La Vida International adoption agency is working with gay and lesbian men and woman who want to adopt children with HIV from South Africa.
From their website:
We are excited to announce that we are accepting applications for the South Africa Special Needs Program. This program is open to single male and females and married couples. LGBT individuals and couples are welcome to apply.
Most of the children available for adoption are living with HIV and/or some have other moderate to severe special needs. In the last 30 years, living with HIV has changed dramatically and with proper treatment chldren are expected to have a normal life span. HIV has never been transmitted in a normal family living environment. Most orphans have contracted the virus through mother to infant pregnancy, birth or breastfeeding.
The South African government has flexible eligibility guidelines to adopt. These include:
Applicant/s are over the age of 25 (USCIS regulation, South Africa only requires that you be over age 18)
While there is no official cut off age, applicants age 50 and over will be accepted by Wandisa on a case-by-case basis
Applicants must be physically and mentally able to care for a child (If there is a significant health concern a doctor’s letter will be required)
Married applicants’ length of marriage should be a minimum of 2 years (at time of dossier submittal)
Applicants with minor criminal histories may be considered.
Male and Female single applicants may also apply
LGBT individuals are invited to apply
UPDATE 2016. Children’s Home | LSS is placing children from Brazil and Mexico with LGBT families. Contact them directly to find out if any children with HIV are waiting
On Sunday, Father’s Day here in America, but Monday in Russia, two men will determine if thousands of Russian orphans will grow up in a family or in an institution. Hundreds of them had already met their families. Many of these precious orphaned children are living with HIV. In fact, at least 20 Russian orphans with HIV had American families in process to adopt them when the adoption ban went into effect.
The G8 Summit is in a few days and although our Congress and Senate have been AMAZING help to families in the adoption process, President Obama has yet to respond. If you would like to write him a note to let him know this matters to you and that it needs to matter to him, that would be great! The link to his correspondence page is below, just click and fill in the info. I placed my comment in the Subject that says Administration at the very bottom under Non Policy Comments. This only takes 2 minutes of your time.
Here is a sample comment, although it is always best to personalize:
Dear President Obama,
I am saddened to know that you have yet to respond to letters written to you about the Russian Adoption Ban that 170 Members of Congress and the Senate have, in a rare show of UNIFIED support, signed requesting your involvement in finding a solution to reuniting the Russian orphans that were promised homes with American families. Please make sure this item makes it on your agenda and is discussed with President Putin at the Summit Meeting. Take just one moment and think of the love you had for Malia and Sasha the moment they were placed in your arms. Now think how you would feel if after holding them and loving on them for days, they were taken from you. Your heart would break as it is now for many American families. I know several of those families, all of which were in the process of adopting children with disabilities such as Down Syndrome and HIV. These are children who may never know the love of a family if they remain in Russian orphanages. It is an urgent human rights matter that Russian orphans with disabilities have the opportunity to be adopted by Americans and other international families.
The Summit meeting is fast approaching. Please make sure this item makes it on your agenda and is discussed with President Putin at the Summit Meeting.
Other ways you can help:
‘Like’ 300 Broken Promises on FB to support the families in process.
Please help advocate for orphans with HIV by adding the photolisting slideshow (see left sidebar) to your blogs and social media. Please contact me if you would like help adding the slideshow to your websites or if the slideshow is too wide for your sidebar. In blogger, I believe you add an html widget (not a slideshow widget).
