Did This Year Really Happen?

This year began just like the two before it, with me standing on one of the balconies of my high-ris

A moment’s wound for one could be a lifetime for others.

With a tone that sounded as if the Earth being round, an officemate of mine heralded to us that in d

 

Did This Year Really Happen?

December 18, 2011 in Personal Stories

Did This Year Really Happen?

This year began just like the two before it, with me standing on one of the balconies of my high-rise condominium, watching the mass of humanity far below ring in the New Year with fireworks that always take my breath away. From where I lived some were so close I could almost catch them in my hand. It was big, it was beautiful, it was exciting – just like my life. 2011 was to be a big year for me. I had just finished a major recording project and signed on with a legendary record producer to launch my career in Asia. My career was finally going the way I wanted it to, and I would finally have enough cash to buy that brand new condo in Eastwood, take my fabulous vacation somewhere exotic, and still qualify for permanent residency.

Except for the small strange rash on my upper lip everything was perfect.

A week later, it started. The headaches, the eye pain, the sore throat. Ten days into 2011, I was sicker than I’d ever been; vomiting, nausea, fever. Little did I know that that was just the beginning of the weirdest year of my life. It’s really funny how these things sneak up on us when we’re least expecting them. Just when I had gotten my life to where I always dreamed I wanted it to be, it fell apart with these words: “All your test results came back negative, except the HIV test.”

That was February 5, 2011 on board the Grand Princess, a beautiful luxury ship sailing in the Caribbean Sea. The next day I was evacuated from the ship home to Manila where the worst nightmare of my life began by finding out that I had been betrayed by one of the people I trusted most, and had been infected with HIV on purpose. After that, it became a blur of “why don’t you go back to your own country” and “you don’t deserve it because you’re white”, rotating doctors, 2-hour bus rides and fear far more real than anything Steven King or Clive Barker could ever dream up.

On February 13, just a day after emailing Migs, the Manila Gay Guy for help, I got a message from someone wanting me to go with him for HIV testing. I did, and soon other people started asking me to do the same for them. So it became a regular thing for me. At least a couple of times a week I’d go with someone for HIV testing and thank goodness, they were always negative. But for the first time in my life, I found strength in helping other people. For me? That was just plain weird.

By March I had taken all I could take and decided once and for all to end it. With a box cutter in my hand I decided to take my revenge on the person who infected me by going to his house, sitting on his door step, slitting my wrists and letting him come home to a bloody corpse. Fortunately, my new friend Marco realized something was wrong and came to stop me. Marco realized the mountain I was facing, being a foreigner with HIV trying to get help. So he took it upon himself to be my friend, my interpreter and even my nurse until I was able to stand on my own again.

March was a big month. I started making new friends. I met Raffy who took me to yoga, where I connected with Paulo and Ben. I met Jericho who connected me with Humphrey. I met Dr. Kate who connected me with my psychiatrist. Marco took me to a Recollection Retreat where I met Brother Dan. And from there, things started to change.

In April I started on ARVs because the virus was eating my retinas and I had started to go blind. The meds made me really sick and looking through my journal now, I remember how hard it was for me to adjust to them. I worked through it though, always keeping hard candies in my bag. They helped for some reason, but I was still really sick for the first couple of weeks. I even fell out of a moving tricycle one time. It was good that Marco was around to help me with simple things like cooking, cleaning and going to the bathroom because I couldn’t even stand up.

Also in April, I met Keith. Keith emailed me because he wanted help getting tested as well. Little did I know that he would be the first person I’d help who would test positive. And, as with Marco, little did I know how important he would become in my life and in my work. We started talking about the idea of a website about HIV where other people who needed help could get information about the virus and where to go for help. Keith is important to me to this day, and we continue to develop ideas and projects together.

