Thursday, May 30, 2013

May 30, 2103-Volume 85: On Being Another Year Older and Maybe Wiser

The Adventures of the Blind/Low Vision/Visually Impaired (BLOVI) Girl- Volume 85:  On Being Another Year Older and Maybe Wiser

Another year older next week brings another set of reflections about where I am at this age. This birthday seems like a big one, 45. No more pretending like I am not squarely into middle age and more than half of my life is likely over. I should probably keep my age a secret. I get told I look under 40, so I could keep turning 39. But in reality I am proud of who I am, where I am and how at look. It seems to only get better. That is the focus of the blog.

I am writing this blog early because next week, on my actual birthday, I will be in NYC celebrating. We have no plans except for The National concert the first night we arrive. I did not think at this age I could be so excited about seeing a band, but I am intensely psyched about being able to have that experience and such awesome seats. We have no other plans except to wing it each day, staying in the living room of my best friend and his partner. We call it “doing NYC single moms on a budget” style. I call it spontaneous and fun. Again, this does not at all feel middle-aged., adventuring our way around the city and letting the days and nights unfold. But it seems like me.

I feel beautiful at 45. I feel confident and confortable in my own skin. This week I had a photo shoot to take new head shots. Amy, the hair and makeup person, was there the whole time. Fixing my hair and touching up my makeup. I was in four outfits, two hairstyles and various poses. It felt good to get that kind of attention. I felt like I was on a real model shoot and that any moment Rachel Zoe would swoop in to style me.  And it was good knowing Ashley would take incredible pictures to capture me at this point in my life. I felt like I was connecting with the camera, even though I had to guess on the location of it and the lens. I was able to hopefully show my inner glow. I think I have that at this age. That glow that comes from both the knowing and the liking of yourself. And in these moments I feel powerful. And being asked to walk in the celebrity fashion show at ColumbiaStyle Week is just another opportunity to “work it.” I plan to show my edgy style and fierce walk. I work hard on my body, working out 5 days a week. I eat really healthy and I take care of my skin. It does not come naturally. The results are worth all the effort, even though I can't really see my face or body that well. I can feel it and others can see it. That is motivation enough for me.

An additional perk is that I am finally getting some boobs. I had heard about this boob phenomena of women all of a sudden having bigger boobs in their 40’s. Some kind of peri-menopausal perk to make up for the rest of the crap.  But I had no hope of it ever happening to me. And I actually didn’t know it was happening until my daughter kept pointing it out. “Mommy, she said, you are finally getting some boobies.” I just never noticed. It is, for me, especially difficult to see going from little to slightly less little. She had been begging me to try on my wedding dress for her. So the other day I found it and donned it and twirled around. It was a little big in certain areas but it was tighter in the bust area. And that is what convinced me that maybe; just maybe I was a little bigger up top. I am glad I beat Sadie to my bust development stage. Hope this growth spurt continues. Remember the line in Grease, “10I must, I must I must increase my bust.”

Am I where I thought I would be at 45. No way could I have predicted that. As I have said many times I would have never thought I would be a visually impaired single mom of a 7 year old at this age. I have no crystal ball or magic wand so I just go with whatever happens. Hell, I don’t plan much of anything anymore. One of the ways I have gotten wiser is that I know that life is largely unpredictable and out of my control and I have to just go with the flow. Ride the current and not swim against it. Or float on top of all the churning waters below me. I have learned to relax and breathe and float. That serves me well every day. When I have obstacles both literally like that series of steps I have to navigate or figuratively like how I can rebrand my business. I am more apt to throw up my hands and say I give up and let the Universe do its work.

I am a better parent as I age. I think I am more patient, more observant and find most things about parenting fun in a dark comedy kind of way. There have been really rough times and I take things day to day. But as my daughter matures and gets wiser I have to be on my toes. She is in need of a sort of sparring partner or a wall to hit up against. And she is always in need of a referee. I can take on all those roles. And I see myself in her more and more. Now that I recognize myself I know what to do. I am blessed that I can give to her all the things that will support her hopes and dreams. Because I had those same dreams. And really she is a money making venture if I am realistic about the possibilities.

I define success differently at 45 because of both age and disability. There is a whole chapter in my book that talks about how I had to redefine what accomplishment meant and how I derived a sense of impact from my actions. Now I feel successful when it is a good day and there are no disagreements. Or when my clients show up or when I write something I like. Or when I have a good conversation.  All those are successes. All those nourish my soul. And yes that is the change in me at this age. I seek to nourish my soul and to do what feels good. I experience curiosity, wonder and amazement. That is what makes me feel alive and vibrant. When you lose your ability to be surprised, amazed or filled with wonder. When you lose your ability to laugh at yourself and at the absurd. When you lose your ability to giggle when you are happy you begin to get old and start the dying in little doses.

