still inside

The college in Detroit where I taught for twenty years is closing for good this week. As I’ve been reflecting back over my experiences there—twenty years is a long time—one event in particular stands out.


It concerns a sequence of eight poems I wrote, titled “still inside.”


I originally wrote these back in 2007. Every so often when I give poetry readings, I bring these out to read because they’re among my favorites. After all these years, I still find them tremendously moving, and my audiences usually do, too.


The poems are monologues written in the voice of a little girl who suffered, as the poems describe, every kind of bad luck a child can have.


The sequence is based on the situation of an actual little girl. The basic events in the poems are true—a baby was born as a twin, but suffered life-altering hypoxia because the medical staff didn’t know there were two babies and she stayed inside her mother too long. She was born into a world of poverty and disregard.


That much is true. The rest is “truly imagined.”


(As Marianne Moore said, poets should create “imaginary gardens with real toads in them.”)


My stepdaughter is an attorney specializing in rights of the handicapped, and she’s the one who told me about this girl. The third poem in the sequence mentions an attorney who steps in because the little girl’s regular lawyer wouldn’t release enough money for her proper care; my stepdaughter is the one who intrudes to help the child. (The other attorney said to her, “What are you, an avenging angel?”)


The story of this little girl affected me for a long time, until it moved and saddened me to the point where I felt compelled to give her a voice that the circumstances of her short life had denied her.


I felt I had to bear witness to all she endured.


But I didn’t just want to focus on her sadness. My grandson Jamie was also born with a number of severe handicapping conditions, and everyone who came into contact with him during his own shortened life was profoundly transformed by his loving nature. I wanted to imaginatively imbue the little girl with some of Jamie’s indomitable spirit as a way of counteracting all the misfortunes of her life.


I had always thought these pieces could form the basis of a multi-media project consisting of words, music, art, and dance. I showed them to one of my friends and colleagues, Geoff Stanton, when we were both teaching at the college. Geoff is a phenomenal composer and musician, and he jumped at the chance to compose music for them.


[image error]The result was a stunning series of eight songs using the poems as lyrics set to music for two voices, piano, and cello. We presented them as part of one of Geoff’s annual concerts, and I was thrilled with the way they turned out. I’m including the poster for the event, left.


(As I write this, I don’t have a recording of the music available, or else I’d include a sample of that, too.)


As these things go, I haven’t moved my multi-media plans forward. Perhaps at some  point in the future they will come to pass.


Until then, I offer this sequence in the hope the pieces will affect you as much as they continue to affect me.


 


still inside  


by Donald Levin


i


another one


 


no doctor saw my momma


before we came


no exam no test


no money no thought


for another waiting


when it was time


it happened so fast


at the poor people’s hospital


my sister came quick


but after she was born


nobody knew


i was still there


awaiting my turn


quiet as i ever was


they turned away


to bathe and weigh the new one


and while i was waiting


i ran out of air


in the dark channel


of my momma’s narrow body


and it wasn’t till later


when she started screaming


that the nurses and doctors


caressing my sister


ran back


and discovered another one


still inside


and they did what they could


but the story of my life


was written by then


 


ii


absence of air


 


hypoxia


the doctors called it


to explain why my sister was good


and i was the bad one


right from the start


which meant no walking


or talking for me


though i could understood


what people would tell me


if only to hum in reply


and i did try to smile


if i thought it would help


which wasn’t often


though i cried at the seizures


that made me go stiff


and roll my eyes


and afterwards whimper


till i fell asleep


the medicine made me so


dizzy and tired


couldn’t see either


no sight in my eyes


except shapes and shadows


and the flashing lights of seizures


the only things i could see


retarded, they said


which probably i was


since i couldn’t learn


the way my sister did


who was always quick


even when she was born


she was the first


and i was last


 


iii


the house we lived in


 


momma bought with the money


they gave her for me


at first a lawyer handled the money


but wouldn’t give us enough


till another one made him


we never could have had


such a big house


there was supposed to be


a ramp and special bath


but momma never had it made


used the money for sofas


i was not allowed to sit on


so i couldn’t ruin them


by drooling which


i couldn’t stop


and she bought the other children


clothes there were two more


after me and my sister


so i stayed inside


for most of the time


and when a nurse came


to care for me


which wasn’t often


i was clean and dry


but when nobody came


i had to wait for gramma


who watched me when momma was out


but she didn’t always remember


so i stayed in my diaper


till it got so heavy with wet


she couldn’t lift me


or turn me over


when she finally remembered


so i had to stay still


inside my room


in pants that were heavy and wet


till someone remembered


and came to take care of me


but i was patient because


i was already such trouble


my momma told me


 


