Saturday, October 12, 2013

Up front in the sideshow




A month ago my life was seemingly stable.  Despite my symptoms I could manage in my power chair, take short walks and do physical therapy, with enough life left in me to perform in my band and commit to my studies for college at Temple for Media and Business. I’m not sure what happened, but I know when it happened. My band had performed a set at The Smokin Gun revue.   It was a burlesque showcase featuring the talents of women dancing the art of feminine seduction.  It differs from stripping because that dance form is designed by the male audience, where as burlesque is designed by the female performers. Submitting vs. Controlling, Expression vs. Exploitation. I’d always wanted to be a dancer, and having a medical condition, I’m no stranger to having to get nude in front of people.  My favorite part of Burlesque is the costumes; many are handmade and personally designed.  So much hard work is put into something people just want to see taken off and thrown to the floor.  We finished our set with “Dr. Verma.”, and being it a burlesque night, I let Jesse take of my top underneath of which I had our band stickers on as pasties.  There’s no better billboard than the female body.  If companies really wanted to make profit, they should pay swimsuit models to get tattoos of their logos. I wiggled a little in my walker, not enough to cause a fall or strain though.  The night ended, and I went home to my apartment to rest.  I woke up to another fire, they’ve been happening every two weeks or so here because PHA is too poor to afford security cameras to identify the arsons.  A while back I took up Buddhism and meditation to train myself mentally to stay calm and not pass out while having to exert myself in evacuation.  Although I was mentally in the right place, physically I was not.  I took a wrong step somewhere and I think something shifted in my back.  Even though I made it out safe, nothing has been the same since.

The first thing was headaches and extreme fatigue.  I slept for almost three days straight, and couldn’t sit up without the feeling that all the blood was out of my head and had severe pounding.  I went to the hospital at UPenn with a blood pressure of 65/30, and stayed there for a week till it went up to at least 85/40.  I had blood work and head to toe MRI’s that were all read to be fine, so I was released with them telling me it was just a strain and would get better.  Even with rest and drastically reduced activity, my issues seemed to worsen.  It became very difficult to move my arms, one day I could not move them at all and had to have a friend work my power chair buttons to get around Market Street. I’ve had the weakness in my legs since the tethered cord surgery, but arms as well makes it hard and dangerous to do just about anything.   I have attendant care coming in to help me with everyday tasks, but they cannot help me with the mental fog and lack of concentration and energy I am currently feeling.  Just writing this blog is almost wiping me out, and I’m supposed to be reading 30-60 pages a day and writing papers for classes.  The pain is agonizing, but I can’t take meds for it because then I cannot access my mind at all.  I had to cancel two upcoming gigs for Great Neck because of this, one of which was Disability Pride New Jersey, an event that meant a lot to me as well as many people I care about.  I had to stay back and not join my friends in the ADAPT National’s trip, a civil protest in Washington DC for disability rights.  I had even bought a bondage outfit costume to wear while we all handcuffed ourselves to the capitol fence. I wanted to paint on myself “Disability: The Ultimate Bondage experience.”  I learned a woman’s car had crashed into that fence after a police chase ended up in open fire shooting at the exact spot hours after my friends had been removed and detained for fighting for our rights.  I wish I could say I was there that day.

The only event I did not cancel was one that I had agreed to be a part of “Carnivolution”, a traveling burlesque sideshow event that I was feeling crazy enough to need to go to.  My friend Erik, who goes by the performance name of “Velvet Crayon” asked if I could play a part in a storyline he’d written for the show.  Erik has osteogenisis imperfect; he is the perfect tiny monster wheeling around in a koala mask with an electric guitar.  In his story he was the President who needed the help of his five ex wives to save the son of David Bowie from Satan in a tutu.  I was to play the first lady wife who commanded the army of cripples in a concentration camp, a place that teaches them to literally concentrate.  I sang a musical duet number with him, something he’d written that we had never practiced before the show except briefly in his van together as he drove me there.  Being my ride made him 15 minutes late, but he did not seem to mind. 

When I got to the venue I was helped in by Jelly boy the clown.  The stage was outdoors, but there was an indoor house like area with couches and pot smoking.  I saw one of my heroes Bunny Savage there.  I told him before I named my kitten after him, he was flattered, and relieved when I told him I wasn’t going to press for child support.  He looked different tonight then when I’d seen him around at the other shows in Philadelphia.  He told me and the others in the room that he’d lost a good friend, and on top of that his bassist suddenly died.  No one ever really knows what to say in those situations, but after which he mentioned that he hadn’t slept in days and the girl next to him responded

“O I know what you mean, that happens to me all the time.”

