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Test Positive Aware Network

Long-Term Survivors of HIV and Wellness

No Longer an Oxymoron

September/October 2008

HIV Wellness Oxymoron
Either of two retroviruses that infect and destroy helper T-cells of the immune system, causing the marked reduction in their numbers that is diagnostic of AIDS -- called also AIDS virus, human immunodeficiency virus* The quality or state of being in good health, especially as an actively sought goal* Something (as a concept) that is made up of contradictory or incongruous elements*

*from Merriam-Webster Dictionary Online


Joey 2001

It was early 2001. I remember thinking it was not like Joey to be late. I'd known him for several years and he always arrived for his appointments early or on time. He was now 15 minutes late and I had begun to worry. The phone rang and instinctively I picked it up, thinking it might be Joey on the other end. "Hello?" Nothing. "Hello?" Still nothing. Then muffled crying. "Joey? Is this you? What's the matter?"

After several minutes, I learned Joey was trapped in a bathroom several blocks away. He had gotten off the bus on his way to see me because he had an urgent need to relieve himself, but barely made it to a gas station bathroom. He had no clean clothes and was too embarrassed to leave. Luckily, he had a cell phone and called me.

Joey was 35 when we met in 1998 and had been HIV-positive since the late 1980's. He had been on various HIV-related medications, but his health continued to deteriorate. Joey worked as an attorney, but the pace of his work was becoming more difficult to manage as his disease depleted him more and more. To complicate matters, he and his partner (also HIV-positive) were addicted to crystal meth and their relationship had become violent. At the time of this phone call, Joey had lost his job, left his home, and was barely managing to survive in homeless shelters. He had resigned himself to a very short future, and was focusing on putting his meager resources in order for his family.

I scurried around my office to find clothing I could bring to Joey where he was stranded. I knocked on my office mates' doors and was able to find a shirt, sweat pants, and a jacket. When I reached the gas station bathroom and knocked on the door, Joey was still crying softly. He opened the door a crack and I handed him the clothing. "I used to be somebody, Jeff," he whispered. "I used to be somebody."


Ken 1998

A 42-year-old transplant to Chicago from New York City since 1998, Ken described his time in New York as the best years of his life. He remembered an active social life, involvement in a 12-step recovery program for substance use, and a career as an emergency room nurse. Diagnosed with HIV in 1991, his health deteriorated rapidly with one opportunistic infection after another. He came to Chicago to make a fresh start, but quickly relapsed on multiple substances and processes (alcohol, narcotics, and sex). He came to see me initially because his nursing license had been suspended for writing false prescriptions to maintain his habit and he was mandated to see a therapist, among other activities, in order to lift the suspension.

Ken had a small apartment on the north side of the city that he managed to keep due to a small inheritance from his parents. He was unable to work in nursing, however, because of his suspended license. His health also compromised his ability to maintain other steady employment. He subsidized his income with short-term temporary administrative jobs, many of which paid him in cash.

"What's the point anymore, Jeff? None of my friends live in Chicago, and most of my friends from New York are dead. I don't have any energy left," he shared with me in March of 2000, after being discharged from the hospital because of a bout with pneumonia.


Mark 1996

"I had to give my dog away," Mark shared with me in our first meeting in 1996. "I can't even take care of her, let alone myself." He stared at the floor and bounced his leg up and down as he waited for my response -- and for the judgment he feared I would share with him. I quietly invited him to tell me more.

Mark had left a successful position in real estate voluntarily. He was 45 years old at the time and had saved enough money to be unemployed for a short while as he explored alternative professions. Originally from a small town in Iowa, Mark had come to Chicago as a teenager who realized that he could not safely be gay in small town Iowa. He worked to put himself through college and was active in Chicago's gay social scene of the 1970s. "That was an incredible time in my life," Mark shared. "But it also resulted in alcoholism and HIV."

During the first year of our work together, Mark exhausted the money he had saved and began doing temporary day labor as jobs arose. Eventually, his health deteriorated to the point of not being able to work at all and he applied for and began receiving disability payments. His body changed as a result of both HIV and the medications he was taking. The pride he once felt from his physical fitness shifted to shame as he described his weight gain, sunken cheeks, and areas of lipodystrophy.

