Little Travellers Blog

Entries from February 2007

Praise for Little Travellers from Stephen Lewis

February 27, 2007 · 2 Comments

Here is a quote from Stephen Lewis about the Little Travellers and Hillcrest from his visit to the University of Manitoba last month.

“I’m wearing a Little Traveller – these wonderful pins that are made in an NGO called Hillcrest in South Africa, which is working with women and orphaned children. The Little Travellers that are available for sale are very, very much worth buying and supporting and they have raised tens of thousands of dollars – it just shows what can be done in a community if you want to make a difference. Hillcrest is a wonderful project and it is terrific that the dollars are going there directly.”
– Stephen Lewis, Former UN Special Envoy to HIV/AIDS in Africa

It is truly an honour to hear such positive words about our project by Mr. Lewis.  For more information about Stephen Lewis and his humanitarian efforts, please visit the Stephen Lewis Foundation.

Categories: AIDS · ARVs · Africa · Blogroll · Canada · HIV · HIV/AIDS · Little Travellers · Manitoba · News · Society · South Africa · Thoughts · Winnipeg

Little Travellers news has been moved to our blog

February 24, 2007 · Leave a Comment

Today we decided to move all our Simunye/Little Travellers news over to this here blog from now on. The latest news is still linked into our website, so you can still get the same news there as well, but this brings it all together in one place.

The blog also gives you guys (our valued visitors) more features and more ways of getting our news to you, including our nifty little email and RSS subscription feature (look to the right). It also gives you the ability to participate by commenting on our news, so it’s more of a conversation now too.

Here’s an archive of the news from our old news page. It’s got some great links in it, so be sure to check them out:

Categories: Little Travellers

Last night's fundraiser was a smash!

February 12, 2007 · Leave a Comment

Last night we had a fundraiser for Simunye and the Hillcrest AIDS Centre at Times Change(d) which raised over $1200! We sold several dozen Little Travellers, which are now making their cute little way around Winnipeg. Thanks to everyone who came out on such a cold night to show your support, Andrew Neville and the Poor Choices for the rollicking entertainment, to the good folks at Times Change(d) for a great time, and Cam for putting this thing together!

And hey Cam, how’s it feel to be 30 now?

Categories: AIDS · Africa · Canada · HIV · HIV/AIDS · Little Travellers · Manitoba · News · South Africa · Winnipeg

South African Diary: “Living With AIDS”

February 4, 2007 · 1 Comment

BY Thembi Ngubane

Thembi Ngubane.
Twenty-year-old Thembi Ngubane.

Editor’s note: Five million South Africans suffer from HIV, the virus that causes AIDS. This makes South Africa the hardest-hit country in the world. Fully three-quarters of new cases are girls and young women between the ages of 16 and 25. One of those women, Thembi Ngubane, agreed to record an audio diary of what it’s like to live with HIV. Thembi, who is 20 and lives in Khayelitsha, a wind-swept township outside Cape Town, spent long hours reflecting on what it’s like to have an intruder in her body and how her life has changed since she was infected. In collaboration with independent producer Joe Richman of Radiodiaries.org, FRONTLINE/World presents “Thembi’s Story,” in a format that is new for us, what we call a Direct Voice Dispatch.

The Trespasser

Every morning when I wake up I run off to my drawer, take out the mirror and look at myself. Then I start to do my prayer. I say it every day, every time when I’m feeling angry, like how when you are angry at someone, you always have that thing inside you that you need to tell that someone what you feel. I say, “Hello HIV, you trespasser. You are in my body. You have to obey the rules. You have to respect me. And if you don’t hurt me, I won’t hurt you. You mind your business, I’ll mind mine. Then I’ll give you a ticket when your time comes.”

I never thought I would worry about HIV and AIDS. It was the last thing on my mind.

I’m going to tell you how I was infected. I had this boyfriend, then we broke up. I went my way, and he went his way. A year later I heard that he died. When I went to his house, his family was gathered there. I said, “What happened? Was he shot? Was he stabbed?” His sister told me no, he was sick. I said, “What?” She told me he was very thin, and he couldn’t talk, then all of a sudden he just lost a lot of weight. Then I asked her, “What if he had AIDS?” She said, “I don’t know.” That’s when I started to get real worried.

I decided, OK, I’m going to go for a test. I went to the clinic. They bring all of the equipment in front of me and just prick all of my fingers. Then 10 minutes passed by. The counselor came back and said, “We need to have another one.” He started to do another one and another one. They did all my five fingers, and I started to worry. I kept thinking, Why is he testing me five times? Then he said, “OK, now it’s time for your report. When your blood looks like this” — he pointed at the test results — “it means you have the virus. You are HIV positive, and you’ve been positive for many years.”

“When your blood looks like this” — he pointed at the test results — “it means you have the virus. You are HIV positive, and you’ve been positive for many years.”