I wanted to say that too, but not about the sleep.  Just about the life being a cold hard bitch and leaving with anything you really care about.  I didn’t want to mention that there’s something very medically going wrong with me and maybe I’m going to drop dead tonight.  But I thought that too, cause I’m a dreamer like that.  Regardless of what was gong on in my central nervous fuck the system, I was going to do Burlesque.  I talked it over with one of the dancers, Miss Rose, who does costuming and burlesque shows around the city.  She was playing the part of one of Satan’s maids, but for my song she was my “helper.”  We discussed the different positions she could help me in in my walker, and the dramatic ways we were going to go about removing my clothes, such as her putting my hand to my mouth so I could bite down on my gloves to remove them.  The song I was performing to was one that Erik helped me choose.  It was “Old Fashioned Morphine”; the perfect fit for my scene.

The acts went by quick and delightfully traumatic.  Helios the fire twirler, Titano the strong man, and Miss Molotov the acrobatic pregnant clown.  People carrying men on their backs walking on glass, human suspension from their flesh, snorting insanity peppers on women’s stomachs, power drills up the nose.   I was not freaked out; I was freaked in.  Each act I imagined what it would feel like, to be on fire, to roll in glass.  In no way could it cover the headaches and spinal nerve pain I am always feeling.  I wondered if it could cut it away.  Then I saw a guy performing with Ehlers Danlos Syndrome, the condition that caused me all this splendor.  He showed the audience the same flexible poses I used to freak out my friends with (not as much now because the fusion rods limit much of my supermobility powers), and dislocated his hands for their amusement.  I got to speak to him afterwards, his fingers swollen, his smiling through the pain.  He told me he was supposed to be in a wheelchair at age 6, but has been able to work through the pain just by being psychotic.  I wonder if I had not gotten the Chiari and Tethered Cord aspects of the syndrome if I would be doing the same.  They cause me to be in a wheelchair most of the time now, so I do not experience the joint and body pain most EDSers do.  But I also do not experience the life.

Although I was having a hard time keeping my body up in the upright position, I felt for the first time totally stressless. Even though it hurt to do anything or everything, here it was accepted to be tortured, to feel fucked, to exist and accept how I really feel.  I find pleasure in the dark, sometimes the happiest thoughts in my head are

“Don’t worry, you’ll die someday.”

Just so I can go on with this living.

Everyone wants me to be positive.  Those who love me, those who look up to me, my friends and all those who help me, the Buddhists and the good people in the city.  I feel judged a lot, and like a lot is expected of me.  I can not not be relied on, I am not in charge.  I’m not driving this life, I’m just surviving.  I get 50-100 messages a day online that I do have the eye power to read almost any of, young people with disabilities wanting advice or creepy old men wanting a creepy new friendship.  I have no problem getting naked onstage for a theatrical performance of self sexpression, but I have a problem with getting naked in front of a man just for money.

I felt healed in a way last night.  When Miss Rose danced around with my floppy ragdoll limbs, I felt more control of self than I’ve had in a long time.  I would have been a dancer.  I am still a singer.  I can do all the things I would have, whether I’m really here or not.  If it hurts to move, move more.  The more it hurts, the less you’ll even notice.  Erik had a fluke happen in his sideshow act of electrocuting a pickle which caused him to get unintentionally electrocuted himself.  He could have died, but instead he was just paralyzed from the neck down, in massive pain and unable to push his wheelchair.  The guy with EDS put his swollen re-located fingers on his shoulder and told him he needed to just take it.  I was concerned for his life; he was concerned that he now couldn’t give me a ride home.  Miss Rose and another dancer took me home instead. 

My life has become a sideshow, it makes sense that this is the only place I feel like I fit.  I don’t fit in with the shells of society, that’s why I picked the name “Anomie” in the first place. I find myself almost tearing up in class sometimes, when the professor talks about making a place in the professional world and preparing for life careers.  The reality is no one will hire someone with my level of disability, and even if they did I would likely not be able to perform a job with any efficiency.  I will be stuck in the Munchausen help of Social Security for the rest of my life as my condition is progressing.   If it were just my body I’d have a chance, look at Steven Hawking, he is more able to live and discover than most able bodied people.  But it’s my mind too, the cloudiness of thought, the fog, it’s becoming hard to remember things, and I can only concentrate when I have not moved at all, otherwise the vertigo sets in and the world spins too much to even think.  I’ve seen many neurologists about this, they are useless, only giving medications that are CNS depressants that knock me out completely and make me sleep all the time and mess with my blood pressure even more.  Here in the sideshow, the less you think, the better.  Also mobility was not an issue, I got to be carried around by Titano throughout the night. No one is shy to suffering, or uncomfortable by the realities of pain, in fact, it is the amusement. 

