I just found some long lost friends through face book. I'm so glad that I've kept up and can use the internet. I hesitated about face book, but now that I do face book I 'm begining to see it's real value that is an easy way to find lost friends and to keep up. It is so nice to be able to say hi to a friend anytime you'd like.
I'd lost my friend Mary, with whom I had gone to school. She had married not once but twice. I had seen her twelve years ago. She had told me her new married name and that they were moving to Florida. I still had not kept up. I am a terrible correspondent when it comes to the mail. I never mind writing. I have been know to write a letter address it and then forget to mail it. I'm hopeless. (But email is instant, and besides there is spell check.) I visited one of my best friend's site and found a long lost pal from our teenage years. Sue had listed a friend who I instantly knew was my friend Mary. I found two friends at once and was able to get another of my High School buddies together too.
We were a three some in our High School, hanging around together. We had a lot of fun and laughs. Pajama parties, movies, going Downtown for lunch or just running a muck. Old friends are the best. It takes you back, and lets you remember and feel like a kid again. Just talking about old times is wonderful. I'm so happy to have found Mary again and can't wait to get together with her and my other cohort Robbie, and talk old times. We might have to do it three ways on face book, because we live so far apart; nevertheless we can get together now.
About the process of producing Art work, as a Mother, daughter, divorcee, caregiver. All about life and being handicapped from childhood and having a life well lived.
Friday, June 24, 2011
Wednesday, March 9, 2011
A Dog's Life
Yesterday My elderly Shetland Sheep Dog, Shep, Had a medical emergency. We rushed to the Vets thinking that this was the end. The doctors there were able to operate on and remove the very large fatty tumor, that Shep had started to try to bite off. Our other two dogs, Tinker and Caesar were both terribly upset. They were use to going places together, and what's more Shep had bled a lot. They jumped up and gave us the once over with their keen noses. Lewis said that Caesar even seemed to have tears in his eyes. Tinker just looked totally distressed.
They operated on Shep, but because the tumor was so big, the size of a tennis ball, they did not have enough skin to seal over the wound. His front leg was shaved down to his paw and up pass his shoulder. When he arrived back home thoroughly doped up, both small dogs shifted him and Tinker sat by his side with his head down watching him. Caesar on the other hand, was scared to get too close, but was obviously very concerned.
Some people think about animals as dumb beast. Dogs (and cats to a point) have a great deal of love and emotions. Shep has wanted to be close to me. He is happy just to be near me, happier still for me to put my hand on him and stroke him. Some how this gives him comfort. Dogs are pack animals and depend on each other. Their master becomes their leader.
My little Tinker, a small Dachshund, needs to be close. He starts out on top of the covers and before the night is over he burrows under the blanket and sheet and cuddles up as close as he can get to me. I hate to think of dogs that can not come into a home. I have three dogs and two cats that live with us. This was not planned it just happened.
Years ago the boys and I found a young golden retriever Samantha at the Gloucester Humane Society. Then I inherited Shep from my middle son, when they could not manage a dog and work. These two were constant companions. Samantha had cancer, for the last 3 or 4 months of her life Shep sat by her and licked her ears or her face giving her love and constant attention.
They operated on Shep, but because the tumor was so big, the size of a tennis ball, they did not have enough skin to seal over the wound. His front leg was shaved down to his paw and up pass his shoulder. When he arrived back home thoroughly doped up, both small dogs shifted him and Tinker sat by his side with his head down watching him. Caesar on the other hand, was scared to get too close, but was obviously very concerned.
Some people think about animals as dumb beast. Dogs (and cats to a point) have a great deal of love and emotions. Shep has wanted to be close to me. He is happy just to be near me, happier still for me to put my hand on him and stroke him. Some how this gives him comfort. Dogs are pack animals and depend on each other. Their master becomes their leader.
My little Tinker, a small Dachshund, needs to be close. He starts out on top of the covers and before the night is over he burrows under the blanket and sheet and cuddles up as close as he can get to me. I hate to think of dogs that can not come into a home. I have three dogs and two cats that live with us. This was not planned it just happened.
Years ago the boys and I found a young golden retriever Samantha at the Gloucester Humane Society. Then I inherited Shep from my middle son, when they could not manage a dog and work. These two were constant companions. Samantha had cancer, for the last 3 or 4 months of her life Shep sat by her and licked her ears or her face giving her love and constant attention.
Thursday, February 24, 2011
Wheelie Blues No More..Permobil c300
OK I've jumped through all the correct rings. I'd spin around in tight circles if I could count on my chair to make tight turns. The batteries are quickly dying and I will not replace them in a chair that is to be replaced. Because of the batteries and the faulty steering, I have had to be pushed into my Van on occasion. Oh the humiliation! I'm a free spirit that deserves to be free! It rubs me the wrong way to be tied down. Yes, I know be thankful for all your blessings. I am, I really am, but I yearn to be more mobile. So much for my gripping and my impatience.
I started this several days ago. Something told me that I needed to check on how the order for the chair was coming along. So I called the Health Care provider to see what was happening. I talked to my contact there. She said that they had not ordered it yet, because they had not gotten all the paper work from my doctor's office. She also said she had called and left a messages for me at work and on my home phone. There were no messages left. She had not bothered to call. I called her boss and she immediately took charge. Thank goodness I called or I would still be patiently waiting for weeks more. I've always been patient but I really need this chair. I have been totally amazed at how callous people who work at Home Health Care Facilities are. Maybe I'm more sensitive because I know what having a working chair means to the individuals; however, don't these people have any empathy? If I was a health care provider, I would expect the people who worked for me to be on the ball. If certain documents were missing then I would expect them to be all over it making sure that everything was in line. She let down the business as well as the client.
After checking and complaining, I think I've finally gotten my chair ordered, after 6 weeks of trying.
The new chair has been shipped. I can not wait, however, my part after medicare is $3800 wow! Being handicapped is expensive at least I have Medicare who pays 80%. My son gave a customer a good deal on a few items saying Mother needs a new wheel chair. Between my credit card and the shop we will make it. Hopefully this is a Cadillac of a wheel chair! I noticed going down the aisle of the shop that I was making a real racket with the old one. At least that chair is moving! I am expecting it either Monday or Tuesday.
This was first published in February 2011. It is now May 2016. I have had a few bumps in the road and I have had some work done on the chair but it is still sturdy. I had to have the seat plate replaced, and when I did I decided to get a raiser for the chair so that I can adjust my seat so it will go up and down. This was well worth the cost which came out of my pocket. I can now think about going someplace and staying in a motel/hotel. Most beds in these were not standard 19" to 20" height any more as they thought the up grade to pillow tops made the place look better. this made it so that people who could no longer stand could not easily find a place to stay with a bed that they could transfer into. One time my son actually had to drag me unto a bed that was too high for me to transfer to. Now I can cook without worrying about fat popping into my eyes, and I can see into taller pots. Also I sit behind the counter at my shop and I can get myself up to a better level there to work the computer and to wait on clients. I can highly recommend this power chair, Permobil c300. By the time my other chairs have gotten to be this age, they were in bad shape and barely working.
