“Hey, do you have a phone?” a woman asks people as they pass by in the plaza.
“They always lie” she says looking my way.
“Do you have a phone? My battery died” she asks me.
“I think my batteries dead too” I say. Which is a partial lie.
I’m sitting in the plaza eating cookies and drinking Chai with my kids. It’s a cold day, us and the woman across the plaza are the only people stationary. Everyone else is walking through, getting lunch or last-minute Thanksgiving stuff.
The woman moves to the table next to us. She has short grey hair, a little beard on her chin, her voice is raspy but almost like a teenage boy, she must be close to sixty years old.
“I’m trying to call my case worker, I need my meds, I need to contact Paul, do you have a phone?” she asks again, this time less than a foot away from me, my kids are watching our interaction. A police car pulls up and the woman gets anxious, she says they are trouble for her. I ask her if she knows the number, she does so I let her use my phone. A woman answers from the city health department in the city north of mine, the receptionist knows Sebra, she transfers her to Paul, her case worker. An answering machine comes on and Sebra leaves a message. She tells him she needs her meds and a quilt for the night. I tell Sebra I have to leave soon, It’s time for the kid’s gymnastics class.
I tell her that I need to take them to class, but that we will come back around and check on her, let her know if Paul called back, and if Paul doesn’t bring the comforter me and the kids will bring one. We go to gymnastics, but Paul doesn’t call back. We realize Fiona left her tiny (her most precious stuffy) at the Indian restaurant where we had lunch. We have to go back downtown no matter what. We pick up Tiny at the restaurant and see that Sebras still there in the plaza.
“Sebra Paul didn’t call back” I say to her.
“You took way longer than you said you would” she says.
“Did you bring the comforter?”
“No, we’ll go get it right now, we wanted to make sure you were still here” I say.
The kids and I drive over to the Salvation army and buy two comforters and two pillows. We drive back and I illegally park in the bus stop. I leave the kids in the car to talk with Sebra. I ask her too many questions and she tells me I’m asking her too many questions she doesn’t know the answer to. I realize she is in crisis. She tells me her legs are stinging because of the pee, that she needs to change her pull up, that she can’t control her bladder, that she needs her meds before the holiday starts, she starts asking me what she should do. We call Paul again and he answers the phone, but his voice disappears. The kids start yelling someone’s on the phone in the car. I had left my car running so the call transferred to blue tooth. Sebras not happy about this. I say let’s try again. We go through the questions again and this time Sebra stops me and asks me what she should do. I realize again this person is in crisis. I take a deep breath. She had told me she’s sleeping at city hall. It’s already four and Sebra doesn’t want to sit in the plaza anymore. But she doesn’t want to miss Paul if he shows up with her meds. She can’t walk all the way to City Hall with her bag of stuff and the new quilts and pillows. She’s also let me know she’s scared of the other homeless people.
I decide to give her a ride to city Hall and call Paul again from inside the car. She likes this idea but is concerned about my car seat, she asks if I have any plastic to put on the seat. I do, she gets in the car and the stench of ammonia from the pee is so strong. I open the windows but Sebra says she’s cold and asks if she can close the window. I have the heat cranked to 80 degrees and Sebra says it feels so good. I take a deep breath and look at Sebra. I tell her we will call Paul again from the car when we get to city hall. I was able to shed my nervous uncomfortable smile on my face and my questioning. I was able to hunker down with Sebra in the situation and grasp the seriousness of it. We got to city hall, I backed into her spot, kept the car running and called Paul again. I took another deep breath; I had been pronouncing Sebra’s name wrong all along and her patience was running thin. I said the name correctly and reversed what I would say to Paul when he answered. Sebra and the kids watched me in silence. The phone rang and Paul answered. He was twenty minutes away and had the meds.
Sebra and I got out of the car. She was amazed her sleeping bag was still there, but someone had put poop on top of it. It was poop on a plastic bag, Sebra wanted me to take it to the trash can by the library, but I wasn’t going to do it. She scooped it up with her sleeping bag and put in by a bush, but she was concerned because other people stash their blankets there and people walk through there. Maybe I should have tried to get rid of the poop, but I’m always leery of needles and scooping up a sleeping bag with poop on it seemed like a risky thing without proper safety equipment.
