Youth leading to achieve an AIDS-free generation


In a recent Lifelong AIDS Alliance press release, a group of advocates wrote:

The CDC found that in 2010, youth ages 13-24 accounted for over a quarter of the new HIV infections in the US whereas in Seattle, only one in every eight people are diagnosed with HIV between the ages of 13-24 years old.

In fact, the CDC reports that approximately “60% of all youth with HIV do not know they are infected, are not getting treated, and can unknowingly pass the virus on to others.”

Last year, Ed Murray, mayor of the city of Seattle, proclaimed April to be Youth HIV & AIDS Awareness Month. In the proclamation, he encouraged “all within Seattle to educate themselves and others of the very real threat HIV/AIDS continues to pose to young people and to contribute their talents to our ongoing fight on behalf of everyone impacted by this disease.”

11079999_1081136428570350_4514214241474059868_n

In truth, it’s the young people who are responding to this health issue that is still impacting youth and young adults. In Seattle, the youth HIV activists who urged for the city proclamation last year are continuing the awareness with hosting an educational community forum in celebration of National Youth HIV/AIDS Awareness Day (NYHAAD) held yearly on April 10th. The forum will be held on April 18th Saturday 1PM-3PM inside the Auditorium at the Downtown Central Library which includes an honest dialogue about HIV and AIDS stigma affecting youth communities in 2015 as well as prevention efforts.

This is a great chance to hear from 4 positive youth in Seattle area and PrEP Advocate Panelists. “This event is so important because it’s youth developed, youth led, and youth run,” Manuel Vengas, Seattle NYHAAD Youth Ambassador from Advocates for Youth, recently said.

Everyone can do something. Engage with your community and family at home. Most importantly, we need to have these discussions with our youth – otherwise we are neglecting them valuable information. Even though Seattle recognizes April as Youth HIV & AIDS Awareness Month, there’s still much to be done here and throughout the US as we strive to build an AIDS-free Generation. If folks can’t attend the community forum that’s understandable but there’s plenty of other ways to get educated and involved. There’s a list below of youth resources to get you started. Also consider joining Seattle area youth HIV activists, and regional community partners in a live twitter chat TODAY from 3-5PM. Join the Twitter chat by following @HEYOYouth and #PNWYouthHIV.

Let’s talk about this!

The forum is presented in partnership with the #MyHIVMoment campaign, a collaborative effort of Lifelong, BABES-Network YWCA, the Center for Multicultural Health, Entre Hermanos, Gay City Men’s Health, Seattle Counseling Services, and We Are 1.

~

Youth Resources

Youth can drop-in for free, confidential HIV testing at Lifelong weekdays from 8:30a.m. to 5:30p.m. For a full list of testing locations, click here.

The Seattle Young People’s Project is a youth-led, adult supported social justice organization that empowers youth (ages 13-18) to express themselves and to take action on the issues that affect their lives. For more information, click here.

Health Education Youth Outreach (HEYO) is Lifelong’s youth education program for youth age 16-24. Through peer-to-peer outreach and education, HEYO reduces stigma around queer issues, promotes healthy sexual choices and makes HIV testing and other resources readily available. For more information, click here.

The Inspire Youth Project (formerly Rise n’ Shine) provides emotional support programs, stability, advocacy and AIDS education for children and teens affected by HIV/AIDS. For more information, click here.

Safe Schools Coalition offers support for LGBTQ youth. For more information, click here.

BABES Network-YWCA offers peer support to women & heterosexual men living with HIV and their families as well as HIV education and resources. For more information, click here.

For information about PrEP and PEP, click here or see the information below.

Harborview Medical Center
M-F regular business hours: (206) 744-4377
M-F outside normal business hours: (206) 726-2619
Or visit the Harborview Emergency Room at 325 9th Ave., Seattle, WA.

For Needle Exchange locations, click here.

For drug and alcohol resources in Seattle & King County, click here.

-Written by Tranisha Arzah, BABES Network Peer Advocate

Living well with HIV


What is HIV?