At 45 I feel young and alive. And maybe even a little on fire. I know myself. I am still learning what I am capable of. I am usually not afraid of what is going to happen next. I am hopefully optimistic. I can forgive and move on. And I can love, really love. I know what I want in a relationship and am really healthy in them. I am continually seeking to learn new things and learn about new people. And I am willing to admit my faults and weaknesses and be held accountable for my behavior. And I hold others accountable for theirs and keep my boundaries tight.

So, here is to being 45. It will sit well with me. And this will be my year. Maybe, if the Universe allows.
Keep Moving Forward,
Beth (BLOVI) Medlock

Wednesday, May 22, 2013

May 22, 2013-Volume 85: The First Chapter of Enlightened

The Adventures of the Blind/Low Vision/Visually Impaired (BLOVI) Girl- Volume 85: The First Chapter of Enlightened

This week I decided, while I am processing some points for the next blog, to share some of my manuscript. The 300 page tome I wrote with the working title of Enlightened: How Losing My Sight Gave Me Vision. As you know, I am in the query and editing process. I am proud of what I wrote and think it has a place in the publishing world. It is, to me, a story like no other. It is both dark and light and always hopeful. What I have shared is Chapter One: The Day of the Blinding.
  
Chapter One: The Day of the Blinding
Loss is permanent, untreatable and unchanging. We can be blind to this. I was, until I was blinded.

The day started out as a good day. In fact, it was one of the first good days in a month of bad days in a whole year of struggling. The theme of that year was loss-- divesting myself of possessions and of people. On that day I felt energized, so I got on my bike, let the sun shine on me and rode hard to think and breathe.

Later that day I had a date to meet a new person. I was in the throes of getting over the loss of someone I loved deeply, and on this day I felt the first blushes of feeling alive.

Just when I thought I was maybe, hopefully, turning the corner on the theme of loss, another loss occurred. On that day I left the world of the sighted and entered the world of shadows, of almost blindness. A healthy, energetic, fiercely independent, positive and confident woman with a mountain of doubts and a need to please became a disabled person who had to rely on others to do the basic acts of daily living. And in a word, it sucked.

I was training for a sprint triathlon. I had decided to attempt this new endeavor to challenge myself and to deal with the pain I was feeling from the loss of a relationship. I turned inward into my body and the self-focus it takes to get ready for an event, needful of the structure it provided that could contain some of my grieving and release some of my pain.  I thought that pushing my body and being in physical pain would distract me from emotional pain.

The year had been rough in general. Changing careers as a self-employed person in a failing economy had left me as a single mom at the poverty line. I sold anything and everything I had of value, which I discovered was not much. I sold my car, which was paid off and had held its value, as well as the diamond from my engagement ring, which I no longer wore, in order to keep our house and to keep my child in her private Montessori school.

I had just begun to turn a corner in my new endeavor, had begun to get by financially and gain some momentum in my career. And I had also begun shaking off the sadness and sludge of a two-year relationship that ended amicably, but felt like a crushing blow.

I woke up that day on July 2010 feeling energized and with a plan. And I could accomplish it because my daughter was at her Dad’s for the weekend and I had “me” time. My plan was to train, to push my body, to do some block sets of different types of exercises and then to reward myself by going out that night.  First I rode my bike about 15 miles.

I was one of those rare people that had never learned to ride a bike as a child. And they don’t make training wheels for adults. I had made a few bike riding attempts, the last at the age of 40, but I always gave into the fear of feeling really out of control. So on my 42nd birthday, I finally overcame my fear of learning to ride and I did it. I learned to ride with the help and guidance of my recent ex-boyfriend, one of the last acts of consideration, kindness, and support that had been the hallmarks of our relationship. In learning to ride a bike I felt a freedom not only of movement but also of overcoming fear.

And on that bike in the three weeks since the end of that relationship, I had been working out my feelings while riding, sometimes angry, and sometimes crying.

That morning I had a ton of energy, and so after the ride, I decided to keep challenging myself. So I went straight to a P90X intense workout using the DVD and setting up in the den of my house.

One of the segments I had been doing was the chest and back. So, on this day, like on others, I rigged my tube bands with handles to do the back work. The video shows a band that is really long, but I had two that were not so long, but had clips on the ends, so they could be clipped together and affixed to the doorframe to accomplish the back pulls. An ingenious fix to my problems, I thought, as I often rig things to work around a problem. And it had worked in the past.

But on this day as I was doing the last rep and “giving it my all” the door frame came loose and the part where the two bands were clipped together, which were made of plastic, hit me at a speed and force which I later found out was 200 miles per hour.

All I remember is a split second sound like a crack, then intense pain and the recoil of my head hitting the hardwood floor, missing the bricks around the fireplace by less than an inch. This all seemed like it took a second.

Then there was darkness, not a pitch black but a muddy gray of shadow. I was on the floor and then sat up as fluid gushed from my eyes into my mouth, which tasted both of salt and metal. I assumed the saltiness was from my eyes and the metallic taste was obviously blood. But in the mix I had no idea where the blood was coming from, just that the mixture was pouring from the top part of my head and eyes.

I knew immediately that this was bad, really bad. I had the sense of that and I knew I needed to get help. So I crawled on the floor, because for some reason I could not seem to stand up, until I found my house phone.