May was when I started getting involved in advocacy, talking with Keith about the website, meeting with artists about fundraisers, attending conferences and forums, and all the while helping people get tested for HIV. In May, I helped at least 1 different person almost every day – some days as many as 3-5. I started considering disclosing my status publicly. When word got out that I was considering that move, suddenly I started meeting everybody because everyone had an opinion. I was threatened with deportation and physical violence. My doctor was worried about the effect it would have on my health. Wanggo and Humphrey were behind me completely. I did my first TV interview on June 8 and made my first public speaking engagement on June 9. After that, I started disclosing my status to everyone I met. It felt amazing!

In June I met Dave, a Buddhist monk back from Taiwan who wanted to get involved in advocacy. Dave and I became fast friends. I had always wanted to become a monk, but really didn’t know how. So as Dave and I started to talk, I started to think that maybe that was the right time for me. I remember I got really sick in June and was confined at PGH. Dave came to visit me and gave me some Buddhist prayer beads made from polished sea shells. He held my hand and chanted for me. That experience made me realize that if I was ever going to be a Buddhist monk, I better do it now, because there’s no day but today, after all. I did it. But clearly, it didn’t last too long because I’m still here in my office writing a blog post instead of sitting in a monastery in Cambodia. (My friends thought I had lost my mind.) But what did remain is my friendship with Dave. And with Dave came Andrew. Andrew was moved by hearing my story and wanted to help me help other people. So Dave, Andrew, Keith, Marco and I started to talk about how we could formalize our operations. Things started to move.

In July, I learned to be a counselor. Yes, an HIV counselor, which is a specialty. But I wasn’t just interested in being limited to DOH forms and risk assessments. I wanted to really help people. I realized that I had been counseling people all along, and just didn’t know it. So with training and mentoring, I started to refine my skills and by July 9th, I was certified as an HIV Counselor by one of the best counsellors I’ve ever known. July was spent learning Pali chants and studying Buddhist texts while at the same time getting people tested for HIV and continuing to do TV interviews, public speaking engagements and organize The No Day But Today Project into a formal organization.

But by mid July it became clear that I was in serious financial trouble. I hadn’t collected a paycheck since November 2010, and had invested most of my savings in my last album, which never got released. And whatever else I had left after that was spent on medical tests and treatment earlier in the year. So by July, I had to start getting creative. So I decided to do what anyone in my position would do. I had a garage sale and founded an NGO.

I sold everything I owned and on August 1st I used the money to get an office for The No Day But Today Project. And since I was now a Buddhist monk, I didn’t need finery like a TV, sofa or a bed, so I moved into the office with my blanket on the floor and smiled myself to sleep…for a while. But it didn’t take long before I realized that the demands of running an NGO, being a counselor and a public figure was way too much to handle as long as I was living the quiet, chaste life of a Buddhist monk. It became a strain that even I couldn’t manage.

As September and October progressed, I started learning the basics of building a good NGO. We had weekly support group meetings, the testing continued, there was more training and more connecting with other NGOs for support and partnerships. I learned that it’s okay to be human in front of a camera when I took Bob the photojournalist to one of the HIV treatment hubs and then let him sit in on one of my sessions with my shrink, during which he heard all my deepest, darkest secrets. Afterwards, when we got in his car, I broke down. Fortunately, his camera was in the back seat. But I decided that maybe it’s okay for me to be a human – with emotions, fears, hopes and dreams, and maybe even to fail sometimes. And if people see that…who cares?

In November I started feeling the pull of romance again, and started considering dating again. But the demands of running an NGO, being an advocate and counselor leaves little time for things like that. The No Day But Today Project became a legal entity on November 8, and I was like a proud daddy with a new baby.

So now, here it is December. 2011 – the weirdest year of my life – is coming to a close and I can’t help but wonder about 2012. I’m still sleeping on the floor of my office without a TV or a chair to sit on. But where at the onset of the year I was a selfish, rich, arrogant hermit, 2011 has taught me to be a friend, advocate, counselor and mentor. And honestly, I couldn’t be happier.