To start, it is the abbreviation for Human Immunodeficiency Virus. HIV is a virus that can only infect people and that weakens the immune system. Unlike other viruses, HIV does not clear out of the body – there is currently no cure for HIV.

According to AIDS.gov,

We know that HIV can hide for long periods of time in the cells of your body and that it attacks a key part of your immune system – your T-cells or CD4 cells. Your body has to have these cells to fight infections and disease, but HIV invades them, uses them to make more copies of itself, and then destroys them.

Over time, HIV can destroy so many of your CD4 cells that your body can’t fight infections and diseases anymore. When that happens, HIV infection can lead to AIDS, the final stage of HIV infection.

It used to be said that HIV was a “death sentence” – but nowadays, there are many options for treatment and medication, and programs throughout the United States to help patients afford medication.

Around the world, there are about 35 million people living with HIV. There are about 1.2 million people living with HIV in the United States, 12,300 living in Washington state, and about 7,300 in King County. In the United States, 16% of those living with HIV don’t know they are – which means they haven’t been tested and aren’t receiving the medical treatment that will help them be healthy in the long-term. What to get tested? Click here for more info on local testing sites.

For those living with HIV, medical treatment isn’t the only way to stay healthy. Having a good relationship with a doctor, and honestly and openly discussing your health is an important part of taking care of your health. And, there are additional ways to live well.

  • Manage your mental health – talk to a counselor if you’re experiencing major stress or just need to talk through some things.
  • Avoid using substances like drugs and alcohol in a way that harms your health.
  • Consider quitting smoking cigarettes and other tobacco products. Smoking isn’t healthy for anyone, but it also can increase your risk of co-infections if you’re living with HIV. Learn more here.
  • Follow a healthy diet – talk to your doctor or a nutritionist about learning how to improve your diet. Are you getting enough veggies? What about protein?
  • Keep moving! Exercise increases your strength, endurance and fitness. It helps your immune system work better to fight infections.
  • Talk about family planning options with your health care provider – there are lots of options for birth control and ways to plan for having children.
  • Learn about how to prepare to travel abroad.

These are just some ideas. What do you need to be healthy and live well? Make sure to talk about your goals with your doctor, and find support to help you be successful!

If you are a woman living with HIV, consider giving us a call at BABES Network-YWCA at 206.720.5566. BABES is here to support women living with HIV and their families. We’re happy to connect with you on the phone or via email. Or, you can join us at a support group or upcoming retreat. We’d love to get to know you and have you join the sisterhood!

WordpressHeader

Take the Test. Take Control.


National HIV Testing Day is Friday, June 27th.poster-nhtd

When was the last time you were tested for HIV?

… Let’s back up. What is HIV? Here’s a really helpful definition from AIDS.gov:

“HIV” stands for Human Immunodeficiency Virus. To understand what that means, let’s break it down:

H – Human – This particular virus can only infect human beings.
I – Immunodeficiency – HIV weakens your immune system by destroying important cells that fight disease and infection. A “deficient” immune system can’t protect you.
V – Virus – A virus can only reproduce itself by taking over a cell in the body of its host.

HIV is a virus – like the flu. But it’s a virus that our immune systems aren’t able to clear out of our bodies. When we have HIV, “we have it for life.”  HIV attacks a key part of the immune system, the T-cells or CD4 cells. AIDS.gov says: “Your body has to have these cells to fight infections and disease, but HIV invades them, uses them to make more copies of itself, and then destroys them. . . . Over time, HIV can destroy so many of your CD4 cells that your body can’t fight infections and diseases anymore. When that happens, HIV infection can lead to AIDS, the final stage of HIV infection.”

There are about 50,000 new HIV infections in the US each year. About 15,500 people with an AIDS diagnoses in the US died in 2010. And while 15 years ago, an HIV/AIDS diagnosis was considered a death sentence, today there are many medications and medical treatments that have been successful in keeping people living with HIV/AIDS healthy and thriving for years and years.

