I recently had an interesting experience. I applied for a position as librarian at my old school. I substituted in the library until they got around to doing the interviews. Unfortunately, the interviews were held on the day that the teachers were testing and so no teachers or staff were on the interview committee.
The interview committee consisted of the Principal and one administrator from the school district central office. The interview went fine. A week went by and I had no word about a decision. By the end of the next week I was on my last day of substituting. That morning I checked the district job list online and found that the position I applied for was no longer listed, but instead a librarian position at a high school was advertised. I knew that the high school librarian had also applied for the same position as I, so it was not difficult to put 2+2 together. I still have not heard from the Principal or the Administrator telling me the position has been filled.
So, my question is: Whatever happened to "professional courtesy"? I stepped in and substituted when needed and was in the same building as the Principal, but apparently he could not be bothered to inform me that they filled the position with someone else.
Perhaps school districts need to make sure their administrators have good people skills and standard good manners. I worked for this district and that particular school for 10 years before I retired. I expected some "professional courtesy" and received none.
There were 7 other people who applied for this position also. I can only assume that they have not been contacted either. An email, a phone call or a letter would have been appreciated.
Monday, September 28, 2009
Wednesday, February 25, 2009
Downsizing!
I have been living in a 2400 sq. ft. house and have just moved into a much smaller house. I now have one bedroom, one bathroom, one living room and one very tiny kitchen! The bonus is the screened in porch (blue door on the left). It is huge! And I have two separate courtyards with a variety of plant life and even a huge apricot tree.
It took me almost a full month to totally get out of the big house! I did have to rent a storage unit to put all the furniture that would not fit in my new tiny place.
My "itty-bitty" kitchen. Yes, it really is as small as it looks!
Wednesday, December 10, 2008
HAPPY!! HAPPY!! JOY! JOY!
Tuesday, October 7, 2008
My "new" car!
Wednesday, October 1, 2008
Damages to car
My car lost in freak accident
Yesterday, September 30th started out pretty good. I drove into town to take my dog to the groomer, had coffee with my sister, applied for a job as a substitute teacher, then, because I still had time to kill before I could pick up my dog, went to Marshalls to do a little Christmas Shopping. I was in the store about 20 minutes. By this time it was about 12:30 and I decided to go get some lunch. I walked out of the store and saw an ambulance, several police cars, two fire engines and a local tv news truck. HMMMMM! What could have happened here? All these vehicles were blocking the view of my parking spot. When I could finally see my car I could not believe my eyes!
Here are photos of the scene.



The red car is mine. The Ford F150 demolished the side of my car and pushed it into the Land Rover, which took care of the other side. Notice the wheel of the truck is on the hood of the Toyota SUV.
The Land Rover and SUV were able to drive away. My car had to be placed on a flat bed because the suspension system was destroyed. I just heard from the body shop. My car will be totaled, sigh......
Now begins the insurance mess! I am sitting around waiting on phone calls from my insurance company who is contacting the Ford F150 owner to demand they pay for an auto rental for me until they can get me another car.
I loved my car! It only had 60,000 miles, no dings and got over 30 miles per gallon!
WHY ME?
Here are photos of the scene.



The red car is mine. The Ford F150 demolished the side of my car and pushed it into the Land Rover, which took care of the other side. Notice the wheel of the truck is on the hood of the Toyota SUV.The Land Rover and SUV were able to drive away. My car had to be placed on a flat bed because the suspension system was destroyed. I just heard from the body shop. My car will be totaled, sigh......
Now begins the insurance mess! I am sitting around waiting on phone calls from my insurance company who is contacting the Ford F150 owner to demand they pay for an auto rental for me until they can get me another car.
I loved my car! It only had 60,000 miles, no dings and got over 30 miles per gallon!
WHY ME?
Friday, July 18, 2008
Hawaii At Last!
I just returned from my visit to see my son in Hawaii. He lives on Oahu up in the mountains, a region called Tantalus. Absolutely gorgeous! The photo above was taken at Paradise Cove where we attended a Luau. It was fun and the food was great!
My son, Geoff, lives high above Honolulu in the rain forest. Below are some photos of the view of Honolulu from the road he travels daily to get to work.
There was so much to see. I took over 250 photos. Here are some of them. The plant life and the trees were incredible.
This was taken on a trail not far from Geoff's house. The roots of these trees are incredible!