In 1999, I remember a session where I asked Mark to imagine what he would like his life to be like -- to close his eyes and think about where he would live, the kind of job he would have, and what his social life would be like. "I can't do that because it's not possible anymore," he said with resignation. With gentle prompting, he eventually shared: "I would live in a high-rise in Lincoln Park with views of the lake. I'd be working in real estate again and I'd feel hopeful. But I don't think that's going to happen, Jeff. It's too late now."


Joey, Ken, and Mark 2008

Joey, Ken, and Mark did not believe they would be alive in 2008. Or, if they were still alive, they thought their quality of life would be severely compromised. They had resigned themselves to illness and our initial work together was more about acceptance than it was about hope, wellness, and the future.

Today, Joey is working as an attorney again. He owns his own home on Chicago's South Side. He has a small circle of close friends, and has connected with a large extended family with whom he spends a great deal of time. He walks and exercises regularly. He plays tennis occasionally. He loves music. He laughs a great deal. His health is still a concern, but when a health issue arises, he is quick to address it.

Today, the suspension on Ken's nursing license has been lifted and he is once again working as an ER nurse. He has a renewed relationship with his sister and has forged a close relationship with a cousin whom he visits several times per year. He has also acquired a cat who he says greets him with anticipation upon his arrival home from work each day. He continues to have health problems, many of which are not a direct result of the HIV. And, he still hopes to increase his circle of friends in Chicago. Still, he says he is grateful for what he has and for how far he has come.

Today, Mark lives on Lake Shore Drive in a high-rise facing Lake Michigan. He works full time in real estate and recently was promoted to manage an office on the north side of Chicago. He has been sober for over 20 years and has a strong connection to the recovery community. In addition to having his own sponsor, he has three individuals whom he sponsors. He exercises three times per week and has lost 20 pounds. Mark has also invested considerable energy in his emotional and spiritual growth, attending a number of weekend workshops and retreats. He remains dissatisfied with the effects medications have had on his body (in combination with the effects of aging), but says he finds himself feeling hopeful more often than not.

Joey, Ken, and Mark, however, are not alone in this journey. Many men, women, and children diagnosed with HIV 10, 15, or 20 years ago were not expected to live long, let alone live with hopefulness and an attention to wellness. Certainly advances in medication and other interventions have played a major role in living "well" with HIV. There are other critical ingredients -- listed below -- to the lives Joey, Ken, Mark and similar others have created for themselves.


Relationships

The power of relationships has been a healing force for each of the men discussed above and remains a healing force for all of us. Tapping into the power that comes from connection with others is a key ingredient to wellness. Of course physical health influences a desire to connect with others, but reaching out to others and, in turn, having others reach out to us creates a powerful synergy that contributes to a sense of purpose and well-being.


Courage

It is no small feat to face imminent death, feel resigned to this destiny, yet swiftly turn on your heels and walk in a different direction. The process of rebuilding a life, in many ways, takes more courage than the initial building. Each of us, when faced with an obstacle, has the choice to become resigned, or to learn and grow. Long-term survivors of HIV such as Joey, Ken, and Mark allowed themselves to be transformed from their experiences and courageously chose to rebuild lives of meaning and purpose.


Humor

Given the stories of long-term survivors of HIV like Joey, Ken, and Mark, it seems difficult to even consider humor an ingredient of wellness. And yet, I remember many instances of laughter even as each man shared incredibly painful and embarrassing experiences. Joey will consistently share with me his family's hardships, economic problems, and illnesses, but through the pain, he is able to make small jokes and sometimes, even chuckle. And now, several years later as he recounts the incident of me rushing clothes to him at the gas station restroom, he grins at me and chides: "Couldn't you have at least brought me some socks?"


Morality

While each person's sense of what is right and what is wrong may be different, the idea of having a sense of right and a sense of wrong serves as a foundation for all of us. Long-term survivors of HIV are constantly faced with others' judgments, their own feelings about their HIV status, and making decisions about self-care and risk. There are no clear "rights and wrongs" in this world, which requires that each person have some internal mechanism for recalibrating this process in response to constantly changing physical health.