Then I had to figure out how to feel the keys and determine through a visual map where the 9 and 1 keys were. I made a few attempts and on the second I called 611, which I knew because it reached Time Warner Cable. On the third attempt I managed to call 911 and reported my accident to a dispatcher who stayed on the phone with me until the ambulance arrived.

I was lying on the floor holding the phone talking to the dispatcher, in a pain that I knew was there but did not register with the adrenaline pumping to keep me alert. I do not really remember what I told the dispatcher about the accident, but I remember using words like “hit hard in the eyes,” “cannot see,” “fell backwards” and “hit head.”

My side door, the one closest to me, was open so the emergency personnel would not have to break down the door. I remember being grateful they would be able to get to me.

I asked the dispatcher to call my sister, one of the only numbers I could remember. Thanks to the age of contact lists and saving numbers, I realized I knew only that one number and the number at my mom’s in Tampa by heart, which I remember thinking was pathetic because I used to know tons of numbers and they made them the length they did so you could easily retain them to transfer them from short to long term memory. But the one number was enough and they were able to reach her.

It took about 12 minutes for the ambulance to arrive. I know this not because I could see the time, but because I kept asking the dispatcher how much longer, how much longer, sensing I could pass out or become less able to articulate what happened as the pain became more and more overwhelming.

The ambulance, a neighbor, and my sister arrived around the same time and I knew it was bad based on their reactions. Even though I could not see anything, I could sense it and hear it in the voices of the paramedics and the fact they very gently strapped me on the neck brace and board because they needed to make sure I had not suffered head or neck trauma.

I remember being in the ambulance trying to describe what had happened and being asked questions about loss of consciousness and level of pain, which was the first time I realized that I was in excruciating pain. Sometimes we do not know how much pain we are in until someone asks us.

I was really in my body on that ride to the ER, my thoughts examining and assessing what was I able to see, where was the pain coming from, and what type of pain it was. I was so present, so in the moment, that I did not think of the next steps or the future, or of informing my ex-husband and my daughter. My only thought was that a really bad thing has happened, I caused it, and I am in incredible pain.

I wish I could tell you I was scared, but that was not the case. With the adrenaline pumping, I was in survival mode and there was no time for fear. That did not come until later, at the hospital, when the amount of damage I had done became clearer.

The ER was chaos on a late Saturday afternoon, which is supposedly the worst time to be in an ER. When they wheeled me in, they had no place to put me and initially I was in a hallway, just like you see on TV where there are people with medical emergencies lining the hallways but you are not really sure that actually happens. It does, on a late Saturday afternoon in a public hospital.
The ophthalmology residents saw me quickly. I got the feeling they don’t get a ton of eye injury calls. They were, from what I could tell, a little blown away and somewhat baffled by what they saw, or rather what they could not see.

I recounted my story again and they communicated they had never seen anything like this. A blunt force trauma to both eyes almost never happens and they were trying to figure out what it was that hit me and how it managed to do so much damage. I kept saying the tube bands were the hardest resistance and I was pulling from a distance of about 8 feet. And also I was really strong. I could tell they had this mix of “How cool!” with “We have no clue what to do.”  I heard them consulting on the phone with several attending physicians.

At the end of the retelling of the whacking-my-eyes-out story, I added, “I have no insurance.” And for some reason I felt it was important everyone in the ER attending to me knew this. I kept repeating that I was uninsured, thinking that maybe they would give me a colored wristband that signaled, “Don’t give this one any unnecessary tests.” Maybe I was afraid they would not treat me the same or cut corners or stick me in the hall. (But wait, I was already in the hallway).

This was a public hospital, so I figured that they treated many others that were uninsured in that ER, probably also hanging out in the hallways. But what I realized was that as a middle-aged white woman that was brought in as Dr. Medlock, they would not assume I was one of the millions not able to afford health insurance. 

I had been dropped from my ex-husband’s insurance as of June 1 of that year because of his remarriage and I could not afford a private policy. I thought I could be eligible for COBRA, but never got a letter or any option to sign up. Later I found the letters had gone to his new house and he failed to forward them to me. I’m not sure, even so, that I could have afforded it.

After the sixth or seventh time I repeated the no-insurance mantra (while visions of hospital bills danced in my head), the residents finally said, “It does not matter, we will do everything we need to do.” They also added, “Most of the people in here are uninsured.”

Later when I saw the billing person, I told her I thought I had a 60-day window for COBRA, and she said that was not true, but I knew better. I got on the phone with someone I knew from Blue Cross Blue Shield, them with the Employee Insurance program through the state.

And guess what? 57 of the 60 days had elapsed and we had three days to get me covered. So, the process of getting coverage began on that day and through the help of many, including someone walking the paperwork through the system on my last day of eligibility, I became an insured American.

If I had listened to the hospital and their incorrect information, I would have been stuck with over $30,000 in medical bills from just the hospital stay. I had tenacity, even in the worst of times. And I won the first in what would be a long series of battles. That was a good sign.

