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You can't care for others if you're not caring for yourself, Estela Mata-Carcamo Estela Mata with Looms4Lupus reminds us in this webinar clip. Watch the full #SWHRtalksAutoimmune webinar online here: ow.ly/BGgx50SGe3f VCU Health

@looms4lupus offers educational and supportive resources for those affected by lupus, fibromyalgia, and mental health conditions. Join our in-person and virtual events on Facebook, X, and YouTube. Available in Spanish & English. Together, we build a stronger, informed community.

HAPPY 10TH ANNIVERSARY HealtheVoices! 🎉 Thank you for including me! Proud to be part of the #healthevoices family, amplifying patient voices & empowering #patientadvocates. Together, we advocate for change, support patients/caregivers & collaborate with healthcare providers! 🎉

Wrapping up a great day at Familia de Sangre with a full house in our advocacy breakout! #bleedingdisorders #advocacy #education #findyourvoice #patientsvoice Looms4Lupus Estela Mata

We loved seeing so many friends a& blood family at Familia de Sangre. Thank you HemoSoCal Hemophilia Foundation of Northern California CentralCa Hemophilia for hosting a great event! Thanks to Estela Mata Looms4Lupus for moderating and panelists - Thalia, Ivan and Andrea for sharing their experience.

Honored to attend the Familia de Sangre conference in Anaheim, CA, for the second year to Moderate on behalf of Hemophilia Council of California "Talk-How to Advocate for Yourself" with Thalia Santiago, Andrea Ramirez, & Ivan Giron Jr. They shared their lived experience as an advocate.

Today is World Suicide Prevention Day! Today and throughout September, let’s raise awareness and support those in crisis. If you or someone you know needs help, call the 988 Suicide & Crisis Lifeline. You are not alone. No estas solo (a)! #SuicidePreventionMonth #YouAreNotAlone

We see you. We know this is hard. You are not alone. #WeSeeYouWednesday Thank you, Juana, for all you do to spread #lupusawareness with your nonprofit Looms4Lupus and work in the community!

Celebrate #HispanicHeritageMonth with Looms4Lupus! The past three years, we’ve celebrated Hispanic/Latino leaders making positive impacts in our communities! Some past guests: Assemblywoman Rubio Senator Susan Rubio Blanca Garza Jacobs medical providers from Hospital for Special Surgery (HSS) Daniel G Garza....

“Celebrating and Learning” Series in Honor of #HispanicHeritageMonth LIVE Spanish Event! Dr. Laura Geraldino-Pardilla will discuss “What you need to know about lupus & the kidneys” 🗓 Wed. 9/18/2024 🕒 12:00 PM PST 📍Facebook Live & YouTube Te esperamos! Unete! Comparte!

Serie “Celebrando y Aprendiendo” en Honor al #MesDeLaHerenciaHispana ¡Evento en Vivo en Español! La Dra. Laura Geraldino-Pardilla discutirá “Lo que necesitas saber sobre el lupus y los riñones” 🗓 Miércoles, 9/18/ 2024 🕒 12:00 PM PST 📍Facebook Live y YouTube ¡Te esperamos!

Looms4Lupus & @lupusla support groups are a great way to connect & get the support you need. Saturday 9/14/2024 at 9:30am PST. Facilitators: JuanaMata Estela Mata Link:us02web.zoom.us/meeting/regist… Grupo de en Español 9/15/24 a las 9:00am PST. Enlace: us02web.zoom.us/meeting/regist…

Attended the Susan Rubio Zocalo Park ribbon cutting in City of Baldwin Park, CA on Sept 14, 2024. Congrats, @sensusanrubio, on the park named after you! A day of amazing performances, including a Mexican Independence Day Grito & live music. Great greenspace for community gatherings!

PBM practices have caught the attention of the Federal Trade Commission and the House Committee on Oversight and Accountability. The committee has been investigating PBMs and their role in rising health care costs for over a year. And an FTC report found that the three largest

Acompañenos este Miercoles a las 12pm PST en vivo via Facebook y YouTube, Celebrando y Aprendiendo juntos sobre Lupus, la Nefritis Lúpica y la importancia de cuidar y hacernos los examenes necesarios para el cuidado de los riñones.

Nos da mucho orgullo de poder colaborar con Lupus LA y brindarles el apoyo a uds y sus cuidadores en español. Las Hermanas Mata JuanaMata quien vive con Lupus y Estela Mata facilitan estos grupos en español. Juntos "Tejiendo Una Comunidad de Esperanza". 🧡

Estoy muy contenta de poder trabajar con Lynne Kinst de @hemocouncilofca! Acompañenos mañana a uno de los de Talleres de Web Gratuitos en español que les puede beneficiar a las personas que viven con enfermedades sanguineas y también enfermdades chronicas y sus cuidadores.

En honor al Mes de la Herencia Hispana, les invitamos a la serie de eventos “Celebrando y Aprendiendo”. Acompáñenos para aprender sobre el lupus y la nefritis lúpica en un evento gratuito y virtual en español. #NefritisLupica

Thank you for sharing Donald Thomas, MD!! GRACIAS!!💜