Tag Archives: cancer

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R is for Resume

I am blogging A to Z about artists, particularly women artists and mostly about my mother, Helen Burling Ottaway.

I find two copies of her resume. One is from 1991 and one from 1993. I will add the 1993 information, but it’s a LOT. My mother was prolific! She complained about getting ready for shows and I did not realize how very many she did! I am so proud of her. She died of ovarian cancer in 2000 and I do miss her still.

Helen Burling Ottaway

  Del Ray Atelier

105 E. Monroe Ave

Alexandria, VA 22301

SELECTED SOLO SHOWS

1991 Nov     Will have solo show at Bird-in-Hand Gallery, Washington, DC

1989 Sept     “Cascades: Watercolors of Washington State”, Bird-in-Hand Gallery, Washington, DC

1988 Nov     “Fantasy Etchings”, National Orthopedic Hospital, Arlington, VA

1987 Oct      “Spirits to Enforce, Art to Enchant”, Fantasy Art, River Road Uniterian Church, Bethesda, MD

1986 Mar     “Prints and Poems”, Poetry by Katy Ottaway, Martin Luther King Library, Washington, DC

1984 Nov     “Forests, Flower, and Fantasies”, Sola Gallery, Ithaca, NY

          Apr     “Birdland and other Lullabies”, Pastels, Gallery West, Alexandria, VA

1981 May    “Fantastical Bestiary”, Etchings and Drawings, Gallery West, Alexandria, VA

          Mar     “The Way of the Brush”, Watercolors, Gallery One, Alexandria, VA

TWO PERSON SHOWS

1986 Nov     Two Person Show, “An Occasional Pair of Claws”, Fantasy Art with Omar Dasent, Gallery West, Alexandria, VA

1985 Apr     Two person Show, “Figures and Foliage”, Pastels, Capital Centre Gallery, Landover, MD

1982 Nov     Two Person Show, “The Four Seasons”, Gallery West, Alexandria, VA

SELECTED GROUP SHOWS

1990 Feb     “Visions 1990” Westbeth Gallery, New York, NY

1989 Feb     “Year in—Year out”, Studio Gallery, Washington, DC

1988 Mar     “independent Visions III”, Metro Gallery, Arlington, VA

          May     Juried Show, Sculpture, The Art League, Alexandria, VA, Juror: Bertold Schmutzart

1987 Dec     Juried Show: “The Best of 1987”, Martin Luther King Library, Washington, DC, Jurors: Dr.

                     Jacqueline Serwer, Sandra Wested, Robert Stewart

1987 Apr     “Independent Visions, Fifteen Women Artists”, Metro Gallery, Arlington, VA

          Feb     “Portraits 1987”, The Art Barn, Washington, DC

1986 Oct     “Juried Show, “Printmakers VIII”, The New Art Center, Washington, DC

          Jan     “Independent Visions”, Metro Gallery, Arlington, VA

1985 Dec    Invitational, “Highlights of the Year”, Martin Luther King Library, Washington, DC. Jurors:

                     Linda Hartigan and Monroe Fabian

          Nov    Invitational, “The Macadam Nueve-Splintergreen Conspiracy Show”, Gallerie Inti,

                     Washington, DC. Curated by Omar Dasent and Ann Stein

          Oct      Juried show, “Printmakers VII”, WWAC, Washington, DC. Juror: Jane Farmer

          Mar     Invitational, “Mama, Don’t Let Your Babies Grow up to be Artists”, The Splintergreen

                      Conspiracy, Martin Luther King Library, Washington, DC. Curated by Omar Dasent

          Mar    “Shakespearean Images”, Hofstra University, Hempstead, NY

1984 Nov     Juried Show, “Printmakers VI”, WWAC, Washington, DC. Juror: Carol Pulin

           July     Juried Show, “Printmakers VI”, WWAC, Washington, DC. Juror: Jo Anna Olshonsky