More bumps in the road. The company from which I order the chair originally has decided to close down their service department. They now say that they have someone who will come to us. I live off the beaten path and would prefer to go where there is a service center. I have called around and most do not know how to work on Permobils. Plus they prefer to work on ones that were ordered from them. I thought that I had found the answer until I got an email saying that they could not work on Permobils. What the heck?
I started this several days ago. Something told me that I needed to check on how the order for the chair was coming along. So I called the Health Care provider to see what was happening. I talked to my contact there. She said that they had not ordered it yet, because they had not gotten all the paper work from my doctor's office. She also said she had called and left a messages for me at work and on my home phone. There were no messages left. She had not bothered to call. I called her boss and she immediately took charge. Thank goodness I called or I would still be patiently waiting for weeks more. I've always been patient but I really need this chair. I have been totally amazed at how callous people who work at Home Health Care Facilities are. Maybe I'm more sensitive because I know what having a working chair means to the individuals; however, don't these people have any empathy? If I was a health care provider, I would expect the people who worked for me to be on the ball. If certain documents were missing then I would expect them to be all over it making sure that everything was in line. She let down the business as well as the client.
After checking and complaining, I think I've finally gotten my chair ordered, after 6 weeks of trying.
The new chair has been shipped. I can not wait, however, my part after medicare is $3800 wow! Being handicapped is expensive at least I have Medicare who pays 80%. My son gave a customer a good deal on a few items saying Mother needs a new wheel chair. Between my credit card and the shop we will make it. Hopefully this is a Cadillac of a wheel chair! I noticed going down the aisle of the shop that I was making a real racket with the old one. At least that chair is moving! I am expecting it either Monday or Tuesday.
This was first published in February 2011. It is now May 2016. I have had a few bumps in the road and I have had some work done on the chair but it is still sturdy. I had to have the seat plate replaced, and when I did I decided to get a raiser for the chair so that I can adjust my seat so it will go up and down. This was well worth the cost which came out of my pocket. I can now think about going someplace and staying in a motel/hotel. Most beds in these were not standard 19" to 20" height any more as they thought the up grade to pillow tops made the place look better. this made it so that people who could no longer stand could not easily find a place to stay with a bed that they could transfer into. One time my son actually had to drag me unto a bed that was too high for me to transfer to. Now I can cook without worrying about fat popping into my eyes, and I can see into taller pots. Also I sit behind the counter at my shop and I can get myself up to a better level there to work the computer and to wait on clients. I can highly recommend this power chair, Permobil c300. By the time my other chairs have gotten to be this age, they were in bad shape and barely working.
More bumps in the road. The company from which I order the chair originally has decided to close down their service department. They now say that they have someone who will come to us. I live off the beaten path and would prefer to go where there is a service center. I have called around and most do not know how to work on Permobils. Plus they prefer to work on ones that were ordered from them. I thought that I had found the answer until I got an email saying that they could not work on Permobils. What the heck?
Sunday, February 20, 2011
But I am a Real Artist
I remember meeting one of my good friends for the first time. We started talking and discovered that we both pursued the art of painting. I told her that I was an artist and she replied that she was a REAL ARTIST. This took me back. I can imagine that my mouth hung open. Was she insinuating that I was not a real artist. Now that I think about it some 15 years later, what she meant was that she took art seriously as a full time pursuit, not just some hobby to be replaced with another. There are so many people who play at art. Neither she nor I played at our art. It was serious business that we both pursued with a passion.
We have grown with our art in very different ways. I have tried to continue painting not matter what my circumstances are. There have been times when I could paint with out interruptions as a full time job. During this time I grew and produced a great number of works. There was a show in Richmond where we both took our paintings to be displayed. The show was judged and awards were given. I only received one ribbon during that time. I'm not sure that my friend received any. It did not matter. The shows were once a month,and we continued to try. This gave us the incentive to paint more and more. We are as different as night and day, but we are and continue to be REAL ARTIST despite all odds.
Recently, I have been working full time with my son, Lewis. Running an antique vintage decorative arts shop both on Main Street and on line is exciting, but leaves me little time to paint.
We have grown with our art in very different ways. I have tried to continue painting not matter what my circumstances are. There have been times when I could paint with out interruptions as a full time job. During this time I grew and produced a great number of works. There was a show in Richmond where we both took our paintings to be displayed. The show was judged and awards were given. I only received one ribbon during that time. I'm not sure that my friend received any. It did not matter. The shows were once a month,and we continued to try. This gave us the incentive to paint more and more. We are as different as night and day, but we are and continue to be REAL ARTIST despite all odds.
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| After Katerina by S. Drake Streetman |
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| Apple Tree Painting by Leigh Lewis Trimble |
Handicap Blues
I don't like to complain. I don't admit to being handicap except when I am desperate. As long as My chair works and my van works I'm "A OK." Occasionally everything goes bad at once. I'm playing the waiting game for a new wheelchair. I called the company to ask how long only to be told that my doctor's appointment had been too far away to work and that although I had been fitted for the chair a doctor's order and visit was necessary. As my Mom says this is ridiculous, "You have been in a chair for ten years! It's not like you'll magically heal and not have to use a chair." So why does medicare not have a provision for people who have a chronic condition? Why do they want to pay for a Doctor's visit that is not at all necessary. Go figure. That's the way things work. People don't always think. My doctor says that she hates filing out the forms for someone who already has a chair and she has to justify that they still need a chair.
At any rate a new chair is on the way. On to problem number two. The handicap van door. The Ramp Van doors are and have been erratic ever since I purchased the vehicle. Last fall I took the van to have the doors fixed again. It seems that every time I have the automatic ramp door fixed it breaks again. The trouble is it is erratic, some times it works just find and other times especially in very cold or nasty weather it just does not close at all. So, when I took it to be repaired the bad news was, "Oh, gee we think you need to by a new vehicle, and here is our salesman to help you out." This does not wash with me. To say the least if you start hard selling me, my ruff goes up and I will not be sold. The alternative was to have it fixed for a tune of $1,800. Well, this seemed better than buying a new van for $50,000 to $70,000 that they quoted. My van had less than 80,000 miles on her. Why is it that the handicap adaptable parts wear out much sooner than the vehicle? The long and the short of it is I bit the bullet and had the van repaired. It worked for about a month and has been a pain in the neck ever since. Right now in February, I can't get it to close most of the time and I feel as though I have to take someone along with me to help with the door. Last week mother and I were rushing to make a dental appointment and I lost patience with the door reopening when I put the car into drive, so I slammed on my brakes and the door slammed shut; however, when we got to the dentist Mother got out of the front seat and I tried the ramp door. It would not open at all. I had jammed the door. I called my son, Chris, and took the car over to his shop where he had to use a crow bar to get the door to open. Then he had to position the door on it's runners so it would at least be able to be closed manually. What does one do with out someone to help them. I've always said that the Good Lord knew what he was doing when he gave me 3 sons. Even though I thought a daughter would have been nice. Thank God for my sons. So now I have to figure out how to get a good second hand Van. I've done some research on the web and it turns out that not all handicap vehicles are 50 to 70 thousand, I found a few newer ones for 30 something and older ones even less expensive. I can tell you this, I will not be buying a new Van from the same people , who fixed this one. I hope with trade in I can afford a good van.