Check out the root system of this Chinese Banyan tree!!!!
This is one of the flowers growing in Geoff's little garden in front of his house.
Besides the turtle, I really didn't get many photos of animal life. But here are a few.
I had such a wonderful time. Geoff took me out to eat a lot and was such a great host! I had lots of fish, Chinese food, Thai food, Vietnamese food, Hawaiian food (I tried poi...once) and one of my favorite things was the Ahi burger and garlic fries we had a little place near the North shore.
I look forward to another visit soon.....if the airline prices ever go down!
Sunday, May 11, 2008
Chemo Is Over
I had my last (hopefully, forever!) round of chemo on April 16th! WhooooHoooo! My PET scan showed I am clear! So no more prednisone, thank goodness! I hate that stuff! I am still not over it's effects!
I have to thank everyone at the UNM Cancer Center in Las Cruces! They are a wonderful bunch of people....always ready and willing to answer any question at any time.
I will still have to go in every six months for 2 years for a Retuxan treatment. It is a targeting drug. It is supposed to ensure that the cancer does not come back.
I have gained weight and am eating like a normal person again. When I started the chemo treatments I weighed 110 lbs. Now, I weigh about 130 lbs. Some of this might come off after all the drugs clear my system. The prednisone causes a lot of bloating and swelling (mostly around my middle!). I never thought I would be happy to put on weight! Now I need to get on an exercise regime.
I am going to visit my son, Geoff, in Honolulu on June 18th. I will be gone for three weeks! I plan to take some leisurely hikes and lie on the beach a lot! I think the sea water will be really good for me. We have had absolutely no rain since December here in the desert! Our humidity ranges on the average at about 5%. It will be nice to get my skin hydrated again! I am really looking forward to this trip!
I will probably post again while I am in Hawaii and will include some photos! So, until then, Aloha!
I have to thank everyone at the UNM Cancer Center in Las Cruces! They are a wonderful bunch of people....always ready and willing to answer any question at any time.
I will still have to go in every six months for 2 years for a Retuxan treatment. It is a targeting drug. It is supposed to ensure that the cancer does not come back.
I have gained weight and am eating like a normal person again. When I started the chemo treatments I weighed 110 lbs. Now, I weigh about 130 lbs. Some of this might come off after all the drugs clear my system. The prednisone causes a lot of bloating and swelling (mostly around my middle!). I never thought I would be happy to put on weight! Now I need to get on an exercise regime.
I am going to visit my son, Geoff, in Honolulu on June 18th. I will be gone for three weeks! I plan to take some leisurely hikes and lie on the beach a lot! I think the sea water will be really good for me. We have had absolutely no rain since December here in the desert! Our humidity ranges on the average at about 5%. It will be nice to get my skin hydrated again! I am really looking forward to this trip!
I will probably post again while I am in Hawaii and will include some photos! So, until then, Aloha!
Labels:
chemotherapy,
Malt lymphoma,
Prednisone
Friday, March 14, 2008
The Wonders of Chemotherapy
The Wonders of Chemotherapy
It has been a while since I have posted to my blog. I have been busy undergoing chemotherapy for MALT gastric lymphoma. Surprisingly, it has been a very positive experience. For those of you who know me, I have been losing weight over a 2 year period and could not find a doctor who would actually look at everything and do a diagnosis. So, I went to the Mayo Clinic in Arizona. The doctors there actually listened to me and did the appropriate tests and came up with the diagnosis of MALT gastric lymphoma.
I have just finished my third round of chemo at the UNM Cancer Center in Las Cruces. The doctors and staff there are incredible! They are available for questions 24-7. They answer emails. They actually answer their phones personally! Because the Prednisone tablets I have to take were so unpalatable, the UNM Cancer Center pharmacist, Traci, actually crushed them up and put them in gel capsules for me and now I am able to swallow them without experiencing the foul taste! The idea for the gel caps came from my dear friend, Carolyn, who is always watching out for me.
Here is the wonderful part of all this. The chemo has not made me sick. I have had no nausea and no vomiting. The Prednisone, which I take for 5 days at the beginning of my chemo treatment, is apparently having a good effect on my appetite. I have gained 15 lbs since the start of chemo! I am eating well for the first time in 2 years. For the past two years I could eat only small amounts of food and then would experience nausea attacks. My doctor in Arizona said I was actually starving. Now I feel better than I have in 2 years! That is not to say that the chemo doesn't make me tired and lethargic, but that part only lasts from 5 to 10 days.