           Oct      Four Person Show, “Just Four”, Galerie Triangle, Washington, DC

                        “The First Great American Camel Show”, Gallery West, Alexandria, VA

1983 Mar      Juried Show, “Printmakers V”, WWAC, Washington, DC. Juror: Barbara Fiedler

          Feb       Juried Show, “Artists – Art Historians: A Retrospective 1972-1982”, National Conference, The Women’s Caucus for Art,m Bryce Gallery, Moore College, Philadelphia, PA

1982 May      Juried Show, “Woman as Myth and Archetype”, WWAC, Wshington, DC. Juror: Mary Beth Edelson

          Feb       Invitational, “Art is where the Heart is”, Gallery 805, Fredricksberg, VA

          Feb       “The Printmakers of the WWAC, The Torpedo Factory, Alexandria, VA

          Jan        Juried Show, “The Eye of Eleanor Monroe”, WWAC, Washington, DC Juror: Eleanor Monroe

1981 Oct.      Juried Show, “Collage and Drawing”, WWAC, Washington, DC Juror: Jan Root  

Numerous juried shows, the Art League, Alexandria, VA

Numerous group shows, Gallery West, Alexandria, VA

EDUCATION

1967 B.F.A Cornell University, Ithaca, NW

WORK EXPERIENCE

1992-currently   Teach Drawing and Watercolor, Capital Hill Arts Workshop, Washington, DC

                              Teach Art Class for Seniors, Recreation Department, Alexandria, VA

                              Teach etching workshops and watercolors at the Delray Atelier, Alexandria, VA

1987-1990           Graphic Artist, Al Porter Graphics, Washington, DC

1985 Fall               Co-Director of Gallery West, Alexandria, VA

1982                       Director of Exhibitions, WWAC, Washington, DC

1982                       Director of Gallery West, Alexandria, VA

1981                       Chair of Exhibitions Committee of Gallery West, Alexandia, VA

                                Taught watercolor classes at Washington Women’s Art Center, Washington, DC

                                Taught children’s art classes for the Arlington Recreation Department

1967-1970             Assistant Curator at the Ithaca College Museum of Art, Ithaca, NY

ATOZBLOGGINGCHALLENGE2022 #art #Women artists #Helen Burling Ottaway #ATOZCHALLENGE #Christine Robbins Ottaway #APRILATOZ

For more information about the #AtoZChallenge, check out this link.

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P is for Paper over

I am blogging A to Z about artists, particularly women artists and mostly about my mother, Helen Burling Ottaway. Today’s post is about my mother and my sister: another woman artist. Christine Robbins Ottaway.

I do not have much of her fine art. She was a landscape architect and historic preservation expert and worked for Caltrans. She also wrote, on her blog Butterfly Soup, and in other places.

The painting is an oil, by my mother Helen Ottaway, done when my sister was 14. This painting seems especially creepy to me, the oranges and blues. I love the painting but it is frightening as well. My sister could write terrifying stories. Here is my poem about one of her stories. The title of her story is “We don’t make good wives”.

Paper over

They are papering over your memory
They want the clean version
The inhuman perfect version
I remember the violent sea serpent
Related to Aunt Nessie: me, I think

He stole your skin, you say
But you lure him to, posing
On the shore naked
And let him take you home
And impregnate you

And then you have six daughters
What did he expect? you say
Cold blooded and beautiful
White skin and greenish hair
Who all can swim like fish
and all seven search
Until you find the skin
and then away

You say, he took my skin
Now I have taken his

Let them paper over your memory
Let them pretend you were sweet
I hold your words in my mind
And I love you wholly

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ATOZBLOGGINGCHALLENGE2022 #art #Women artists #Helen Burling Ottaway #ATOZCHALLENGE #Christine Robbins Ottaway #APRILATOZ

For more information about the #AtoZChallenge, check out this link.