If anyone out there reads my blog and has any advise, I sure could use some help here. Please comment or email me. Thanks
.
At any rate a new chair is on the way. On to problem number two. The handicap van door. The Ramp Van doors are and have been erratic ever since I purchased the vehicle. Last fall I took the van to have the doors fixed again. It seems that every time I have the automatic ramp door fixed it breaks again. The trouble is it is erratic, some times it works just find and other times especially in very cold or nasty weather it just does not close at all. So, when I took it to be repaired the bad news was, "Oh, gee we think you need to by a new vehicle, and here is our salesman to help you out." This does not wash with me. To say the least if you start hard selling me, my ruff goes up and I will not be sold. The alternative was to have it fixed for a tune of $1,800. Well, this seemed better than buying a new van for $50,000 to $70,000 that they quoted. My van had less than 80,000 miles on her. Why is it that the handicap adaptable parts wear out much sooner than the vehicle? The long and the short of it is I bit the bullet and had the van repaired. It worked for about a month and has been a pain in the neck ever since. Right now in February, I can't get it to close most of the time and I feel as though I have to take someone along with me to help with the door. Last week mother and I were rushing to make a dental appointment and I lost patience with the door reopening when I put the car into drive, so I slammed on my brakes and the door slammed shut; however, when we got to the dentist Mother got out of the front seat and I tried the ramp door. It would not open at all. I had jammed the door. I called my son, Chris, and took the car over to his shop where he had to use a crow bar to get the door to open. Then he had to position the door on it's runners so it would at least be able to be closed manually. What does one do with out someone to help them. I've always said that the Good Lord knew what he was doing when he gave me 3 sons. Even though I thought a daughter would have been nice. Thank God for my sons. So now I have to figure out how to get a good second hand Van. I've done some research on the web and it turns out that not all handicap vehicles are 50 to 70 thousand, I found a few newer ones for 30 something and older ones even less expensive. I can tell you this, I will not be buying a new Van from the same people , who fixed this one. I hope with trade in I can afford a good van.
If anyone out there reads my blog and has any advise, I sure could use some help here. Please comment or email me. Thanks
.
Saturday, February 5, 2011
Keeping on Track and Keeping Order
New business plan in order. I don't have children to take care of but now I have my Mother living with me. Lewis has been camping out at my house to help with Mom and with finances. We have tried to spent as little as possible on ourselves. Starting up a new business takes funds. Fortunately Mother helps us with household finances. We have lived on a shoe string for the last two years. This past month January 2010 has seen us coming ahead in the business, maybe we can pay ourselves. Because the business is teetering on the edge of becoming big, we find ourselves overwhelmed at times. We have less walk in business, but tend to be extremely busy with the internet. I answer emails, phone calls, attempt to find shipping quotes talk to customers and hurry up and wait. Sometimes decorators especially the famous ones tend to take you for granted. The hard part here is keeping track of everything at once. My office has been behind the checkout desk, but we are beginning to find it necessary to establish another more extensive desk. Mother serves as a greeter, she does a great job, but sometimes she tries to help with straightening. This can be a disaster, because she will throw things away or misplace items that we need. I get distracted when she starts moving around shuffling items on the counter. Then I have problems keeping on track. Because I need to keep track of what is going on I get brain overload. After work and after dinner when I could possibly find time to paint, I tend to have no energy or creativity left.
Thursday, February 3, 2011
Keeping on track
Sometimes it is hard in life to keep on track. That is keep doing all the right things at the proper time. Sometimes life throws at you more than you can handle. It is easy to become overwhelmed. Believe me I have learned all about this by the school of hard knocks. The best thing to do is to slow down and take several deep breaths and then keep on going hopefully with some sort of order.
I jumped into running businesses several times in my life. Actually I believe that this is part of God's plan for me, why else would I find myself thrust into being in a business? I love dealing with people particularly chatting and visiting with the public. I never much liked or felt comfortable going to big parties where I knew very few people. But being in my shop is like being in my home and it is easy to be gracious to people who come into your home, shop.
Our first shop was a gift shop that I ran with my husband. I was responsible for ordering the merchandise for the shop. We had bought a preexisting shop and I was able to use the example of what was previously purchased in order to figure out what would sell. I soon was connected with the various salesmen who represented these companies. Then I relied on my up bringing and personal inherent taste. Being a Virginian I was aware of the type of items that Virginians would buy. Unfortunately I never had any training in business. Perhaps, I should have taken a course or two in Business. My Art History background helped me with buying. It taught me to look for quality and good design. Where I had problems was keeping up with the book keeping. I ordered items for resale and projected sales. As long as I was the only one doing the ordering I was able to keep up. When my husband started to order framing materials we began to run into some problems. I kept records in my head, that was not a good plan. I still tend to have this bad habit.
All the while that I was running the gift shop, I had small children at home. Lewis was a baby when we bought the business, Chris was eight years old and Scott was five years old. Some how we maneuvered running a business and a family at the same time. Actually, I ran the gift shop with help from the ladies that worked for me and my husband ran an extension of my father's art gallery. I took Lewis to work originally in a baby seat and play pen, years later people would come in and asked about the cute little baby. Thinking about this now I have to stop and wonder that I could do all this. Some how I did manage. I would leave work and head home in time to be there for the boys to get home from school and pick up Lewis from baby day care. Then I would start dinner and help the boys with their home work. There were bullies to deal with hurts to heal, swim team and soccer practice. Games to go to. As I write this I am marveling at how I could have done all this.
I have to admit that at this time I was only restricted to wearing a brace on my left leg and I walked with crutches. I guess I could have done this from a wheel chair too. You never know what you can do until you have too. My motto has always been to do whatever is needed to be done come what may.
I think that when I consider how much I had done at that point in my life, that it helps me deal with the now. I still have another type business to deal with. With this business, I learned not to go on credit and not to gamble on projected sales as much. We prepay everything that we purchase so that our inventory is paid for. But we still have to gamble on the amount of business we might do. We started out as an Antique Mall renting spaces and selling other people's merchandise with two or three part time employees. I had four or five ladies working for me at the gift shop. The great thing about this business was that we purchased a program for our computers that made keeping track of everything easy. As long as we wrote up the items sold, correctly, all we had to do at the end of the month was to push the right buttons and the computer did the rest. Oh, I do love computers. I would never be writing this if I did not have the ease of writing on the computer and God bless spell check! Now I have less and more to deal with. Life would not be interesting if everything went along easily.
So now we changed our business from an Antique Mall to a partnership. Lewis and I decided that we would do much better going it alone. The economy sort of dictated it. With the drop in the economy we realized that the dealers were leaving and we could not easily find new dealers to replace them that carried the type of merchandise that we required in our shop. We did not want to go the way of many Antique Malls who allowed their dealers to sell anything including flea market type items. We wanted to be a real antique shop. We began slowly to take over the spaces in our shop. As the dealers left we would fill their spaces. We finally mid 2009 got a load against my house and stared buying for real with the idea that we would have a single shop. We also bought a van and designed a logo and picked a new name our name. The die was cast.