Spirituality

None of the men I've described here would consider themselves religious, in the traditional sense of this word. But all of them, at this point in their lives, would say that spirituality plays a major role in how they currently live. Each has found a way to connect with some force that is greater than themselves. Ken's relationship with his cat is a nontraditional example as, for him, his cat represents a connection to all living things and some source of energy and "spirit" larger than his own. Joey has created this sense of connection with extended family, and Mark taps into "spirit" through AA and prayer. Regardless of the source, a belief in and connection to a source of energy beyond ourselves is a great source of wellness.


Living Well

Long-term survivors of HIV face innumerable challenges. In many instances, the medical challenges of living with the effects of HIV take a back seat to the emotional and psychological challenges of dealing with impending death. For those people who have spent years preparing to die, finances have been exhausted, careers have been compromised, and loved ones have died or moved on in other ways. The prospect of continuing to live may become a frightening one, fraught with existential questions about finding purpose and meaning -- and a process of dealing with both tangible and intangible losses. Wellness takes on a new and different meaning for long-term survivors who are now looking at living indefinitely. While still comprised of what we traditionally consider wellness activities (healthy eating, exercise, entertainment, work-life balance, and other forms of self-care), wellness with long-term survivors is equally comprised of meaning-making and purpose-finding.

I didn't think that I would be using the word "wellness" in referring to long-term survivors of HIV, and yet here I am, discussing three people, each of whom have lived with HIV for close to 20 years. Advances in medicine have contributed to living with HIV, but attending to "wellness" with HIV is the task of each individual who chooses to live well. In a recent session with Joey, he ended as he has on many occasions: "Well, Jeff, it looks like I'm going to live."

Yes, Joey, it looks like you're going to live -- and it looks like you're going to live well.

Joey, Ken, and Mark are composites of some of the long-term survivors of HIV with whom I have worked. Their names are not actual client names and their stories have been constructed from the common challenges faced by long-term survivors of HIV.

Jeff Levy, LCSW, is a psychotherapist and the Chief Executive Officer of Live Oak, Inc. in Chicago's Lakeview neighborhood. Live Oak provides psychotherapy, consultation, and professional training. To learn more, visit www.liveoakchicago.com.

*from Merriam-Webster Dictionary Online.


Got a comment on this article? Write to us at publications@tpan.com.

This article was provided by Test Positive Aware Network. It is a part of the publication Positively Aware.
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See Also
More on HIV Medications
More Stories of People Living With HIV

Reader Comments:

Comment by: Innocent (Kenya.) Sun., Sep. 27, 2009 at 10:58 am EDT
I got infected in 2007 during my 1st year in law school when i was 19 yrs old, to the guy i lost my virginity to. (He dumped me soon thereafter.) I didn't know of my status when i met the love of my life but i found out a few months after we started dating. At first i held back bcoz i felt that i didn't deserve him and I tried to push him away but he wouldn't leave me finally i told him of my status but he didn't believe me so we took a test together bcoz i wanted him to know what he wud be getting himself into so he finally believed me and dumped me. That was last week but am hanging in there i know there is a man out there who will love me for myself so am still grieving 4 losing him and right now all i can think of is if he doesn't love me then who will? But I am taking courage in all the success stories u guys post and i know I'll be o.K.

Comment by: Ray (South Africa) Fri., Sep. 4, 2009 at 6:02 am EDT
Recently diagnosed - very disappointed that funding for cure research in SA is zero, whereas globally lot of funding has been cut back. Surely we the sufferers must lobby for funding merely to have hope of living. It is our human right to live in and with dignity.