I’ve started dating again with what little time and money I do have. But I’m married to my work, so it’s more like having an affair than dating. I’m still Jake, still doing TV interviews, public speaking engagements, building bridges and helping people get tested. The only difference now is that I have a team of people who help me with all of it. In fact, you wouldn’t be reading this if it weren’t for them. You think I have time to run a Facebook page, Twitter, Tumblr AND a website? Are you kidding? That’s all Keith. I just write the material. And the testing part? That’s becoming more and more about Marco, who’s also a great counselor by the way. Dave is responsible for making us legal and Andrew is trying to bring money into the Project. Wow, what a year.

This morning I spoke to a group of students at UP Diliman about the power of positive thought, speech and action. I love students, and I probably would’ve been a teacher in another life. I really didn’t realize that I understood the subject so well, but it felt really great to step outside my comfort zone and do something different. Oh, who am I kidding…I don’t have a comfort zone anymore! Afterwards, as the taxi driver was taking me on a scenic tour of the villages, barangays and barrios of Quezon City, I was planning our first General Assembly for next February. What do I know about General Assemblies? There’s still so much I don’t know. But I’m learning as I go. And after the year I’ve had, I’m sure that the right people will be there to help me when I need them, just as they have been all year.

To all who have loved me, cared for me, helped me, mentored me, sheltered me, held my hand, laughed with me and have generally helped me become who I am still becoming…thank you all. I love you!
Here’s what 2011 taught me:
- Life lived only for ourselves isn’t worth living.
- Helping people is worth more than a 7-figure salary.
- I don’t care how long I live – I care about what I do with whatever time I have.
- I’ve learned that no one should face life with HIV alone.
And the moral of this story is this: If you want to bet against Jake Lopez…don’t! I certainly won’t anymore!
Here’s wishing you and those you love Happy Holidays and a happy and healthy 2012!

+Jake

A moment’s wound for one could be a lifetime for others.

November 9, 2011 in Personal Stories

A moment’s wound for one could be a lifetime for others.

I wasn’t really minding the dude since it’s midday and work is starting to nail us. If not because of the shrieking “OMG” of another lady officemate, I would go on ignoring them.

I turned to where the commotion was. Blood. I saw blood. Blood that spewed and unsightly at the finger of my officemate sitting next to me. And not just blood, a finger of his was covered with scotch tape in a vain attempt to substitute for the loss of bandage. So that was his announcement. Pwede rin pala ang scotch tape, no? he said.

The wound he’s nursing was all too perfect for me to do the cringe: my neck muscle strained, one of my leg folded and suddenly raised, and my eye twitched. My cringe strings always get the pulling whenever a badly mended wound is in sight.

He took some time in explaining what happened. Apparently, the metal label of his netbook created a nasty slice on his finger without him knowing when he was pulled out the contraption. As things happened quickly, it was painless. The next thing he knew was he was looking for a band aid but the good secretary offered a pathetic solution to none that is scotch tape. He said the bleeding stopped, which was good, but his appendage was still soaking in sanguine splendor.

I and Ms. OMG haven’t stopped cringing yet. Slightly irritated with our proof of disgust, Mr. Wounded Finger took the offense of a six-year-old kid whose ego was badly injured and bellowed somewhere from the pits of his vendetta, looked to me, and hollered, “Hoy, ah, wala naman akong AIDS.”

It was a gun fired at point blank. As soon as his words registered in my head, I saw myself bleeding, this time, in what could be a mix of shame and self-pity. His bullets came round. If only I could muster the shattered courage, I would have snorted, “Well, in case you have Sir, would my simple nonchalant sitting here infect me?”

But of course I didn’t tell that straight to his face. The most adult thing to do is to shut up. So I tied my tongue and let silence restore disturbed peace. After all, Mr. Wounded Finger didn’t know the kind of wound I too am carrying after all. He didn’t know about my status. And I guess with that sort of snicker made against me, against people living with HIV, I wouldn’t let him ever know.