I just stared at him and said, “OK.”

Now I’m considered stage 4. When you are stage 4, you are no longer HIV positive anymore. They say you’ve got AIDS.

The doctor told me I was very much at risk of getting sick. He said it’s like swimming in a lake where you have crocodiles. You can swim for some time without getting bit, but if you stay for a long time, at some point you’re going to get bitten.

Getting Sick

For a few months, I stopped recording. I didn’t want to hear my sick voice. I didn’t want people to see me like this and hear me like this. I couldn’t even look in the mirror — the way that I looked, my face was sort of becoming like bones and dark, and my eyes were kind of big, and I was shaking. I couldn’t walk. All the things that were happening, I thought they would never happen to me. And my boyfriend, Melikhaya, was very, very worried. He would plead with me to go to the hospital, but I didn’t want to go. I was afraid of the way people were going to look at me. People would stare and start to point, “Look at her, look at her.”

I just wanted to hide myself. Then my mother showed up. When she came into the house, she stared at me because the last time she saw me I was fine, and now I’m thin like this. Than she said, “Child, why are you like this?” I just looked into her eyes — she was very afraid. I looked at her and said, “I don’t think I’m going to live long.” And she said, ‘OK, don’t worry. I’m going to take you to the hospital.” Then she put me on her back and took me to the hospital.

Thembi uses a radio recorder.
Thembi prepares to record another radio diary installment at her home near Cape Town.

A few weeks later, I visited another doctor. His name was Dr. Abrams. He asked me how I was doing. I was coughing. I told him, “I have pains in my neck and in my head.” He took some blood and looked for signs of infections. He tapped on my chest and told me it was dull and hollow in there. He told me I was too thin and very short of breath. Then he told me I needed to be on ARVs, to bring down the virus count.

I am very lucky to be in a community that supplies ARVS because in some areas they are not available. “ARV” stands for “anti-retroviral.” Anti-retrovirals are medicines that help to fight the virus. You must take them for the rest of your life.

Relationships

My boyfriend’s name is Melikhaya. We live together. We’ve been together for two years. Everyone knows we are very close. If they see Melikhaya, they see me. He met me and I met him and that was it. I remember when I found out about my HIV status — it was very painful to tell him. I thought, What if I’ve also infected him? Now I’ve ruined my life, and I’ve ruined everybody’s life.

He doesn’t want to blame me. He says that I didn’t chase after AIDS. He tells me he loves me and to just be strong. And then he teases me: He jokes that my biggest fear is that if I die first, he’ll find another girlfriend.

Now I have to tell you something that will come to you as a surprise. Melikhaya and I have a baby. Onwabo is almost a year old. She has many toys.

“I thought, At least I will have a child to leave behind, even if I die. And my family will see me in that child. I just wanted something to call my own, something to live for.”

When the doctor told me that there were things they could do to help prevent the baby from being infected, I decided I wanted a baby.

Onwabo is fine. We gave her a drug called AZT when I was in labor. [By using AZT and other drugs and by not breastfeeding, the transmission rate can be reduced dramatically.] She’s been tested, and she is HIV negative. At first I didn’t want people to know that I was pregnant. I felt I didn’t have the right to have a baby. I thought if I had a baby, maybe in the hospital they would arrest me. Sometimes I think maybe it wasn’t the right thing to do, but I just wanted it so bad. I thought, At least I will have a child to leave behind, even if I die. And my family will see me in that child, everyone will see me in that child. I just wanted something to call my own, something to live for.

Thembi in the arms of her boyfriend Melikhaya.
A pregnant Thembi with her boyfriend Melikhaya. Their child, Onwabo, is not infected with HIV and is now a year old.

The way that I care about Onwabo and the way that I love her makes me think about how my mother feels about me. My mother has clothed me, fed me, raised me and now, at the end of the day, she must also bury me. I was supposed to be the one to look after her. She had put me on her back when I was young, and now that I am an adult, she must again put me on her back. That is not right.

My parents don’t live together. They live in different townships, but not far. My father is kind of an old-fashioned person. He doesn’t know that I have AIDS. I haven’t told him. I feel like I could tell the whole world, but not him. And now I feel like I’ve been hiding for so long, I just have to tell him because he’s my father. I want him to hear it from me.

Here we are at my dad’s house, and it is raining a lot. The roof of my father’s shack is made of tin. I told him, “OK, Dad, before, in the past, there was no epidemic like AIDS, but now people are suffering from it. How do you and the other old people think about it?” He told me, “It’s hard for us old people. You clothe the kid now, tomorrow the kid is dead.” I told my father, “I have news. I was trying to tell you, but I just couldn’t. But I don’t want you to feel as if I am hiding something from you. Three years ago I was discovered HIV positive. I have AIDS. But everything is under control. I’m on ARVs. My health is fine. I’m going to the good doctors. So I don’t want you to worry about anything. Just for you to know because it has been kept a secret for a long time.”

