More than 2.6 million servicemen and women have deployed to Iraq or Afghanistan since September 11, 2001. Many veterans return home from their service with symptoms of post-traumatic stress, depression, chronic pain and traumatic brain injury. These symptoms are also common among civilian trauma survivors.
Now researchers from Harvard Medical School and other institutions will embark on a five-year-long project, the Aurora study, to better understand and treat these disorders. The research will utilize the efforts of 19 institutions and more than 40 scientists.
Trauma survivors will be enrolled in the study in the immediate aftermath of trauma and followed longitudinally for one year using sophisticated adaptive sampling methods to perform a comprehensive, state-of-the-art assessment of genomic, neuroimaging, physiologic, neurocognitive, psychophysical, behavioral and self-report markers.
In addition to its unparalleled scope, the study differs from previous studies in that it will assess neuropsychiatric effects of trauma broadly rather than focus on only one or a few diseases.
“We want to be patient-centered and not diagnosis-centered,” said Samuel McLean, lead principal investigator of the study and an emergency medical physician at the University of North Carolina at Chapel Hill.
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Funding: The five-year-long project is funded by the National Institute of Mental Health.
Raise your voice in support of expanding federal funding for life-saving medical research by joining the AAMC’s advocacy community.
Chronic illness, chronic pain, and mental illnesses can create a sense of low energy in those who suffer from them.
The spoon theory is a way to discuss the use of energy in tasks as a kind of currency. People who do not have energy draining conditions have, in theory, infinite spoons to expend on whatever they please. People who have chronic conditions may awake with 10, 5, or 2 spoons on any given day.
A stat that gets me every time: “If current diagnosis rates continue, 1 in 6 gay and bisexual men will be diagnosed with HIV in their lifetime, including 1 in 2 black/African American gay and bisexual men, 1 in 4 Hispanic/Latino gay and bisexual men, and 1 in 11 white gay and bisexual men.”
One of the most important things you can do is get tested and know your status; here’s a tool that can help you find a nearby testing site. Note that the option for selecting your gender isn’t quite right, but the wealth of testing locations in their database is still helpful.
If you’re in a donating mood, you can also support the work of some organizations doing excellent things for those affected by HIV/AIDS, including GMHC, AIDS United, Planned Parenthood, Lambda Legal and amfAR. (And please add your favorites; there are so many!)
We’ve been fighting this fight for upwards of 30 years. We’re not stopping now.
Graphics created by: @eclecticjessica
Black Community we have to be careful. Protect our Girls! Spread this!
Yale professor Timothy Snyder explains how democracies fall.
The original, established, symbol is on the left and the “new” symbol is on the right.
So what’s the problem?
Well, the biggest problem is that the newest symbol wasn’t designed by someone in a wheelchair. It was designed by two artists who don’t use wheelchairs who thought that they could speak on behalf of people who do.
Who cares, it’s a good symbol, right?
Nope.
See the original symbol, the one that’s been around for decades and has been embraced by the disabled community, works for both people in manual wheelchairs and people in electric wheelchairs. The second one is obviously someone in a manual chair, excluding those who use electric ones.
There’s also ironically an ableist message behind their reasoning that the person on the right symbolizes an active member of society, whereas the non-moving person on the right can be depicted as lazy. This reasoning is extremely ableist and ignorant, artsy for the sake of being artsy without giving thought to what they’re actually implying.
The real kicker?
My college has the new signs everywhere. New York State as a whole adopted these new signs. A ton of different buildings around the nation are putting up these new signs because people are just sort of assuming that everyone with a disability approves, even though most people in wheelchairs are objecting to it and the people who are advocating for it aren’t in wheelchairs in the first place.
And guess whose voices are the ones being heard?
And guess whose voices are the ones being ignored?
I wanted to post this from my other blog and I think it’s important that other people learn what SPD really is so they can notice it and catch it early. It’s not easy to have this and my everyday life can be hard some days but other days it’s much easier. Please educate yourself and others about SPD so you can help them if they need it.
This is exactly why I was terrified, and still am.
Stay safe. Fight back. And sit tight because these next 4 years are gonna be one hell of a ride.
Struggling with mental illness after a traumatic event most likely caused by mental illness. Sexual Assault Survivor.
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