I thought his line of thinking was a kind of oddball that it hit my sarcasm button. Why, tell me? Who in his right mental frame ever sprinkled his blood on everybody? Are we really entering the civilization of vampiresque and zombiesque that we’d feast on someone else’s blood? Having seen his wound, my cringing would be inevitable but I wouldn’t surely partake on his blood–whether he’s a healthy man or an HIV carrier. Thank you for informing me that you are HIV-free but that’s your wound. You keep it to yourself. Some things aren’t gladly shared.

Was there any prejudice committed against me with his slur? Looking back, still I’d say there was none. For he was clueless about the personal wound I am carrying, he didn’t know the severity of his words. The flight of his utterances were not intentional spears hurled at my status or against my humanity. His flush of irate was, I surmise, a vengeful f-you for the sheer, nay immature, disgust toward the sight of blood that I and my lady officemate displayed, but it wasn’t a personal stab against me and my disease. Nonetheless, reading between the lines, I clearly can sense that in the depth of his collective consciousness, his words are not but reeking of stigma.

It’s unfair to dissect or psychoanalyze him here and trace why he uttered such kind of innuendo. From lack of information, from stereotypes or from the equally incompetent media whose reportage seem to spread the malicious word that HIV is a death sentence, who knows? But it seems to me that his words would just add a great deal of obscurity to the already dumbfounded: that HIV-positive people doesn’t have the right to be wounded? Or even bloodied?

For crying out loud. How many people living with HIV out there can still manage to have their face pricked at beauty centers? How many can still have their tooth extracted? How many still have managed to keep the virus to themselves despite being wounded one time in their lives?

Surely, what draws the line between a wounded healthy man and a wounded HIV carrier for my office mate to tell me that? Both need access to medical care, or the very least, first aid, but misinformation is making it doubly hard for the sero-positives because there is judgment made against them quickly. There is already the fear in the uninfected that a mere sight of blood is already infectious, and the non-medical practitioners are easy victims of this maligned information. And when this baseless factoids snowball what you get is stigma.

Down the lines of the most basic science of HIV, blood really is infectious. But really now, who would be infected by the mere sight of it?

All has the right to medical attention, even the most corrupt needs doctor, but stigma makes a difference altogether. While stigma on the sending end means to look down upon on someone, to discriminate others, to consider a person an entirely different being, on the receiving end it is shame, self-pity, and guilt. Stigma is a double-edge sword that has done no good on both ends: one reinforces stereotypes, the other wallows and becomes the victim of a supressive ideology.

What started as an office mate’s wound ended up with a barrage of questions of my own and others’ security. What should I do if I cut myself like that? Would I lift a monobloc chair and parry anyone who’d come near me? Would I go on a screaming fit and just run to the faucet like a deranged madman? Would I call for a freaking ambulance? Or better, I thought, I shouldn’t just wound myself. I should do everything to not wound myself. Without knowing it, I have given in the mold of stigma–which is ironic, because even if with utmost care, I might still cut myself whethere I like it or not. Even the untimely, they say, has its time.

But if everybody would just treat a wound as a wound, a wound that needed serious medical attention, a wound that must be dealt with great care, be it from an HIV carrier, or a healthy man or a diabetic, we can all do away with that one great wound that’s for a lifetime, and that is the wound that drills the heart of every people living with HIV whenever they come across prejudice, stigma, and disparaging swipe made against them.

If only people were aware of how hard it is for HIV-positive people to rise above themselves on times when it seemed the world crashed in on them because of the disease, I guess they wouldn’t add another round of hardships on us, call our wounds as an HIV person’s wound, and dwell on their hang-ups. They’d just call it, “a wound.”

As for me, I’m doing everything I can so as not to cut myself, and I starting by gently pulling out my laptop from its sleeve.