Much of what I remember about the ER was the pain, the neck brace burrowing in deep and the board under me hard and unforgiving, causing me more pain and an inability to move. Even more painful and jarring were the lights they kept shining in my eyes, which I could tell were there along with just shadows, and nothing else.

At some point my sister called my parents and my ex-husband. But the only story she could tell was that there was severe trauma and lots of blood in the eyes, so the doctors could not see anything and have no idea of how much damage was done.  At least I thought that is what she was saying. Later I found out she significantly downplayed the accident.

There was also an unknown about whether the recoil where I hit the back of my head or the blow to the front of my head had caused any brain trauma. My brain seemed to be working fine. I was alert, asking tons of questions and making snarky comments. I just needed the pain to stop, which I knew would be a whole other issue.

Pain and managing it is a theme in my life. My body does not respond to opiate painkillers. So for me taking a Vicadin or Oxycodone or anything else is like taking a placebo.

I know this from other hospital stitch ups, like my C-section. Let’s just say that by the time they got my daughter out, the epidural had worn off, so I could feel every stich going in and pulling through in the 45 minutes it took to close up the incision. And afterward they could not control my pain and I shook for 6 hours. There have been other post op and injury related sources of pain where no amount of painkiller seemed to work, or knock me out.

Knowing this about my body I knew two things: it was going to be deep breathing and meditation for my short-term future, and I was going to be asked if I was a drug addict.

So they hung the bag of Percocet and I thought, “Great, this one does not work.” After a while I got the pain level question using the 1-to-10 scale. “My pain is an 11,” I said.  And they responded with their first set of hems and haws and “What’s up with that?”

Then they switched to morphine, which I knew had no chance of touching the pain, but I thought, “Hell, I will give it a go.”  What I have learned is that you can’t actually say out loud things like “There is no way that crap is going to work,” because then they are assured you have a drug problem.

After the morphine there was another round of “How is your pain?” To which I answered coherently, “An 11.”  “Impossible!” said the doctors. “You should be feeling less pain and be a little sedated.”  “Do I look sedated?” I asked.  “Well, no,” said the resident, who would become my go-to doctor for the rest of the stay.

At this point I decided to recount my numerous other horror stories with the theme of “I am in a boatload of uncontrolled pain.” This, for some odd reason, led them to think I was drug seeking.

I had been through this rodeo before, though, so I answered the “Is she a druggie?” questions convincingly enough to get what I call “the good stuff.”  For me the good stuff is really not that good, but it does take the edge off. It is something that used to be an over-the-counter 19th century go-to drug. And it is the drug that most closely mimics heroin. It is called Dilaudin.

After the Dilaudin and some admonishments that this was all I was getting, because they could potentially put me in a coma-like state, the doctors asked the pain level question. So I said, “It’s about an 8 or 9.” They did not like my answer at all because doctors do not like for their patients to be in pain. They tend to want you to be injured in comfort.

“We have given you the maximum dose we can give,” they said. “To a normal human,” I thought.

So my pain containment strategies, which began in the ambulance, continued: not talking, focusing on meditating, and trying to stay in control. And I did this for not only hours, but days.

Finally, after five hours of waiting, I had my CT scan. A lot could have been going really wrong in the five hours I was waiting. I could have had a brain bleed.

Also, the trauma team was supposed to consult with me because I had experienced what they considered to be a trauma, but when the CT came back clean, they bypassed me. That ER sure was crowded, and I guess an eye injury did not seem all that exciting. But hell, I was blinded.

Then something way better happened. They took me off the neck brace and board, and that relief was almost as good as the sense of relief I felt when I defended my dissertation.  “Now my pain is a 7, lucky me,” I said to myself.

After 8 hours they moved me into a temporary holding bed. The ER was kind of like hell, so I guess this temporary holding room was like purgatory.

Even stranger was when I realized it was the room I was in when I miscarried 6 years earlier. The wallpaper, a specific picture, where the TV was placed in the room led me to a flood of memories and I knew that was the room.
Word of the freak-accident-girl was spreading like wildfire through the bustling ER, and so, lucky me, I got lots of unexpected pop in visitors to gawk. I was trying to ignore all of this, staying focused on breathing and meditating, but I knew it was happening. 

Then suddenly I was just bored, just lying in the hospital bed, wanting to move, and waiting for something to happen. The thing about trauma is that it can actually be pretty boring once the shock wears off. And I felt a mix of anxious waiting for something to happen and boredom for the rest of the hospital stay.

 


Wednesday, May 15, 2013

May 15, 2013- Volume 84: Why I Do Not Date (or at least the why I tell myself)

The Adventures of the Blind/Low Vision/Visually Impaired (BLOVI) Girl-Volume 84: Why I Do Not Date (or at least the why I tell myself)

I like to tell people that I have taken myself out of the dating scene. Mostly because I have not been on an actual date since September 2012. This is partly true. But it is also true that frankly, in Columbia, South Carolina, there is really nothing out there. Or nothing that looks good to me. The lack of interesting potential dating partners is the focus of this blog.  But first………….

