Joanne Golombos (Western Region)

Walk with Us to Cure Lupus as we raise funding for vital lupus research and spread awareness in the USA western region.
@lupusresearch

[Joanne Golombos (Western Region) @LRAwestregion]

Walk with Us to Cure Lupus, Los Angeles is 25 days away.
Have you signed up to make a difference in the lives of those with lupus?!
Join us and be a part of the movement  https://t.co/mYSzZe4yly
#lupus #lupie #spoonie #lupusawareness #chronicpain #fibromyalgia #walkforacure

[Lupus Research @LupusResearch]

Los Angeles! The Lupus Research Alliance will be participating & sharing about our resources and upcoming events at #TheLupusProject 2019! Hope to see you there! Register at https://t.co/wzNN66UTvD or The Lupus Project on Facebook
#tlp #tlp2019 #lupus #lupushealth
@LRAwestregion

[Joanne Golombos (Western Region) @LRAwestregion]

#LupusAwarenessMonth is just a few weeks away. Join us in #Seattle on May 4 at the Great Wheel (Pier 57) as we #LightItUpPurple!

[Amanda G @LAlupusLady]

Thank you @LupusResearch and @LRAwestregion for another Twilight #WalkWithUs in Southern California.

It’s not too late to support #LupusResearch via my team.
https://t.co/Df9194JvKM

[Holly Baird @thathollybaird]

#Lupus is an autoimmune disease that disproportionately affects women: 9 out of 10 adults with lupus are women and most women who develop lupus are between the ages of 15 and 44.

[Holly Baird @thathollybaird]

On top of the increased risk factor young women already face, black, Hispanic and Asian women are more likely to get lupus than white women—and often experience more severe side effects #lupusfacts

[Lupus Research @LupusResearch]

Each person with lupus has slightly different symptoms that can range from mild to severe and may come and go over time. However, some of the most common symptoms of lupus include painful or swollen joints (arthritis), unexplained fever, and extreme fatigue. #symptomsoflupus

[Peter Morley @morethanmySLE]

Last Day!

Please Vote For Our @Netroots_Nation Panel:

@HealthCareVoter co-chair @lpackard submitted a panel on healthcare w/me, #healthcare heroes @ElenaHung202 (@LittleLobbyists), @AdyBarkan & #SteveGomez this AUGUST.

Vote here➡️ https://t.co/J3Zgb8K8Eg

Thank you!

[Joanne Golombos (Western Region) @LRAwestregion]

Post it. Share it. Spread the word. April 14th Los Angeles Lupus Warriors take over the @RoseBowlStadium 💪🏻💪🏼💪🏽💪🏾💪🏿💜 #lupus

[Joanne Golombos (Western Region) @LRAwestregion]

@mandifanci Make Lupus tired. You’ve got this! 💪🏻

[Holly Baird @thathollybaird]

@LupusResearch @PUMA @selenagomez Awesome! @LRAwestregion 💜 can’t wait for the LA stroll! #april14

[Joanne Golombos (Western Region) @LRAwestregion]

@LupusResearch @PUMA @selenagomez LA come out and represent! 💜🏃🏾‍♀️💪🏻 #lupus #april14

[Lupus Research @LupusResearch]

Learn more about the @PUMA and @selenagomez collaboration benefiting Lupus Research Alliance https://t.co/1oRAjlTIRk

[kasper @Nas_Jackson]

Count your blessings 🙏🏽 Im dedicated to this work it’s not a game it’s a lifestyle 😈@LupusOrg #lupus

[Minority Health @MinorityHealth]

Please share OMH’s latest FOA. Approximately $2M is available to help reduce #lupus related disparities among minority and/or disadvantaged communities. The deadline is March 30. https://t.co/g7eh37zPYK

[Joanne Golombos (Western Region) @LRAwestregion]

@morethanmySLE @AynRandPaulRyan @Genosworld @RepMaloney @DavidYankovich @Alyssa_Milano @harveyjkaye @ASlavitt @RenaSofer You’ve got this!

[Peter Morley @morethanmySLE]

I've had a bit of a setback to my health due to my #Lupus

But like the #ACA, I will continue to fight and persevere! #HealthCareVoter

[Megan Smith @meganl_smith]

"Lupus is so hard to explain to people, a lot of the time you don't look like anything is wrong with you". An incredible story about the realities of living with #Lupus: https://t.co/seLBg470Ho One for you @selenagomez.