I set up her bed, I put an old beach blanket I had in my car down, then one quilt, then the other and the pillows. She kept saying they were too nice to be used outside. She asked if I had an extra room, she could sleep in. I said no. She wanted to know If I could stay longer or come back, I said no. At the plaza I had touched her shoulder when I was apologizing for upsetting her by asking so many questions and she had said don’t touch me. But now, as I was leaving, she said Thank You so much several times and gave me a hug.
I got home and had to start making dinner right away, it was my husband and my anniversary, and I had promised him stew. He had called me on my way home wondering if he should just order his own food. I felt bad but have an instapot! Stew can be ready in an hour and a half! I got the stew started and kept thinking about Sebra. I had to take a shower, it just felt like I had that smell on me. But I felt, I can’t really explain how I felt. Just thinking that we, as a society are willing to let our fellow humans sleep outside in freezing cold in their own piss is what I thought about. How could we do that? Sebra really didn’t know what to do, except that she needed her meds, she needed help. At least ten people walked by her in the plaza as she asked people to use their phones. Everyone said no. Then a cop car showed up, someone must have called the cops, but by this time Sebra was sitting by me. The cop stayed for maybe fifteen minutes then drove off.
Last night the kids kept asking me questions, where do homeless people sleep, where do homeless people eat, why can’t Sebra get a bed? I had told them about the beds at St. Vincents, but that they only have a small number of beds. Jack asked why can’t Sebra put the quilt on the floor? I said it doesn’t work like that. He couldn’t understand. When I told them about the soup kitchen, I said we could go help one time and Fiona said YES I WANT TO DO THAT! Jack said, no, I don’t want to see that homeless person again.
I think it’s scary to see what we all are, that innate humanness that’s in all of us. Some of us luckier than others. But we don’t know what Sebras circumstances are, how she arrived at this place. But I think it can happen to anyone. I think Jack and Fiona can see that too, and that they are lucky. They are lucky to sleep in a warm house. I just got a freeze warning on my phone from tonight until Friday. I hope the city does something to take in the homeless people tonight. I think I need to make a few calls today.
Tag: life
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I walked over the green hill, past the ice cream truck, I felt good, I was on time to pick up my kids from summer camp. I parked at the very far end of the park so I could enjoy the walk. It was a beautiful day, a bit windy, hot and dry. August quickly approaching. I expected my kids to be super happy they weren’t the last ones to get picked up, I’m always running late, savoring that last minute of alone time.
“Mommy!” Fiona said. “Jack mommies here”
Fiona gives me a big hug.
Jack leaned against a tree.
“Can we get ice-cream?” Jack said.
“No, Not today. You had a special treat in your lunch box.” I said.
Yesterday I bought them each one of those cute sandal cookies with blue frosting from Panera bread.
“I hated it; I hated the cookie” Jack said.
Fiona was playing with a bottle of sunscreen a kid had left, she was spraying it on the grass. I told her it wasn’t good to do because of the chemicals and that it would hurt the birds and bugs and grass, Fiona understood. The whole time Jack began to cry and whine and ask over and over again why we can’t get ice cream. I tried to reason with him, explain to him why not, as he kicked Fiona’s camp bag, smashed a hat left on the ground by another camper, then he threw an acorn at me that almost hit my face.
I told him that was very bad behavior and I began to walk towards the car with Fiona. Jack cried the whole way, having a meltdown. Right before we got to the Ice Cream truck, I said to Jack that he better walk by without incident or there would be no ice cream the next day either. He agreed and I gave him a hug and he hugged me back and held my hand. Fiona ran to the Ice Cream truck and wanted to show me the picture of the ice cream she wanted to get the next day. Jack had calmed down enough to do the same. I thought I was in the clear.
When we got to the car another meltdown took place because Jack wanted to sit where Fiona was sitting, even though it was her turn to sit there. I sat there in the car as Jack melted down and I waited until he decided to get strapped in. It was horrible. During this time Jack hit Fiona multiple times. Then Fiona hit Jack back. I don’t know what to think of this behavior. I don’t understand it. I try to stay positive most of the time or at least calm. I get anxiety and stressed, but I don’t yell or hit or say mean things to people. I don’t know why Jack is like this and it is starting to bother me.
I thought it was maybe because I spend more time with Fiona, she’s always had her doctors’ visits and the extra explanations I do and giving her that extra attention she needs. I started making sure I would give Jack special time and play basketball with him, but Jacks never satisfied and the end goal for Jack is always a toy or a treat. Or to watch u-tube. I hope this is a phase. Because I need Jack to be on my team.