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memorial

Today is my sister’s birthday, Christine Robbins Ottaway. She died of breast cancer in 2012 at age 49. She had gotten stage IIIB breast cancer at age 41. She went through mastectomy, chemotherapy and radiation and was clear for two years. Then it recurred and she returned to treatment, rounds of chemotherapy, a gamma knife radiation, another gamma knife and whole brain radiation. She was very very strong and tough and fought the cancer right up until the end.

This photograph was taken at my father’s 70th birthday party, in 2008. My friend Maline took the photograph. She and other old friends gathered and we sang the family folk songs.

Here is a drawing that my mother Helen Burling Ottaway did in 1978 of Chris. My mother always had a sketchbook. This is one she sent to me, because I was an exchange student in Denmark that year. At Christmas I received the wonderful sketchbook with my mother’s comments. My sister was 14 when I went to Denmark and I was 17.

Chris Ottaway by Helen Ottaway, 1978
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abuse, enabler style

I am raised by a family of triangulating enablers and enablees.

The enablers are my mother and two uncles. They are very very smart. Let me qualify that: they are very very smart intellectually. Emotionally, not so much.

The two uncles have PhDs and are professors. They marry wives that are lessor in their view. One tells my mother that he wants a woman who is not as bright as he is. I don’t know if she is less bright, but she is a hella better athlete. I also have the impression that she had a time where she drank too much.

The other uncle marries a woman who tends to be a hypochondriac. He takes her to India, where she gets polio while pregnant. She is then a sick hypochondriac, which is very difficult. The ill can control their families by planning things and then getting sick at the last moment. On the other hand, chronic fatigue and fibromyalgia are very real and we are on the edge of figuring them out. That uncle divorces his wife and I instantly like both of them better. They stop being a weird unit and are suddenly individuals.

My mother tells me, when I am in college, “I wondered if your father was an alcoholic when I married him.” I want to hit her. She won’t leave him, she won’t stop enabling him, they scream at each other at 2 am often. Now I wonder about that and conclude that either screaming at someone was something she needed or she was an alchoholic too.

After my mother dies, I ask my uncle, what about his parents? After all, the three of them learned enabling somewhere and it pretty much has to be at home.

My uncle tells me his parents had a PERFECT marriage and that my grandmother LOVED being the wife of a physician and professor.

Um, so, then, why did she pay my tuition to medical school, uncle?

And I think about my mother’s stories. Once, she says, your Uncle Jim bet his friend Dick that Dick was too chicken to shoot a cigarette out of Jim’s mother’s mouth. Ooooo. With a rubber band shooter. Yes, my grandmother. Bob took the bet and succeeded. My grandmother roared with anger and the two boys ran like hell and hid.

And someone in the family tells me: your grandfather helped your grandmother control her temper.

There it is. The enabler/enablee.

The enablers die first. My grandfather of cancer at 79, my mother of cancer at 62. The cousins are all angry at me because I won’t follow the family rules and triangulate in a satisfactory manner, and I don’t care any more. I am ignoring them. I got my father’s banjo back and I am done. The two cousins I own land with jointly are not the worst triangulators.

I have to remind myself: for them, this is love. For some people, controlling or being controlled is what functions as love and intimacy. Fighting and tears when person A talks to person C about person B and person C then lets person B know, that is how they feel close. It is not only families, but communities. Clay Shirky’s description of a group being it’s own worst enemy describes the same patterns: identify an enemy inside or outside the group and then everyone comes together against the enemy. The enemy says the wrong thing, doesn’t worship the right god/desses, wears different clothes, looks different. And the group feels safer once the scapegoat has been killed, the guy has been burned. It would be nice if we could burn a ritual guy instead of torching each other.

The real anger is in the enabler. They control it by having the enablee express it. Then it is not “theirs”. They can feel superior to the enablee who is out of control. Sadly, the problem is only fixed temporarily and they will need their anger expressed again and again and again.

The cycle can be broken. It is a lot of work.