iv


school


 


when the bus came to take me


every morning


they would strap me inside


in my wheelchair


so i wouldn’t bounce


on the trip to school


with the driver and an aide


who cleared my throat


if i needed it


and when i got to school


my teachers were so happy


to see me


when they rolled me off the bus


they’d take my coat


and change my pants


and my teacher who is very tall


held my hands to say hello


and later they all sang


good morning to you


good morning to you


and sang about


my bright shining face


which i had because


i was so happy to see them too


every morning i also saw


my friend zach


who was in my class


and who liked me too


our teacher wheeled us together


so we could sit and hold hands


even though we couldn’t see


we felt each other’s hands


which were both crooked


because our muscles were so tight


but the touch of our fingers


twisted together


kept us warm


till it was time to go to music


which i also loved


 


v


momma always wanted


 


to be where she wasn’t


before we bought our house


we lived in different places


and she always wanted to be


someplace where we weren’t


when we moved to the city


from the town we were born in


she wanted to go back


to our old home town


and when she went back


at night to meet friends


she wanted to be back


inside our new big house


and when she was with us there


she yearned for jamaica


where she came from


she said she never was happy


since she left jamaica


if she had stayed there


she said her life would be


completely different


she must have been right


because i never remember


seeing her smile


or hearing her laugh


except when her friends were around


and i thought she must have


lots of friends


in jamaica


to miss it so much


 


vi


on valentines day


 


one year i got to eat chocolate


which i never had before


i never ate by my mouth


always got formula


through the button in my tummy


when i tasted the chocolate


i couldn’t breathe


gramma called an ambulance


momma wasn’t home


and gramma had to stay


with the other children


so I went by myself


to the hospital


they said i couldn’t breathe


because i was allergic to


peanuts in the chocolate


they gave me medicine


which i was also allergic to


the doctor gave me something else


that worked this time


and i could breathe again


so he sent me home


but i couldn’t breathe again


at home my throat closed


so i had to go back


in the ambulance


the doctor wanted to put


something in my throat


a little hole


an always open o


so i could keep breathing


but he couldn’t do it


without momma’s permission


and nobody knew where she was


so the doctor called the lawyers


in charge of my money


they must have said sure


go ahead then the doctor said


well you know


this will be permanent


it’ll mean round the clock care


from now on


it will mean a nursing facility


it will be pretty expensive


i just wanted you to know


he listened


and hung up


and told the nurses


who were holding my hand


her trust won’t fund the care she’d need


let’s try something else


he sent me home


with a machine


to suction my throat


and now when the mucous


collects in my throat


i get suctioned


if anybody’s there to do it


the lawyers must have said


they would pay for it


but somebody has to remember


to suction me


which doesn’t always happen


and i wind up coughing


until i can spit out the mucous


and sometimes i can


but sometimes i can’t


and i just have to lay there


and cough and cough


 


vii


sailing


 


my momma didn’t want


nursing care for me


didn’t want people around


telling her how to take care


of her daughter


but once when a nurse came


her name was nancy


she took care of me for a while


brought a big boat


and hung it from the ceiling


i couldn’t see it


except as a blur


but she described it


it was different colored ribbons


like a rainbow


with sails so big


when the breeze blew in


when the windows were open


in the warm weather


nancy said the boat would float


back and forth like a real boat


sailing on the waves


of the ocean


and after the company


nancy worked for took her away


to care for another child like me


who they said needed her


more than i did


she left my boat


hanging in my room


and when i laid in bed at night


waiting to be turned over


i would think about the boat


waving in the breeze


and pretend i was the captain


sailing around the world


on my boat of colored ribbons


and everywhere i went


people would wave


and clap as i sailed by


 


viii


still, inside


 


though everyone did


the best they could


i was not to live long


scoliosis twisted my spine


like a cane’s bent handle


in my fifth year


and as it curved around itself


my organs compressed


till one day


my lungs couldn’t move


enough air


and all my spit pooled


in the back of my throat


and i inhaled it


and got pneumonia


a speck of mucous


was all it took


hidden like a grain of sand


in my chest


the bright red ring of sickness


pearled around it


and because i couldn’t rise


or blow it away


the infection overwhelmed me


and the fever


made my seizures so bad


i couldn’t breathe at all


and before anyone knew


to call the ambulance


i died


but at my funeral


everyone came to say goodbye


momma my sister my gramma


the rest of the family


the lawyers and doctors and nurses


who took care of me


and i could feel them all


standing crying


over my coffin


as i lay still


inside


 


©2019 Donald Levin


 

 •  0 comments  •  flag
Share on Twitter
Published on December 16, 2019 12:12
No comments have been added yet.