I have, however, lost my hair! No big deal, it will grow back! And I am having fun wearing all kinds of hats and big earrings! My other dear friend (since 3rd grade), Martha, came for a visit and was with me for my last chemo. She brought me a variety of hats and scarves to play with.
I want to thank all my local friends for being so supportive during this process! Diane, you are my rock! You are always ready to help. And Cathy and Mary Helen, thanks for all the phone calls to check up on me.
And finally, to my two wonderful offspring, Geoff and Joy, although you are so far away you call almost daily to check in and make sure I am alright. I am so blessed to have such wonderful children!
I have just finished my third round of chemo at the UNM Cancer Center in Las Cruces. The doctors and staff there are incredible! They are available for questions 24-7. They answer emails. They actually answer their phones personally! Because the Prednisone tablets I have to take were so unpalatable, the UNM Cancer Center pharmacist, Traci, actually crushed them up and put them in gel capsules for me and now I am able to swallow them without experiencing the foul taste! The idea for the gel caps came from my dear friend, Carolyn, who is always watching out for me.
Here is the wonderful part of all this. The chemo has not made me sick. I have had no nausea and no vomiting. The Prednisone, which I take for 5 days at the beginning of my chemo treatment, is apparently having a good effect on my appetite. I have gained 15 lbs since the start of chemo! I am eating well for the first time in 2 years. For the past two years I could eat only small amounts of food and then would experience nausea attacks. My doctor in Arizona said I was actually starving. Now I feel better than I have in 2 years! That is not to say that the chemo doesn't make me tired and lethargic, but that part only lasts from 5 to 10 days.
I have, however, lost my hair! No big deal, it will grow back! And I am having fun wearing all kinds of hats and big earrings! My other dear friend (since 3rd grade), Martha, came for a visit and was with me for my last chemo. She brought me a variety of hats and scarves to play with.
I want to thank all my local friends for being so supportive during this process! Diane, you are my rock! You are always ready to help. And Cathy and Mary Helen, thanks for all the phone calls to check up on me.
And finally, to my two wonderful offspring, Geoff and Joy, although you are so far away you call almost daily to check in and make sure I am alright. I am so blessed to have such wonderful children!
Monday, January 7, 2008
Prospects for 2008
2008 is here and I have some health issues to take care of. I have been going back and forth to the Mayo Clinic in Arizona since October. I have had a lot of tests done and they finally came up with a diagnosis in December. I have what is known as MALToma or MALT lymphoma, a non-hodgkins lymphoma in the stomach. That was quite a shock to hear! No one in my family has ever had cancer and I wasn't prepared. So, I begin chemotherapy on January 14th. I will hopefully be through with chemo by the beginning of May. After that, I hope I can begin to put on weight again and feel like eating again.
Friday, October 12, 2007
Wildlife in my Backyard
One of the many rabbits I see every day.
I looked this bird up in my birding book. I think it is a PYRRHULOXIA. Or Cardinalis sinuatus. In other words, one of the cardinal family. It is a beautiful bird.
Saturday, September 22, 2007
New Mexico Roadrunner
This little guy was cruising around in my backyard. Fortunately I have very large windows in my back room, so I managed to snap these photos without spooking him. Roadrunners are very fast...as you know...beep!beep!vrooooom!
Monday, September 17, 2007
Sunday, September 2, 2007
Harvest Wine Festival
Yesterday my friend, Diane, and her sister-in-law, Bernadine, and I went to the Harvest Wine Festival in Las Cruces at the fairgrounds. We tasted a lot of wine and I was pleasantly surprised by many of the New Mexico wines. New Mexico has a lot of good vinyards.
Anyway, It was a great afternoon and I do recommend New Mexico Wine. I found a very good Sangiovese from a Tularosa Winery and a couple of good Pinot Noir from the Deming Area. The St. Claire winery had a sort of blush wine called "prickly pear" that wasn't bad at all. There were a lot of sweet wines, which I do not care for....and several sparkling wines that were really pretty good! No, I did not buy any. My little wine rack is full and I can purchase these New Mexico wines anytime I want around here. Tularosa is having its own little festival on September 15th....maybe I will go to that and buy some of the Sangiovese.