However, 1 in 6 people living with HIV/AIDS don’t know that they’ve contracted HIV. In order to receive medical treatment and stay healthy, it’s super important to know your HIV status.

Friday is National HIV Testing Day. Before Friday, find an HIV testing site near you to take a test. You can find HIV testing sites and other services near you with the AIDS.gov HIV Testing Sites & Care Services Locator. It’s quick and often free. Knowing your HIV status is the first step to prevent the spread of HIV.

timthumb

Born with HIV


How can we educate more people about what it is to live with HIV? How do we spread the word about HIV prevention? How do we build a society where there is no HIV stigma? 

A young woman, 18 years old, was interviewed by WebMD.com to tell her story of having been born with HIV, living with it as a child, and living with it now as an adult. She asked that the interview be anonymous. Read her story below.

“I was born with HIV. My father gave it to my mother before I was born. I have an older brother but he does not have it. When I was born, my father was in the hospital. They didn’t know what he had, and they never suspected he was HIV positive. That was the last test they tried.

“My mother was in one hospital while I was being born, and my father was in another hospital. They tested my mother and she was positive. They found out when I was born that I was HIV positive, but they weren’t sure at first if it would go away [hyperlink added]. So they kept testing. It never went away. I have been living it my whole life. I can’t say it is a horrible thing. It is sad because my father passed away a couple of months after I was born. And I still worry about my mother.

“A lot of my family still doesn’t know. They wouldn’t be understanding, so we kept it away from them.

“Growing up I had to go to the National Institutes of Health and get blood drawn. I knew something was wrong, but I never understood the extent of it until I was in fifth grade and began understanding that people were not comfortable and did not understand my situation. The worst part was taking the medications and not being able to eat after it. That was my biggest complaint until I reached middle school.

“I knew my mom had it, too, and she was all I had. I worried about her dying and leaving me alone.

“My mom always told my teachers [that I had HIV] because if I got a cut on the playground they would have to take care of it. And when [I entered middle school], my teacher couldn’t handle it and said she didn’t want to teach me.

“I was so scared in middle school. I thought, ‘I can’t tell anyone, no one wants to be my friend.’ And it still is like that sometimes. I am OK. I am really healthy. My doctor tells me I am doing really great. I am thankful for my positive mindset. But it is hard having friendships and relationships. By now you’d think people would know a lot about HIV, but they don’t. I would never tell someone I was not close to. Even when I do feel close enough to someone to tell them, I wonder. Are they going to say, ‘Get away from me! Don’t touch me!’ The truth is that people really do look at you differently when they know you are HIV positive.

“It is hard. I have a boyfriend now and he knows and is understanding. But I know people’s ignorance is not going to go away. I still think people are going to hate me or not want to be my friend when they learn I have HIV.

“I worry about my mom, still. My brother, he has told me he wishes he had it instead of me. But I say, ‘No, don’t wish for that, it isn’t something I would ever want.’ It is something you can take and make it a great thing to live your life to the fullest, or you can just be depressed about it. It would be different if you are used to living without it and then have it. I think that would be much harder.

“I do not know what it is like not to have it. I have never been sick. I’ve been taking the same medicine for 13 years. They changed the medicines only once because I was on the same regimen for so long. That was the only time I got sick, [which] was in reaction to the change in medicines.

“I never really got sick enough to go to the hospital. There are days I feel sick, but I have hope. I thank God because I look at others and see how much worse my situation could be. I look normal and am normal in every other aspect of my physical health.

“I plan on keeping on trucking. I plan on doing great. I wouldn’t be this way without the medicines and theoretical advances and technology. And I haven’t gone through half of the drugs yet, and that makes me happy. But it is a hard disease to have.

“It is a lot better now. Because I know I am going to be OK. I know it has gone this far and it is only going to get better. It is a bad situation, and I am making the best of it.

“I know now that people know more about HIV and AIDS. It is not now a hush-hush thing. On TV there is AIDS awareness. People want to help others and care. But I am not one to say, ‘Look at me, this is what I have.’