- J

Just be there

October 16, 2011 in Personal Stories

Usually when I write, it’s directed to my brothers and sisters living with Harvey. But this time, I want to talk to everyone else – those whose friends, partners and family members get diagnosed with the virus.

I do not speak for the HIV+ community as a whole. In fact, I can only speak for myself, based on my experience. So if you’re one of my poz brothers or sisters, please don’t think I’m trying to speak for you. But feel free to agree with me if you feel the same as I do. I always welcome your thoughts and opinions, whether you agree with me or not.

I was recently contacted by a guy whose friend was just diagnosed with HIV, and he wanted advice on how to support his friend. Since being diagnosed, his friend has become angrier and angrier, and more and more distant. He emailed me to ask what I thought he could do for his friend.

This is more common than I’d like to admit. Many people get so angry at everything and everyone that they decide they’re going to spread the virus to as many people as they can before they die. Other people cut themselves off from their friends and family, choosing instead to hide their status and consequently, themselves. Still others progress all the way down that same slippery slope to the brink of suicide.

This causes great pain and fear for the people who care for the infected person. Often times they don’t know how to help, and they’re paralyzed by that fear, afraid to say or do the wrong thing. Fear is a natural mechanism that warns us of potential dangers, and it should be acknowledged and heeded. So it’s important to know how to handle the person who’s falling apart.

From now on, I’m referring strictly to my own experience. But I’ve learned that I’m not all that unique in my struggle, so there are probably others who will agree with me.

At the time of my diagnosis, I was alone, sick, in tremendous pain and mightily afraid. For the first 5 days of my new life with Harvey, I was totally alone. I was either in a lonely hotel room or on an airplane with hundreds of strangers who were all staring at me. I would double over in pain or just bust out crying for no apparent reason. I was quite the spectacle, I’m sure.

I was flying from Miami to Los Angeles, and I was seated on the plane next to a wonderful woman from one of the US Virgin Islands. She was, well, voluptuous with smooth skin the color of dark chocolate and had the sweetest Caribbean accent. From the moment I got to my seat beside her I let her know to expect me to cry and maybe double over in pain during the flight. She told me that she was a nurse, and that if I needed anything at all, she was there for me during the flight. We were 3 hours late leaving Miami before we could even begin the 5 hour flight west to LA. During those 8 hours sitting next to the woman, named Christine, I had many terrible abdominal cramps that would send me screaming into my pillow, and this was between random fits of seemingly-unprovoked tears. And Christine, this random stranger, would simply stroke my hair and tell me, “Go ahead honey child, you go ahead an’ let it all out. E’ry-tin’s gonna be alright.” She comforted me all the way to LAX – 8 hours. I’ll never forget her.

At that stage, that’s what I needed: a soft voice, a warm hand and a soothing spirit. She didn’t say anything profound, she was just there. And there’s so much healing power in the human touch. That’s important to remember.

When I arrived home and found out that I had been infected on purpose, I learned the definition of the word “rage”. I had been betrayed by one of the closest people to me, and “anger” doesn’t begin to describe what I felt when I lost all self control, kicking, hitting and screaming at my friend like a crazy person. Afterwards, with the blood still drying on the dining room floor, I went into my kitchen and just sat on the floor alone, rocking back and forth, and wailed. I have never experienced that before, and I hope to God I never do again.

When I calmed down a bit, I texted my best friend who came running to my side. He sat with me as I yelled and cried. He let me express the hurt over the unimaginable betrayal that had just been revealed. He didn’t say anything profound, he was just there. And knowing his love for me was comfort enough. It didn’t take away the pain, but it soothed my spirit to be with him.

Soon after that, I started treatment – much to the chagrin of the people at the clinic who had never dealt with a foreigner before. Their uncertainty in dealing with me was, in the end, more than I could bear. Even after managing to gain coverage by PhilHealth, they refused to honor it, telling me instead that I didn’t deserve it because I’m not a Filipino. And then, one afternoon, they informed me that I was going to have to pay P20-30,000 per month if I needed medicines. That scared me and I headed downwards towards a breakdown when one of them said, “Why don’t you just go back to your own country?” Well that was just the end of it!

