We get it. We’re not for everyone. Our brand of advocacy is a little too in your face for some people. We’ve been rocking some boats with the Truth Pandemic, apparently. Some might prefer we sit down and shut up.
We’d like to sit down, shut up, and maybe take a load off while we’re at it. Project HOPEFUL has been working since 2006 to help find homes for orphans, educate about children living with HIV/AIDS, and support families who would seek to adopt these children. It’s tiring work. You see, we all might like a little break.
It is not likely to happen any time soon, though. Not while the Stigma Double Standard exists. Believe us. THIS is personal.
Have you heard of the Stigma Double Standard (SDS)? It is an insidious “little” double standard that isn’t really small at all. We believe its implications are profound. SDS starts out like this: Parents of children with HIV/AIDS shouldn’t disclose their child’s status if they want to combat social stigma. This only turns their child into a cause. The best way to handle this is to lobby in other ways.
Then, SDS takes another turn and assumes that every parent on the front lines of advocacy for orphans/adoption of children with HIV/AIDS must be in it for all the lovely attention they get.
The Stigma Double Standard truly baffles us as a staff. Do parents running races to raise funds for a cure for Leukemia face this? What about those with public care pages outlining their child’s congenital condition or an upcoming surgery in detail? Are parents breaking their child’s trust in this way?
Honestly, we want to know if any parent advocating for their Autistic child was told to sit down and shut up, to stop turning their child into a cause. Have those parents been told that the way to help their Autistic children is to keep their child’s Autism a secret? Keep the condition nameless and faceless so people can never put the pieces together and SEE that their ignorance effects REAL LIVE CHILDREN?
Yet ALWAYS this is the case with our children with HIV/AIDS. People continually want us to keep them out of it. They want us to shut up and not speak about our children as the real children they are; children living and THRIVING with HIV/AIDS.
What about any other conditions?
We could go on and on.
Hmmmm, what about a child with Tourette’s Syndrome? Should that child’s parent shut up about Tourette’s and stop educating others because it makes some people feel awkward to have to learn the facts and admit they didn’t know anything about Tourette’s before? Would critics argue that the parent’s efforts to educate the public about Tourette’s is actually damaging to their child? That somehow this child is needlessly being exposed to stigma through their parent’s efforts to educate the general public?
The truth is we can’t think of any other disease children might have where people would ask their parents to hide the fact and keep it secret. And why? Why should we? Is HIV/AIDS anyone’s dirty little secret?
It is not for our children!
Do parents who are serious about advocating for their children in such a public way encounter more criticism? YES. Do their children? Possibly, though so far our staff doesn’t have any battle stories to tell you. Likely because most stigmatizers (this may or may not be a word but for our purposes let’s go with it.) are cowards and don’t usually dare try anything in person. These people prefer the shadows, talking behind backs and whatnot.
Is this increased potential exposure to stigma a reason to stop advocating? Well again, that’s a personal question everyone must ask themselves. Of course our staff considers EVERY member of our family in making these decisions. (Anyone who assumes otherwise is crazy!) We guess it comes down to how high a family’s tolerance is for criticism, attacks, and just general (excuse our crudeness) CRAP.
No one loves to deal with the above mentioned things. Believe us, if, as a staff, we could wave a magic wand and remove all the nasty and unpleasant bits from our work we would. IN.A.HEARTBEAT. But we can’t.
So, it comes down to a few things:
Someone’s got to be in the line of fire if anything is ever going to change.
As parents we do our best to ensure it is US and NOT our children who take the heat.
Yes, we know our children might feel the heat sometimes too. We’re not happy about that by any means! We do our best to limit the heat factor for them. And we do a pretty darn good job of it.
Most of our advocacy happens online, and at our workshops. It’s not like any of us trot our children out every weekend for an HIV/AIDS parade down our neighborhood street.
Besides all this, we rather think our children are up to the challenge of facing stigma.
So far, none of our children who are old enough have told us they would choose life to be any other way than it is. In fact, all of the ones who are old enough tell us that life before disclosure was much more stressful. They were filled with fear that someone might find out. Now they can just “be”.
That’s because we surround them with a loving support network where they don’t have to feel ashamed about their status. They are raised to know that IF a problem exists with their positive status it lies with others and not themselves. We talk openly about the trials and struggles that come along with being HIV-positive.
We are actively working to build in our children the character and life skills we believe are necessary to thrive with HIV/AIDS. One of the ways we do this is by allowing them to see us work through challenges. And by working through them together as a family.
When adjustments need to be made for the sake of our children we, as parents, make them. In everything we try our best to serve our children’s needs first. THE KIDS ARE THE CORE OF OUR WORK. period.
We’ve said it repeatedly that we believe advocacy is the best way to make the world a more friendly place for our children with HIV. We know this to be true through experience. After all, Project HOPEFUL has a track record of proven effectiveness. God sure has blessed our work. We are thankful for that!
We’ve written extensively on the topic of disclosure before. Project HOPEFUL believes it is an intensely personal decision with many factors for parents to consider. It’s not a decision that should ever be taken lightly.
Our staff understands that there will always be people willing to believe the worst in others. For these people it won’t be a stretch of the imagination for them to believe we are attention hogs carelessly flinging our children to the ignorant public to be eaten alive; that we love the “cause” more than our children.
To these folks there’s only one thing to be said: If our work doesn’t illuminate things for you… well, then we don’t know what to say. But at least cut us some slack and don’t criticize us for being different from you. Don’t assume things about us that aren’t true. Especially about our children! And please stop acting like you’ve got all the answers. None of us do.
We’re all just working through this one day at a time. We can’t say for certain how our children will feel about everything we do when they are grown. We can be sure we’ll make some missteps along the way. But our intentions are pure. And we’re confident we know how to get back on track if we stumble.
In the end we believe: