Please read my latest blog here. http://adapadvocacyassociation.blogspot.com/2011/03/adap-crisis-lawmakers-stop-bickering.html It covers the ADAP Crisis and the harshness of partisan bickering. I wrote this for the ADAP Advocacy Association (aaa+).
The idea behind this blog is to show the world that HIV doesn't have to be a scary topic and it must be discussed. I talk about my life and how much of it I have to live. I welcome all comments and questions from followers and supporters out there.
Showing posts with label ADAP. Show all posts
Showing posts with label ADAP. Show all posts
Wednesday, March 30, 2011
Friday, November 19, 2010
BEING RESPONSIBLE IS IRRESPONSIBLE
At least that is what I'm starting to believe in our country. I'm a responsible citizen: I pay my taxes, I bring home an honest paycheck, I take care of my heath, I volunteer, I even vote. However, I am starting to understand that trying to stay ahead and doing the right thing is working against me.
Let me explain. I work a full time job through a temp agency. The agency has an extremely limited benefits package that will not cover my specific HIV medical needs. I also work part time at night at a hotel of which is my only medical coverage. This part time gig is a union job. Regardless of your opinion of unions I will say this: I believe unions are necessary solely for the purpose of employers and employees having equal opportunity in an environment that would have otherwise. Sure, there are abuses on both sides, but I digress. My union benefits differ from regular medical benefits in a number of ways. I cannot choose my medical care. Instead, it is required that I see their doctors and their specialists in order to be covered. The problem with that is that it can take as little as a few months to see a doctor for a sore throat. Their response is if you need to seek help go to the emergency room. Being HIV positive and required to submit bloodwork every three months in addition to my primary care follow up of said work, it is a necessity that I am able to schedule my appointments in a reasonable matter. Of course there is no HIV specialist under my medical plan. Finally, if I want to see a specialist not only would I need a referral to see that specialist (every time I need to see him), but I would also need a referral to get bloodwork drawn (again, every time I need it done.)
For the time being, I have been paying for my blood work as well as my doctor visits out of pocket. Thousands of dollars later and I still owe a significant amount. Unfortunately, until we find a cure, or I quit my jobs all together, this cycle will have no end. Naturally, I can see how the world outside of HIV take this illness less and less seriously given your "once-a-day" medications and living longer lives. This side of the epidemic isn't spoken about enough to the general public. I've had endless meetings with social workers over months on end. It has come to the point where I have pleaded with them with what I should do. "Give me an ultimatum," I say.
Scenario One: IF I quit my part time job and have no medical benefits I will qualify for New York's ADAP (Aids Drug Assistance Program.) Consequence to Scenario One: my income will be significantly less and I may be forced to leave my home and move back in with my parents. My temp job is above the poverty level, but just enough to barely make ends meat, so I don't qualify for government assistance. Food will become a luxury. My parents live outside New York City, and our state is under the radar for falling into the ADAP "waiting list" category. For further information regarding ADAP and the waiting lists (if there is one in your state) and what you could do to help, click on the website here: http://www.adapadvocacyassociation.org/
Scenario Two: IF I keep both my jobs I will not qualify for ADAP. Consequence to Scenario Two: Not only will I run myself down with fatigue working 60 hours a week like I currently do, but I will somehow have to conjur up $750 every three months. At least my medicine is still covered with my current part time job. That is, they haven't questioned my prescriptions at this point. Praise be to God that I don't have to ever pay for my medications out of pocket. Seeing how much each individual pill costs turns my olive skin to snow white.
There should be a law of some sort where employers only have a certain time frame to decide whether or not they'd like add a temp employee to payroll. There should be consquences should they string hardworking professionals along. Maybe there is, but I doubt it.
I haven't reached my offical one year mark being HIV positive and I'm already exhausted. I'm tired of closed doors and "we can't help you" answers. I try to do the right thing by working hard and paying my dues with no end in sight. I was once taught to aspire to a world with a house and a white picket fence and landscaped gardens. For all the Americans on waiting lists, live hours and hours away from medical care or try to do the right thing and still get spit on like me I say this: even in a metropolis like New York City, you can feel alone.
We really are all in this, together.