It was a religious experience for me.  Jesus was a woman with a fake beard stripping down to a holy trinity thong with three hot dog dicks, and hell was the exit out the end of the night.  After I got home I heard the devil, that voice in my head saying to me

“Ok you’ve had your fun time, now go back to school and help the world become a better place.”


I really got to get my non-profit organization started.

Sunday, August 25, 2013

Failure is a possibility; surrender never is.


My neurologist awkwardly laughed when I told her I was going back to college in a few days.  I'm constantly spinning and in a ton of pain without medication, and for unknown reasons I have no more reflexes in my legs and vestibular ocular reflex. She says I need another MRI, and we're going to work out a plan for medication to hopefully raise my energy levels and concentration abilities through the neuropathic storm in my central nervous system. She doesn't think I'll be able to handle school right now, she didn't say that, instead I got a

"Well, good luck with that."

I know there's something very wrong still.  But I don't think it's curable.  Considering my track record, any more experimental surgery will likely make it worse, and take more life away from me.  In 2008 I dropped out of college with a 4.0 to undergo the first round of chiari surgery.  It's been five years of that.  Five years of not being able to build up any momentum in life, becoming trapped in others lives, feeling like a burden and hating myself for needing help with everything.  I'm finally free, living independently in the city despite my disability.  I use a power wheelchair for long distance transport, I have my own apartment through subsidized housing, and am having attendant care services set up through the government so i no longer have to put pressure on friends and family.  I can go to school again finally.  I don't even care how sick I am still, I'm not contagious, and I can take a lot. I just want the chance to get out during the day and feel like I'm where my life would have been had this shit never happened.

I don't know what going to happen to me or my future, but I'm glad I don't.  Just a chance is enough to keep me going.  A chance to feel whole.

I'm sorry to anyone I've hurt in this process.  I appreciate all of the help I've gotten to get here.  

Sunday, August 4, 2013

The Importance of "Disability Pride"



Tonight while eyeball waddling through the public wonderfucks of facebook I came across a post on the “Disability Pride Philadelphia’s page.  The admins unearthed an article written by accredited internet guest blogger Edward J. Heaton, titled “stupidity rolls on”, the level of profound intellect of content could be grasped within the first sentence:

“Just what the !#$(@#$?! is “Disability Pride” and, more importantly, why should we be throwing a parade for it?”

Heaton’s dispute is that a positive event such as a parade or festival should not be held for a negative aspect of a person’s life, supporting his argument purely on semantics of the word “disability”.  What I find funny is that myself and friends have said pretty much the same thing:

“Am I really “proud” to be disabled???”

As much as we’ve said that, we’ve never argued that they should cut funding and not celebrate.  That’s like saying “Our lives suck, so no matter what, we shouldn’t try to lighten up and have fun.”

Another conclusion that Heaton puts forth is that since there are so many cross disabilities, having an event for all of them together is futile because there is no “commonality”.  Many agree with him;  and there are not many general broad spectrum “disability” events being held.  Possibly unrelated, but there are also no big wave united movements going on presently to change barriers that all of us with disabilities must face, especially oppression on the social and socio-economic sub-levels of living.  We are the largest minority, and we are the most persecuted.  Overcoming suffering together is way more bonding than sharing a favorite sports team or a dislike of the Twilight series.  Also, saying that because there are different disabilities that they don’t belong in the same festival is like saying that Latin Pride Philadelphia has too many different countries involved for everyone to be considered the same ethnicity. Just because individuals do not share a culture does not mean they do not belong to the same community. 

You might be thinking that I’m biased and writing all this because my band got to perform at Disability Pride Philadelphia, and afterward was asked to play at Disability Pride New Jersey.  Well, you’re totally right.  Do you know how many people with disabilities turn to art and music for coping?  Many.  Do you know how many venues there are accepting to disabled artists? Almost none. When we play at local bars and music places around Philadelphia people either stare at me like a make-a-wish alien or drink away their attention and get angry that I’m not performing Pat Benetar covers.  Stages aren’t even wheelchair accessible, I have to be helped onstage for every show.  Not only having an accessible accepting venue to play at, but one where there’s going to be a large crowd of folks who can fully appreciate what you are doing is a super-yay for the talented creatives of crippledom.