Comment by: Stephen (Houston, TX) Sun., Aug. 2, 2009 at 1:37 am EDT
My goal is to live to 52. That way I will have lived 26 years uninfected and 26 years HIV+. I know -- seems weird to look at life this way. However, August of 2009 will be my 22nd year of my new life. I have been told I am one of the lucky ones. Shortly after being diagnosed in 1987 I met the love of my life. He is HIV- and we've been together for almost 22 years. I suppose we could be poster children for safe sex. My current situation is ideal: healthy, non-reactive, tolerating the same medical regimen for the past 9 years and relatively financially well off. What has changed, however, is my mental state. I feel totally trapped. Living my life as carefully as possible, never missing any medications, and doing everything to keep myself as healthy as possible is almost like never coloring outside the lines, but obviously worse. Can any of you relate? I feel trapped and dead inside, as if venturing out to do something different would be pointless. (And for those of you who may be feeling something similar, don't see the movie "Revolutionary Road.") I love to travel but wonder if one can travel to certain countries with a bag of medicine. Know what I mean? I guess I should just stay put, be happy and get on with my life. I understand intellectually that I do not have anything to complain about considering the the unusual blessings bestowed upon me, but I still cannot get rid of feeling rather useless. I really had no idea I would live this long. Maybe it's time to seek professional mental help. 50 is almost here and perhaps I'm dealing with that too.

Comment by: Raffael (Spain) Sat., Jul. 4, 2009 at 6:51 am EDT
I have been diagnosed hiv + since 2004 and it was really hard in the begining especially as doctors found my defense system collapsed "CD3" YES! thats true..so i got treatment right away and care, and had to face the death of my father few months later from cancer, two months later from fathers death the loss of a friend 25 year old and a year later the loss of my ex boy friend. Of course all this was a hard time for me as could be for anyone of us, but I got the strength and courage to survive the loss of my dear ones, and learn to live with hiv+ with patience. I am 38 year old, my friends many times tell me how good I look and thats because I take care physicaly by a healthy nutrition and some sports as much as i can, no smoking, no drinking exept a glass of wine from time to time and a cup of coffe some times, and take care my slef emotionaly, be with people they love me and as I always care for others. I encourage people to ask help if they can and need from a special or good friend, and underdstand that they have to think positive and have love in their lives. Live healthy and rest well and enjoy life with a big big smile. :-) Love to all of you! It took me 3 long years, and today i hardly get a cold, i feel tired sometimes but with enough energy to work, to

Comment by: jayson (melourne australia) Thu., May. 28, 2009 at 7:18 am EDT
i'm newly diagnosed HIV positive (april 15, 2009) it good to know a lot of people have live longer having the HIV, but my question is " what quality of life?.. i just thought that the longer u live the longer u suffer of the stigma attached to HIV.. living with fears, uncertainly and rejection is not a life that we aim to live....blessed to all HIV positive people who has hopes!!!!

Comment by: summaliangela (Mauritius) Mon., Apr. 13, 2009 at 5:07 am EDT
This is quite a hot information. I?ll share it on Twitter.

Comment by: Attetevoill (Eritrea) Wed., Apr. 8, 2009 at 4:22 pm EDT
FANTASTIC!

Comment by: GIFT (SOUTH AFRICA) Thu., Oct. 2, 2008 at 10:48 am EDT
Well this is very interesting to see and know how one can live long with the virus, in fact Iā??m only three years with HIV but I have realize that I can still achieve my goals, obstacles are there like any other person just have to find a way of solving it, Iā??m born asthmatic and Iā??ve been on different medication actually each and every day I have to drink a pill, I used to be discriminated against when growing up ,could not even participate in sport activities just because my doctor sent a letter to the school stating my health status. Teachers and students will make a joke of it. Hey Iā??m 24 years and I survived that now Iā??m HIV +. When I found out about my status, I nearly collapsed. I was well informed about the virus but my worry was how in godā??s name will I manage two incurable diseases within me ? Then I discovered why not treat HIV like any other chronic disease? Because itā??s not the only disease/virus that has no cure If I survived 24 years of asthma and still feel strong with HIV so can any hiv+ person .The secret is knowing whatā??s right for you, the choices and the attitude we have against these diseases will determine your chances of survival, being hiv+ does not change anything ,positive thinking can beat the virus .I have a 7 year old daughter and I am determined to see her getting old and will love to hold my grandchildren and you know what? If I have to die before that, it will definitely not by hiv/aids nor suicide, could be anything else .So to all those living with the virus, donā??t loose hope that a cure will be found one day and keep on lecturing those who are ignorant --hiv is there it does not kill you if you take care of yourself but it does kill you if you are still reckless and ignorant. You do not need to be rich to live a healthy lifestyle, but be wise and make the smart choices!!!!!!!!!!!!!!!