Let me explain. I work a full time job through a temp agency. The agency has an extremely limited benefits package that will not cover my specific HIV medical needs. I also work part time at night at a hotel of which is my only medical coverage. This part time gig is a union job. Regardless of your opinion of unions I will say this: I believe unions are necessary solely for the purpose of employers and employees having equal opportunity in an environment that would have otherwise. Sure, there are abuses on both sides, but I digress. My union benefits differ from regular medical benefits in a number of ways. I cannot choose my medical care. Instead, it is required that I see their doctors and their specialists in order to be covered. The problem with that is that it can take as little as a few months to see a doctor for a sore throat. Their response is if you need to seek help go to the emergency room. Being HIV positive and required to submit bloodwork every three months in addition to my primary care follow up of said work, it is a necessity that I am able to schedule my appointments in a reasonable matter. Of course there is no HIV specialist under my medical plan. Finally, if I want to see a specialist not only would I need a referral to see that specialist (every time I need to see him), but I would also need a referral to get bloodwork drawn (again, every time I need it done.)
For the time being, I have been paying for my blood work as well as my doctor visits out of pocket. Thousands of dollars later and I still owe a significant amount. Unfortunately, until we find a cure, or I quit my jobs all together, this cycle will have no end. Naturally, I can see how the world outside of HIV take this illness less and less seriously given your "once-a-day" medications and living longer lives. This side of the epidemic isn't spoken about enough to the general public. I've had endless meetings with social workers over months on end. It has come to the point where I have pleaded with them with what I should do. "Give me an ultimatum," I say.
Scenario One: IF I quit my part time job and have no medical benefits I will qualify for New York's ADAP (Aids Drug Assistance Program.) Consequence to Scenario One: my income will be significantly less and I may be forced to leave my home and move back in with my parents. My temp job is above the poverty level, but just enough to barely make ends meat, so I don't qualify for government assistance. Food will become a luxury. My parents live outside New York City, and our state is under the radar for falling into the ADAP "waiting list" category. For further information regarding ADAP and the waiting lists (if there is one in your state) and what you could do to help, click on the website here: http://www.adapadvocacyassociation.org/
Scenario Two: IF I keep both my jobs I will not qualify for ADAP. Consequence to Scenario Two: Not only will I run myself down with fatigue working 60 hours a week like I currently do, but I will somehow have to conjur up $750 every three months. At least my medicine is still covered with my current part time job. That is, they haven't questioned my prescriptions at this point. Praise be to God that I don't have to ever pay for my medications out of pocket. Seeing how much each individual pill costs turns my olive skin to snow white.
There should be a law of some sort where employers only have a certain time frame to decide whether or not they'd like add a temp employee to payroll. There should be consquences should they string hardworking professionals along. Maybe there is, but I doubt it.
I haven't reached my offical one year mark being HIV positive and I'm already exhausted. I'm tired of closed doors and "we can't help you" answers. I try to do the right thing by working hard and paying my dues with no end in sight. I was once taught to aspire to a world with a house and a white picket fence and landscaped gardens. For all the Americans on waiting lists, live hours and hours away from medical care or try to do the right thing and still get spit on like me I say this: even in a metropolis like New York City, you can feel alone.
We really are all in this, together.
Sunday, August 22, 2010
PRIDE: DOES IT HOLD NEW MEANING?
The year was 1969- a year that’s forever frozen in LGBT history worldwide. The location was Greenwich Village, New York City. It was a hot summer night in June when we came out of the “closets” and stood against the corruption of the police and said we were not going to hide anymore. Windows were smashed, trash cans were burned, people were beaten and arrested, but that didn’t stop the now called “pioneers” of our community from getting their voices heard. These radical days mark a time period when anger and frustration lead us one step closer to our freedom- the freedom to be who we are today.
It’s a shame that I was not around at that time, but I am fortunate enough to know some of the gentlemen who were front and center of the Stonewall Riots. To hear them speak so passionately of their eye witness accounts today is such a treasure for me because I know if I was there I would be right beside them. It’s been forty years since the first Gay PRIDE Parade was held and I had wondered if my generation has become complacent and forgotten what so many of our brothers and sisters before us had to go through to allow us to parade around city streets in flashy rainbow colors and Speedos? Even more so, with my generation practicing riskier behaviors and taking HIV less seriously because of their “treatable-with-one-pill-a-day” attitudes, have we lost all context of the word PRIDE?
I’ll admit when I was in my early twenties I used PRIDE as an excuse to party all day and to socialize. Back then, I was still getting comfortable with the idea that I was a gay male. I thoroughly enjoyed being able to hold a guy’s hand in public without hesitation. Then, as PRIDE’s have come and gone my own personal attitude of the holiday became stale to say the least- until this year’s PRIDE. This year was the first time I was going to celebrate the events being HIV positive. I worried for days prior as to whether I can truly have a good time or was my focus was going to be on my HIV status? Can I remember that I am still a gay man who would one day hope to see a world where we are treated as equals?