“I feel like people are more aware now than they ever have been. But just because there are medicines out there, and things like MTV spots and speakers who come to schools and speak to the students – even so, young people still don’t think it will happen to them. You still have to be careful.

“I think, especially for younger generations, they couldn’t even imagine knowing someone with the disease. They all sleep around, they don’t care. They protect themselves, but that doesn’t always help. They think nobody they know could ever have HIV. They would never guess I do.

“My message to other people with HIV is that I know it is hard for people to cope with. But, living though my experience, I know it is livable. You have to keep yourself healthy and be smart. You are going to be scared. It is only natural to feel that way. But your truest friends and those who love you will be OK. If you care about them enough, they will be understanding. From what I have seen, everyone has been understanding, even though I thought they wouldn’t be. Everyone has loved me more, not less, from knowing how strong a person I am. So don’t be scared is pretty much my message.

“If people don’t understand, it is their loss. That is how I think of it. There are people out there like that, but I have not met them. Like my middle-school teacher, they just don’t know. They think if you get it, you are going to die. They don’t know enough about it still. Their education level on it is slim.

“I love my doctors so far. I appreciate them and know that without them I would not be here today. People say doctors just do it for the money. But what they have done in terms of research and treatment has saved my life. I say thank you.

“Looking forward? Honestly, I don’t know. I don’t think there will be a cure. Eventually, maybe there will be a cure, but more likely it will be you can live with it and you will be fine.”

“We promised them we would tell the world.”


Last year, the National LGBT Cancer Network surveyed LGBT cancer survivors to learn more about their experiences in the health care system. More than 300 individuals from across the country participated in the survey and shared their stories.

After connecting with LGBT cancer survivors and conducting their research, the National LGBT Cancer Network made recommendations that fall beneath these six themes:

  1. Stigma plays a prominent role in LGBT healthcare. (pg. 8)
  2. The local healthcare environment determines one’s experience and is highly variable. (pg. 10
  3. Disclosure [to healthcare providers] is often related to perceived safety. (pg. 13)
  4. Respecting LGBT patients means respecting their support teams. (pg. 17)
  5. The pervasive expectation of gender conformity can be alienating. (pg. 21)
  6. LGBT survivors need more culturally appropriate support and information. (pg. 24)

In the report’s conclusion, they write:

Cancer doesn’t discriminate, but the healthcare system often

does, as evidenced by the many experiences reported here by survey respondents. These experiences, while taking place at one of the margins of the healthcare system, offer a rare glimpse into the opportunities for change in the entire system. A well-intentioned one-size-fits-all approach too often gives a message of unwelcome to LGBT patients, leading those who can avoid the system to do so, and suggesting to others that they need to remain silent about their lives, their support systems and their needs.

For more information and to read the recommendations, read the full report here.

Know Your Status!


WomensTesting_v3b

BABES @ AIDS Action & Awareness Day


This Tuesday, BABES Network-YWCA joined our partners at WHACAN (Washington HIV/AIDS Community Action Network) for this year’s AIDS Action & Awareness Day.

BABES staff – Tonya, Brenda, and Nicole – traveled down to Olympia to advocate on behalf of Medicaid expansion, keeping WSHIP, and to preserve funding for HIV/AIDS prevention, education, and other services. We loved connecting with other HIV/AIDS advocates, hearing from legislators like Ed Murray and Jeanie Darnell, and telling our stories to State Senators and Representatives from our districts! It was a long day, but throughout, we felt energized and empowered!

Governor Jay Inslee even spoke at the event – just after BABES member Tranisha spoke, shared her story, and inspired us all to take action for people living with HIV/AIDS. We are so proud of Tranisha for her bravery and courage!

pictures

BABES in Olympia!

BABES Network-YWCA Program Manager Nicole Price speaks at AIDS Action & Awareness Day

BABES Network-YWCA Program Manager Nicole Price speaks at AIDS Action & Awareness Day

Tranisha, a member of BABES Network, speaks at AIDS Action & Awareness Day

Tranisha, a member of BABES Network, speaks at AIDS Action & Awareness Day

Governor Inslee gives Tranisha a big hug after she speaks!