Blessings.

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Sorrow

I used to stop by more

but the people were less and less

the interactions faded to grey

I didn’t feel loved

I used to be ok with that

not feeling loved

not feeling valued

but now I want to be loved

And I am loved, to my surprise

as if a little love

has opened longing

so that I want more love


I want to be loved and feel loved

I send everyone love

even those who have been mean

and the incessant downvoters

and those who have me blocked

or don’t answer or ignore

or leave the catbox when I show up

I send love to you too


but now that I have a small crack

of love in my life, like the sun

shining on a crack in concrete

the seed stirs in sun and water

and grows

written 12/26/17. I wrote this about another writing site. It is falling to bits, like a old building not maintained. It makes me sad, because it is where my sister used to write. She died in 2012 and I still often miss her.

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Damaged or blessed?

Am I damaged or blessed to have PANS?

Damaged because it has put me out six times? Four times with pneumonia, once with preterm labor, and once with mononucleosis. Plus getting really sick with strep A as a kid, an earache that had me crying with pain at age 8, coughs in medical school that would hang on for six weeks and not respond to albuterol. Only rest would help. A year this time and not better yet, 6 months out last time and then seven years working half time. In 2012 out two months. 2005 out two months. Preterm labor out 6 months. Mononucleosis: dropped ten pounds and did not feel better or gain it back for two months. How much income have I lost? A lot. Am I damaged?

Blessed because I am not dead? My sister dies of cancer at 49, my mother at 61, my mother’s father at 79. All three married people who had “anger issues”. And all three got cancer.

I think that they had anger that they could not reach.

I do not think that ALL cancer is buried, unexamined, unresolved anger. But I am starting to see a medical pathway that could lead from buried anger or other buried emotions to illness and death. The buried emotions are stressful. The body tries to hold the stress. The body works very hard at it. The conscious mind is not aware. This is the realm of the unconscious. The stress, the unresolved trauma, anger, grief, whatever, triggers antibodies. Heightened sympathetic nervous system, higher adrenaline and higher cortisol. Cortisol is the steroid system. Steroids help to lower inflammation but they also impair the immune system. The immune system is chronically suppressed, trashed, and then it can’t do its job. Anti lysoganglioside antibodies form and block the lysogangliosides. The lysogangliosides are supposed to clean house in the brain. They can’t clean house, they are paralyzed. And the brain forms plaques: dementia. Or some other antibody forms that blocks cancer removing cells in the immune system: and there it is. Cancer.

We all have cancer all the time, that our immune system is removing. That’s a little weird to think about, isn’t it? So we need healthy immune systems, we need the parasympathetic nervous system, we need to relax, we need to play, we need to laugh ourselves silly at stupid cat videos, we need to make ridiculous memes go viral on TikTok, we need to use the power of the internet to drive the cost of a share up just to fuck with the rich Bosses, because we are tired of them fucking us over.

So, says my sig other, or he who used to be. You need to avoid stress, in order to not get sick again.

Well. I stopped eating on Saturday a week ago and ate minimal calories and mostly high protein and fat. Because I was pretty sure he was breaking up with me. He felt the same about me. I was terrified when we walked two days ago, so I wore the dragon shirt. Most of all I wanted not to yell.

Neither of us yelled. We both listened. He doesn’t know why he has shut me out of three areas of his life, and the three most important ones. It isn’t me. He is aware that it is him. He was not really aware that he was doing it. I am trained to hide emotions, from childhood in my crazy family and then physicians are trained as well. I cry with patients sometimes, when we find that their cancer is back, or other things like that. The child dying. But I can hold a calm expression even when a person tells me that they are hearing voices telling them to kill themselves and would I please take out the antenna in their tooth. So I sat hard on my emotions for ten months. Until I thought the right time had come.