Sunday, July 29, 2007
My medical problem solved
Finally, after six weeks, I have blood pressure and a pulse in my left arm. The wonderful people at Memorial Medical Center in Las Cruces took great care of me. Everyone was wonderful and it was a very positive experience.
I have to thank my friend, Diane for taking me to the hospital and hanging around while they put the stent in and bringing me a capuccino in the recovery room and then spending the night with me. I also want to thank my friend Cathy for taking over when Diane had to leave and for calling me twice a day since to make sure I was alright. Friends are wonderful!
I can't forget Carolyn, who called me at least twice a day before the procedure was done to make sure I hadn't dropped dead at home alone.
I am so thankful to have two wonderful kids who care about me and wonderful friends who have given their time to help me!
I have to thank my friend, Diane for taking me to the hospital and hanging around while they put the stent in and bringing me a capuccino in the recovery room and then spending the night with me. I also want to thank my friend Cathy for taking over when Diane had to leave and for calling me twice a day since to make sure I was alright. Friends are wonderful!
I can't forget Carolyn, who called me at least twice a day before the procedure was done to make sure I hadn't dropped dead at home alone.
I am so thankful to have two wonderful kids who care about me and wonderful friends who have given their time to help me!
Wednesday, July 18, 2007
Nightmare at Mountain View Medical Center
My visit to Mountain View Regional Hospital
(An experience to forget)
www.mountainviewregional.com/
Prologue
Before I relate the events of July 6, 2007, I should go back in time two weeks so you will know the complete history of this experience to forget.
On June 13th I had just finished mopping floors and was in a bit of a sweat. I decided to sit down with a glass of water and rest a bit. Within five minutes I experienced extreme dizziness and my tongue, the inside of my mouth, and my lips all went numb. Then my hands started shaking uncontrollably. Needless to say, I got scared. After several tries I finally got my fingers to work on the telephone keypad and called a friend to come and get me and take me to the emergency room at Mountain View Regional Hospital. When we arrived there were about 3 people in the waiting room. I had to register then sit and wait…..about 20 + minutes. They called me in….sat me in a room….could not get the blood pressure from my left arm until they had tried about 3 times. (HINT! CLUE # 1)
Finally a Dr. came in, asked me what had happened. I told him. (By now the numbness was gone and my hands had quit shaking) He said, “Well, I don’t think you had a stroke. But you might be having “mini-strokes”. Try taking some baby aspirin and go see your primary doctor tomorrow.” He sent me out to the desk where I paid them $75.00, for nothing.
So, I went to see my primary doctor the next day. She immediately ordered an MRI of my head and an ultrasound of my carotid artery. (She, apparently got the hint right away when her assistant could not get a pulse or a blood pressure reading from my left arm)
I leave with the orders and drive immediately to Mountain View Regional hospital, where I am told that it is 5 o’clock and they are closed. They have no MRI techs in the building and that I need to make an appointment for tomorrow. Okay. So I said, who do I call to make the appointment? Oh, that department is closed until tomorrow. You need to come in early in the morning with your orders.
Next day, Friday, June 15: 8 am: I arrive at reception desk with the MRI orders, which, by the way, say STAT. I show them to the girl. She says, “Do you have an appointment? You have to have an appointment ahead of time for an MRI.” So, I make the appointment. It won’t be until 11 am. By this time I am beginning to get woozy again…and decide to go sit in my car and wait. Oh yes, when I got the appointment they had me pay $238.00 right away.
Fast forward to Monday, June 18th…a 9 am appointment with my primary doctor. She has the results from the MRI and ultrasound. She refers me to a vascular surgeon, because the ultrasound showed carotid artery blockage. Tuesday morning I call the surgeon’s office to set an appointment. Uh oh! I’m sorry , our computer system is down. I can’t make any appointments until the IT guy gets here and fixes it. Leave your number and I will call you back. That day passes with no call back…I call at 4:45…and get an automated message that says to “please call back during regular office hours…8 am to 5 pm. Hmmmm…..guess they had nothing to do since their computers weren’t working, so went home.
Tuesday, June 19th….No call back still. So, I call them. I need an appointment as soon as possible….these are my symptoms…..I have the results from the MRI and Ultrasound. She says, “Oh, it sounds like we really need to get you in here…..BUT….the doctor only sees patients in the office on Tuesdays, as that is the only day he isn’t in surgery. “ So I told her that I tried to make an appointment yesterday, which was Tuesday, only they couldn’t make appointments because their computers were down. At this point I am silently screaming! Well….nothing to be done but wait a whole week for an appointment.