Governor Inslee gives Tranisha a big hug after she speaks!

Governor Jay Inslee speaks at AIDS Action & Awareness Day

Governor Jay Inslee speaks at AIDS Action & Awareness Day

HIV/AIDS Advocates from around Washington State

HIV/AIDS Advocates from around Washington State

Let’s Talk About Sexual Health


“Sexual health is about having a positive and respectful and responsible approach to sexuality and a relationship.”

The CDC asks young people to talk honestly with their doctors about their sexual health. It’s important for each of us to build trust and a good relationship with our doctors.

“Learning about sexual health issues and issues around it make it easier to talk with a partner or partners. The more you talk about it [with your doctor], the more comfortable you get talking about sex [so you’re not at risk for] HIV or herpes or gonorrhea or chlamydia or syphilis.”

Talk to a doctor, get tested at a local clinic, or find one at gytnow.org.

AIDS: Am I Doing Something?


December 1st of every year marks World AIDS Day, when folks from around the globe join together in the fight against HIV/AIDS. This year, BABES Network – YWCA is collaborating with other community organizations to host an awesome World AIDS Day symposium titled AIDSAI Doing Something?

The symposium will feature speakers on relevant topics such as stigma, how issues of race and gender intersect with HIV/AIDS,  and the latest scientific research – as well as a group of HIV-positive panelists who will discuss their personal experiences. The focus of this event is to provide information, raise awareness, and empower individuals and communities to take action against HIV/AIDS.

The event is free and open to the public. It will take place at All Pilgrims Church on Capitol Hill (500 Broadway East Seattle, WA 98102) from 1-4pm this Saturday, December 1. Light refreshments will be provided. Please join us!

Let us know you’re coming! RSVP on Facebook!

Partner organizations for the Am I Doing Something? event are Gay City Health Project, Planned Parenthood of the Greater Northwest, Public Health of Seattle and King County, POCAAN, Social Outreach Seattle, UW ACTU, Seattle Counseling Service, Lifelong AIDS Alliance, Entre Hermanos, and HIV Vaccine Trials Unit.

For general information on HIV/AIDS, click here. To find out where to get tested at a location near you, follow this link. And to learn more about the World AIDS Day Campaign, visit their website.

HIV and Homelessness: Brenda shares her story


Last week, Firesteel published the following blog post, written by Brenda Higgins. Brenda is a Peer Advocate with BABES Network – YWCA, a sisterhood of women facing HIV together. July is National HIV Awareness Month. Firesteel wanted to recognize the bravery of women living with HIV and facing many other challenges including homelessness.

Brenda Higgins, Peer Advocate at BABES Network-YWCA

I was homeless, abusing substances and making very poor choices when I was diagnosed with Human Immunodeficiency Virus (HIV) in May of 2007. I thought being homeless was hard enough, but receiving an HIV+ diagnosis while homeless was completely unbearable. My diagnosis did not stop my behaviors right away, for a short period of time I continued to take myself further and further down and in a completely life-threatening and self-destructive manner. I always did what I could to convince myself that I would never contract HIV and, that “It will never happen to me”; almost an invincible type of attitude. Yes, I knew HIV existed, but, I was ignorant to the fact that there were so many new medications and that people were living healthy, productive lives with HIV.

I was tested at Spokane Regional Health District. The day that I was given my results, was a very difficult day. I was alone. I had nowhere to go. I had no one to turn to. I could have stayed and participated in the results consultation/counseling, but the first thing that came to my mind was “I really need to get out of here!” I felt as though the walls were closing in on me and I ran.