Even then, I did my best and screwed up. We’d opened up one thing and I thought the rest would be ok. I sent an email. Whoa, boy, it was NOT ok, and I got yelled at. I burst into tears. I didn’t feel like yelling at all, I was crushed. But it is ok, it had to come out. The Year of the Ox is almost over. I hope the Year of the Tiger is less horrible. But at the same time, I would not trade the time with him for anything.

Damaged or blessed? Cursed or blessed?

Both, I think. All of us.

I am submitting this to today’s Ragtag Daily Prompt, though it is not a hawk.

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practicing grandmother

My sister sends me a t-shirt years ago.

It said, “I don’t know if I am the good witch or the bad witch.”

I burst into tears and put it in the trunk of my car. I never wear it. I am the designated bad witch for half my family. We won’t go into that.

She gets a shirt too. Hers is the green one. Mine is black.

She is dead, in 2012, breast cancer. It’s hard to describe the fallout. Toxic and radioactive. But… I have decided not to be a witch.

Instead, I am a practicing grandmother.

Really I’ve been one for a while. There was a young couple who lived down the street with two children. This was in 2014. I was a Facebutt friend, so sometimes noted what was happening. The father has to travel for his job. The mother is trying to care for two kids and work and so on… been there.

In 2014 I am recovering from my third round of pneumonia. This third round it takes six months before I can return to work. Short of breath and coughed if I talked. The state medical watch doctors went to disable me but I fight them tooth and nail. I win.

I wander down to the neighbor and offer my services. She already knows me. She is instantly grateful and two year old T is introduced to me, again. He doesn’t really remember me. She explains that he is coming to my house for a little while and then back home.

T and I walk towards my house.

A nuthatch calls.

I stop and reply. In college I took ornithology and the teaching assistant could do a barn owl call so well that the barn owls would do a territorial fly over at night to see who had the weird accent. Marvelous.

The nuthatch and I went “enh” back and forth. T is amazed. This woman talks to birds. Then we see the nuthatch! I point out how nuthatches come down a tree head first. “If you hear that call, it’s a nuthatch. Look for it.” The nuthatch is very cooperative. Magic.

We get to my house. T is clutching a book. “He’s taking it everywhere,” sighs his mother. “I’m not sure why.”

So first we read the book. It is a board book about a farm. Each page has a central picture and then there are pictures around the edges with the word under each picture. On one page T says, “Haaaaay.”

“Oh!” I say, delighted. “You can read HAY!”

His face lights up. An adult who gets it! Yes! He can read HAY!

On another page he says HAY. “Oh,” I say, “That is straw. Straw is a lot like hay but it’s not exactly the same.”

He is very serious absorbing that information.

I show him my closet. There is a stick horse. Only it isn’t a horse: it’s a unicorn dragon, with a forehead horn and wings. When you press a button it’s eyes flash and it roars.

Ok, that’s pretty scary. He wants the closet door closed and he does NOT want to play with the dragon.

Next is pouring. I get out a towel and put it on the kitchen floor. I get out a rather nice expresso set. Bright colors. Orange and green and yellow and blue. I fill the coffee pot with water and invite him to sit on the towel. “You can pour the tea.”

He looks at me with surprise. He picks up the coffee pot. He looks at me again. “Go ahead. It’s ok.” He starts pouring into a cup. He pours until the cup overflows and the saucer overflows and he keeps pouring. The coffee pot is empty. He looks at me a little warily. This is technically spilling and he knows it.

“Would you like more in the teapot?”

He nods.

I refill the coffee pot with water and he starts again, with a different cup.

When I return him to mom, after two hours, he’s damp. “Sorry, he got a little wet, but it’s just water,” I say cheerfully. Mom is too harried to do much more than look resigned at a change of clothes.

Next time he comes with a change of clothes and his large stroller, in case he goes down for a nap.

And first off, he goes to the closet. Time to hear that dragon roar again.

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chronic fatigue

I am realizing that I have had chronic fatigue since 2014. Or possibly 2012.