Comment by: Chevy (Dallas, Texas) Wed., Oct. 1, 2008 at 6:07 pm EDT
Thanks for those stories; I think it's so important to stress that many people live long lives with HIV. I was diagnosed in 1989, yet I've never really, really been sick. I lead a life that is supported by those principles you stated: humor, relationships, the notion that I am alive --not just surviving another day, and above all, honesty and frankness about my challenges. Now that we've reached this "landmark status" we should share with others what we know about staying well, and living well. That's not being smug, that's being a public lesson.

Comment by: Irving (Springfield, MO) Wed., Oct. 1, 2008 at 12:31 pm EDT
Thanks for sharing this piece with us as. It is inspirational to hear stories of people who have hit bottom and made their way back to the top. I hope that everyone who reads this sees a bit of themselves in these three courageous men and feels encouraged to continue on with their dreams! I too am a long term survivor and when I get down and think I'm done, it hits me that I am still here, there must be a reason, and that excites me!

Comment by: Mike (Perth.W.A.) Mon., Sep. 29, 2008 at 8:24 pm EDT
Great thought provoking article. Being new to HIV acceptance, i would like to read others stories on a more regular basis. I feel out in the woods, and find reading such stories helps me to see the road which I want to one day be back on. It's hard work "remaining positive when positive."

Comment by: Lori Powely (Peoria,IL) Fri., Sep. 26, 2008 at 10:26 pm EDT
I have been living with this disease for 19 yrs. My first and only medication I took then was AZT. Then it was the only treatment given. However, I developed toxicemnia. I have experienced clinical trials, and was a guinea pig for my doctor of the new medications. For the first time, my levels are at the awesome levels.My viral load is undetectable and my T-cell count is 4oo.I consider myself, as well as other long term survivors the time capsules to this pandemic.

Comment by: Hans (Africa) Fri., Sep. 26, 2008 at 6:14 pm EDT
Once I dreamed of a deadly epidemic and was infected in that dream, but I never believed I was going to die rather I was shouting ā??ā??Jesus save me, I shall not die, I shall live and proclaim the goodness of the lordā??ā?? obviously I did not die in that dream even when the things I was infected of attacked me and blocked my respiratory system in that dream. Now since I diagnosed positive to HIV, I maintain that thought, words and prayer. I SHALL NOT DIE, I SHALL LIVE AND PROCLAIM THE GOODNESS OF THE LORD I believe there is nothing God cannot do for me and the entire world confronted by HIV/AIDS.

Comment by: Kirk (Dallas) Thu., Sep. 25, 2008 at 4:57 pm EDT
Jeff, The article was inspiring and enlightening. I have been poz for three years now; however, I am not on meds. I have experienced so many emotions that the above contributors felt. I too feel that I am happier, in some ways, healthier, and certainly more spiritual (not bragging) than I was in pre-hiv. I do not wish this on anyone but my 12 step group(SAA), bestfriends and friends, TheBody articles, my Higher Power, and my sponsor have have caused me to laugh, live, and have hope. A BIG THANK YOU for sharing this most wonderful-power-packed article. Well, Jeff, it looks like I am going to live!!!!

Comment by: garski (Seattle WA) Thu., Sep. 25, 2008 at 4:05 pm EDT
This seems to be so much about material success -- the well-paying job, self identification as a professional -- that it doesn't really relate to me. I've been HIV positive for more than half my life and facing the continuing erosion of everything that I've ever believed in has been very difficult. Everything? The possibility of a meaningful relationship in a climate of fear and concealment, the notion of purposeful self determination after years of being an object of sympathy and pity, the harsh limits of employability. Yes, everything -- these aspects touch all corners of my life. How do you return to work without the risk of sacrificing health care coverage? I seems that no one can answer this simple question. In every situation the circumstances are different, I realize -- but I can't get around the punitive intent of the whole system, ever trying to deny, minimize, or institutionalize my struggle. No matter how you look at it I remain hostage to medications that I could never hope to pay for without public assistance. This is untenable. In the early years I never imagined that survival would end up feeling so much like punishment. Those of you in healthcare seem to have no idea of the psychological toll paid by survivors such as myself. Pick up my mat and walk, yes, I've done that indeed, but it gets harder and harder with the burden of the entire healthcare system planted squarely upon my mortal shoulders. My survival has never been intended as a political act. As far as politics impinge upon healthcare reform, it makes me literally sick to my stomach to watch television, or to participate in any kind of political discussion regarding the 'culture wars.' I am not a pawn. I am not a tool. I am not a statistic to justify any particular point of view. I am a human being -- is it too much to ask to be so recognized?