Here are the Codes:
STANDARD SLIDESHOW CODE:
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WordPress.com: (via Gigya) REMOVE THE SPACES FOR END-CAPS
[ gigya src=http://www.slideroll.com/player.swf?s=0jjqnyh0 ]
Google Gadget URL:
Facebook Static FBML (?) for Pages:
<fb:swf swfsrc=’http://www.slideroll.com/player.swf’ imgsrc=’http://slideroll.com/users/group708/user708504_20110217224539/thumbs/proj440300.jpg’ flashvars=’s=0jjqnyh0&cs=1′ wmode=’transparent’ swfbgcolor=’ffffff’ waitforclick=’false’width=’250′ height=’250′ salign=’tl’ scale=’showall’ /><div align=”center” style=”width: 250px; color: #999;”> Click image to view slideshow.</div>
NEW MYSPACE CODE:
<div align=”center”><object type=”application/x-shockwave-flash” data=”http://www.slideroll.com/player.php?s=0jjqnyh0″ id=”slideshow” base=”http://www.slideroll.com” width=”250″ height=”250″ wmode=”transparent” scale=”noscale” salign=”tl”> <param name=”movie” value=”http://www.slideroll.com/player.php?s=0jjqnyh0″ /> <param name=”allownetworking” value=”internal” /> <param name=”allowScriptAccess” value=”never” /> <param name=”enableJSURL” value=”false” /> <param name=”enableHREF” value=”false” /> <param name=”saveEmbedTags” value=”true” /> <param name=”base” value=”http://www.slideroll.com” /> <param name=”wmode” value=”transparent” /> <param name=”salign” value=”tl” /> <param name=”scale” value=”noscale” /> <param name=”allowFullScreen” value=”true” /> </object></div>
Simple Embed Code:
NOTE: If your slideshow runs slowly, remove the wmode=”transparent” and <param name=”wmode” value”transparent” /> tags from the code.
Here are 2 stories written by 2 different families on opposing sides of the disclosure topic.
Written by a family who chooses to disclose their child’s HIV status:
When my husband and I were considering adopting our daughter, who has HIV, one of the first things that we discussed was the issue of disclosure. Whom would we tell? How would we go about telling people? I had volunteered for five summers at a camp for children with/from families dealing with HIV. I had also worked for two years as a case manager at an AIDS service organization. I had witnessed many, many individuals and families who kept the status of their HIV+ family member secret, and I had watched many individuals and families struggle greatly with the stress of doing so. I met children who lived in fear of accidentally “outing” an HIV+ sibling or parent. I met HIV+ children who lived in terror of their friends finding out their secret and abandoning them. I met parents who felt that they had no one to trust and who carried the burden of their and/or their child’s status alone. My husband and I considered these scenarios carefully, both to determine what we wanted for our child but also what we wanted for ourselves. We felt that living with HIV was not just our child’s issue; it would become a family issue, and it would affect the emotional climate of our family.
What we determined was that we did not want our child to live in fear. We did not want her to fear that her friends and the people in her life only loved a part of her and that they would disappear if they knew all of her. We did not want her to live with a huge secret. We did not want her to wonder what people would think if they knew she had HIV. We wanted our child to be secure in the knowledge that the people in her life loved and accepted her, all of her, exactly as she is that no one in her life is afraid of her. In addition, we didn’t want our younger children to feel that our family lived with a secret that might destroy us if it were found out. We did not want our kids to feel responsible for being the gatekeepers of such a secret. We did not want our children, any of them, to feel isolated and alone with the stress of living with HIV. And finally, neither my husband nor I felt comfortable with the idea of perpetuating the stigma of HIV by living as though it was something that needed to be a secret. We are familiar with the argument that HIV isn’t a secret but that it is personal information that shouldn’t be shared. We asked ourselves whether we would disclose that one of our children had cystic fibrosis or diabetes or any other health issue that would affect our children’s lives and emotions. Our answer was yes, we would, because no one blames children for having these illnesses, and everyone expects that the child and family living with these illnesses needs support. We feel that HIV is the same and that it’s the social stigma of HIV that makes it seem different. My husband and I did not want to have to come up with ways of stretching the truth when necessary. We did not want to have to lie if our child were to become ill and need to be hospitalized. We did not want those in our lives to feel betrayed if/when they found out that we had kept this information from them. We had the feeling that, if we told people that our child had HIV, it might be a big deal, but if we didn’t tell people and then they found out, it would most likely be a HUGE deal. We felt that the backlash from keeping such a secret would most likely be far greater than the reaction to an initial disclosure.