I tried to find some professional help – someone who could help me deal with everything that was happening to me. But I couldn’t find anyone to help me at any of the four hospitals I visited that day. Again, my best friend came to the rescue. He left work to meet me at KFC. I was so angry and scared I was visibly shaking. I didn’t want to go on. I didn’t want to live anymore, and I didn’t want to face anymore abuse or betrayal or discrimination. Once again, my best friend didn’t say anything profound, he was just there, and let me rage and shake until I was spent.

Over the next several weeks, the frustration with my clinic’s reluctance to treat me boiled into pure fury. In the background I had also been wrestling with how to deal with the person who infected me. Blood wasn’t justice enough for me. I wanted him gone forever, and I was tired of the pain of my life, and I was reaching my breaking point. A friend invited me to go to yoga with him and there, I met a guy who had been at my clinic the day I had my meltdown about the cost of medicines. During the yoga session, I collapsed. That was the end of my mental and emotional strength. I had been sick for two months and had lost a lot of weight – almost all muscle, and I was weak. I was so depressed, I just wanted to give up. I went down to the front steps of the office building in Ortigas, sat in the rain and cried until the class finished.

The guy who had been next to me during the yoga class stayed with me until the early hours of the morning as I cried and yelled and expressed my deepest pain and fear as I drank Red Horse beer in the rain outside the 7-11. He didn’t say anything profound, he was just there.

There have been many times since that day in February, when Harvey became part of my life, when I wanted to explode, collapse, disappear and even just cease to be. And at every turn, there’s been someone there. They don’t say anything profound, they’re just there.

For those of you with loved ones and friends who have just learned that they have HIV, just be there. There’s no need to say anything profound. Let them express whatever it is they need to express, for as long as they need to express it. Don’t try to correct them, contradict them or scold them for saying something you don’t think they should say. It’s important that someone just beginning life with HIV is allowed to be a little crazy and say and feel and think outrageous things for a while. Let them know that you love them, that things will get better, that you will help them through their hell, and that you’re always available to them. And when they emerge from the storm, you’ll have a stronger, more precious relationship than you ever imagined. And then someday, when you need someone, they’ll be there.

One life to give

October 16, 2011 in Personal Stories

I am an American citizen and a veteran of the US Navy. I could easily go back to America and have access to the latest HIV treatments and medicines available. Some have encouraged me to do just that.

But the Philippines is my home. My heart is here. I will die here. The best people I’ve ever known are here. People who love me, accept me, support me and care for me are here. The best friend I’ve ever had is here. I wouldn’t be alive if it weren’t for ‘bayanihan’, and for that I’ll never leave your side. Even though the immigration laws now ban me from becoming a permanent resident of the Philippines because I am HIV+, I will stay and fight with you until the end. No fear, and no backing down. As Randy Jackson on American Idol says way too much, I’m “in it to win it!”

I’ve been researching the current issue of the Free Trade Agreement between India and the European Union. This is truly disturbing. The large pharmaceutical companies in Europe and the US are putting profits above human lives. Modus operandi for them. That’s why 48 million Americans can’t afford health insurance or medical care.

I realize that every company is in business to make money for their share holders. I get that. I realize that big drug companies spend a lot of money on research, development and testing, and profits from branded drug sales offset those costs. I get that too. I also realize that proprietary information such as patented intellectual property should be protected. I get all of it!

However, I also understand that by manufacturing generic drugs through “reverse engineering”, India is keeping me – and about 700 others of us in the Philippines alone – alive by providing the generic ARV meds we depend on. The European Union is now trying to take those medicines away from us, claiming that India is infringing on intellectual property laws by manufacturing generic ARVs.