I jumped into running businesses several times in my life. Actually I believe that this is part of God's plan for me, why else would I find myself thrust into being in a business? I love dealing with people particularly chatting and visiting with the public. I never much liked or felt comfortable going to big parties where I knew very few people. But being in my shop is like being in my home and it is easy to be gracious to people who come into your home, shop.
Our first shop was a gift shop that I ran with my husband. I was responsible for ordering the merchandise for the shop. We had bought a preexisting shop and I was able to use the example of what was previously purchased in order to figure out what would sell. I soon was connected with the various salesmen who represented these companies. Then I relied on my up bringing and personal inherent taste. Being a Virginian I was aware of the type of items that Virginians would buy. Unfortunately I never had any training in business. Perhaps, I should have taken a course or two in Business. My Art History background helped me with buying. It taught me to look for quality and good design. Where I had problems was keeping up with the book keeping. I ordered items for resale and projected sales. As long as I was the only one doing the ordering I was able to keep up. When my husband started to order framing materials we began to run into some problems. I kept records in my head, that was not a good plan. I still tend to have this bad habit.
All the while that I was running the gift shop, I had small children at home. Lewis was a baby when we bought the business, Chris was eight years old and Scott was five years old. Some how we maneuvered running a business and a family at the same time. Actually, I ran the gift shop with help from the ladies that worked for me and my husband ran an extension of my father's art gallery. I took Lewis to work originally in a baby seat and play pen, years later people would come in and asked about the cute little baby. Thinking about this now I have to stop and wonder that I could do all this. Some how I did manage. I would leave work and head home in time to be there for the boys to get home from school and pick up Lewis from baby day care. Then I would start dinner and help the boys with their home work. There were bullies to deal with hurts to heal, swim team and soccer practice. Games to go to. As I write this I am marveling at how I could have done all this.
I have to admit that at this time I was only restricted to wearing a brace on my left leg and I walked with crutches. I guess I could have done this from a wheel chair too. You never know what you can do until you have too. My motto has always been to do whatever is needed to be done come what may.
I think that when I consider how much I had done at that point in my life, that it helps me deal with the now. I still have another type business to deal with. With this business, I learned not to go on credit and not to gamble on projected sales as much. We prepay everything that we purchase so that our inventory is paid for. But we still have to gamble on the amount of business we might do. We started out as an Antique Mall renting spaces and selling other people's merchandise with two or three part time employees. I had four or five ladies working for me at the gift shop. The great thing about this business was that we purchased a program for our computers that made keeping track of everything easy. As long as we wrote up the items sold, correctly, all we had to do at the end of the month was to push the right buttons and the computer did the rest. Oh, I do love computers. I would never be writing this if I did not have the ease of writing on the computer and God bless spell check! Now I have less and more to deal with. Life would not be interesting if everything went along easily.
So now we changed our business from an Antique Mall to a partnership. Lewis and I decided that we would do much better going it alone. The economy sort of dictated it. With the drop in the economy we realized that the dealers were leaving and we could not easily find new dealers to replace them that carried the type of merchandise that we required in our shop. We did not want to go the way of many Antique Malls who allowed their dealers to sell anything including flea market type items. We wanted to be a real antique shop. We began slowly to take over the spaces in our shop. As the dealers left we would fill their spaces. We finally mid 2009 got a load against my house and stared buying for real with the idea that we would have a single shop. We also bought a van and designed a logo and picked a new name our name. The die was cast.
Monday, January 31, 2011
My Father's Influence
July 21, 2015 was my Dad's birthday, Donald Sykes Lewis Sr.. He would have been 96. He did a lot of wonderful things in his life. Not the least being bringing up a daughter and a son who loved him very much. His love for art has enriched all our lives.
Dad brought beauty and the understanding of good design to everything he touched. He established Auslew Gallery, in 1952 in Norfolk Va. Against the better judgment of all the rest of our family. As a child I remember everyone telling him that there had never been a successful art gallery in Norfolk. Richmond was the capital and maybe he would be better there. He persevered. In the beginning he ran two businesses at once. He still maintained an adding machine business while my mother ran the newly formed art gallery. The first summer my little brother and I went to work with her so the business could get off the ground.
The Gallery became one of the largest in the southeastern states. Dad specialized in American Art. He had only a few years of College letting his older and younger brothers go in his place, but when it came to art his thirst for knowledge was insatiable. He studied books on art and read every bit of information he could get on American art. Without a degree in his field he became recognized as an authority. He could spot a great painting even under layers of old varnish and dirt. He both cleaned and restored paintings. He was good friends with local College professors Charles Sibley, artist and professor at Old Dominion , and Parker Lesley, Art History Professor and adviser to the Queen on renaissance jewelry. He was deeply respected.
Dad was also an inventive artist in his own right. He came up with something he called "cloutage". This was a process of using found metal pieces and combining them with paint to produce some wonderful pieces of art. An example of one hangs in my living room next to the large one by his grandson Lewis' large painting (1st photo). When I was in college he had a show of his work some where on Madison Avenue in New York City. The show was successful. Leo Castelli wanted to handle his art, but told him he must do much larger pieces. His work was done on board with metal and was extremely heavy as it was. (One of his paintings is in the photo above and to the left.) My brother and I were both in the middle of our education. Dad was worried about supporting the family. After showing in New York he felt that somehow he had made it. Little did he realized what Leo Castelli could do for an artist's career.
Dad never pursued his art career any further. The Gallery thrived he bought estates of artists, one of the largest being that of Herman Herzog. He had paintings by most of America's well known Artist of the 19th and early 20th centuries. One of the last estates that he purchased was the Eliot Candee Clark estate.
At one point he sold a Renoir to the Norfolk Museum. My mother brags about having slept over Monet and Renoir. Dad had them on consignment and he worried about their safety. So, he stashed them under their bed at night. In fact, when they left for a trip my husband and I were entrusted with their keep and we also slept over both a Monet and a Renoir. We carried the Renoir around with us wrapped in our dog's blanket. Later it was put on display at the Virginia Beach Board Walk Art Show, as art having been donated by the school children of Norfolk. There was a guard and ropes to keep people back. If only they had know.
My Dad was the caretaker of our family. He was the middle child but he was the one the whole family looked up to even his older brother. Our house was where they all gathered.
Before he died he was intent on making sure that his family was taken care of. He worried particularly about me and my sons. Being a divorced mother of three sons, he worried about how we would survive without his support. He purchased the building, that houses our shop, thinking that we could have an art gallery. There were not enough paintings to fill 8,400 sq feet. But antiques and art go together. Two of my sons got their start in very good businesses from that building. How pleased he must have been. We all feel as though he is still taking care of us. Scott my middle son has his own auto repair business thanks to a loan from Dad's trust. Chris, Lewis,and I feel as though he watches out for us giving us nudges in the right direction toward finding our treasures. I personally miss being able to ask his advise, but know that somehow, with his guidance, I'll make the right choices. He spent his life teaching us.
