Search results for #LiftUpLupus
#LupusAwarenessMonth Starts Today !! 💜✋💜 #MesDelLupus comienza Hoy!! Who do you wear purple for? Por quien tu usas morado? #LupusChat 🦋 #Lupus #LupusFeelslike #LHandSign #LupusWarrior #POP #KellyFundForLupus #KnowLupus #100Lupus #FFpaciente #LADAorg #LiftUpLupus
#LupusAwarenessMonth Starts Today !! 💜✋💜 Who do you wear purple for? #LupusChat 🦋 #Lupus #LupusFeelslike #LHandSign #LupusWarrior #POP #KellyFundForLupus #KnowLupus #100Lupus #FFpaciente #LADAorg #LiftUpLupus
Alison Lee is an inspiring #lupuswarrior and activist, that underwent a kidney transplant in 2016. She shares her story to help #LiftUpLupus and support others who are going through their own #lupusnephritis journey. Watch now: bit.ly/AlisonLee-LN #NationalKidneyMonth
Tye battles neuropsychiatric lupus, which makes him more susceptible to seizures, strokes, anxiety and mood changes. Tye emphasizes that building a strong support system can be valuable, helping to #LiftUpLupus both emotionally and physically. Read more: bit.ly/Tye-Weitman
To help elevate the conversation on #lupus and mental health for those who may be struggling, we got personal with @selenagomez as she shared her challenges and her success stories to #LiftUpLupus. Read the full interview here: ow.ly/E0Oq50HbNo9
Tye battles neuropsychiatric #lupus, which makes him more susceptible to seizures, strokes, anxiety and mood changes. Tye emphasizes that building a strong support system can be valuable, helping to #LiftUpLupus both emotionally and physically. More: bit.ly/Tye-Weitman
Stress related to chronic conditions, like #lupus, can be frustrating. Here’s ten of our favorite tips to help manage #stress. #LiftUpLupus
Lupus warrior Miah SantaCruz first experienced symptoms at 7 years old and wants people to know that lupus can affect anyone – even children! She is an incredible young advocate and voice in the #lupus community and shares her inspirational words to #LiftUpLupus!
As Lupus Awareness Month 2021 has come to a close, LRA President Ken Farber takes a look in this video at the many ways we came together to #LiftUpLupus. Take pride in all the #lupuscommunity accomplished and hope in the tremendous progress underway. Watch now!
RT @LupusResearch: Lupus underdiagnosed survey by LRA and National Kidney Foundation 51% of people with lupus nephritis said they had not been previously diagnosed with lupus. See our survey here: bit.ly/LN-Gaps #LiftUpLupus #LAM2021 #riseforrare
Thank you all for joining us for such an empowering #LupusAwarenessMonth. We will continue to #LiftUpLupus together with more scientific research and innovative discoveries, the ongoing support from our community and your inspiring stories as lupus warriors.
Candy Brown has been involved with the Lupus Research Alliance for many years as a walker, advocate, and fundraiser. On her own or with her incredible family, Candy is a light in the lupus community. #LiftUpLupus #LupusAwarenessMonth
#MemorialWeekend As May ends, so does #LupusAwarenessMonth But #LiftUpLupus & fundraising never stop #Memories and THANKS to those who always gave just because they knew. #johnsonandjohnson #AtlanticHealth @LupusResearch @KellyFund4Lupus @CaringForLupus
Whether as a walker or participating on the LRA’s Young Leaders Board, Ruth Wilson is a strong force that goes above and beyond to #LiftUpLupus by raising vital funds needed for research and raising lupus awareness. #LupusAwarenessMonth
Thank you @KathleenArntsen for all that you do to #LiftUpLupus and support the lupus community!
Thank you @KathleenArntsen for all that you do to #LiftUpLupus and support the lupus community!
RT @LupusResearch: This month we honor #AANHPI Month. 2020 research found that people of Asian ancestry tend to develop lupus at a younger age and have more severe disease than whites. #LAM2021 #LiftUpLupus by sharing our post and spreading awareness.