So, I made the appointment for the next week, met the vascular surgeon and set up a date and time at Mountain View Regional Hospital to do an angiogram and put in a stent if needed. And here is where the nightmare begins.
JULY 6TH DAY OF THE ANGIOGRAM
My daughter was concerned for me and took time off and spent the money to fly in from Philadelphia to be with me before and after the angiogram. I arrived at the appointed time for the angiogram and even though I was pre registered they had me go back to admitting all over again. So, I got a number and waited. I finally got back to the Cath Lab at 10:30 am. They put in an IV with saline and gave me two benadryl and shaved my groin area and left me. My daughter was not allowed to stay with me. They told her she could go home and they would call her when the procedure started. I was scheduled for 12 noon.
12:30 comes around and finally someone comes to check on me and let me know that because of a schedule glitch with the anesthesiologist it would be another two to three hours before they could get to me.. Well I felt like crying at that point. My head was killing me, the lights in the room were bringing on a migraine. I asked for something for my headache. Two hours later someone came and gave me two Tylenol. At 2:30 I called my daughter and told her I was still just waiting. Finally at around 2:45 they came to get me. No one introduced themselves or told me what I could expect them to be doing. I got no warning when they pushed the catheter into my groin and I screamed because it was very painful. “Oh, does that hurt? Let me know when it stops.” Then, “okay we’re going to take an x-ray now.” They moved a machine next to me and that is when I got hot all over and thought I had wet the bed. They gave me no warning about the effects of the dye being pushed in. Then….”okay, we’re done”
I said I wanted to talk to the Dr. I said he was supposed to put the stent in today. He told me that in his office and I had to sign a release that allowed him to put in a stent if needed. He denied telling me that and refused to talk to me about it. He told me to make an appointment at his office and we would schedule a time to put the stent in. He said due to the fact that I was under the influence of medication he couldn’t speak to me about this now. I said, “What medication? I got two benadryl at 10:30 am and 2 tylenol at 2:30 and I was fully aware of what was going on around me. He just backed off and told me to call his office on Monday.
Now they roll me back to the same room I started in so that I can be observed for 2 hours to make sure the puncture site in the groin did not bleed. This was about 3:10 pm. I lay there listening to an endless amount of gossip and personal phone calls. No one came and checked on me until 4:30 pm. Finally I was allowed a glass of water and some apple juice and a sandwich. They called my daughter to come after me then and took out the IV and let me get dressed. Then they went over directions about taking care of the incision. In the meantime my daughter comes to pick me up and is told at the nursing station that I am not there. They think I am on the 4th floor. So up she goes and of course I am not there. At this point I asked the nurse to wheel me outside to wait for her and we ran into her at the end of the hall. I was wheeled outside, my daughter got the car and we drove off with me using some four- letter words.
I think that pretty much tells about my ordeal at Mountain View Regional Hospital. I am now trying to locate another vascular surgeon at a different hospital.
(An experience to forget)
www.mountainviewregional.com/
Prologue
Before I relate the events of July 6, 2007, I should go back in time two weeks so you will know the complete history of this experience to forget.
On June 13th I had just finished mopping floors and was in a bit of a sweat. I decided to sit down with a glass of water and rest a bit. Within five minutes I experienced extreme dizziness and my tongue, the inside of my mouth, and my lips all went numb. Then my hands started shaking uncontrollably. Needless to say, I got scared. After several tries I finally got my fingers to work on the telephone keypad and called a friend to come and get me and take me to the emergency room at Mountain View Regional Hospital. When we arrived there were about 3 people in the waiting room. I had to register then sit and wait…..about 20 + minutes. They called me in….sat me in a room….could not get the blood pressure from my left arm until they had tried about 3 times. (HINT! CLUE # 1)
Finally a Dr. came in, asked me what had happened. I told him. (By now the numbness was gone and my hands had quit shaking) He said, “Well, I don’t think you had a stroke. But you might be having “mini-strokes”. Try taking some baby aspirin and go see your primary doctor tomorrow.” He sent me out to the desk where I paid them $75.00, for nothing.
