Mathewson Street
United Methodist Church
134 Mathewson Street Providence, RI 02903

 401-331-8900










Here is a sampling of the creative writing produced in ArtsReach's Creative Writing Workshops, led by Linda Louise King.  Enjoy!


*****************************
LOVE (by Alexi)

Pay attention.
I’m looking into you.
I don’t want to forget this part.
My inner beauty is yours
Your divine wisdom is mine
I see you
Love is nothing to strive for
We don’t have to strive for love
You are not my prize
You are my gift.

*****************************
LIGHT (by Alexi)

I am very lovely, but I did not always think so. There were many reasons for my take on myself,  but what it came down to was this. I could not see myself. Many tried to reach me but I was not willing to be seen.  If I could be seen, I could be hurt, yet invisible, I was condemned to loneliness.
            The first day I let in the light, I wept. I wasn’t weeping in pain or out of being hurt. My heart cracked open. And the gush of all there was inside poured out. I couldn’t even think about hiding in this experience. I felt relieved. At last my self imposed exile was over. I could be reached.
            I felt so intensely aware of the ways I can hurt, and yet the sharing of my vulnerability and the connections made, became a souce of inspiration. When I shared my experience other people actually recognized themselves. They opened up to me and I to them. I had never heard about such things, telling my story right out in the open and people cheering.
           I am a hero. We are a heroes. It’s simple. Just share who you really are, inside. How is it that this never occurred to me? If I go back to my old ways, I hope some part of me will remember this moment and pull me back to the possibility of receiving love.

 *****************************

THE EVENT THAT CHANGED MY LIFE (by Mike G.)

I had never seen an angel before. She came just in time. I was in a car, outside a fast food place, bickering with my friends. I just couldn’t relax.  A disheveled woman stood near the door.  I was about to scream at her. I thought she was begging. Something about her presence calmed me down.. With quiet reverence, she gave some found money to our over-stressed driver. I truly relaxed.
           
Even now, when I am stressed, and I remember that woman’s presence, it restores my peace. I was touched by an angel. I have learned that they’re never in disguise. They appear for you and your eyes only. The woman who taught me that angels are real had followed my friend out of McDonalds, to return the money he had dropped.

 *****************************

EULOGY TO A SWEET SOUL (by Mike G.)

We remember Mike G.  He was kind. He was sweet. He was mean. He was insulting as well as obstinate. We all feel sorrow for his passing. We all try to remember his goodness, even when he was not good, and mad at the person who was his friend.
            His friend said that Mike was a cantankerous S.O.B. Yes, he did, to the shame of all who were present. Yet, this was also the person who said. He always provided me with water when I was thirsty and flowers while I could still smell them.
            The tears begun in sorrow swept me up with joy, in rememberance of him. Hopefully, I should be so bold. Mike G. is a friend for more than his lifetime.

*****************************

VISUAL THESAURUS (by Vorteci)

Nelson’s shadow, like my own always seems dark, yet there is light (bright light) in it’s contrast. It’s a search within the bottomless pit of self. In its solitude it haunts me. I see a profile of self, of separation, of uniqueness, of quiet, loudly broken by its own silence. Still a silhouette, still solo, still strong. This is my shadow, unlike others. Sometimes frightened by its hollowness, still a reflection of substance fills its emptiness.
            Yet to see someone else’s form, I can deeply reflect the me, myself and I and the essence, imagined or real of other entities. One’s beauty, beyond self, imposed flaws, and knowing the scars and marring, is what we perceive to be true.
           
After self reflection and acceptance of others vitality, I can then enjoy my surrounding senses. Like the smell and texture of a rose. Like the shimmering waters of a brook. Like the face of life in a rock, a pebble, a boulder.
           
The anticipated taste of a fruit, the surprise of bitterness to the tongue, The garnishing of life eaten or absorbed,  its life force, its love light. As art created to stay forever in one’s mind, yet tightly held in form. The colorful ribbonous hues of movement, stagnant and fleeting grasp of moments. To stand at one’s crossroad and choose a path based on wisdom. So for whom does the bell toll?  It  tolls for me. And these are a few of my favorite things.

*****************************

ON HOLY GROUND (by Vorteci)

 Strangely, these moments are shared with strangers, but familiar souls. The sweetness of single words, conversing with people with special needs. Ha! They are most pleasant.
            I’m rewarded by “hello.” Experiencing someone’s worth with a story. Yes, greater is the pleasure when they share themselves. The limited world in which we live makes me honor what they say.
            Speaking of special movies, books and people. I feel proud that though somewhat socially limited, I receive the gift. My caregiver smiles from deep inside. Pleasure. This makes me a better person.
            Social politeness belongs to all. Should it fail a mean streak appears, but quickly vanishes in the wind, controlling me and the world. Oh what a pleasure it is to walk a mile, trot a stairwell, dash the time when late, knowing to always get an early start. Remember, some days are longer than others, but each day has its own presence.