My WTF of the week is the infestation of the flies--part three. Yes, for the third year in a row I have a fly problem. They are back and they are bigger than ever. There is an unusual and unfortunate story as to how the flies got into my house. And it is not pretty. My daughter is in her playroom trying to get out some art supplies when I hear a cry then horrible screaming—flies, flies. Here is what I see--large black things all over the floor, some moving, some not. She keeps horror movie yelling, “Flies, flies, get them.” So I move fast and grab the vacuum and begin sucking up the black insects I see which are partially on the floor and partially in a—wait, is that an Easter basket. It is the missing Easter basket from like 7 weeks ago. When I look in it I see lots of huge black things. They cannot be flies. They are bees or small birds. But somehow they are flies. Here is what happened, or at least my theory. The missing basket which had opened up plastic eggs and candies got trapped under something else allowing the flies to develop and feed off the sugar, making them the largest flies I have ever seen. Some of them died of gluttony and maybe lack of oxygen, but the strong survived. And they were monstrous. So I tossed the whole basket into the trash outside and continued sucking up flies. But, alas, some flew off, as flies implies. A friend arrived to bring over miniature knifes and swords for the diorama project (see next story) and I was still sucking up the dead and dying flies. She made a gagging noise at the sight. This was one of those moments I was glad that I don’t see so well. I wrote about that in my memoir. The fact that visual impairment makes gross things, like the state fair and operation shows, less gross. Now the loose super flies (not Superfly in a 70's way) are roaming freely about the house and I am guessing they are breeding. They are difficult to kill and I can see them well. It took me like 7 swats to bring one down. Another actually played dead and then arose to fly again. Vampire flies, and cunning too. There seems to be nothing I can do to avoid the yearly infestation of the flies. They very much like our house. Right now as I write I can hear one of them buzzing loudly and I need to kill it.

This week I can’t get enough of the fact that yes, oh yes; we finished the dreaded diorama project and turned it in. And we survived. But the last days of the project were tense. First, the Little Bear figure was late arriving. I had shelled out the extra 4 bucks to get it here between the dates of May 10 and 11. And yet, on May 11 he was not here. So I started tracking him. That day, when he was supposed to be at my house and being glued into the diorama, he was in transit heading out of Missouri. And this was worrisome. On Monday morning he was in Columbia being sorted. So I knew or hoped he would get here just in time to be placed in the diorama the night before the due date. I already concocted a backup plan of going on a hunt for a Native American figurine. When I got home Monday the mail had come and I tensely reached in to the mailbox, holding my breath. Yes, the damn little figurine was that important. There was a bigger package. That was my raw green organics detox products so I was momentarily distracted by my joy in being able to start my detox. But I saw no other package. CRAP. As I flipped through the rest of the mail there was a little bubble envelope. I knew it was our Little Bear and I ripped it open immediately and felt relief. But then came the task of getting him in the diorama. The day before my daughter and I had a meeting of the minds and decided there could possibly be other objects in the boy's pocket where Little Bear was brought to school. At first she said the book says there is nothing in the pocket, but the diorama needed to be jazzed up. So we glued coins and wrappers to the bottom because she said boys have change and gun wrappers in their pockets. And then she decided there should be a love note in there. Yes, still locking her up at 12. So the last step was Little Bear and his sword thing he would be using to cut his way out of the jean pocket. The day before my gagging at the flies’ friend brought over an assortment of play swords and knives (she has boys) and Sadie chose one.  And she gave us the idea to make Little Bear a marionette so he is the moving part. So we got the Popsicle stick and the string so he moves up and down to cut at the jeans. Popsicle stick, poke hole, string, easy peasy. Making it look like he was not hanging from a noose, not as easy. I gathered the string into a lovely belt and that worked. Last step, placing sword in hand. First I tried to tie the string around it, Impossible-could not see enough to do this. Then I tried to tape the sword in place. No go, it kept falling out. Then I tried regular Elmer’s glue. Also not working. I am gluing a plastic tiny sword to a tiny plastic figurine, how hard can this be. Really hard. An hour later I remember I have Gorilla Glue. I cannot read the label but know this stuff can hold anything. So I proceed to use the gorilla glue and get it on my hands which I think (looking back on the superglue peeling the stuff off your burning fingers days) is not a good thing. I can’t read the bottle but assume it says something like “Do not let glue come in contact with skin. If this occurs proceed directly to an emergency room where a plasma cutter may be needed in order to pry any stuck together body parts loose.” So I wash it off quickly and check the sword situation and it is still loose. There is no way this is happening. But then I held it there and blew on it and waited for some binding process to occur and after a few minutes the sword is no longer moving. And with a tug of the stick at the top of the diorama, Little Bear is bobbing up and down, sword erect, cutting the jeans. This is when I realize I forgot to make the cut in the jeans, which is also not easy but somehow gets accomplished. Victory is mine. Why does every project have to be so hard? Oh, I forgot, it’s because I can’t really see small things.  Another chapter in my book—my dislike of all things small like head lice, Playschool toys parts and of course, flies.