So, I went to see my primary doctor the next day. She immediately ordered an MRI of my head and an ultrasound of my carotid artery. (She, apparently got the hint right away when her assistant could not get a pulse or a blood pressure reading from my left arm)
I leave with the orders and drive immediately to Mountain View Regional hospital, where I am told that it is 5 o’clock and they are closed. They have no MRI techs in the building and that I need to make an appointment for tomorrow. Okay. So I said, who do I call to make the appointment? Oh, that department is closed until tomorrow. You need to come in early in the morning with your orders.
Next day, Friday, June 15: 8 am: I arrive at reception desk with the MRI orders, which, by the way, say STAT. I show them to the girl. She says, “Do you have an appointment? You have to have an appointment ahead of time for an MRI.” So, I make the appointment. It won’t be until 11 am. By this time I am beginning to get woozy again…and decide to go sit in my car and wait. Oh yes, when I got the appointment they had me pay $238.00 right away.
Fast forward to Monday, June 18th…a 9 am appointment with my primary doctor. She has the results from the MRI and ultrasound. She refers me to a vascular surgeon, because the ultrasound showed carotid artery blockage. Tuesday morning I call the surgeon’s office to set an appointment. Uh oh! I’m sorry , our computer system is down. I can’t make any appointments until the IT guy gets here and fixes it. Leave your number and I will call you back. That day passes with no call back…I call at 4:45…and get an automated message that says to “please call back during regular office hours…8 am to 5 pm. Hmmmm…..guess they had nothing to do since their computers weren’t working, so went home.
Tuesday, June 19th….No call back still. So, I call them. I need an appointment as soon as possible….these are my symptoms…..I have the results from the MRI and Ultrasound. She says, “Oh, it sounds like we really need to get you in here…..BUT….the doctor only sees patients in the office on Tuesdays, as that is the only day he isn’t in surgery. “ So I told her that I tried to make an appointment yesterday, which was Tuesday, only they couldn’t make appointments because their computers were down. At this point I am silently screaming! Well….nothing to be done but wait a whole week for an appointment.
So, I made the appointment for the next week, met the vascular surgeon and set up a date and time at Mountain View Regional Hospital to do an angiogram and put in a stent if needed. And here is where the nightmare begins.
JULY 6TH DAY OF THE ANGIOGRAM
My daughter was concerned for me and took time off and spent the money to fly in from Philadelphia to be with me before and after the angiogram. I arrived at the appointed time for the angiogram and even though I was pre registered they had me go back to admitting all over again. So, I got a number and waited. I finally got back to the Cath Lab at 10:30 am. They put in an IV with saline and gave me two benadryl and shaved my groin area and left me. My daughter was not allowed to stay with me. They told her she could go home and they would call her when the procedure started. I was scheduled for 12 noon.
12:30 comes around and finally someone comes to check on me and let me know that because of a schedule glitch with the anesthesiologist it would be another two to three hours before they could get to me.. Well I felt like crying at that point. My head was killing me, the lights in the room were bringing on a migraine. I asked for something for my headache. Two hours later someone came and gave me two Tylenol. At 2:30 I called my daughter and told her I was still just waiting. Finally at around 2:45 they came to get me. No one introduced themselves or told me what I could expect them to be doing. I got no warning when they pushed the catheter into my groin and I screamed because it was very painful. “Oh, does that hurt? Let me know when it stops.” Then, “okay we’re going to take an x-ray now.” They moved a machine next to me and that is when I got hot all over and thought I had wet the bed. They gave me no warning about the effects of the dye being pushed in. Then….”okay, we’re done”
I said I wanted to talk to the Dr. I said he was supposed to put the stent in today. He told me that in his office and I had to sign a release that allowed him to put in a stent if needed. He denied telling me that and refused to talk to me about it. He told me to make an appointment at his office and we would schedule a time to put the stent in. He said due to the fact that I was under the influence of medication he couldn’t speak to me about this now. I said, “What medication? I got two benadryl at 10:30 am and 2 tylenol at 2:30 and I was fully aware of what was going on around me. He just backed off and told me to call his office on Monday.
Now they roll me back to the same room I started in so that I can be observed for 2 hours to make sure the puncture site in the groin did not bleed. This was about 3:10 pm. I lay there listening to an endless amount of gossip and personal phone calls. No one came and checked on me until 4:30 pm. Finally I was allowed a glass of water and some apple juice and a sandwich. They called my daughter to come after me then and took out the IV and let me get dressed. Then they went over directions about taking care of the incision. In the meantime my daughter comes to pick me up and is told at the nursing station that I am not there. They think I am on the 4th floor. So up she goes and of course I am not there. At this point I asked the nurse to wheel me outside to wait for her and we ran into her at the end of the hall. I was wheeled outside, my daughter got the car and we drove off with me using some four- letter words.
