adults monitor kids playing games while on summer break. I seem to recall the kids came and went freely. The adults appeared to pretty much just be there to get games out, organize groups, and keep the peace. I think there were also some crafts and stuff the adults did with the kids.
I didn't want to buy a special deck of cards and I had tons of face cards around, so I just used them. You could use any deck of cards that has multiple suits and has at least 10 cards in each suit. I will explain the game using face cards.
The Premise of the Game
The game is kind of like Skip Bo and multi-player Solitaire rolled into one game. The object is to play as many of your cards as possible and get rid of your Dutch Blitz pile as fast as possible by playing them ace through ten of the same suit on common piles in the middle that everyone plays on. Once one person has gotten rid of their Dutch Blitz pile, then everyone counts up the number of cards they have played to get their score.
Set Up
- Get a deck of face cards for each player and remove all cards except the cards ace through ten.
- Each person shuffles their deck and then deals a pile of ten cards face down, with the top card facing up. This is their Dutch Blitz pile.
- Next to the Dutch Blitz pile deal three single cards face up.
Playing
- Players play any aces they find during play into the middle of the table. If they find a two and there is an ace of that same suit they can play it. It does not matter who placed the ace. Do the same for cards three through ten.
- Once a pile has been completed in the middle the person that played the ten is responsible for taking it out. Game play does not stop to wait for them.
- Cycle through the cards that were not dealt three at a time. Placing the three cards in front of them in a pile.
- The top card of the three is the only one that can be played and once you put another three down on top of them, you can't go back.
- Once you have cycled through all the cards in your stack, pick them up and turn them over and go through them again.
- When you play the top card of the cards you are cycling through you may then play the one under it.
- When you play one of the three face up cards that are next to your Dutch Blitz pile, you may move your top card from the Dutch Blitz pile into that spot.
- When you play your last card from the Dutch Blitz pile call "Dutch Blitz" or "Blitz" or "Done" or whatever you all agree on. Even if the last card you played was moving a card over from the Dutch Blitz pile to the three face up cards, you are still done.
Scoring
- Once someone has called Dutch Blitz then collect all the cards from the middle and give them back to each player.
- Each player counts the cards they played.
- Each player deducts the number of cards left in their Dutch Blitz pile. The difference is your score for that round.
- One player will keep a sheet of paper with each players name and their score each round.
- Before you play, you should agree on what score you are playing to in order to declare a winner. Once someone's cumulative score from the rounds reaches that amount they win.
Sunday, December 18, 2011
Randall Bennett
I just found out I go to church with Randall Bennett. Ok, I didn't just find out, since we have been in the same congregation for a long time and we frequently have small group meetings together and talk. But he told me today that he is on the TWiT network every so often. He mentioned Tech News Today, which is not one of the TWiT shows I generally watch, but I looked it up and sure enough, he is semi almost famous.
Since I am a geek, this is almost more cool than when I was in a congregation with Rob Morris, defensive lineman for the Indianapolis Colts, and my wife use to go visit his wife each month to fellowship and give a spiritual message.
Since I am a geek, this is almost more cool than when I was in a congregation with Rob Morris, defensive lineman for the Indianapolis Colts, and my wife use to go visit his wife each month to fellowship and give a spiritual message.
Tuesday, September 13, 2011
Mouse Without Borders
Microsoft has released a free tool for managing multiple machines. It allows you to use one mouse and keyboard on multiple machines. It also lets you drag files between those machines.
Once you install Mouse Without Borders you get a control panel where you can adjust settings. Mouse Without Borders must be installed on both machines. Once you have given the client machine the name of the host machine and a security code that the first machine establishes you can then slide the mouse off the side of the host screen. The mouse pointer then appears on the side of the client machine.
From what I understand, it was created by a software developer at Microsoft, who built it on his nights and weekends. Interesting that Microsoft encourages their employees to do this on their nights and weekends, whereas Google generally give their employees a percentage of their work time to work on creating new products of which the employee envisions.
Mouse Without Borders can be downloaded from Microsoft here.
