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There is no single blood test to diagnose lupus. But tests and several criteria are available to help a doctor make a diagnosis. The Lupus Research Alliance has funded studies aimed at finding more definitive diagnostic tools.
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
ONLY ONE WEEK LEFT TO HELP IAN REACH HIS GOAL!!!
If you can, purchase an exclusive “It Was Always You" Tee because the proceeds benefit the Lupus Foundation of America. It’s a wonderful cause and it’s a wonderful tee and Ian Harding is a wonderful guy.
https://represent.com/ianhardingalways/ian-harding-30-birthday-for-lupus-foundation-of-america
If you can, you should donate to the Lupus Foundation of America. It’s a great organization dedicated to an incredibly worthwhile cause: discovering the cause of lupus and hunting for a cure. Together we can solve the cruel mystery of lupus. Visit lupus.org/know and donate today!
May is Lupus Awareness Month
May is #LupusAwarenessMonth + @LupusNC Fayetteville Walk to End Lupus on 5/14/16 #latasharjonesblog #thisislupus
  I’m Walking to End Lupus. Join Me? Click the image above to support Team TaTa. Click above to learn more! You can help us raise awareness about this cruel and mysterious disease by playing the game and challenging others to KNOW LUPUS.
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The 21st Century Cures Act has passed through Committee and is up for a vote in the House. Right now, it’s just a bill on Capitol Hill but YOU can help make it a law.
Don’t just like or reblog this. Take a moment and email your State Representative. Urge them to vote to pass the bill and send it to the Senate.
Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
Free to watch • No registration required • HD streaming
Hey guys, FYI--as always, I’m sorry to not be around so frequently, but finally one of the reasons I’m not around is relevant!!! (although I’d argue that End Times’ themes of chronic illness make it relevant ;-) [link])
I’m lucky enough to be interning with the Lupus Foundation of America right now, and just finished up a two day advocacy event on Capitol Hill! I wanted to thank everyone there that made it such a great first internship experience for me, foundation members and advocates alike, and all the reps we met with for their support (right...?).
In the meantime, I’ve been tweeting about the event here [link] and hopefully will continue to be tweeting throughout my internship experience!!
As usual, I’m afraid, blog on hiatus, but feel free to send in questions or just let me know how you’re doing. I’d love to hear from you.
(and who knows... maybe this new greater level of involvement with the autoimmune community will give me an excuse to take the time away from Mad Manatee Productions again and start back up. We’ll see.)
KNOW LUPUS Public Service Announcement
If we're going to say "NO" to lupus, we must first KNOW LUPUS. Created through the generosity of LIFETIME Entertainment by Insomnia TV for the Lupus Foundation of America, the campaign features celebrities from television and movies appearing along side people with who are living with lupus. Learn more about our KNOW LUPUS campaign at lupus.org/know.
KNOW LUPUS - Public Service Announcement.