I think that pretty much tells about my ordeal at Mountain View Regional Hospital. I am now trying to locate another vascular surgeon at a different hospital.
Labels:
Health Care New Mexico,
Hospitals,
Medical Care
Sunday, June 10, 2007
Librarians and NCLB
Some notes on Cataloging Books and NCLB
When I took my cataloging class in college, I really hated it. But, I learned how to do it and swore that I would never accept a job as a cataloger. I imagined being buried deep in the bowels of the library with no sunlight and nothing but rows and rows of books. I couldn’t imagine doing that for a living! So, I did not accept the first job offer I got. I turned it down and later accepted a job as a children’s librarian.
As much as I hated cataloging, I was good at it and in later years I found that I did need to do it. When I started working for the public school system I discovered that I needed to catalog the books for the school library. Sometime in the 1970’s I found that certain book jobbers would add catalog cards with book orders…for a price. So, when my library budget was good enough I would spend the money and order the cards. I still had to give them a local call number, sort and file them in the card catalog, but I didn’t have to type each card. That was a great help.
By the mid 1980’s computers were coming to the libraries and there were programs that were helpful for typing and printing catalog cards. And finally, in the late 1980’s companies came out with MARC record programs and barcodes were put on books. This really was major. A librarian could order books complete with barcodes and full processing. Sometimes we would have to change the call numbers or subject headings to match our particular library, but this development was a real turning point. It saved so much time and that time could be spent reading to and teaching children.
By the 1990’s most school districts had processing departments to do the cataloging of materials. At first this was great and then all of a sudden, it seemed we were not allowed to do our own cataloging. When the online web based programs came about, most school districts opted for that system and hired a person to be in charge. The school librarian was no longer in charge of her own school library. We couldn’t even buy paperback books. If we did, we got them back with notes saying they were not worth cataloging. Apparently now we had rules about how thick a book could be, how old the copyright date could be, and were told which publishers we could not purchase from. So, I began wondering why I bothered with all those classes on cataloging and why I took that class in Book Selection. I actually know some librarians just out of school who never had to take a cataloging class.
So now here we are in the 2000’s and school librarians are handed curriculum guides and scripts on how to run the school libraries. What ever happened to individual library programs? My main objective was to show children the wonders of books and how to use them. Somehow this was all disappearing. My last school was very small, only 300 students, so I had a limited budget. My library budget was about $7.00 per student. You can’t buy a lot of hardback books with that kind of money. So, it was all very frustrating. When I did buy books and send them in to be cataloged sometimes it took months to get them back and then some of them were banded together with a note that they were not good enough to be cataloged and that I should give them away as prizes.
And while all this is going on, the teachers are being handed scripts to follow. Teachers used to bring their classes to the library to do reports on countries, animals, and science projects. But with the advent of NCLB this all stopped. The teachers no longer had time in their days to bring their students to the library for research projects. It seemed to me that NCLB really was put there to automate teaching. Teachers are becoming robots and so are librarians. I chose not to be a part of this system, so I retired. I was fortunate that I could retire. I feel for the individual teachers and librarians who became teachers and librarians because they wanted to teach children and thought they had something to offer. Now the various levels of government are telling them what to teach and how to teach and leaving no room for individual creativity. How is this going to help our children? My children are grown now, but if I had small children now I would not send them to public schools. I would home school them or find a good private school that still encourages creativity in their students and teachers.
When I took my cataloging class in college, I really hated it. But, I learned how to do it and swore that I would never accept a job as a cataloger. I imagined being buried deep in the bowels of the library with no sunlight and nothing but rows and rows of books. I couldn’t imagine doing that for a living! So, I did not accept the first job offer I got. I turned it down and later accepted a job as a children’s librarian.
As much as I hated cataloging, I was good at it and in later years I found that I did need to do it. When I started working for the public school system I discovered that I needed to catalog the books for the school library. Sometime in the 1970’s I found that certain book jobbers would add catalog cards with book orders…for a price. So, when my library budget was good enough I would spend the money and order the cards. I still had to give them a local call number, sort and file them in the card catalog, but I didn’t have to type each card. That was a great help.