I still feel the need to pick up my phone and call Dad to ask his advice. I could always count on good advice. It was not what I always wanted to hear but, never the less his advice was right on. I see him now in my sons, Lewis in particular. All my sons felt as if Dad was their Father too. When I got my divorce Chris was a senior in High School, Scott was Fifteen and Lewis was ten. We went to live with my parents. He was always there for the boys and myself.
The father's day before Dad died, I had the good fortune of writing him a note to tell him how much I loved and appreciated him. After he died I found that note tucked into his things. I realized how much it had meant to him. I was truly lucky to have had him as my father.
Dad brought beauty and the understanding of good design to everything he touched. He established Auslew Gallery, in 1952 in Norfolk Va. Against the better judgment of all the rest of our family. As a child I remember everyone telling him that there had never been a successful art gallery in Norfolk. Richmond was the capital and maybe he would be better there. He persevered. In the beginning he ran two businesses at once. He still maintained an adding machine business while my mother ran the newly formed art gallery. The first summer my little brother and I went to work with her so the business could get off the ground.
The Gallery became one of the largest in the southeastern states. Dad specialized in American Art. He had only a few years of College letting his older and younger brothers go in his place, but when it came to art his thirst for knowledge was insatiable. He studied books on art and read every bit of information he could get on American art. Without a degree in his field he became recognized as an authority. He could spot a great painting even under layers of old varnish and dirt. He both cleaned and restored paintings. He was good friends with local College professors Charles Sibley, artist and professor at Old Dominion , and Parker Lesley, Art History Professor and adviser to the Queen on renaissance jewelry. He was deeply respected.Dad was also an inventive artist in his own right. He came up with something he called "cloutage". This was a process of using found metal pieces and combining them with paint to produce some wonderful pieces of art. An example of one hangs in my living room next to the large one by his grandson Lewis' large painting (1st photo). When I was in college he had a show of his work some where on Madison Avenue in New York City. The show was successful. Leo Castelli wanted to handle his art, but told him he must do much larger pieces. His work was done on board with metal and was extremely heavy as it was. (One of his paintings is in the photo above and to the left.) My brother and I were both in the middle of our education. Dad was worried about supporting the family. After showing in New York he felt that somehow he had made it. Little did he realized what Leo Castelli could do for an artist's career.
Dad never pursued his art career any further. The Gallery thrived he bought estates of artists, one of the largest being that of Herman Herzog. He had paintings by most of America's well known Artist of the 19th and early 20th centuries. One of the last estates that he purchased was the Eliot Candee Clark estate.
At one point he sold a Renoir to the Norfolk Museum. My mother brags about having slept over Monet and Renoir. Dad had them on consignment and he worried about their safety. So, he stashed them under their bed at night. In fact, when they left for a trip my husband and I were entrusted with their keep and we also slept over both a Monet and a Renoir. We carried the Renoir around with us wrapped in our dog's blanket. Later it was put on display at the Virginia Beach Board Walk Art Show, as art having been donated by the school children of Norfolk. There was a guard and ropes to keep people back. If only they had know.
My Dad was the caretaker of our family. He was the middle child but he was the one the whole family looked up to even his older brother. Our house was where they all gathered.
Before he died he was intent on making sure that his family was taken care of. He worried particularly about me and my sons. Being a divorced mother of three sons, he worried about how we would survive without his support. He purchased the building, that houses our shop, thinking that we could have an art gallery. There were not enough paintings to fill 8,400 sq feet. But antiques and art go together. Two of my sons got their start in very good businesses from that building. How pleased he must have been. We all feel as though he is still taking care of us. Scott my middle son has his own auto repair business thanks to a loan from Dad's trust. Chris, Lewis,and I feel as though he watches out for us giving us nudges in the right direction toward finding our treasures. I personally miss being able to ask his advise, but know that somehow, with his guidance, I'll make the right choices. He spent his life teaching us.
I still feel the need to pick up my phone and call Dad to ask his advice. I could always count on good advice. It was not what I always wanted to hear but, never the less his advice was right on. I see him now in my sons, Lewis in particular. All my sons felt as if Dad was their Father too. When I got my divorce Chris was a senior in High School, Scott was Fifteen and Lewis was ten. We went to live with my parents. He was always there for the boys and myself.
The father's day before Dad died, I had the good fortune of writing him a note to tell him how much I loved and appreciated him. After he died I found that note tucked into his things. I realized how much it had meant to him. I was truly lucky to have had him as my father.
Tuesday, January 25, 2011
Still Working on My Art
I am sustaining and continuing to work on the quick oil beginnings to my newest painting. I did a quick sketch of my dark tones to begin with getting tree lines and fields arranged. This lined up my perspective and worked to begin to draw the eye back into my painting. Gaining perspective in your art is one of the most important things in your design particularly in a landscape.
I had used muted greens and earth tones to sketch in the dark tones. Next I began to work in the sky. I did not want to have too much contrast in color and tone. The day that I am portraying was somewhat gray and overcast. I was careful to mix my blue with my white toning it with ocher and senna tones. I used my darkest color highest in the sky and defused this with lighter variations of similar colors toward the horizon. By doing this I was able to give a suggestion of light clouds.
Next I worked with the ocher and senna toned with some white and green in the fields. The furthest field was lighter than the closer fields. You get glimpses of this through the trees. I worked planes of these colors through the fields in the mid ground and in the fore ground I began to break up these same tones some what brighter and using my brush strokes to suggest grasses and weeds. Writing about how I go about painting actually makes me clarify in my mind how I go about approaching my paintings. I'm trying to find time and energy to finish this painting. The trees in the middle ground have only the darkest tones on them now. I need to go back and add medium tones careful to retain my freedom of brush stroke. In the foreground where the grasses are depicted I need to work a little more. The final touches in a painting are always the hardest. These need to be considered and added careful not to over do.
Monday, January 24, 2011
Back to making Art
I've written before about the difficulty I've been having about starting and even sustaining an art project. Painting has taken me through some really tough times. It helped me get through my divorce and raising three sons as teens alone. Art is my Salish. It has been my refuge from problems it has allowed me to regain what sanity I could garner in troubled times. It has kept my calm. To paint one does need a clear mind. I have never before had to contend with a crowed mind. My elderly Mother is loosing her memory and her short term memory is so bad that I am forced to think some for her. I do this because I love her, and because she so often took care of me selflessly. We were each others best friend and now I try to understand how she is feeling. I see glimpses of Mom as she use to be. Her voice echoing the past. This can misled and confuse because you could expect her to be as she once was. This is just an illusion. Come back to reality and accept the current reality do not expect too much. It has taken months if not a year for me to accept our reality. Once accepted then life does become easier and less difficult. If this is confusing for me just think how terrifying it has to be for her. With my somewhat hesitant acceptance of our reality comes a clearing of my mind. I can not change reality so make the most of what you have, live life, and love.
With my acceptance of our reality I have begun to experience some freedom of thought. Gradually I have attempted to finish some of my paintings that I had started. Last night I found a photo of a fall field that I had attempted to paint maybe ten years or more ago. I had done a large painting that I was never satisfied with. The house where I had painted this was too dark. When your lighting is not right nothing seems to work. Colors are off. Once you belabor too much with a painting, you loose the freshness. At any rate that painting did not turn out to be good. Last night I sketched in my dark tones of this field with loose brush strokes. This is a fall scene but fall with muted tones of greens and browns. The interesting thing is that the hedge rows and tree lines all help to describe visual space. I also have a beginning of atmospheric perspective in the early stages of this painting. This is exciting and I can hardly wait to get back to my painting tonight.
