Hyperbaric oxygen chamber therapy needs to be approved for #lupus patients @US_FDA@NIH@WHO. We need more clinical trails to prove it works @NIHClinicalCntr. My experience with the treatment has been amazing fatigued decreased, mentally lifted, decreased pain etc
Hope in action @LupusResearch Millions of people worldwide are affected by lupus but there is hope, and more importantly, there is action. Hope is not passive it’s powerful when we use our voices, share our stories, and push for progress in research
Every story matters.
💜 May is national lupus awareness and it is not a month it's a movement. As someone living with lupus, I know firsthand the strength it takes to navigate this journey. Thank you for standing with our community not just in May, but every day.”
I’m here with Judith Mills, co-chair of the Lupus Voices Council, during Lupus Awareness Month. Lupus is a chronic autoimmune disease, and we must keep raising awareness and funding research for a cure.
Fatigue, joint pain, rashes, and fevers can be signs of lupus.
Thank you @SenatorCory_ for standing up against Medicaid budget cuts that will affect many in the #Lupus community that depend on Medicaid. See you on the Hill with in May.
An honor to stand with activists and advocates this morning to make clear to Donald Trump, Elon Musk, and Congressional Republicans: Medicaid cuts will have devastating effects on New Jerseyans and raise costs for all Americans.
May is Lupus Awareness Month. Yesterday on Capitol Hill advocating with LFA was a blast. I made new memories & cried at @CoryBooker office after story telling. I literally bumped into @BernieSanders in the cafeteria. I nearly wanted it to scream. He then said I know I know….
Tune in Tuesday, Nov. 8th at 11am PST! Season 2 Episode 13 of the #YourStoryOurFight® podcast features Judith Mills, a Biomedical scientist, TEDx speaker and adjunct professor - as well as a #lupus & disability advocate. Catch up on past episodes at: https://t.co/xTxE5L526K