We know that chronic fatigue can be kicked off by infection. One in ten people with a severe infection is diagnosed with chronic fatigue. Severe stress can also kick it into gear or a combination of stress or grief or attack or assault and infection can kick it in to gear.

We don’t really understand it, though I am finding experience to be a very great teacher.

As far back as medical school and residency, I was curious about it. I love the edges of things: it is the things that we don’t understand that I study. I pick up bits of information like a crow or magpie. I add it to the pile of things related to it in my brain. Sometimes I will add just one more small piece and the entire pile of puzzle pieces with suddenly, in just a blink, rearrange itself into a picture.

The pieces won’t arrange themselves until I have a complete picture. Or, well, until something in my brain is satisfied that it is complete enough. Since nothing is every complete or completely understood, is it? Nothing fixed and we make up all the words.

Anyhow, chronic fatigue would explain why running my own clinic, I did not see more than ten patients a day. Also I do have some OCD, hidden under a messy packrat gene. You would NOT look at my house two months ago and think that I have some OCD. Messy and chaotic. But I am a precision demon about patient charts and I am always thorough. In 2009 our local hospital let me know that my reputation was of a brilliant diagnostician. Ironically, this was right before they fired me for arguing about the patient quota of 18 per day. I ran late because I could not stop being thorough. I cut my work from 4 days a week to 3.5 but that was still two hours of dictating and paperwork for every day of clinic. So clinic was 28 hours plus the dictating and paperwork and calling specialists and calling insurance and a one hour meeting at lunch with the administration EVERY DAY FOR MONTHS, so really clinic was 8 hours of patient contact plus the one hour lunch meeting. Redo the math: 28 hours plus 4 one hour lunch meetings plus 7 hours of the generated deal with stuff AND do not forget about call nights. 39 hours plus call. At least one call night a week, 6 pm to 8 am, so that is 51 hours or more. I felt that I was working flat out as fast as I could every single day in clinic and I still was not keeping up.

I also really really resented the one hour lunch meetings because I was only allowed 20 minutes for a patient and was to see them “for one thing”. Seeing people “for one thing” is unethical and dangerous because for example: a diabetic with a toe infection. That is already two things. But you’d better calculate the third: kidney function, because you have to dose the antibiotic for the toe based on the kidney function, and diabetes is the number one cause of adult kidney failure in the US. Oh, and you’d better check on the diabetes too, because if their blood sugar is whomping out of control, the toe won’t heal and that’s how they got infected in the first place. So I might have ranted a bit about seeing people “for one thing” because I think it is an UNETHICAL DANGEROUS LOAD OF CRAP. DO NOT PUT UP WITH IT, DOCTORS AND PATIENTS OF THE UNITED STATES. It is corporate trying to maximize profit and they can frankly go to hell and stay there. Single payer. ‘Nuf said.

Even more ironically is that two years after they fired me for vocally disagreeing with the quota (I would add that I was not diplomatic and I was vociferous), the hospital dropped the quota down. To what I had asked for, 16 patients a day. I actually had kept track through my career and knew that I averaged 16 patients a day. One partner usually saw 20 or 21, but the problem was that he kept the chart in his head. When I would get one of his patients, I’d have to say, “Um, you have some heart disease, right? You’ve had a heart attack or a bypass? What year was the bypass? How many vessels?” I’d be guessing from the medicines and clues… but the past history was not entered into the chart. So, yeah, I only saw 16 patients a day but my charts were solid and thorough and the charts on his patients were a lot more comprehensible every time I saw one of his patients and did the chart for him. He owes me. Pay up.

Anyhow, I have worked really hard for the last seven years, in spite of some chronic fatigue and fibromyalgia. Which I rather refused to admit to myself. I thought I was “well”. I felt bad that I didn’t clean up my chaotic house.