With my acceptance of our reality I have begun to experience some freedom of thought. Gradually I have attempted to finish some of my paintings that I had started. Last night I found a photo of a fall field that I had attempted to paint maybe ten years or more ago. I had done a large painting that I was never satisfied with. The house where I had painted this was too dark. When your lighting is not right nothing seems to work. Colors are off. Once you belabor too much with a painting, you loose the freshness. At any rate that painting did not turn out to be good. Last night I sketched in my dark tones of this field with loose brush strokes. This is a fall scene but fall with muted tones of greens and browns. The interesting thing is that the hedge rows and tree lines all help to describe visual space. I also have a beginning of atmospheric perspective in the early stages of this painting. This is exciting and I can hardly wait to get back to my painting tonight.
I have Post Polio
Once the pronouncement has been made. You have Post Polio. What do you do? The first thing that I did was to start making plans. I had no insurance. I was self employed. I had an old wheel chair but it was manual. They had told me that all my limbs were involved, that was a lot to take in. My Dad helped me get a used handicapped van and a used jazzy wheel chair. I don't think I could have done it without help. My son,Chris and I were doing Antique shows. We did the outside Brimfield Ma. Show. We step up in a tent. They did have outside handicap restrooms. Thank God for little blessings.
There are some things that are easier to do from a wheel chair than walking with crutches. This was amazing. I could do grocery shopping on my own. I did not need help carrying boxes. In the past I had a lot of baskets and bags, so that I could carry things from one place to another. Having a motorized chair and a vehicle to carry both myself and my chair actually gave me a lot more freedom. I had to give up visiting my friends who had steps going into their homes. We now meet for lunch or dinner out, and do our visiting there or at my house. I've had to make charges to accommodate being in a chair. The chairs work well unless they are not charged or something happens to them. If the chair is disabled you are up the creek without a paddle. Fortunately I had three sons, all of whom would help out their mom in a pickle. Chairs can be disengaged and pushed when necessary. I learned about this the hard way.
Shortly after having to use a chair full time I was able to get disability. Two years later I got medicare. This sure did help out with expenses. I was finally able to get a chair that was right for me. There still is no help with vehicles. A new handicap van runs between $50,000.00 to $70,000.00. I've been lucky finding two used vans so far. It seems that the handicapped parts go bad before the actual van goes. I end up fighting doors and ramps that don't want to close, and power seats that short out. Never the less I am extremely fortunate and happy to be able to have a handicapped van even with all the frustrations.
I love to cook and my kitchen is at normal height. I learned to use a kitchen work table to chop and mix on. I have an electric fry pan that I can use on my table. I dream of being able to design a kitchen for my needs. I think that I would lower the cabinets and have large draws that pull out rather than shelves. I have not been able to use the upper cabinets in my kitchen at all. I purchased an antique Chinese cabinet for my living area that I use to store my china plates, bowls, glasses,etc. This looks great and works well. The table is butcher block and looks good. I think I would like to incorporate more counter tops of this type with a shelf underneath. I.'d like a gas counter top range at table level, a built in oven, and a lower country kitchen sink that is open underneath so I can get close to the sink with a dish washer with drawers as well. I'm not sure what I want in a refrigerator and freezer.
I moved into a 55 and older community. Everything is on one floor. I had a ramp built for the entrance and a small deck with a ramp to the back yard. I was very fortunate that my backyard was already fenced in. So I could just let my two dogs out to do their duty.
There are some things that are easier to do from a wheel chair than walking with crutches. This was amazing. I could do grocery shopping on my own. I did not need help carrying boxes. In the past I had a lot of baskets and bags, so that I could carry things from one place to another. Having a motorized chair and a vehicle to carry both myself and my chair actually gave me a lot more freedom. I had to give up visiting my friends who had steps going into their homes. We now meet for lunch or dinner out, and do our visiting there or at my house. I've had to make charges to accommodate being in a chair. The chairs work well unless they are not charged or something happens to them. If the chair is disabled you are up the creek without a paddle. Fortunately I had three sons, all of whom would help out their mom in a pickle. Chairs can be disengaged and pushed when necessary. I learned about this the hard way.
Shortly after having to use a chair full time I was able to get disability. Two years later I got medicare. This sure did help out with expenses. I was finally able to get a chair that was right for me. There still is no help with vehicles. A new handicap van runs between $50,000.00 to $70,000.00. I've been lucky finding two used vans so far. It seems that the handicapped parts go bad before the actual van goes. I end up fighting doors and ramps that don't want to close, and power seats that short out. Never the less I am extremely fortunate and happy to be able to have a handicapped van even with all the frustrations.
I love to cook and my kitchen is at normal height. I learned to use a kitchen work table to chop and mix on. I have an electric fry pan that I can use on my table. I dream of being able to design a kitchen for my needs. I think that I would lower the cabinets and have large draws that pull out rather than shelves. I have not been able to use the upper cabinets in my kitchen at all. I purchased an antique Chinese cabinet for my living area that I use to store my china plates, bowls, glasses,etc. This looks great and works well. The table is butcher block and looks good. I think I would like to incorporate more counter tops of this type with a shelf underneath. I.'d like a gas counter top range at table level, a built in oven, and a lower country kitchen sink that is open underneath so I can get close to the sink with a dish washer with drawers as well. I'm not sure what I want in a refrigerator and freezer.
I moved into a 55 and older community. Everything is on one floor. I had a ramp built for the entrance and a small deck with a ramp to the back yard. I was very fortunate that my backyard was already fenced in. So I could just let my two dogs out to do their duty.
A New Chair is on it's way.....hurrah!
Never in this world,did I think that I would get excited over A WHAT?! A Wheel chair, but I think they are finally getting it. I use a chair or maybe we should say I abuse a chair. What I really do is live my life just the way I would if I still could walk.
So Friday Robin from West Home Health Care in Richmond came to our shop with a new chair for me to try out. It had front wheel drive! It would drive differently from my Invacare chair. My Invacare chair had lasted six really good years, but all f a sudden I found that a lot of little things had started to go wrong. If you depend on a chair, you really need one that works.
The new chair was designed in Sweden. And much like some European cars, this seemed to be built to last. The clincher was for me that I took it out into the back of the shop and it ran easily through our gravel drive. We often go to outdoor antique shows such as Brimfield Ma. A lot of the fields there were gravel and it would wear my batteries down in no time. I would have to find a plug and sit and charge. As you might guess I don't like to sit still a lot. I also felt bad about imposing on people for an electric charge. Everyone, however, was nice about assisting. I got over being embarrassed about asking for help a long time ago.