My mother always said that you must be tough even if you are feeling hurt. You must not always be jelly belly, cry, cry, cry, cry. Telling my dad was one of the hardest things that I have ever done. But I didn’t want to cry. He must see just a tough face. I wanted him to see that I was not afraid. That I was going to be OK.

Plans

It’s been about a month now since I started on the ARVs. In about two weeks, I could walk and breathe and do things. So when I look back, I just think it was some sort of miracle or something. Let me see outside, what the day looks like. I’ll show you around my neighborhood. It is a bright, beautiful day. People are starting to wash their laundry, putting it on the line. Music is coming from every house. I just love it today.

“In the past, our parents were suffering from apartheid. They wanted to be free. And now it is the same with HIV and AIDS. This is the new struggle.”

My neighborhood is very crowded. There’s this shack behind another shack. Or there’s this house, and behind the house is a shack, and behind the shack is another shack. Noxola is one of my friends. She lives nearby. She was diagnosed HIV positive in 1999. She has two daughters. There are a lot of us here in Khayelitsha who are sick, but they don’t disclose it because they are scared of discrimination. People do talk, do point, do whisper. Sometimes if they hear if someone is HIV, they burn your house down so you can’t stay there anymore. In the past, our parents were suffering from apartheid. They wanted to be free. And now it is the same with HIV and AIDS. This is the new struggle.

Right now I am making a bottle for Onwabo. Now it’s almost half past 10, and we are preparing ourselves for sleep. Goodnight. Where is the other blanket? She is already asleep. Melikhaya is already in bed. As always, I’m the last person to sleep.

I’m just imagining what this world would be like without me. I’m not scared of dying, but I’m scared of not being here. Leaving my baby behind. I just want enough time to see her grow a little bigger.

AIDS is not going to bring me down. I am the one who’s got hands and feet and a mind. And it is only something that is inside my blood. So it will try to rule maybe inside, but outside I’ll be the boss. I want to study further. I want to have a great job. There are a lot of things I want to get done.

I’m just going on with my life.

**********Listen to Thembi’s Radio AIDS Diary **********

HIGHLY RECOMMENDED!!!!!!

Categories: AIDS · ARVs · Africa · Blogroll · HIV · HIV/AIDS · Human Rights · International Development · Politics · Social Justice · Society · South Africa · Thoughts · Uncategorized

Where is your Little Traveller?

February 2, 2007 · Leave a Comment

Take a minute to tell us where you and your little traveller are at our new little travellers map! The map is another step to increasing our web-based promotional/advocacy efforts around here, so check it out. You can also see where other little travellers are, anywhere in the world. You might just find other little travellers right in your own neighbourhood :)

Categories: AIDS · Blogroll · HIV · HIV/AIDS · Little Travellers · News · Uncategorized

Finding hope in South Africa (about the Little Travellers & Ilan!!!)

February 2, 2007 · 1 Comment

Finding hope in South Africa
February 02, 2007 | Myron Love | The Medical Post

Each summer, medical student Ilan Schwartz volunteers at an AIDS clinic in South Africa, the country of his birth, and finds creative ways to help the afflicted

Ilan Schwartz’s home may be Winnipeg, but his heart is in South Africa and, more specifically, the Hillcrest AIDS Clinic near Durban.

For the past two summers, the 24-year-old University of Manitoba second-year medical student has volunteered at the clinic, which is located in a predominantly white town 30 minutes from Durban in KwaZulu-Natal, South Africa, one of the hardest hit areas on the continent.

In addition to volunteering his time in the summer, he is also raising money to help support it through the sale of “Little Travellers”—South African-made dolls on pins. The dolls are made by women who are caregivers at the clinic and whose families and friends have been affected by AIDS.

Thus far, Schwartz, with the help of colleagues and friends, has raised more than $50,000 through the sale of the $5 dolls. The money, Schwartz says, helps Hillcrest maintain its programs and provides economic empowerment to the women who make the dolls.

“We often hear references to the AIDS disaster in Africa, but what does this really mean? It is difficult to put a face to the tragedy, because we learn only of sweeping generalizations.” Schwartz is originally from South Africa. His parents, veterinarian Dr. Peter Schwartz and mother, Hilda, came to Winnipeg 19 years ago. While Schwartz had been back to visit a few times, he says his images of the country were more from pictures than from memory.

“I wanted to go back to South Africa and do something in the public health area,” he says. “The most pressing public health issue in South Africa today is AIDS. I contacted an organization which put me in touch with the Hillcrest AIDS Centre in KwaZulu-Natal in eastern South Africa.”