My first encounter with an HIV/AIDS Service Provider was at CHAS – Community Health Center of Spokane. I went in because I thought I was going to just waste away and die; I was so terrified and had no idea what to expect. I soon learned from CHAS – Community Health Center of Spokane that HIV is manageable and, during the same visit I was also told that we were going to forego Antiretroviral Therapy (ART) at this time because of the fact that I was homeless and not living a healthy lifestyle. I had no stability and not at all a full understanding of what being HIV+ really meant. After a couple of months of being completely lost, something inside of me said that it was time to make changes. I realized that if I did not make any attempts to take care of myself and build a better life; I was not going to be around for much longer (not only because I was positive, also because of the lifestyle I was living).

I moved back to Western Washington and placed myself in the Everett Gospel Mission Women and Children’s Shelter. One week later I went to Catholic Community Services to apply for housing assistance, and through this amazing organization; I was referred my wonderful, HIV savvy internal medicine doctor: Dr. Dreyer with The Everett Clinic. I also entered myself into an out-patient recovery program at Evergreen Manor. Even after these attempts to better my stability, Dr. Dreyer and I both agreed that it was still too soon to start Antiretroviral Therapy (ART) because I did not have adequate housing and it was too early in my recovery. I am so grateful for Housing Opportunities for Persons with AIDS (HOPWA); this program provides the funding that makes it possible for Catholic Community Services to provide the financial assistance that afforded me to be placed into my own apartment within the next month. Within six months I was on Antiretroviral Therapy (ART) thanks to all my forward progress including the fact that I was stable, mainly in housing, but also because of each and every attempt that I made to better my quality of life.

It was shortly after that that I met the wonderful women of BABES Network – YWCA at the Seattle AIDS Walk in September, 2007. I was overjoyed that I now knew that there were other women out there just like me. BABES Network – YWCA heightened my spirit, my drive, my self-confidence and aided me in my ability to remain stable. It was in May of 2010, that Nicole Price (my Peer Counselor; now Program Manager) saw my potential, sent me the job announcement and encouraged me to apply; which is the reason that I am now a Peer Advocate with BABES Network – YWCA and am able to provide referrals and resources to other women that are currently in or have been homeless and in similar situations as myself.

According to a report provided by King County Public Health in June 2009, Facts about HIV/AIDS in Homeless Persons KCPH (most recent), out of 6283 homeless individuals, 105 had an HIV and/or AIDS diagnosis. Accessing and remaining in care while homeless, while not impossible; is very difficult to do when you don’t know where you’re laying your head at night, when you don’t know where your next meal is coming from and when you do not know if you are even going to make it to see the next day because of unsure and unsafe conditions. Among the before mentioned and so many other things; HIV is one of the most serious issues that the homeless population has to face. Intravenous Drug Use (IDU): the sharing or re-use of unclean needles, unsafe sex (mostly for a means to survive on the streets), and the use of recreational drugs that lead to unsafe sexual behaviors are major factors that play a role in the contraction and transmission of HIV and other Sexual Transmitted Infection’s (STI’s).

This is a nationwide issue and something that can be changed through persistence, commitment and with the proper use of advocacy. According to the HIV/AIDS and Homelessness Fact Sheet provided by the National Coalition for the Homeless in July 2009 (again, the most recent), “Preventative and educational programs need to be provided at shelters, soup kitchens, and other locations that are easily accessible and comfortable for homeless people. Currently, many shelters only minimally address HIV/AIDS. Sex and drug use are strictly forbidden at most shelters, so many shelters do not allow outside HIV/AIDS education and prevention programs to openly discuss those topics or to distribute condoms.”

There are measures that each individual must take in their own care, but when one doesn’t even know where to start, where do they turn when they don’t even have a roof over their head?

July is National HIV Awareness Month. What steps will you take to advocate for an end to HIV and homelessness?

Additional Resources
HIV/AIDS Epidemiology Semi-annual Reports Provided by a joint effort with the Washington State Department of Health and Public Health –Seattle & King County
United States HIV Surveillance Report provided by the Centers for Disease Control (CDC)

Housing Resources for PLWHA (People Living With HIV/AIDS)
LIFELONGAIDS Alliance – Housing
Lyon’s Building Apartments – DESC
Catholic Community Services Housing
Plymouth Housing Group
Rosehedge/Multifaith Works Housing