This is a tintype. “Tintype photography was invented in France in the 1850s by a man named Adolphe-Alexandre Martin. Tintypes saw the rise and fall of the American Civil War, and have persisted through the 20th century and into modern times.” — from here.
I do not know who this young man is, nor the year. I asked my maternal uncle before he died and he denied any knowledge of the person. He was the family historian and archivisit.
However, I have four tintypes in the box of china doll furniture clothes and accessories. My sister and I received a box of jewelry and the tintypes from my Great Aunt Esther Parr. She was my maternal grandmother’s sister and married Russel Parr. Her maiden name was White, a daughter of George White, the Congregationalist Minister who ran Anatolia College in Turkey and then moved to Greece. My sister and I divided the box of jewelry and the tintypes. There were eight so we took turns picking. We used them for dollhouse portraits, not realizing that they were real photographs. I wonder if the tintypes are from the Parr side of the family.
Last month I was missing my father on February 12. I was a month off. His birthday was today, Malcolm Kenyon Ottaway, born in 1938. I miss him now, too.
I will label more photographs, since I appear to have inherited the maternal family paper archive. There are people that I don’t know, though, and my parents are gone. My mother’s siblings have died as well. I am so glad I still have my father’s sisters.
Ask your parents about the pictures and the objects they keep, before they are gone and you lose the story. Time marches on.
Wait, another? We don’t go through the stages of grief once. We go around and around, like a spiral. Some days we want to lie down in the driveway and just not move. Others it seems like the there might be a tiny bit of sun in the world after all. A mourning handout from the American Academy of Family Practice writes about a culture where one is considered “legitimately crazy” for a year after the death of someone loved. The person is allowed to be emotional, complain, wear their bathrobe all day and call people at 3 am.
Maybe we are all in that stage right now.
Stages of Grief Playlist 2
Denial
The Offspring: Pretty Fly for a White Guy
Bargaining
Kate and Anna McGarrigle: Hard Times Come Again No More
My sister had breast cancer for 7 years. She said that the five stages of grief missed two. She adds βActing Outβ and βRevengeβ. I am planning a series of stages of grief playlists, because we are coming up on one million US citizens dead of Covid-19 and we are at six million world wide and counting. We need help grieving. I have other stuff going on to, so my go to is music.
My theme for the April AtoZ blog challenge this year is art. I think it will mostly be my mother’s art. She died in 2000 of ovarian cancer. My only sibling died in 2012 of breast cancer and my father in 2013 of emphysema. And I have the art: my parents were both packrats and trying to deal with the house and an out of date will took about three years. Moving stuff around, getting rid of stuff. The art initially went in to a storage unit and then into my house. My mother Helen Burling Ottaway was prolific! And she kept every single piece of art and her diaries back to high school! I found a suitcase with my grandfather’s poetry as well: that will be for another day.
This painting is of my sister. My mother started oils later in her career and Michael Platt, a DC artist, said something like, “Quit doing tiny things. Do something big.” My mother started doing life size and larger than life portraits in chalk pastel and in oils. This painting captures my sister when she was twenty: emotions. I like it but I also think that it is frightening.
Christine Robbins Ottaway age 20, by Helen Burling Ottaway, oil, 1984
I wrote this poem a long time ago. I was thinking about how being a physician and taking care of other people let me avoid my own feelings. Doctors are trained to hide their feelings. When I was an intern, a patient died on my day off. I came back to find the person gone. No one on the team said anything. I was afraid I’d done something wrong. Was it my fault? Finally I screwed up my courage and spoke the the attending physician. “Oh!” he said, “I meant to talk to you about that patient. They had a lethal pulmonary embolus from the clot in their leg. They were appropriately anticoagulated. You did nothing wrong. This happens.”
I think the war is more of the same. Chaos, to avoid feeling. Let’s not do that. Let us grieve as a world. Let us not melt down in a conflagration. That is my prayer.