What I have written about thus far is much more exciting than the dating scene (for the over 35 crowd) in our famously hot city. A city which is less than tepid in the available not ugly, not unstable, not a cheater or a douchebag categories. My friend who does not go out much recently went on our ladies night out venture. She looked around and looked around and finally said, “If this is what is out there, I have not been missing much.” My friends and I often joke that if you throw a rock in Columbia you have no chance of hitting a decent looking guy. Take that rock to Charlotte and you can hit 10 good looking men in almost any bar or restaurant. There is also an adjustment in the hotness rating scale (1 to 10) for guys in Columbia. For example, a guy that is an 8 in comparison to other guys in Columbia would probably only be a 5 in Charlotte or any other larger city.  And I rarely go out and see an 8 or above Columbia rating. And if I do, the guy is like 25 and I could be his mother. So I do not date. Not because it would not be nice to go on a date, but because there are, or at least there seems to be, no date-able men. And also, as I have said time and time again, I am not very approachable. What I really think is that I am busy, selective and not at all willing to settle. I don’t have much time to go out and I am not crazy enough to Internet date again. The dating chapter of my book would scare any woman away from that.   So, I am going to meet someone the old fashioned way, through a mutual friend. And for a long time that just did not happen because none of my friends knew any decent available guys. But one day a friend did. And that may be a story for another blog. We shall see.

Keep Moving Forward,
Beth (BLOVI) Medlock


Wednesday, May 8, 2013

May 8, 2013-Volume 83: Query Quandary, Am I Really A writer?

The Adventures of the Blind/Low Vision/Visually Impaired (BLOVI) Girl- Volume 83: Query Quandary, Am I Really A writer?

In these past weeks, as I have been sending out queries trying to convince some agent, any agent, to want to represent my book I have realized that I am not very good in marketing myself. And, when it comes to being a writer, I have no track record. I am trying to sound convincing and self-assured and confident; things I usually am. But I am thinking, “What the hell am I doing. Am I really a writer?” That process of owning my identity as a writer is the focus of this blog.  But first………….

My WTF of the week is that we got two school projects in the last 3.5 weeks of school. And one is the dreaded diorama. I knew this would be coming at some point, along with the volcano project I had hoped would come later. All year I have finessed my way through helping my daughter with school projects and some have been challenging. But all of them I could manage with my limited vision. But a diorama is not an easy task because it contains small things. And I cannot see small things. The project came with four pages of instructions, which would have taken a long time to read with my magnifiers or the zoom camera. It is also on green paper, making reading it even more difficult. So I did the right thing and made my daughter read the instructions, given it is her project. Let’s just say she paraphrased the instructions so that I have some idea of what we are doing, but not really. We have a scene from the Indian in the Cupboard. It has to be three dimensional, and have at least one moving part. Great, small things with moving parts, not at all a problem. So we Google images of Little Bear (I thought that was an actual bear cartoon) and see that there is a Little Bear action figure from the movie, which is three dimensional and I am hoping has moving parts. This figurine came with the 1995 VCR tape (for you young folks, in the olden days we had tapes which came before the DVD) and they are collectible. But I manage to get one on eBay and pay a few extra bucks to get it here at the last possible second to glue him into the scene. Then we come up with a great idea for the diorama which involves my ripping up some old jeans. So even though I am still not sure what we are actually doing or will be able to really see the final product in its awesomeness, we will have some kind of diorama to turn in next week, And with that the first grade projects will hopefully be completed. I may not make it through second grade.

This week I can’t get enough of the fact that someone, somewhere has decided I am a local celebrity who will be walking in the local celebrity runway show at ColumbiaStyle Week. That is right folks; I will be walking my kind of blind ass down a runway. Let’s be clear, I can stomp down a runway-attitude and all. But I probably, with the lights down and cameras flashing (I am assuming it will be am actual runway show and that there will be paparazzi of some sort) there is no way I will be able to see the runway or the end of it. But you know I love a challenge and have a plan. I will count steps. One time or two down the runway making sure I stride the same way and in my best “Miss J would be proud” walk, I should be able to get to the end, look fierce and walk my ass back to from whence it came. And don't think I won't be jockeying for a really good outfit to wear. I will fight like it’s a Filene's basement super sale or one of those bridal dress smack downs. I am also having new head shots done. My last pictures are great and these really do, hopefully still look like me. But we all know that I have no clue since I can’t see myself that well. It has been 2.5 years and even though I have not aged a bit (I had some assistance here) it is time to have updated pics. So I have to make sure my hair is freshly colored, my eyebrows are not unruly, my manicure is flawless and my skin is glowing from a microdermabrasion. I have scheduled all these interventions with precise timing to be ready for the headshot day looking as best as I possibly can. Sadie is getting hers done too. She has decided to be the next a little less Latina version of Selena Gomez. So I am supporting her in her dream.  But since she just naturally looks good I will wash and straighten her hair and put some lip gloss and a little blush on her. Oh, to be young again. Recently she was doing a friends hair on the playground and the helpless little girl says, “Ouch, you are hurting me.” And my daughter says, “Beauty is pain.”  How did she learn this (it was not me)? But she is right. It also takes time and money. And you know what they say-it takes a village---people.