Most of our close friends and family members knew that we were sponsoring an HIV+ child. Disclosing to them consisted mainly of telling them that we would be adopting this child and offering the opportunity to discuss their concerns with us. I wrote up an information sheet about HIV, how it is transmitted (and how it is not transmitted), how it is treated, and the likely prognosis for our daughter. I offered this to our friends and family when we told them of our plans to adopt our daughter. No one took the information sheet, and with very, very few exceptions, everyone was extremely supportive. We presented the information in a straightforward manner and with the expectation that our friends and loved ones were already educated about HIV or would be willing to become educated. We did have some family members who were quite opposed to the idea and concerned that we were putting them, their children, ourselves, and our other children at risk. One family member was concerned about how it would affect her children if our child died. We handled people’s concerns by continuing to provide factual information in a calm manner while communicating clearly that our decision was our decision and that we were committed to adopting our daughter with or without their blessing. Although some family members remained opposed to the adoption to the very end, all of them have ended up welcoming our daughter into the family and none of the threats of ceasing contact with our family have materialized.
We had planned to homeschool our daughter, so we felt that the situation would be fairly well controlled. All the families in our homeschool group were aware of our daughter’s status before she came, and all were supportive. In the end, the best choice for our daughter was to go to school. We have been open with both of the schools she has attended, and the the administration and the teachers have been very supportive. We have presented the information in the context of the whole picture of our daughter and how her life experiences have affected her emotional and educational life. Our daughter has chosen not to disclose to her school friends. She has told me that she doesn’t trust her school friends well enough to disclose to them, and we recently had a very anxiety-inducing situation when our daughter was invited to spend the night with a school friend and was very anxious about her friend discovering her medication and asking about it. Although we talked about various ways of handling the situation and the medication was never discovered or commented on, we felt that this situation gave us a glimpse into what life would be like if we had chosen to keep our daughter’s status a secret, and we remain satisfied with our choice to disclose. Our daughter’s opinion is that although she chooses not to disclose to school friends, she is glad that “everyone else” knows that she has HIV and that they “aren’t afraid” of her.
My husband and I both know that disclosure is an issue that will affect different families in different ways, and we respect that different families will handle it differently. As a guest blogger for Positively Orphaned, I welcome the opportunity to share my family’s journey in the hope that it would be of benefit to other families who are considering this issue.
Written by a family who chooses NOT to disclose their child’s HIV status:
I am a very open person, and have been known to share probably more than is necessary throughout my life. In late 2006 my husband and I made a decision that would ultimately challenge and limit my open nature. Our decision was to adopt another child. This time we were adopting an HIV positive child and there was another layer of research and decision making to be done that reached far beyond the experience we had with our first adoption. One of the most important decisions to make was whether or not to disclose our child’s HIV status.
We started the process being fairly open about the fact that we were adopting an HIV positive child. A few friends, some colleagues at work and our immediate family were informed. Our news was always received with support and interest. We live in a very diverse and socially progressive part of the country and most of the people we interact with are well educated and knowledgeable about HIV/AIDS. We felt comfortable talking about it, and did not meet any ignorance within our closest circles.
Things started to change after we brought our daughter home. We learned that she was completely unaware of her own HIV status and really had no understanding of this disease. We began having regrets about our initial rush to disclose. We realized that we, too hastily, had made an important life decision about a small child that we did not even know. We did not feel confident that our disclosing had even had any impact on reducing the stigma. We simply could not find a compelling reason to disclose anymore.
I began doing some research to gather information about how children, whose status had been exposed by their parents while they were young, were faring as teenagers and adults. There was not much data to gather, and the little I did find was not very encouraging. Most of the adoptive families I have connected with during our process have chosen to disclose, but their children are young, just as mine are. I felt that I did not have insights from young adults on how their parents decision to disclose had affected their self image. We decided that we were not willing to take a risk with our daughter’s self image and her trust in us as her parents.
We spent the next many months getting to know her and falling in love with her. She began immersing herself in her new life and in school. In the summer we spent time with our extended family and unfortunately, it turned out that some of the family members who initially were understanding about her status were now treating her differently than they treated our other kids. It was subtle, but our daughter noticed it. I noticed it. It broke my heart. My relatives had a new baby and would not allow our daughter to touch her. The parents guarded over their baby and refused to interact with my daughter. It was shocking to me and once again I regretted ever having disclosed her status. We had spent countless hours educating this family about HIV prior to them meeting her. They even expressed quite a bit of knowledge about the disease themselves. Even with knowledge of the facts about HIV and stigma, the fear still abounds. Seeing the hurt and confused look on her little face that day made me vow to myself that I never again would use my daughter to educate others about HIV. This is not my job. If anyone asks me if my daughter is HIV positive, I answer honestly by saying that she is healthy- because she is.