The new chair is by Permobil. One of the harder things that I had to decided was a color. Ok, color is not that important, except that this has mag wheels and colors like Baby Blue, Burgundy, Silver, Hot Pink, and Chili Pepper Red! In the past I've been sedate, choosing Dark Green, and Black. Come on, everyone needs to live a little! So, you guessed it I'm going to bite the bullet and go for CHILI PEPPER RED! I justified this because I sometimes take my chair to work and I'll be more visible crossing RT. 3, or Main Street. Our town is not that big, but there is a little traffic and it would be safer than say Blue, or Silver, both of which were also tempting. What can I say, my wild side just took over. Besides, this is my version of a sport car. Imported no less.
Getting parts was a concern, however the rep let us know that they now have an American factory in Tennessee, and that getting parts would only take a day or two once ordered. Lewis, my youngest son and partner said it looked like a sports car in comparison to my old chair. Don't get me wrong there was nothing wrong with how my last chair lasted or handled. This one is just a better choice for me.
So Friday Robin from West Home Health Care in Richmond came to our shop with a new chair for me to try out. It had front wheel drive! It would drive differently from my Invacare chair. My Invacare chair had lasted six really good years, but all f a sudden I found that a lot of little things had started to go wrong. If you depend on a chair, you really need one that works.
The new chair was designed in Sweden. And much like some European cars, this seemed to be built to last. The clincher was for me that I took it out into the back of the shop and it ran easily through our gravel drive. We often go to outdoor antique shows such as Brimfield Ma. A lot of the fields there were gravel and it would wear my batteries down in no time. I would have to find a plug and sit and charge. As you might guess I don't like to sit still a lot. I also felt bad about imposing on people for an electric charge. Everyone, however, was nice about assisting. I got over being embarrassed about asking for help a long time ago.
The new chair is by Permobil. One of the harder things that I had to decided was a color. Ok, color is not that important, except that this has mag wheels and colors like Baby Blue, Burgundy, Silver, Hot Pink, and Chili Pepper Red! In the past I've been sedate, choosing Dark Green, and Black. Come on, everyone needs to live a little! So, you guessed it I'm going to bite the bullet and go for CHILI PEPPER RED! I justified this because I sometimes take my chair to work and I'll be more visible crossing RT. 3, or Main Street. Our town is not that big, but there is a little traffic and it would be safer than say Blue, or Silver, both of which were also tempting. What can I say, my wild side just took over. Besides, this is my version of a sport car. Imported no less.
Getting parts was a concern, however the rep let us know that they now have an American factory in Tennessee, and that getting parts would only take a day or two once ordered. Lewis, my youngest son and partner said it looked like a sports car in comparison to my old chair. Don't get me wrong there was nothing wrong with how my last chair lasted or handled. This one is just a better choice for me.
Monday, January 3, 2011
Polio and Post Polio
I had polio at the age of four in 1948. Today if I smell wet warm wool it takes me back to being in the hospital as a child. They tapped my spine to find out if I had polio, and then they put me into isolation so no one else could have been affected. In order to keep my body from contracting and hurting they put wet warm wool compresses over my body.
I remember being sick at home that July with measles and then with a strep throat. One morning after a particularly fretful night, the doctor came to the house and asked me if I could walk. I remember saying, "put me on the floor I can crawl." After that my parents whisked me off to the nearest hospital mom holding me in her lap. Mother sat by my hospital bed and read to me. At one point they transferred me to De Paul Hospital, here the Sister's of Mercy helped with the nursing and there was a whole ward of children mostly affected with polio. There had been an outbreak of Polio in North Carolina and Norfolk Virginia was just a ways across the border. I remember the other children our beds were lined up. Several children were in iron lungs to keep them breathing. Several times while I was there we had electric storms, and the electricity went off. My father, doctors, other parents, any one who could help crank a generator to keep the iron lungs working. Other children came into the ward too. One girl had fallen off a horse while riding and had a steel plate in her head. A little chinese girl came in she had been burned terribly. I remember a little boy who had polio and his arm had been paralyzed, in later years we actually met again.
During this time my parents would do anything they could to keep me happy, because all I wanted to do was to go home. So they would ask me what I would like them to bring me. I most have really upset them when I asked them to bring me a real fairy.
That night mother went home and tried to figure out how to handle that request. Finally she decided to make up a story for me about my own fairy, and to take a small doll and make that doll into a fairy. Every day after that she would bring me tales of my fairy who lived in my grandparents back yard. I was thrilled I had my own personal fairy.
I was in the Hospital for several months when I finally came home my brother was almost a year old. My parents still took me for therapy to De Paul Hospital. Dr. John Vann was my doctor he had had polio himself as a boy and he became an orthopedic surgent. He sent me to Warm Springs Georgia, where Franklin Roosevelt had his Little White House. The doctors there were some of those that had worked with President Roosevelt. After examing me they sent me home saying that Dr. Vann was one of the best.
Now what was left for me to do was to live my life as normal as possible. In the beginning I had a brace on both legs and a corset to hold my back straight. I used crutches to walk with. Eventually they did away with the right leg brace and the corset. It was not until fifty years later that I knew the true extent of my paralysis. Mother had told me that I had been paralysised from my sholdiers down. Silly me I never realized that my arms were included in that area. I used and abused my arms. After all I used my arms rather than my legs to walk with.
When I reached Fifty, forty five years after coming down with polio, I began to experience some weakness. Going up and down steps had become more difficult. My arms had begun to ach sometimes. I put this all up to aging. Actually several years before when I was working out at the "Y" I felt some weakness in my arms after swimming for a long time. I register this, but tucked this worry away refusing to think about it until another time.
Around fifty five I really started to worry. The term Post Polio had been batted about. Did I have Post Polio? I neede to know. I began to be fearful, and a little depressed. I needed to know. I also needed to get disability. I was afraid to go places without a son or a friend for fear of falling. I needed help getting around, a scooter maybe? How could I make a living if I was dependent on others to get me places?
So I took matters into my own hands and made a appointment to be evaluated for post polio. The die was cast, there was no turning back now. My son, Chris, took me up to Richmond Virginia to the Sheltering Arms Hospital to see Dr Wooten. She specialized in Post Polio. They ran me through a battory of test. The result was yes I did indeed have post polio. Both legs were involved and both my arms. MY ARMS!!! I never really knew that my arms had been affected. She said it would be best if I did not over use my muscles. I needed to use a wheel chair. She said I should get an electric wheelchair, that my regular one was too much for my arms. This was a relief in a way. But I had no insurance and how could I afford an automatic chair. Once you use a Scooter or automatic wheel chair how do you get around? All of a sudden I had a whole new set of worries.
I did notice after that somethings had become a little more difficult. I tended to ignore and go on. I did start sitting some in my old wheel chair just so I would not burn myself out. Eventually you do have to retrospect and look at what is happening in life
I remember being sick at home that July with measles and then with a strep throat. One morning after a particularly fretful night, the doctor came to the house and asked me if I could walk. I remember saying, "put me on the floor I can crawl." After that my parents whisked me off to the nearest hospital mom holding me in her lap. Mother sat by my hospital bed and read to me. At one point they transferred me to De Paul Hospital, here the Sister's of Mercy helped with the nursing and there was a whole ward of children mostly affected with polio. There had been an outbreak of Polio in North Carolina and Norfolk Virginia was just a ways across the border. I remember the other children our beds were lined up. Several children were in iron lungs to keep them breathing. Several times while I was there we had electric storms, and the electricity went off. My father, doctors, other parents, any one who could help crank a generator to keep the iron lungs working. Other children came into the ward too. One girl had fallen off a horse while riding and had a steel plate in her head. A little chinese girl came in she had been burned terribly. I remember a little boy who had polio and his arm had been paralyzed, in later years we actually met again.