Comment by: STACEY SMITH (Baltimore md) Thu., Sep. 25, 2008 at 3:12 pm EDT
I received a transfusion in 1984 I was 2 .. and would love to tell my story. I agree giving up is NOT an option, you have to fight if you want to live.

Comment by: Adam (Phoenix) Thu., Sep. 25, 2008 at 2:10 pm EDT
As someone who has lived with hiv well over twenty years, I agree with Mike. The people who aggressively pursued information to improve their health issues survived and in many cases thrived. Those who focused on the negative possibilities had outcomes that were not favorable. HIV for me was an opportunity to address some areas of my life that needed work. I plan on being around for a long time.

Comment by: Norris (Winnipeg, Canada) Thu., Sep. 25, 2008 at 8:06 am EDT
I passed the 70 mark this year, have been poz since 1989 (guess that makes it 19 years) and have been coasting for the last year with T-cells in the 800s. I still work, half time. As I live in a small town and in a vocation that would quickly end if my status were known, I am still closeted. I am most thankful that I have done so well, but in the last week I acquired a respiratory infection triggered by allergic sinusitis My own fault; I should have known better than to attend a study conference at a lakeside in September when mold is everywhere). This past week have been hell: alternating fever, and chills that made it almost impossible to do simple things (like typing at the keyboard, inability to keep food down. I am now on antibiotics, and slowly recovering. If I didn't know before, I do now, that opportunistic infections can bring an otherwise quite healthy poz guy down very quickly. I have never felt I might die tomorrow, or the next day. Rather I have greeted each new day with enthusiasm. I have forgotten what life was like before HIV meds, so accustomed as I am to the regimen. Now I am determined to use more discretion in where to travel, enclosed places where many people are present, any circumstance which might expose me to life-threatening pathogens.

Comment by: Bill Hemmer (Los angeles) Thu., Sep. 25, 2008 at 6:29 am EDT
These precepts about living with HIV could equally be applied to someone with cancer or lupus or any number of "fatal" diseases. It isn't just about "living with HIV", it's just LIVING.

Comment by: GOVIND B. CHAUHAN (INDIA) Thu., Sep. 25, 2008 at 6:07 am EDT
I HAVE BEEN SUFFERING FROM THIS DISEASE SINCE 2006 BUT I AM HEALTHY BY SOME MEDICATION. IF YOU COULD KINDLY GIVE ME YOUR CONTACT E-MAIL I.D. FOR MY MAILING YOUR GOODSELF MY TREATMENT HISTORY AND OTHER NOTES FOR YOUR VALUED GUIDANCE. I AM HAILING FROM KANDLA PORT, GUJARAT STATE, INDIA. AWAITING YOUR REPLY PER RETURN MAIL ON : kamlesh_gc@yahoo.com Tks & Brgds. Govind Chauhan

Comment by: Mike (Washington, DC) Wed., Sep. 24, 2008 at 9:10 pm EDT
I myself am now up to 19 yrs, I can say from my own experience and from what I've witnessed is that the attitude with which one approaches the disease has a lot to do with survival. I knew in 1989 when I was diagnosed that the odds weren't in my favor, but I also knew that there were things I could do to help myself, and that folks were working hard to come up with effective treatments. My goal from the beginning was to live long enough to be able to take advantage of those improved treatments. I sought out forward thinking physicians, did a lot of research, and pushed hard for the most aggressive treatments available. I can't say whether I've just been lucky, or it all paid off, but I've never been sick, and never had any kind of HIV-related health issues. Now, thanks to so many different advances, I look forward to many years to come. I wish I could say that for everyone I knew back when. What I have noticed though, is that people who aggressively pursued their own health, lived longest, and were happiest. Those who panicked, and decided that they were going to die, did.

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