My daughter is only 7 years old and going through an immense transition right now. Together with our Pediatric Infectious Disease doctor we are still in the early stages of explaining HIV to her. This is our priority right now. Informing those around us of her status is not important. They are not at risk, and I take comfort in knowing that the law is on our side. When she is a teenager and an adult I want her to look back on this time knowing that we focused on building her self confidence and empowering her to make strong decisions about her own life. That we protected her privacy, just as we protected her sibling’s and our own privacy. That we would not let her be known by her status and that the decision to disclose would be fully hers to make. I am not HIV positive and I do not presume to know what it is like to live with this disease. I can only try to guide her to a place where she can find the strength and the courage to be comfortable in her own body- with this disease. When she is mature enough to understand the medical and social aspects of this illness and is able to make an informed opinion about disclosure, it will be with the support of her parents.
We also do not regard our daughters HIV status as a secret, just as we do not regard our other child’s ADD status a secret. This is just private information. Should someone find out about anything private in our family we will certainly use that opportunity to educate. If one of our children tells someone about a sibling’s status, we will use that opportunity to teach our children about respecting other people’s privacy. We will not make a big deal out of it.
I have found that joining the effort to fight HIV stigma without disclosing my child’s status is not difficult. I have been involved in various efforts to remove the HIV immigration ban, I have met with policy makers as well as with HIV positive people in our community. I am in the process of starting a non-profit and with this will continue to do whatever I can to raise HIV awareness and fight discrimination. Perhaps one day my daughter will join me, but I will let it be entirely up to her.
Adeye, otherwise known as No Greater Joy Mom is hosting a fabulous giveaway which includes fantastic prizes such as a new Kindle, $100 Amazon gift card, $50 and $100 Gift Certificates, artwork, jewelry, Vera Bradley bag, quilts, girls clothing and accessories, and tons of other stuff – more than 100 prizes total. She is raising funds for an adoption grant for Vanya with HIV in Ukr*ine, to help him find an adoptive family. The giveaway ends April 13th, so CHECK IT OUT, spread the word and enter to help Vanya and win some fantastic prizes! It’s very easy to enter – even a $1 donation or blogging about the giveaway will get you entered into the giveaway. At the time of this writing, Adeye has raised $7,000 with a goal of $20K.
One of the big questions I hear when people are considering parenting a child with HIV is “what will their life expectancy be?” Dr. McComsey says “relatively normal life expectancy” and Dr. Gallant says “close to normal”. Medical professionals don’t know the exact answer because children born with HIV/AIDS are nearing 30 years of age at the most (HIV/AIDS was first discovered in this country in the early 1980s). Sadly, many of the children born with HIV in the early days died of AIDS because there were no adequate treatment options. However, children born today with HIV have an excellent prognosis due to the antiretroviral medications. Studies regarding life expectancy are done on adults and it is extremely important to remember that the participants in these studies are often in vastly different situations than children growing up in adoptive families. For example, they have other risk factors that affect their life expectancy in addition to HIV such as poor nutrition, co-infections, IV drug use, homelessness, low socioeconomic status, unhealthy lifestyles and poor adherence to treatment.
Only the most recent studies are worth reading since HIV/AIDS research changes all the time as the treatment options get better. Studies from 2005 indicate anywhere from 6 years less than normal to 21 years less than normal. The average between these 2 extremes is 13.5 years less than the normal US lifespan (78) which is an average life expectancy of 64.5 years (2005). These studies are already 6 years old and the numbers get higher all the time as the medications get better. This means that children born with HIV can live long enough to meet their grandchildren. The best thing we can do to increase life expectancy is encourage our children to lead a healthy lifestyle and diligently adhere to their medications.
There is a new section of links in the right column titled “Grew Up with HIV”.