*****************************

NEW LIFE NEW ME (by Sonny)

I’m looking forward to attending Pittsburgh Culinary Academy, which is a dream of my life, to become a restaurant manager. As far as I know things are going well. The school is going to set me up with a job, financial aid and an apartment. And the Sally May foundation is supporting my efforts.
          I had gone on line to apply to colleges. The Atlanta Culinary Academy referred me to the one in Pittsburgh. I was going for a bachelors since I already have an associate’s degree in culinary French cuisine. They recommended that I would be a good candidate for the restaurant management class.
            I am already a graduate of the Atlanta Culinary Academy in Dover New Hampshire. It took me two and a half years to earn an associate’s degree in 2004. I’ve continued to be a learner. Life is so short and I want to be a good role model for my nieces and nephews, to let them know that anything is possible, if you put your mind to it. My nieces and nephews range from 9 to 30 years old. I got a lot of them and I’m a good role model for my great nieces and nephews, 2 months to about 12 years old.
            I am 44 and I also recently graduated from a program called “Positive Speaking” for Gay men. We talked about life on life’s terms, relationships and how we can become more positive about ourselves, knowing that we are living with H.I.V.
            We were the first graduates of the program. There were eight of us. These meetings were held once a week for five weeks. This is what I got out of them; meeting new people who have the disease, as I have, meeting the staff, very nice people, watching videos about how we can be safe to tell our partners and friends about our disease, and also tell our family.
            Just joining that program showed me that I can get up and do anything I want to do. The disease is not going to make my life miserable. I am going to fight for my life. I’ve had this disease for twenty-three years and I’m still here.
            Before I leave the face of this earth, I want people to know the good Sonny that I am and my accomplishments from three colleges. I got sick and tired of being denied SSDI, six times. I was feeling bad and alone. I decided to get up and get a fast food job and then what came along was the college, and I’m going to pursue that.
            I’m happy. I’m not stressed, just a few problems with family members, but I’m going to live my life and keep going to the day I die. I have all the love I need. I’m loving myself and I have all the love I need from my higher power.

 ***************************** 

A LETTER FROM DOCTOR LOVE (anonymous)

Well, I look at it this way. Life is what you make it. I don’t take life for granted. It is what it is. It’s what you make of it. It’s up to you to put in respect and live the right way, as you go on in your life.
            My story is that I’ve been through enough, to understand enough, about what is going on in the circle. My life can be complex and I have learned to live with a lot of situations, in my life, that have been hard. And there’s times where I just want to call it quits, but I’m around strong people, that keep me going, that believe in me.
            And it makes my life a little bit more easier. I feel that without the people that I’m around, who believe in me and trust me, I don’t think I would be alive today. They give me strength, energy, hope, to carry on another day.
            Well my inner feelings is a strong spot for me. All I can do is express, in the best  way, how I get through, day by day. The word love. If you care about another person no matter what their situation. That’s love. Love and caring together can bring a whole lot to you.
            Love to me is caring for somebody, getting appreciated by them and getting feedback from them. The word love to me is the same thing as caring for someone, no matter who they are. You gotta have that in your heart. Being true to yourself means a whole lot. Being faithful and real helps you get through in life and in your situation, as you go on.
            I try to leave all my worries behind me and follow through with a brand new day. And the right people around me, it helps me get through that day. Every since I been in the community, I feel a lot of love, a lot of caring, a lot of respect, that keeps me going through another day. As long as I have that, I feel I can keep going.
            I’ve been through a lot in life to understand right and wrong. To keep that other person in contact with life, you have to express your feelings with them and help them understand where they’re at in their life. Help them stand up. Give them hope and make sure they never lose faith in themselves. Yeah.