By the mid 1980’s computers were coming to the libraries and there were programs that were helpful for typing and printing catalog cards. And finally, in the late 1980’s companies came out with MARC record programs and barcodes were put on books. This really was major. A librarian could order books complete with barcodes and full processing. Sometimes we would have to change the call numbers or subject headings to match our particular library, but this development was a real turning point. It saved so much time and that time could be spent reading to and teaching children.
By the 1990’s most school districts had processing departments to do the cataloging of materials. At first this was great and then all of a sudden, it seemed we were not allowed to do our own cataloging. When the online web based programs came about, most school districts opted for that system and hired a person to be in charge. The school librarian was no longer in charge of her own school library. We couldn’t even buy paperback books. If we did, we got them back with notes saying they were not worth cataloging. Apparently now we had rules about how thick a book could be, how old the copyright date could be, and were told which publishers we could not purchase from. So, I began wondering why I bothered with all those classes on cataloging and why I took that class in Book Selection. I actually know some librarians just out of school who never had to take a cataloging class.
So now here we are in the 2000’s and school librarians are handed curriculum guides and scripts on how to run the school libraries. What ever happened to individual library programs? My main objective was to show children the wonders of books and how to use them. Somehow this was all disappearing. My last school was very small, only 300 students, so I had a limited budget. My library budget was about $7.00 per student. You can’t buy a lot of hardback books with that kind of money. So, it was all very frustrating. When I did buy books and send them in to be cataloged sometimes it took months to get them back and then some of them were banded together with a note that they were not good enough to be cataloged and that I should give them away as prizes.
And while all this is going on, the teachers are being handed scripts to follow. Teachers used to bring their classes to the library to do reports on countries, animals, and science projects. But with the advent of NCLB this all stopped. The teachers no longer had time in their days to bring their students to the library for research projects. It seemed to me that NCLB really was put there to automate teaching. Teachers are becoming robots and so are librarians. I chose not to be a part of this system, so I retired. I was fortunate that I could retire. I feel for the individual teachers and librarians who became teachers and librarians because they wanted to teach children and thought they had something to offer. Now the various levels of government are telling them what to teach and how to teach and leaving no room for individual creativity. How is this going to help our children? My children are grown now, but if I had small children now I would not send them to public schools. I would home school them or find a good private school that still encourages creativity in their students and teachers.
Saturday, May 19, 2007
MUSIC

I was giving my stove a good cleaning this afternoon and while I was cleaning I was listening to the Adult Alternative music channel on TV. My son was good enough to connect my tv to my stereo speakers while he was home at Christmas. The sound is so much better.
Anyway, I was thinking how lucky I am to be 63 years old and have such a rich history of music. Oh, I know, most young people today have heard all the music from the 50’s, 60’s and on, but they have no personal history of that music as I have. They can’t hear Elvis sing “Don’t Be Cruel” and remember the night they first heard it and what they were doing. I, on the other hand, can remember it well. I was at a party and had a fight with my boyfriend, and that song made a lot of sense to me. Every time I hear a song from one of those eras I remember some of my personal history. I can even remember being very young and listening to my mother’s music, jazz and swing and opera. My father liked country, blues, Tennessee Earnie Ford, Harry Belafonte, and the Kingston Trio.
We were a dancing family. I hope my two kids enjoy dancing as much as I did (do). I danced a lot at home, though it seemed to embarrass my daughter. It is good exercise and sometimes I still stop what I’m doing when I hear a good Rolling Stones song and dance a little bit. I can still dance swing, waltz, two step and do the twist.
I know both my kids love music. I learn a lot of the new things out there from them. My son mixes and DJ’s as a hobby. I like the drum and bass. Some of the other stuff is too repetitive for me, but I can listen and enjoy it for short periods of time. My daughter has sent me CDs that she thought I might enjoy and I think she has good taste.
So, if you don’t have music in your life now, do something about it! It is so important. Play music for your babies and continue to have music in your home for them until they leave and make their own homes. Let them experiment with it and make their own musical history. Try not to judge what they might listen to. Let them figure out what they like and dislike without your judgment. If you don’t like it, ask them to put on earphones or keep the music in their room. Let them make their own choices. You brought them up. Trust that they will make good decisions.
Now, back to the kitchen!
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