Once you install Mouse Without Borders you get a control panel where you can adjust settings. Mouse Without Borders must be installed on both machines. Once you have given the client machine the name of the host machine and a security code that the first machine establishes you can then slide the mouse off the side of the host screen. The mouse pointer then appears on the side of the client machine.
From what I understand, it was created by a software developer at Microsoft, who built it on his nights and weekends. Interesting that Microsoft encourages their employees to do this on their nights and weekends, whereas Google generally give their employees a percentage of their work time to work on creating new products of which the employee envisions.
Mouse Without Borders can be downloaded from Microsoft here.
Tuesday, March 09, 2010
Wednesday, September 17, 2008
TeamViewer Remote Desktop Software
I've been looking for ways to access my files at home from work or where ever I am. I have also been looking for a way to support family members with their computer problems and helping to teach them how to do the things they want to do with their computers.
I tried several things that had limitations. Some of them were complicated to walk others through installing and sometimes never actually worked on their older software.
I found one that I am very happy with. It is called TeamViewer.
Pros
Cons
I tried several things that had limitations. Some of them were complicated to walk others through installing and sometimes never actually worked on their older software.
I found one that I am very happy with. It is called TeamViewer.
Pros
- Free for personal use.
- Remote Desktop - Basically you can take control of another machine and the user on the other machine can see what you are doing. This is helping for fixing problems on a remote machine and also for training.
- File transfer. No need to share directories. Once you connect you get access to both machines file system. You can do file transfers without opening up a full remote desktop session.
- You can set up a VPN. I haven't done a ton with this, because it seems to be a little different than VPNs I have used. Most times when I have used a VPN when you browse the web it goes out through the VPN's network. So far it doesn't work that way for me. I think the idea is that you can share printers and operate on files as if they were on a local network.
Cons
- As far as I can tell there is no way to pipe sound from the remote machine to your local machine.
Tuesday, August 05, 2008
Tricks to Deal with ADHD
Although I have not been officially diagnosed ADHD I find that I am very distracted and have trouble gathering my thoughts. Here are a list of things that I have found help.
-Make lists of short attainable steps to get done what you want to do. The list will probably pop into your head in the wrong order, but once you have captured them all you can go back and organize them. At least this way you capture what needs to be done before you mind gets distracted and you forget what you were doing and what the steps were.
-If you are working on a computer shut down notification icons like email, social networking sites, and so forth. You are likely to lose focus and be distracted when a notification comes in or you will be tempted to go check sites for changes.
-Exercise. My dad often says that teachers told him that they could tell a big difference between when I walked to school and when I got a ride.
-Make it interesting. ADHDers are capable of hyper focus if it is something that interests them. Find ways to use that to your advantage to get lots done quickly. Find ways to make it interesting or even entertaining without creating more distractions for yourself.
-Make lists of short attainable steps to get done what you want to do. The list will probably pop into your head in the wrong order, but once you have captured them all you can go back and organize them. At least this way you capture what needs to be done before you mind gets distracted and you forget what you were doing and what the steps were.
-If you are working on a computer shut down notification icons like email, social networking sites, and so forth. You are likely to lose focus and be distracted when a notification comes in or you will be tempted to go check sites for changes.
-Exercise. My dad often says that teachers told him that they could tell a big difference between when I walked to school and when I got a ride.
-Make it interesting. ADHDers are capable of hyper focus if it is something that interests them. Find ways to use that to your advantage to get lots done quickly. Find ways to make it interesting or even entertaining without creating more distractions for yourself.
Monday, December 31, 2007
How to Play the Card Game Frustration
A few months ago my wife's sister and her boyfriend taught us a card game, which they call Frustration. While they were over this weekend for Christmas they refreshed us on it. I thought it might be useful to some, but possibly mostly to myself if I detail the game here for reference later.
Object of the Game
Do not get points. End the 6 hands with the lowest amount of points.
Game Play
Object of the Game
Do not get points. End the 6 hands with the lowest amount of points.
Game Play
- Use standard 52 face card deck. Not sure, but I think when you get more people you may add more decks. We played with a single deck and four people.