Ok, but what is the point of a parade? 

I’d love to go on a profound literary march here, but I think it’s stated best with just saying: parades are fun; we need fun shit to do. 

Heaton says

“When I was growing up in the 1960s and ‘70s, there was no such thing as “Disability Pride”. What I and my compatriots growing up have pride in was achievement in spite of the disability.”

I totally agree.  There’s no pride in adult diapers and medicine pumps. We need not to focus on the disability itself, and perceive this as a just celebration of life. 

Unfortunately “achievement in spite of a disability” does not fit as well on a t-shirt,

just sayin,

and just because it doesn’t, doesn’t mean that it does not deserve funding and appreciation.


Saturday, April 13, 2013

Acceptance: the truest form of strength.


It’s nights like last night that make me realize how far I’ve come with accepting the symptoms with a neurological condition.  I woke up at four am with the majority of my vision gone replaced by squiggling zigzag colored lines, flashing lights, and fizzling dot images.  I also had nausea, head pounding, and heart palpitations.

The disturbances rarely take over this much of my field of vision. A few years ago when they got this bad I would run around freaking out trying to shut my eyes only to see them brighter.   I can’t run anymore, so that’s a plus, but even if I could it does not affect me like it used to.  I got up and went to my computer and did online math problems through the little circle of reality I had left.    It’s all about doing what you can, and not worrying about what you cannot control.  If I felt the symptoms were posing a critical threat, I have phone numbers I can call and a life alert system.  My vision has returned to its normal levels of semi-psychedelic now.  My head is still womping, but it’s a duller pulse of pain that I am very used to by now.  I recognize it as the ouch-ouch heartbeat in my head.  If I did not feel it, I would think there was something wrong.

I’m not sure if I’m strong or just desensitized.  I think it’s neither, I think it’s just acceptance.  Everyone has agony.  Yours is unique, but not special.  The moment you focus into it is the moment you lose sight of everything.  Keep to the little circles, and remember those you love.

Monday, April 8, 2013

Never give up. Never try.


After four years of not physically being able to work at all, I thought my dream had come true when I found part time employment at a center for independent living for people with disabilities.  Here was an environment where it was not only okay to be disabled and have limitations, but it was respected.  My job was to be a “Youth Initiative Coordinator Assistant”, a fancy title for a position that meant helping kids get through college despite their disabilities.  I certainly had not been able to up until now.  I felt like I was dong my part, and finally integrating into the real world.

I got my own desk and a name tag.  I could not legally use “Anomie Fatale”, so when I was not among staff I would turn the tag around so I didn’t have to see the name on it.  It felt like wearing a dead persons underwear.  I got to go around to schools and give presentations on leadership and advocacy.  I told the kids my real name now, and the story of how it became that way. Anomie is a term in nihilism for one cut away from society, but recently I was feeling more connected to the world than ever. 

I got a letter in the mail from social security.  I am on SSI recieveing benefits of 710$ a month.  I had followed protocol and told them that I would be working part time and gave them a list of hours and income.  I knew that for every two dollars someone makes, that one dollar is reduced out of their SSI payments.  I did not know that “dollars you make” did not actually mean dollars made, it meant dollars you earned before taxes.  My income was around 1,000 a month, but in actuality was 760.  Nevertheless, 500 was taken out of my SSI payments. Because I’m on subsidized housing my rent was increased, and part time work had a dramatic negative effect on my food stamps, and the payment of OVR for my college in the fall.  I was being punished for trying.  Barely breaking even, losing all financial assistance and aid, and exerting my body with a chronic illness when I could have stayed home in bed and not been hurting, this was the reward for hard work and will to succeed. 

If I leave my job now, I will have to live on SSI payment of only 200$ a month for two months until my benefits are reset to the original 710.  The woman I met with told me it’s based on a two month system after the individual has ceased work as I broke down crying in her office.  This is not enough to cover any of my living expenses, if I did not have help from my family I would become homeless and starve. If I stay at my job, I might not be able to have college paid for by OVR in the fall, and whenever my job does stop, it will be the same story of 200$ a month and destitute poverty.

We are in a society where submission and sloth are celebrated.  Disabled people that can work part time can’t really because then they’ll be impoverished and totally screwed. This will change someday, and I will not stop working until it does.  I might have to leave this job, but there will be another someday for me, in a better system and a more just world.  Until then I do not mind being an Anomie, cause seriously, fuck you America. Fuck you fuck you fuck you!!!!!!