When I dropped Fiona and Jack off at camp this morning, Fiona’s friend was already sitting down. For some reason this friend doesn’t say hello or anything, she barely acknowledges Fiona is around. I feel bad for Fiona because she loves this little girl with all her heart. They went through the Early Start program together. There was one chair by the little girl and Jack sat there. Even though I’ve already told Jack to give Fiona space with her friend and that he should make some new friends. He didn’t listen. I tried to encourage Fiona to sit by another little girl at the table. I want Fiona to make new friends. But instead she squeezed another chair in between her brother and her friend. That’s when I left.
This is not easy. I feel very sad today. For the past month I’ve joined several ASL groups and Deaf/HH groups on Facebook. I learned a ton. But yesterday in one of the groups there was a post about mixed group, hearing/non-hearing dinner parties. It talked about everything I know, how it’s very difficult. I live in that world everyday at home. I see all the things Fiona misses when the family is all together talking at once. I can only hope that when my family is fluent in ASL Fiona will feel like she’s totally included, even though I’m not sure she will ever use ASL 100% until she’s older? Anyhow the post the person made was so depressing to me I left that group and all the other FB groups I’ve joined lately. I just can’t take the salt in the wound right now. I’m trying to figure out what else I can do to ensure Fiona has a chance and has an enjoyable time in Elementary School. I’m at my breaking point. And when I left Fiona in that room, clinging to her one friend, knowing she would have a very difficult time understanding what anyone said, with her brother being kind of a jerk, I just feel sad. They are only five, I can’t expect him to have the kind of empathy and compassion I need him to have. Even though Fiona does. Her whole being is empathy, compassion, love, all good.
She has to work so hard and she’s so nice and so sweet and the world is pretty sucky and people can be really sucky. Really sucky, even her own twin. I have noticed the unthinkable lately. Jack was always so good about repeating things when Fiona asks “what did you say” to Jack. He was so good at helping her pronounce words she could understand. It was so sweet. For those reasons I wanted them to even be in the same class in Kindergarten. I thought Jack would always have her back. At least she would have her brother, I thought. Now they will be separated in Kindergarten. I really hope this is a phase for Jack. I hope it doesn’t last long.
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Things have progressed in my fight, battle, request? I have no idea now what the right word to describe what I’ve been working towards. You’ve read it, the pilgrimage to the place I am now. WOW! What a ride. Now my whole family is signed up for a twelve-week ASL course starting in two to three weeks. When Fiona was born and I received all the literature from the National Institute for Newborn hearing screening I knew immediately that I wanted total communication for Fiona, that I wanted us to learn sign language, I didn’t know the difference between ASL and SEE sign, really. In the Early Start program we were in we did TC. I never expected Fiona’s dad or brother to need to learn sign. I knew I would no matter what and I would make sure Fiona knew sign, but never really expected other members of my family to, or my friends.
When I dropped Fiona off at camp this morning and the music was blaring, and her friend wasn’t at camp yet, Fiona looked so unhappy. I felt so bad. I told the camp counselors and they turned down the radio, I felt bad suggesting this too, like changing things for one person when everyone else was fine with the loud music. I told the camp counselor, just so you know Fiona won’t be able to hear anything when it’s this loud. I tried to get Fiona to talk to another little girl who looked as lost and uncomfortable as Fiona. But it was just too loud. I thought, if Fiona was fluent in ASL and had an interpreter she wouldn’t be totally isolated unable to communicate or make new friends. That’s crazy! Fiona was in a position where she was surrounded by 60 plus kids, all having fun, dancing, laughing, talking, but Fiona was unable to communicate with anyone. Theoretically Fiona could have gone and tried to play with some kids, but if they said anything Fiona wouldn’t hear them. It’s hard for kids to make new friends without a disability.
I’ve often heard people saying ASL is the first language for deaf people. Regarding Fiona I’ve heard from her teachers and other experts that English is Fiona’s first language. Because she wore hearing aids and learned English, (with sign language back-up always, but it was SEE sign) that English is Fiona’s first language. But if everyday there are multiple situations where Fiona can’t hear correctly with her hearing aid, but if she was fluent in sign language and there was at least one other person fluent in sign language always Fiona would never be without a way to engage. So, in a way, even for Fiona who has a hearing aid and residual hearing on her right ear, who spent the first five years wearing two hearing aids and is at grade level when it comes to English comprehension, sign language is the only way Fiona will have access to full communication consistently. We can’t count on the hearing aids or the environment to be one that lets Fiona have full access to language.