Now I forgive myself for the house. Because the truth is I couldn’t clean up the house. Not after 7-10 patients and running my own clinic, CEO, chief cook and bottle washer, dealing with the covid changes, trying to figure out medicare’s arcane language, fielding malpractice insurance, business insurance, insurance insurance and phone company scam calls.

I have been sick at home for 6 weeks. I have been on oxygen for 4 days? 5 days? I would have felt a lot better and been able to think better if I had been on oxygen the whole time. Meanwhile, turns out I CAN clean up and organize in spite of being hypoxic. My house is now a very different place and the garden has changed enormously very quickly.

I am sending more money to India, via https://www.pratham.org/ . I can hardly bear to think about the people who cannot get oxygen. It feels terrible and terrifying to not be able to breathe. My chest hurt and lungs and heart when I even sat up, much less walked. If I walked slowly enough, it was bearable, just barely. I walked anyhow. Those edges, I am always there.

It is very weird being on oxygen. I have told people in the past when I had pneumonia. I’ve almost died from it four times. Heart rate of 135 holding oxygen level, but it doesn’t feel good. I am confident that I do not have coronary artery disease, because if I did, I would have had a heart attack the first week. A heart rate of 135 is running a marathon. It is exhausting. Right now on oxygen, my heart rate is 86 and oxygen at 98%. My normal heart rate is more like low 70s. Normal is 60-100, you knew that, right?

It is very weird being on oxygen. Because now I have a visible signal that I have been/am sick. Somehow this is making people more kind, more concerned. I keep thinking, but I told you I was ill before. Why does being on oxygen make people kinder?

I think that is the difference between having an illness where there is not much comprehension and one that we think we understand. So chronic fatigue and fibromyalgia are dismissed, disrespected and discriminated against, while cancer and sepsis and covid-19 and massive trauma in the military are supported. People send gifts.

In the past, tuberculosis was thought to be an illness of sensitive poets. Then the tuberculosis bacillius was discovered and it morphed into a disease of the poor dirty overcrowded low scum of humanity. My mother had tuberculosis, but luckily it was when we’d moved on to sanitoriums, because it is airborne, so stop the spread and take care of people. There was also medicine. My mother had to take 36 pills a day. At one point in the hospital, someone brought her a medicine.

“What is it?” asked my mother.

“Don’t worry about it.” said the nurse.

“No,” said my mother. “I want to know what it is.”

The nurse got the doctor. He came in and said, “Take the pill.”

“What is it?” said my mother. She was 22, 8 months pregnant, very poor, and a student at the University of Tennessee.

“Don’t worry about it.” said the doctor.

My mother threw it at his head. Because not only was she 22, 8 months pregnant, very poor and a student at the University of Tennessee, but she was also the daughter of F. Temple Burling MD, a psychiatrist, physician and professor at Cornell University.

And he had told her, don’t take anything unless you know what it is…..


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The picture is of my mother, Helen Burling Ottaway, in 1945. Helen Temple Burling II at the time of the picture.

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I think the final straw that made the hospital fire me was me singing “The 18 Patient Blues” which I’d made up, to the tune of 16 Tons, into the Chief Financial Officer’s voicemail and at the open mike at the Upstage, here in town. I admit, it was not diplomatic.

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Ottaway back porch

My parents’ time warp Beatnik household, 1978, before I went to be an exchange student in Denmark.

We had a German exchange student living with us. She had been placed with a couple with no children, a military family, and was unhappy. My parents agreed that she could move in with us for the rest of her year. I decided to apply as an exchange student. I have not heard from her in years. Blessings, where ever she is.

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happy sister

I am home sick and it looks like it will be a long haul. Months. Sigh.

Anyhow, I am going through photos and found this. I do not know who took it, I don’t think it was me. I have my parents’ photos and they had my maternal grandparents’ photos, or at least it seems like it. Anyhow, I am floating in a sea of pictures.

I love this one. She is so happy.

Hope you are that happy now, sisty.

Music: William Prince