Now that HIV/AIDS has been around for nearly 30 years, there are adults who have had HIV all their lives. Thankfully, they are speaking out about their lives and inspiring others. These people were born at a time when anti-retroviral medications were not yet available (before 1996) and they know the heartbreak of losing loved ones who did not live long enough to access ARVs. Those who survived the early days with very few treatment options eventually got access to ARVs and many lead normal healthy lives now. However, some adults in this same situation were not as lucky and their disease progressed to AIDS before ARV treatment was an option which has lead to health problems or cognitive issues. Others did not grow up in advantageous living conditions (some examples – parents who were not attentive to medication regimes, neglectful situations, and/or living with HIV+ parents in extremely low socio-economic positions without nutrition among other disadvantages)…their stories can also be found online, but I am choosing to feature individuals who grew up in optimal environments similar to those that adoptive families provide, as I feel their stories are most relevant to our topic. This post is open to comments and discussion.
I interviewed Hydeia Broadbent and published the post on my old blog in February 2009. It’s not an active link anymore so I’m republishing the interview here with a few extras.
Interview With Hydeia Broadbent
Hydeia ~ Thank you so much for this opportunity to interview you. I admire you and your family so much. Your story is fascinating to me, as this website is all about finding homes, families and sponsorship for children with HIV/AIDS. To my knowledge, you may have been one of the very first babies in the United States born with HIV and adopted. What year were you born? Also, do you or did you know of any others born before you who had HIV and were adopted or fostered?
I was born in 1984 to a woman who was addicted to intravenous drugs. I was left in the hospital and turned over to the state of Nevada. My family was told I was the first child born with HIV in the state of Nevada. I don’t know of any children born before me who were adopted. My mother worked together with parents of children born after me to start a daycare center for children infected and affected by HIV/AIDS.
You and your family have been very open about your HIV status since you were first born, which was extremely rare in the 1980s and 1990s. Did you ever feel upset that your parents didn’t give you a ‘choice’ about disclosure?
I feel my parents made the right choice because I’ve seen so many kids my age dealing with depression and trying to cover up lies because they were keeping secrets about why they were at the hospital or why they were taking medicine. Being public showed our family who was loyal and which friends weren’t quite as trustworthy. Take me as I am! Being public made it easier for me as an adult dealing with dating because I never had to sit someone down and have the “ I have AIDS speech.” They already knew what they were getting into…well somewhat!
For me growing up, I really did not face any problems which I can remember. My mother and father dealt with some things, like my kindergarten teacher spraying me with bleach because I sneezed and she mistakenly thought the virus was air born! In another incident, people changed seats on an airplane because I told them I had AIDS after they nosily asked why I was taking medicine. My mother played it off and said “oh look we have an extra seat – now we can stretch out and get some sleep”. My parents never made a big deal of things when people were acting weird because they did not want me to feel like something was wrong with me.
My prognosis now if fine; I just have to take care of myself and stay on top of my medicine and eat well. When I was three, the doctors told my parents I would not make it past the age of five! I even coded blue a few times, but after living past what the doctors feared would be my final days, we decided that no one really knows when your time is up until your time is up.
Hydeia Broadbent was one of the earliest pediatric HIV patients at a time when only a handful of children had the infection. At the time, AIDS was just being named and HIV, the virus that causes AIDS, had not yet been discovered. To date, about 9,000 children have contracted the virus from their mothers in the United States and more than 2.3 million worldwide. Hydeia is a living testament to the incredible progess that has been made in HIV research and treatment. More information about Hydeia’s life can be found in the mother/daughter memoir You Get Past The Tears (synopsis) and you can also see her on Extreme Home Makeover. She can be reached through HydeiaBroadbent.com. Many thanks to Ms. Broadbent for her time and for her honesty and insight. I hope that this interview will show the excellent quality of life of people born with HIV and lead some adults to a child with HIV in need of parental care.
Here are the extras:
- Hydeia on Twitter
- Hydeia on Facebook
- Hydeia on CNN
- Hydeia Broadbent – HIV/AIDS Activist Video
- I would have loved to link to the video of Hydeia and Magic Johnson on a Nickelodean show when she was very little and the Extreme Home Makeover edition she was on, but I can’t seem to find either of those online anymore.