- Go around the table from person to person laying down a single card. Once you go around you determine who gets the trick based on who had the highest card of the suit that was led. Much like what you do in Euker.
- They is no trump.
- Aces are low.
- Play six hands and add up the scores to determine the winner based on who has the least amount of points.
- The six hands are as follows:
- Hand One - Each trick you take gets you ten points.
- Hand Two - Each heart you take gets you 10 points.
- Hand Three - Each queen you take gets you 25 points.
- Hand Four - The king of spades gets you 100 points if you take a trick containing it.
- Hand Five - The last trick of the hand gets you 100 points.
- Hand Six - All previous five rules. In the previous hands each rule only applied to that hand and did not apply to subsequent hands. In
Saturday, July 01, 2006
Patrick Norton's Wardrobe on DL TV
I was watching a recent episode of DL TV today and they read a viewer email about Patrick dressing like a gas station attendant. He commented that he has two shirts like that and he said that apparently wore them too often. I had noticed the shirts as well, but to me this was like Patrick's trademark. It is not unheard of to have personalities have clothing they always wear during appearances.
The other point that was attempted in the viewer email was that it was making geeks look bad by him dressing down. Are we geeks really known for our fashion sense?
I have a few friends like Patrick, who are into tech, but also know their way around an engine. I find that it enhances their abilities when working on computer hardware. Someone thinking that looking like a grease monkey invalidates any opinions one has about technology is short sited.
The other point that was attempted in the viewer email was that it was making geeks look bad by him dressing down. Are we geeks really known for our fashion sense?
I have a few friends like Patrick, who are into tech, but also know their way around an engine. I find that it enhances their abilities when working on computer hardware. Someone thinking that looking like a grease monkey invalidates any opinions one has about technology is short sited.
Sunday, February 26, 2006
Star Wars Battlefront II
It took me a while to figure out what was going on with the game. At first I wanted to be a jedi all the time, but I think I like the concept of mostly just being regular soldiers.
Here were some questions I had that I think I figured out and some questions that I still don't understand.
-How do I be a Jedi in this game? You can earn points or be the server and set the server to spawn the heros more frequently and set a lower level of points that are required to become a hero.
-How do I pick which hero I can be on a given level or is it set? Mos Eisly assult comes up as Heros vs Villians, which allows you to pick any of the heros or villians, depending on which team you are on. That still doesn't answer how to pick a jedi when in Jaba's palace rather than being Boba Fett.
Found a FAQ site on this game that looks like it might be a little helpful. http://pc.ign.com/objects/737/737696.html#reviews
Here were some questions I had that I think I figured out and some questions that I still don't understand.
-How do I be a Jedi in this game? You can earn points or be the server and set the server to spawn the heros more frequently and set a lower level of points that are required to become a hero.
-How do I pick which hero I can be on a given level or is it set? Mos Eisly assult comes up as Heros vs Villians, which allows you to pick any of the heros or villians, depending on which team you are on. That still doesn't answer how to pick a jedi when in Jaba's palace rather than being Boba Fett.
Found a FAQ site on this game that looks like it might be a little helpful. http://pc.ign.com/objects/737/737696.html#reviews
Monday, January 30, 2006
Linux Bootable CD/DVD
I haven't wanted to take the time to do a Linux install and don't know much about recompiling the kernal, BUT I have wanted to learn how to use Linux. What I have elected to do for the time being is use versions of Linux that I can just boot from a CD and go.
The go part has been a little rough as I have been having trouble getting any version of Linux that boots from a CD to use my WIFI adapter. Nonetheless I have been able to learn a few things.
Here are links to the bootable CD Linux distributions I have been trying.
http://www.ubuntu.com/
http://www.knopper.net/knoppix/index-en.html
The go part has been a little rough as I have been having trouble getting any version of Linux that boots from a CD to use my WIFI adapter. Nonetheless I have been able to learn a few things.
Here are links to the bootable CD Linux distributions I have been trying.
http://www.ubuntu.com/
http://www.knopper.net/knoppix/index-en.html
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