There was only one way to find out. That Sunday afternoon I got my PRIDE outfit together, which consisted of nothing more than a white beater, suspenders, and cut up denim shorts, and headed downtown to the Village to meet up with friends and watch Manhattan’s 2010 PRIDE parade. For those not familiar, this particular parade lasts for several hours. I took many pictures of various floats and spoke with many individuals all of which share different ideas of PRIDE. Many of the marchers held political signs explaining current corruptions of government’s treatment of the LGBT community. However, I couldn’t help but notice that there were just as many signs that pertained to the HIV and AIDS community. These leaders were creating awareness to all on the importance of issues regarding healthcare, prevention, HIV and Congress, etcetera. A couple of cocktails and introductions later it dawned on me that I was having a great time! I quickly realized that my definition of PRIDE has not changed because I have HIV. If anything, it has enhanced its’ validity and I felt welcomed again in my own world- a world that is no longer suitable for 1969, but for the present day LGBT community.
I am still new to the HIV community, relatively speaking, but PRIDE has reminded me of my passion for wanting to make a difference in both equality as well as the treatment of this chronic illness. I want the world to know that I am an openly gay male who is NOT a second class citizen. I want the world to know that I have HIV and there is no reason to fear me. I want the world to know that Washington’s plan to cut healthcare budgets for government programs (such as ADAP) is unacceptable and I refuse to have my voice go unheard. I want to the world to know that I plan to educate the generations to come how to take care of themselves and live healthy lives. But most of all, I want the world to know that I’m here.
The Stonewall Riots is a reminder that even though we celebrate forty years of being openly gay that there are still battles to be fought in 2010. With the help of my generation it is time for me to give back what was privileged to us back in 1969- the freedom to be ourselves no matter who we are.
It’s a shame that I was not around at that time, but I am fortunate enough to know some of the gentlemen who were front and center of the Stonewall Riots. To hear them speak so passionately of their eye witness accounts today is such a treasure for me because I know if I was there I would be right beside them. It’s been forty years since the first Gay PRIDE Parade was held and I had wondered if my generation has become complacent and forgotten what so many of our brothers and sisters before us had to go through to allow us to parade around city streets in flashy rainbow colors and Speedos? Even more so, with my generation practicing riskier behaviors and taking HIV less seriously because of their “treatable-with-one-pill-a-day” attitudes, have we lost all context of the word PRIDE?
I’ll admit when I was in my early twenties I used PRIDE as an excuse to party all day and to socialize. Back then, I was still getting comfortable with the idea that I was a gay male. I thoroughly enjoyed being able to hold a guy’s hand in public without hesitation. Then, as PRIDE’s have come and gone my own personal attitude of the holiday became stale to say the least- until this year’s PRIDE. This year was the first time I was going to celebrate the events being HIV positive. I worried for days prior as to whether I can truly have a good time or was my focus was going to be on my HIV status? Can I remember that I am still a gay man who would one day hope to see a world where we are treated as equals?
There was only one way to find out. That Sunday afternoon I got my PRIDE outfit together, which consisted of nothing more than a white beater, suspenders, and cut up denim shorts, and headed downtown to the Village to meet up with friends and watch Manhattan’s 2010 PRIDE parade. For those not familiar, this particular parade lasts for several hours. I took many pictures of various floats and spoke with many individuals all of which share different ideas of PRIDE. Many of the marchers held political signs explaining current corruptions of government’s treatment of the LGBT community. However, I couldn’t help but notice that there were just as many signs that pertained to the HIV and AIDS community. These leaders were creating awareness to all on the importance of issues regarding healthcare, prevention, HIV and Congress, etcetera. A couple of cocktails and introductions later it dawned on me that I was having a great time! I quickly realized that my definition of PRIDE has not changed because I have HIV. If anything, it has enhanced its’ validity and I felt welcomed again in my own world- a world that is no longer suitable for 1969, but for the present day LGBT community.
I am still new to the HIV community, relatively speaking, but PRIDE has reminded me of my passion for wanting to make a difference in both equality as well as the treatment of this chronic illness. I want the world to know that I am an openly gay male who is NOT a second class citizen. I want the world to know that I have HIV and there is no reason to fear me. I want the world to know that Washington’s plan to cut healthcare budgets for government programs (such as ADAP) is unacceptable and I refuse to have my voice go unheard. I want to the world to know that I plan to educate the generations to come how to take care of themselves and live healthy lives. But most of all, I want the world to know that I’m here.
The Stonewall Riots is a reminder that even though we celebrate forty years of being openly gay that there are still battles to be fought in 2010. With the help of my generation it is time for me to give back what was privileged to us back in 1969- the freedom to be ourselves no matter who we are.
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