For the past few weeks I have queried agents, trying to get them to represent my book, which at this stage is only a manuscript. Like that bill, on Capitol Hill who wants to be a law someday. And my not yet a book is all about me. So I am trying to sell me as a central figure in a story and me as a writer. And I am trying to prove I have a platform which essentially means I can make people be interested in, fascinated by and ultimately care enough about me to buy my story. And I am thinking two things, one I am not very good at tooting my own horn and second, I have not considered myself a writer. So to sell myself as a writer is a double whammy of being out of my comfort zone. Way out.

I write. I put words on paper (well actually type them into a computer). My words taking the form of book, of poetry and of lyric. In all these ways I am expressing my creativity. But does that make me a writer, a poet or a songstress. I have published nothing. I have not even sung my songs or read my book or performed poetry in front of others. Very few people have seen my work. This includes this blog thing I do each week. But I am ready to share my manuscript. In part because some of it has been shared in blogs and in my talks and in part because I know what I did can have impact. But I have to see myself as writer to sell what I know. I not only have a damn good story, I wrote a damn good story. How did I do this?


The truth is, and I have come to realize, that I have been writing most of my life. I wrote in my super-secret journal as a teenager and also wrote sons and poetry in my 20’s. I wrote articles through undergrad and graduate school. I wrote countless papers, a comps paper, a dissertation proposal and a dissertation. After school I wrote an evaluation manual and countess evaluation reports, strategic plans and community assessments. I also developed at least 15 different training programs. As a life coach I have written workshop materials for 10 different workshops and almost four years’ worth of newsletters. I have written thousands and thousands of pages. Some of which, holy crap, have been published. But nowhere in those thousands of pages did I see myself as writer. I saw myself as angry adolescent, student, and consultant and life coach. It was work and it was academic or evaluation based or written for money at the end of a process. It was not creative expression of my thoughts or opinions. Or was it, because there is no way to be objective.

But not even when I began to blog and blog and blog did I even consider I was writing or that I was a writer. “I have a blog”, I would say.  When I was writing the book I still did not consider myself a writer. I was compelled to slice myself open and rip out my guts in a process of healing I thought could help others. My accident and its aftermath was a good story with lessons to be learned and maybe it was even inspirational. When asked if I would write other books my answer was always, and may still be, “No.” I am supposed to tell this story and it is the only one I have to share.

But again, that is not really true. Each week I write new material and think of other topics and yes, even other books. And I am compelled to write. I process my emotions through poetry and song first and then through narrative. And more than anything the need, the desire, to write words makes me a writer. And according to my creative coach Cassie, a good one.

So now that I am a writer I must put on my writer sash and mix and mingle with other writers. Holding my head high and wearing my heels higher. Dipping my toes in the waters of the published and learning their secrets. This means sharing my work and selling myself as author. And to do that I must write a new script for myself, create a new avatar. It looks like there is more writing to be done. And maybe another version of my query letter.


Keep Moving Forward,
Beth (BLOVI) Medlock

Wednesday, May 1, 2013

May 1, 2013-Volume 82: I am Crass and Past the Point of Caring

The Adventures of the Blind/Low Vision/Visually Impaired (BLOVI) Girl- Volume 82: I am Crass and Past the Point of Caring

Recently I was accused of being crass and I have decided to own it. I tend to say what I am thinking. I love to be snarky. And my mind can be in the gutter, I admit. To me being able to be crass and quick witted is a sign of intelligence. Think about Bill Maher, Jon Stewart, or Tina Fey.  They are funny because they are wicked smart and they really don’t care about what other people think. I have some of this, passed down to me genetically. Two recent outings typify this point.

On a shopping trip yesterday my dad started reading the labels off my Trader José purchases and was I surprised. There is a huge perk in being visually impaired. I can’t tell what food is in the Trader Joe's unless I really spend time putting on my magnifiers and holding each item up to my nose. And that just looks weird so I don’t do it. This means I don’t go crazy buying chocolate covered anything. I tend to bit the same items over and over when I like them and memorize their location in the store. Thus, I don’t impulse or over buy. Being visually impaired also means I can’t read the labels. So I don't look at the calories or fat or carbs or sugar. I just tend to buy items that sound healthy and taste good. But then I went shopping with my Dad, reader of all labels and shunner of all things not good for you. And he burst my bubble.