During this time my parents would do anything they could to keep me happy, because all I wanted to do was to go home. So they would ask me what I would like them to bring me. I most have really upset them when I asked them to bring me a real fairy.
That night mother went home and tried to figure out how to handle that request. Finally she decided to make up a story for me about my own fairy, and to take a small doll and make that doll into a fairy. Every day after that she would bring me tales of my fairy who lived in my grandparents back yard. I was thrilled I had my own personal fairy.
I was in the Hospital for several months when I finally came home my brother was almost a year old. My parents still took me for therapy to De Paul Hospital. Dr. John Vann was my doctor he had had polio himself as a boy and he became an orthopedic surgent. He sent me to Warm Springs Georgia, where Franklin Roosevelt had his Little White House. The doctors there were some of those that had worked with President Roosevelt. After examing me they sent me home saying that Dr. Vann was one of the best.
Now what was left for me to do was to live my life as normal as possible. In the beginning I had a brace on both legs and a corset to hold my back straight. I used crutches to walk with. Eventually they did away with the right leg brace and the corset. It was not until fifty years later that I knew the true extent of my paralysis. Mother had told me that I had been paralysised from my sholdiers down. Silly me I never realized that my arms were included in that area. I used and abused my arms. After all I used my arms rather than my legs to walk with.
When I reached Fifty, forty five years after coming down with polio, I began to experience some weakness. Going up and down steps had become more difficult. My arms had begun to ach sometimes. I put this all up to aging. Actually several years before when I was working out at the "Y" I felt some weakness in my arms after swimming for a long time. I register this, but tucked this worry away refusing to think about it until another time.
Around fifty five I really started to worry. The term Post Polio had been batted about. Did I have Post Polio? I neede to know. I began to be fearful, and a little depressed. I needed to know. I also needed to get disability. I was afraid to go places without a son or a friend for fear of falling. I needed help getting around, a scooter maybe? How could I make a living if I was dependent on others to get me places?
So I took matters into my own hands and made a appointment to be evaluated for post polio. The die was cast, there was no turning back now. My son, Chris, took me up to Richmond Virginia to the Sheltering Arms Hospital to see Dr Wooten. She specialized in Post Polio. They ran me through a battory of test. The result was yes I did indeed have post polio. Both legs were involved and both my arms. MY ARMS!!! I never really knew that my arms had been affected. She said it would be best if I did not over use my muscles. I needed to use a wheel chair. She said I should get an electric wheelchair, that my regular one was too much for my arms. This was a relief in a way. But I had no insurance and how could I afford an automatic chair. Once you use a Scooter or automatic wheel chair how do you get around? All of a sudden I had a whole new set of worries.
I did notice after that somethings had become a little more difficult. I tended to ignore and go on. I did start sitting some in my old wheel chair just so I would not burn myself out. Eventually you do have to retrospect and look at what is happening in life
Saturday, January 1, 2011
So What is Handicapped?
If you would ask me if I was handicapped, I probably would say that I am not. I came down with polio as a four year old. I do remember being able to walk without crutches or a brace, but now being in a power chair is my reality. My parents did an amazing job of not spoiling me. I'd sure that it would have been much easier to pick me up when I fell rather than watch me try to figure out how to get up on my own.
My brother was a baby when I contracted polio. As I was learning to walk again, he was learning to walk on his own. When I would fall down he would come over a let me lean on him in order to help me up. We had a symbiotic relationship, I would translate what he was trying to say. Unfortunately this was not as good for him. He started talking in sentences, and I was the only one who could understand him. My parents made me stop.
Walking with crutches seemed like an adventure, especially when I discovered that with crutches I could swing my legs and jump way far off the curbs. Off course this was not the proper way to use crutches, but it was fun. I don't think that I ever really learned " the proper way to walk". I walked with crutches in my own way for a very long time. I carried my book bag to school sometimes filled with books. Eventually I walked across campus at Old Dominion College with books etc. I lived my life like any other child, teen, young adult with no excuses.
I had several operations to keep by body straight. I have never thought of myself as handicap. I remember being offended when someone referred to me as paralyzed. I never thought of myself that way.
I think this was probably easy for me to feel this way, because I was so young. Having a handicap happen to you as an older person must be more difficult to accept, to a child life is an adventure.
Sometimes I think now what my life would have been like if I had not had polio. I'm afraid that I would not have met my husband. I would not have had the same children. I might not have had the insight that I like to think that I have on life, and that I would not have done as much with my life or my art. Sometimes adversities that happen in life are a blessing. I think that I am somewhat fatalistic. I feel that there was a plan for my life that I need to fulfill. I have been thrust into the public, not nationally but locally. I have run businesses with the help of first my husband and then my sons. Years ago in 1980 I was awarded handicap Professional woman of the year by the Pilots Club in Williamsburg, Virginia. I feel that people who see me realize that people, who have handicaps are just like them. Needless to say that I have never dwell on being handicapped. It's just the way my life is and I have always tried to live life to the fullest.
My brother was a baby when I contracted polio. As I was learning to walk again, he was learning to walk on his own. When I would fall down he would come over a let me lean on him in order to help me up. We had a symbiotic relationship, I would translate what he was trying to say. Unfortunately this was not as good for him. He started talking in sentences, and I was the only one who could understand him. My parents made me stop.
Walking with crutches seemed like an adventure, especially when I discovered that with crutches I could swing my legs and jump way far off the curbs. Off course this was not the proper way to use crutches, but it was fun. I don't think that I ever really learned " the proper way to walk". I walked with crutches in my own way for a very long time. I carried my book bag to school sometimes filled with books. Eventually I walked across campus at Old Dominion College with books etc. I lived my life like any other child, teen, young adult with no excuses.
I had several operations to keep by body straight. I have never thought of myself as handicap. I remember being offended when someone referred to me as paralyzed. I never thought of myself that way.
I think this was probably easy for me to feel this way, because I was so young. Having a handicap happen to you as an older person must be more difficult to accept, to a child life is an adventure.
Sometimes I think now what my life would have been like if I had not had polio. I'm afraid that I would not have met my husband. I would not have had the same children. I might not have had the insight that I like to think that I have on life, and that I would not have done as much with my life or my art. Sometimes adversities that happen in life are a blessing. I think that I am somewhat fatalistic. I feel that there was a plan for my life that I need to fulfill. I have been thrust into the public, not nationally but locally. I have run businesses with the help of first my husband and then my sons. Years ago in 1980 I was awarded handicap Professional woman of the year by the Pilots Club in Williamsburg, Virginia. I feel that people who see me realize that people, who have handicaps are just like them. Needless to say that I have never dwell on being handicapped. It's just the way my life is and I have always tried to live life to the fullest.
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