  *****************************

THE PLACES I FEEL LOVED    (by Charlie)

I feel loved. Every morning I wake up, its the love of God granting me one more day. The first thing I do in the morning. Before I even get out of bed,  I give thanks for God giving me one more day, to meet and possibly help old friends and new people, to bring happiness, hope and love into their world. God gives it to me and I do my best to give it to them.
          I try to be open to everyone, listen sympathetically to their problems. If I can help them solve them, I try. If I can’t, I tell them not to give up hope. I wasn’t always like this. I was very self centered, concerned only with my own feelings, not my effect on other people. I didn’t care if I hurt them. It was all about me and I only changed when I needed a helping hand or a person to be there.
        It was like God reached out from the sky and said look how the world is. That’s when I began to notice and accept people, because in helping them, I helped myself. This didn’t happen overnight.
          Even though I had already been sent home by my supervisor at work on sick leave, I kept saying. I’m going to be all right. I’m going to be all right. I had worked with this group for over twenty years, as a fashion designer. We were like family. I’d go to their weddings and company outings but they always felt I did not attend enough.
          My color was bad. My body was broadcasting but I was refusing to receive the signal. If it wasn’t for the help of friends I wouldn’t be here. A guy who was sitting next to me in a bar I used to go to, the man who became my close friend, was the kind of person who talked a lot to other people, but only occasionally to me.
        He said. “You can’t go on like this. I will pick you up tomorrow and take you to the hospital. ”We weren’t even that close. We went to the same bar, that’s all. A forceful person, he was very gentle to me. And something about the way he spoke to me convinced me that he was right.
          I got so drunk that night, when I got home I just fell out. The next morning, I was dressed and ready. My friend showed up at about 9 am, casually dressed. He had been drinking too, in the same bar, but not with me.
          He drives me to the hospital. We didn’t talk much in the car. But I didn’t give H.I.V. a thought. I had friends around me who were dying of AIDS and here I was still out partying. I was in my early 40’s and I thought I was invincible.
          I get to the hospital, the emergency room, with my friend and a few doctors come in to examine me. They said if I had gone without medical care one more day I could have died. I had no strength. My mind was blank. My white cell blood count was down to 12.
         But for three weeks they didn’t know what form of pneumonia I had, because I had traveled abroad, to China. It could have been a virus. I had also visited India and Thailand during the same period of time. On these were business trips completing my assignments depleted me. But I was so committed to the job, I didn’t want to stop.
        That was 1994. Three weeks later they called the Communicable Disease Council from Chicago, because they couldn’t pin down what this was and why I wasn’t getting better. They had given me all kinds of drugs and I wasn’t responding. Three different doctors looked at my blood work and came to examine me and they all determined that I was H.I.V. AIDS, positive.
            My friend is coming to the hospital to see me every day. He thought he was going to be able to take me home and a month later, I’m still there. And my assistant from work would come  every day to visit me. I never told her or the company that I was H.I.V. AIDS.
          In 1994, AIDS was a relatively unknown disease that people thought they could catch by using the same cup or breathing the same air. I told them that my doctor gave me two options. I could either work or go on disability.
          My health was deteriorating and the nerves and cartilage in my hips had died. My bones actually rubbed together when I tried to walk. If they had not cured the P.C.D. I would have died. I was in tremendous pain.
            My company wanted me to continue to work for them, under the table. I did it, for about a month. They sent a driver to pick me up and bring me to work. And I could work three to five hours. I felt at home. My boss and my assistant showed me how much they thought of me by being there every day. I felt loved and needed. I wasn’t this worthless lump of disease. I was a gifted fashion designer with necessary talent, despite the disease.
            Things kept deteriorating. Now, I’m over 12 years diagnosed and within the last six to eight months I have noticed a deterioration in my overall health and my walking ability that I didn’t notice before.
            After the first year of my diagnosis, I realized I was alive because God had a mission for me. I told my immediate family about my diagnosis.         My parents were in their late 60’s. They only knew what they saw on T.V.  My brother and sister, all of them, coped very well. It was a blessing. They came to my house, constantly  to give me moral and spiritual support. Very few friends remained.
            The friend who took me to the hospital, unbeknownst to me,  had AIDS. He died about five years later. His legacy lives within me. He gave me the gift of understanding how a friend can help you to accept something that is too hard to bear alone
            He went back home when he was getting very ill, to be with his family, but he came over to say, Goodbye, and wish me the best. But he never mentioned once that he had AIDS. Then it was like being a leper. We couldn’t even talk about having the disease, even though he had saved my life. That's where my family came in. I could talk freely about the HIV and how I felt with them. They were more educated because my sister was a nurse and her husband was a doctor.
            I feel very loved. Coming to AFIA makes me feel loved, wanted and needed and has become an integral part of my life. Here, we all share the same disease and problems. You’ll always find someone who had the same problem and will discuss how they dealt with it. I come twice a week.Without this program, I would feel lost.
 

*****************************

Return to ArtsReach-Info ... or ...to  Homepage