Some of the labels he read in the store. After I put two containers of my favorite dip (the spinach and kale in Greek yogurt), he reads the label. “Oh no” he says. “What does that mean” I say. “You don’t eat some of these ingredients.” “What ingredients?” “It just has something in it you don't like”. “What is it”, I demand. “It has sour cream”. My dad despises sour cream, but I just don’t love it. “What about the calories” I ask. “You don’t want to know that” he says. A bad sign. After I place more items in the cart he ceases the label reading. But once we are unpacking at home it starts again. “Holy crap”, he keeps saying. “What is it now?” I say. “This trail mix has 1200 calories in the bag and these power berries have like 1500 calories and 150 grams of sugar.” That explains the day my daughter ate the whole bag and went nuts. After I shove about four pieces of the dehydrated coconut strips in my mouth he says “This bag is like 1300 calories and it looks like it has about 20 pieces.” And I am still chewing. And before I could stop and think I ask, “What about the Joe Joe's.” Another “You don’t want to know that; you really can only eat two a day.”

What prompted all the calorie talk was that my dad had watched a PBS special on health and longevity. He said that the conclusion was you are healthier and live longer if you reduce calorie intake to no more than 1600 calories a day. Maybe I am screwed in this case. I have eaten 10 to 15 Joe Joe’s in one day. And half the container of dip and about a third of the bag of chocolate covered power berries. I am so glad they were out of mochi that day because I still have no clue how many calories each one of those sugar doughy ice cream balls of wonder have and they have not been ruined by my knowing their dirty little calorie secret. I am going to continue to eat my favorite things and I don't give a damn what is in them or how many calories they have. Ok, maybe I will eat them in smaller portions.

Another fun outing occurred this past weekend. My once a month night out where I again realize I am old enough to say whatever the hell I want to practically anyone. I think I have just moved past the point of caring. My partner in crime and I are bold when we go out. On our last outing the night started out great when one of our favorite bartenders (and by this I mean really cute) has a wonderful reply to us asking if there are any specials. He says, “I am on special.”  To which I say “I’ll take one of those” and my partner in crime says “to go please.” Ha, ha, we are all laughing. But really I will take that to go, please.

Next my partner in crime beckons over a man with a prosthetic leg. She wants to know what happened. He says “Iraq” and tells the story of what he does now, which is work for the company that sells his prosthetic. She asks how far it goes up and can she touch it. I must admit at this point I started to feel protective of him, thinking “don’t ask him that”. I think I identified with him because we were both disabled. And this is the first time I get that. He says “OK”, so she gropes him until she reaches his hip. Then we ask about when he does not wear the leg. By this point really in shape Italian guy from Pennsylvania who is a little handsy comes up to join the conversation. Turns out one of the times he takes off his leg is to let’s just say make love, although they seem to prefer using the f-word here. We ask him what would happen if it was on. This is when the other guy, who also sells the prosthesis, says “Because we could program it to do all sorts of things during the making love session like kick you in the ass.” This leads to a derriere discussion which led to us demonstrating our in shape parts and some patting. Which is also the most action I have gotten in a long time.

The conversation yields some gems. Talking to the veteran makes me think. Loss of limbs is the number one injury for combat veterans. Number two is eye injuries and visual impairment. Then, holy crap, I think of a totally new way to pitch my book. I also was not questioned when I said I was 36, got compliments on my looks and yes, for the first time in a long time how I looked like Marisa Tomei. She is always my Facebook doppelganger picture.

And that was just about 20 minutes of the evening. Other conversations of the night included artistry in grooming, strange pictures appearing on partner in crime’s phone, TED talks on internet pornography (watched it—The Demise of Guys) and how some guy, on his 50th birthday, was going to find someone half his age and punch them in the face. We saw him later an asked him, “Hey, have you found someone to punch yet.” “Why do you think I am walking fast” he says. Oh yes, another strange and funny might in the Cola town.

Next outing will be a mom’s night out I am organizing. I will be on my best behavior. And if I am not I am going to have some rules; Fight Club rules. The first rule of mom’s night out is that you don’t talk about mom’s night out. The second rule of mom’s night out is that you don’t talk about mom’s night out. I will blend that with what happens on mom’s night out stays on mom’s night out. If I don’t establish some rules I will never be able to show my face at my child’s school again.

Saying what I feel and being crass is part of my genetic makeup. Case in point, my mom says to me, after my last boyfriend dunked me, “I thought he looked like a stork, was boring and really did not look like he would be good in bed.” My grandmother had a recent hospital stay and my sister went to visit. She said she knew our grandmother was feeling better because “She is back to calling everyone a shit-ass.” The first song my grandfather taught me that I can remember was, “In 1492, Columbus had to poo. He sat on the grass and tickled his ass, in 1492.” And of course my dad and his siblings are the superstars of scatological humor. And my Dad is just snarky. After the Trader Joe’s trip my daughter shows him the bikini picture I have on the frig and says “This is what mommy wants to buy.” Dad says “Not if she keeps eating this crap.” And when I say “Tomorrow is May Day, and I am a maiden so should be dancing around a May pole”, he says, “Yeah, right.”

And I contend my snarky wit is because I am the offspring of a long line of smart, wise ass, quick witted ancestors who seemed to lack the ability to censor themselves. And I am glad for it. Except that my daughter has this gene. Maybe I will think differently about it as she gets less cute and mouthier.

Keep Moving Forward,
Beth (BLOVI) Medlock