The HIV infection rates in South Africa are astronomical, Schwartz reports. The provincial adult infection rate in KwaZulu-Natal alone is 36%. “Yet you would never know that so many people have HIV and many are dying of AIDS, because there is still such an enormous amount of stigma surrounding AIDS,” he notes. “People don’t talk about it, and they don’t want to acknowledge its presence in their communities. The stigma is the main reason why the AIDS centre is in Hillcrest, a posh and predominantly white town just 30 minutes from Durban, and not in the communities most affected.”

Most of the people the centre serves are from the poor communities in the Valley of a Thousand Hills surrounding Hillcrest. If the centre were in those communities, Schwartz points out, it would go unused because people would fear being seen by their neighbours as they entered the facilities.

“They did try to open an office in one of the nearby communities, but no one used it and it was vandalized, so it was closed down.”

Although many people come to get tested and counselled there, the Hillcrest centre is not a medical clinic per se, Schwartz points out. The services it provides are holistic and cover many of the different facets of the struggle against AIDS.

The centre, for example, operates several income-generating schemes. “Healing the physical manifestations of the disease is of limited use if the patient does not have anything to reward their recovery,” Schwartz says. “Most of the patients—or ‘clients,’ as they are known—are poor, living from meal to meal, unemployed, with limited social support. The centre therefore aims to tend to psychosocial well-being as well.”

The centre also has a food program where needy client families are provided with weekly food packages from a horticulture program, where clients are taught how to grow their own food. The hope is that they can grow enough to put food on their tables, and surpassing that, be able to have a surplus to sell in local markets.

For AIDS patients who are very ill and bed-ridden, the centre has a compliment of 50 home-based caregivers who live in the communities. Each caregiver has as many as 15 patients who they visit twice a week, feeding them, cleaning them and supervising their medication adherence.

“I spoke to two of them, both in their early 20s, like myself, about what drives them to do what they do,” Schwartz says. “It seems that in many cases, they just don’t have many other options. With a 60% unemployment rate (and much higher in many of these communities), you do what you can. They do receive a stipend, a meager R500 ($100 CDN) a month, just as of this past December. I have a lot of respect for them.”

Schwartz’s assignment in his first tour of duty at the centre was to design and administer a survey in order to understand the socioeconomic and family profiles of new clients. “In other words,” he explains, “I was aiming to find out features of the clients, such as if they work, their education levels, how many children they have and if those children are in school, how often and what they eat, etc. This endeavour has given me the opportunity to go with the nurses on visits to patients’ homes. I’ve seen some very sad and frustrating things. It is difficult to express the impotence that I feel, entering one house after another where a young person—not much older than myself—is lying in bed, with sunken eyes and hollow, jutting cheekbones.”

What Schwartz found most frustrating is that many South African AIDS victims are not receiving the treatments that could really help them. The way antiretrovirals (ARVs) are being delivered is just not effective, he says. To begin with, the patient needs a referral to go to a clinic to get a CD4 count. Then they need R150 ($30) to get the count done. It is worth mentioning that many of the patients do not even have the R10 to take a mini-bus taxi to the hospital. Then, if they are below 200 CD4 cells/Ml, necessitating anti-retroviral therapy, instead of getting the ARVs they are sent off with three months worth of antibiotics, to prove their adherence to the medication regiment. Only once they have completed this placebo-esque treatment can they begin their ARV therapy. By this time, many people will have died, or their AIDS will have progressed beyond hope.

Still others get their ARV treatments, Schwartz observes, suffer some side-effects, visit the sangoma (traditional healer), who gives them something to make them vomit, picks up the ejected tablet, and explains authoritatively that it is this poison that is making the patient sick.

“This is a serious problem,” he says. “I went one night to the medical school in Durban, where I heard a sangoma speak. There seem to be two schools of thought among the sangomas. Some, such as the one I heard, take courses and get educated about HIV, ARV therapy, and even some basic virology and immunology. The other school, the more dangerous of the two, believes that all of their knowledge is inherited from the ancestors. They have no desire to learn about AIDS. That willful ignorance is costing lives.”

Schwartz says he would like to return to Hillcrest again next summer. He is considering returning to South Africa to live after he finishes medical school. He would like to specialize in AIDS research and treatment.

“Despite growing up here and feeling Canadian, I still feel a connection with South Africa,” he says. “Despite the high incidence of AIDS and high crime rate, South Africa is an exciting place to be right now. A wonderful social experiment is taking place there and most people are hopeful about the future.”

He wants to let readers know that they can make a world of difference by buying Little Traveller dolls (www.littletravellers.net).

Myron Love is a writer in Winnipeg.

Categories: AIDS · ARVs · Africa · Blogroll · HIV · HIV/AIDS · Human Rights · International Development · Little Travellers · News · Politics · Social Justice · Society · South Africa · Thoughts · Uncategorized