Chaos
So familiar
If there’s a mess And chaos Home that’s home Busy busy Run around Fire fire Fix it Crisis Now what Deal with it
No time for feelings
No no
No time
I don’t want chaos Liar liar
Chaos is so safe
Hero hero Put out the fire Catch the baby Confront Not a hero really Scared Hiding
If I stop the chaos I will have to feel
Maybe it’s ok To feel a little
I forgive myself I understand the chaos I can let go of it by degrees
I feel so vulnerable In the quiet clean safe place Take your time sweet self
I had the heart echocardiogram bubble study. Normal. I really really did not like having the mix of blood, saline and AIR injected and I COULD FEEL IT. My logical brain knew it was going into a vein, but my emotional brain kept yelling “Air embolisms kill people!” Yes, but that is arterial. My emotional brain did not care. Anyhow, it was fine.
Saw the cardiologist who said he can understand why I feel PTSD going into my local hospital. He says I should not need oxygen at age 60 with no smoking. He says “Not your heart.” Yeah, duuuude, I know. He suggests I go to the Mayo Clinic. I agree.
Meanwhile, my primary sent a referral to rheumatology to have me seen at Swedish to confirm chronic fatigue. This is to keep the stupid disability off my back. Swedish rheum doesn’t call me. I ask my primary’s office. Swedish STILL doesn’t call me. I call them, as follows.
“Hi, I was referred to Swedish rheum and I have not been called.”
“Name, serial number, date of birth, length of little toe. Ah, we just received the referral yesterday.”
“Um, I don’t think so. I was referred over a month ago.”
“Uh, oh,” scrabble noises, “Oh, uh, we got a referral in December. We were not taking new patients in December.”
“When did you start taking new patients?”
“Oh, um.”
“When did you start taking new patients?”
“Oh, uh, January. But we only took the ones that called us, because after they call, we then review the notes.”
“So you ignored the referral until I call? How am I supposed to know that?”
“Oh, uh, we will expedite your referral. Maybe even today.”
So THEN I get a message from my primary that they have REFUSED the referral. Great.
Meanwhile I read the cardiologist’s note, which pisses me off. “We will refer you to Mayo Clinic since you have unexplained hypoxia and you think you have PANS.”
I send my primary a very pissed off note saying, could we please phrase this as “a psychiatrist suggested PANS in 2012 and while no one likes this diagnosis, no one else has suggested an overarching diagnosis since that time in spite of her seeing four pulmonologists, neurology, cardiology, infectious disease, four psychiatrists, allergy/asthma, and immunology”. Saying “the patient thinks she has PANS” automatically labels me as crazy and obsessed.
So, it seems I should write a book, about how the medical communities treat patients, including a fellow physician, horribly. Of those doctors, three have treated me with respect and were grown up enough to say, “We don’t know.” The neurologist, the infectious disease doc and the present pulmonologist. All the rest are dismissive and disrespectful. Oh, and the one psychiatrist, but the next one says, “I don’t believe in PANDAS.” I stare at him in disbelief, thinking “they are animals related to raccoons that live in China, you moron”. I did not even know it was controversial until that moment. Holy PANDAS, Batman.
My primary has suggested I write to the Mayo Clinic myself, and I am going to. Because the present people aren’t listening, except my pulmonologist and she is short staffed and looks like death warmed over post call every time I see her.
So it’s all annoying as hell. The cardiologist seemed pretty nice, but damn, he put the same damn rumor down about me self diagnosing. Most of the doctors apparently think I might be a tolerable person if they could just drug me with psych drugs. And from what I have seen, there are many patients who are in this situation.
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 2012and I still often miss her.
Discover and re-discover Mexicoβs cuisine, culture and history through the recipes, backyard stories and other interesting findings of an expatriate in Canada
Engaging in some lyrical athletics whilst painting pictures with words and pounding the pavement. I run; blog; write poetry; chase after my kids & drink coffee.
Refugees welcome - FlΓΌchtlinge willkommen I am teaching German to refugees. Ich unterrichte geflΓΌchtete Menschen in der deutschen Sprache. I am writing this blog in English and German because my friends speak English and German. Ich schreibe auf Deutsch und Englisch, weil meine Freunde Deutsch und Englisch sprechen.
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