In the Philippines, we are facing an unprecedented epidemic – I don’t have to tell you that. We are at risk of losing an entire generation of young Filipinos to HIV, not to mention the children they won’t have or the children they will have who could be born with HIV. With the number of confirmed infections expected to top 40,000 within the next 5 years, according to some reports, this country is looking at an insurmountable crisis not just in lives lost, but in the impact to our healthcare system and our economy.

(Yes, I use the words “we” and “our” when referring to the HIV+ community, young people and government. Just because the law tells me I can’t be a permanent resident or even a citizen here because of my virus, doesn’t mean I’m not one of you!)

Something MUST happen. This is a call to action for ALL Filipinos infected with and affected by HIV and AIDS to lobby the government to encourage India not to sign that free trade agreement with the EU. If they take away our generic medications, where will we all be? Call, write and email your representatives in Congress. They are elected to do what the people mandate. And if the people don’t speak up, then we are the losers. And while I have no vote, I do have a voice. And I’ll use my voice to cheer you on and to raise as much awareness about this dangerous issue as is humanly possible.

The American patriot Patrick Henry once said, “We are not weak if we make a proper use of those means which the God of Nature has placed in our power… the battle, sir, is not to the strong alone it is to the vigilant, the active, the brave.” We must fight together as one positive community now. Future generations depend on how we stand up for ourselves today, and in the days to come.

The great Filipino hero, Dr. Jose Rizal once wrote, “One only dies once, and if one does not die well, a good opportunity is lost and will not present itself again.” With that, I make this commitment to you: I will fight this fight with my Filipino brothers and sisters living with HIV. I will live with HIV just as you live, I will take the medicines you take, I will receive the same treatments you receive. I am here for good. I’m here for life. I’m here with you until the end.

To cite one final American, the revolutionary war spy, Nathan Hale, said as he was being hanged by the British, “I only regret that I have but one life to give for my country.” If you know me at all, you know that I do not think of myself as an American. And though I look as different from you as night looks from day, though I crave different foods and though I struggle with your language, I think of myself as a Filipino by choice. I am one of you. This is my home, and I will stand with you and fight for what’s right and best for all of us.

God bless us all.

+Jake

 

Do you have hope?

October 16, 2011 in Personal Stories


I’m Jake.  I was diagnosed with HIV in February 2011 – just about 2 weeks before my birthday.  Hmpfff… Some birthday present I gave myself this time…
My story has been pretty well documented by this time, so I won’t dig up the past.  But I’m excited about this site.  This site has been a dream of mine for many months, and to see it up and running has really put me on cloud nine.  So since I have a blog here, I wanted my first post to be something profound – something to set the tone.  So here goes…my very first blog post!The first 5 months of this year were the worst months of my life.  I thought I knew what suffering was before, but man – nothing compares to being told you’ve got HIV!  HIV is the only thing in my life I’ve ever been truly afraid of.  And when I found out that I had it, it was like I could hear a big steel door being slammed shut on my future…on my hopes, my dreams, my beautiful condo with the killer view, my P250,000 a month salary, my budding music career…everything.
I was diagnosed on a ship at sea after being deathly ill for more than a month.  My liver was failing.  I was dying, and didn’t even know it.  I was evacuated from the ship and it took me five days to get home to Manila.  I knew I needed help – lots of it!  But I didn’t know where to find it.  So for the first week of my new life with HIV, I was totally alone, lost, sick, and scared out of my mind.When I went for treatment, all I found was more torment.  The language barrier, the apparent lack of support, the patchwork system, the dread of ever telling my parents, compounded by just about every obstacle you could imagine, and then some…it was literally more than I could handle on my own.  Then there was the anger.  Wow…I had plenty of that to go around!But eventually, I started getting help.  I started getting healthier physically, but mentally, emotionally and spiritually, I was wrecked!  Support was nowhere to be found – at least none that I could find outside the realm of cyberspace.  Life had become a waking, never-ending hell, and I wanted it to end.  And I decided that the only way I could escape the pain was to slit my wrists and get it over with.Fortunately for me (and for everyone who loves me), someone I had just met – a virtual stranger – was there to stop me.  He saw the problems I was having, and became my personal psych nurse, putting me under 24-7 suicide watch.  He helped me navigate the system, taught me where to go, how to understand medical tests, get insurance, and even worked as my interpreter.  I never would’ve made it without him.Over time, I started to meet others who supported and helped me.  And in time, I had a new circle of friends.  Everything in my life was still uncertain, and I still hadn’t faced my parents (and I swore that I never would), but every day seemed a little better than the one before it.
Finally, with the help of a psychiatrist, a wonderful doctor, spiritual guidance, and the new friends I had made along the way, I emerged from the blackness.  But there was another story playing out at the same time I was fighting my battle, and that’s the story where this site, and The No Day But Today Project, was really born.
After arriving home from my hellacious 5-day trip from Barbados to Manila, I went online looking for help.  I didn’t know words like “treatment hub” and “ARVs” at that time.  I didn’t know what a PAFPI or a Pinoy Plus was, so the Google searches only made me feel more desperate.  The only thing I understood was “blog”.  So I emailed a blogger, told him my story and begged desperately for help.There were posts of encouragement and support, even some information that helped.   But the one that stands out in my memory was from a guy saying that he was also sick, alone and scared.  I decided that if we were in the same predicament, at least I wouldn’t suffer alone, so I responded.  Next thing I know, I’m going with him for his HIV test.  We spent the day together talking about what I had learned about HIV.  We watched some TV together, and even cried over a Richard Gere movie about a dog that died.  Later that day, we went for his results, and when I learned that he was negative I cried like a baby.  I don’t know why, for sure.  But the important thing here is that that was the first time in my life I ever cared about what happened to another person.He posted on the blog that I had gone with him and had helped him, and soon other requests were coming in.  So I went with them also.  And every time I went with someone for a test, I felt this surge of love and compassion that I didn’t even know I was capable of!  And the more I helped people, the more I wanted to help people.
Many months have passed now since those first very dark days of my new life with HIV.  And as it turns out, the life that I thought I wanted…I really didn’t.  It turns out that the life I thought was ruined, finished, shattered?  It wasn’t.  I just was going in the wrong direction.So now, 7 months after being diagnosed with HIV, I have sold everything I have, moved out of the condo, resigned my job and shut down my career.  I’ve faced my parents and they were more loving and supportive than I would’ve ever imagined, and I’m actually looking forward to going to the US to spend Christmas with them, my crazy old grandmother, my brother-in-law, sister and 3 nephews for the first time ever. I’ve discovered the true meaning of love.  I’ve discovered the true meaning of friendship and family.  I’ve discovered that the solution to my unhappiness was right in front of me all along. I was just too stubborn to look at it.  And I’ve realized that I have infinite love and compassion waiting to be set free.

Enter – The No Day But Today Project.
No one should have to go through what I went through.  And so I, and now my team of volunteers are reaching out to make a difference, and to let every Filipino know that they don’t have to face life with HIV alone.  If you know you need to get tested, but you’re afraid, we can help with that.  If you’ve been diagnosed with HIV and you feel alone and afraid, we can help with that too.  If you’ve had HIV for a long time and you’re looking for a place to help others, or even if you still struggle with your condition, we can also help with that.

I have huge hopes for The Project.  I want to change the way people think about HIV, and how people treat people who have it.  I want people not to be so afraid to get tested, and to do it regularly on their own.  So with this first blog post, I am filled with hope for the future.  I have made it through the worst storm I ever could’ve imagined, and I’m a much better person for it.  I have a reason to wake up every morning, and that is worth more to me than anything.
How about you?  Do you have hope?  Can you imagine yourself with HIV living a beautiful life?
We are The No Day But Today Project, and we can help with that.

Love & Peace,
+Jake