🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

Gracias a Lynne Kinst de Hemophilia Council of California por invitarme para ser la oradora de el taller virtual sobre el tema de la abogacia y como utilizar tu voz para obtener el cuidado medico que se meresen cuando viven con enfermedades sanguineas, y abogar para la comunidad entera!

Thank you, Donald Thomas, MD, for sharing this virtual symposium. It was completely in spanish and will remain on YouTube and Facebook in Looms4Lupus channels for those who missed it. Celebrando Y Aprendiendo, we are Celebrating and Learning together!

Join us for a community event hosted by California Life Sciences (CLS) & Looms4Lupus! Discuss #HealthEquity with leaders like Senator Susan Rubio Rick Chavez Zbur & experts. 🗓️ Oct 4, 11 AM-2 PM 📍 Baldwin Park Arts & Rec Center. Free lunch & Spanish interpreter. Register: bit.ly/CommunityHealt…

Emocionados de atender a la conferencia del 10º Aniversario de HealtheVoices 🎉 Encantadas de representar a la comunidad hispana. Abogamos por el #Lupus #fibromialgia #SaludMental los #cuidadores y #equidadensalud. Nos unimos con otros pacientes! #Looms4Lupus J&J Innovative Medicine

Joaquin Duato highlights Johnson & Johnson efforts to improve patients’ health journeys & emphasizes the vital role of patient advocates as ‘Change Agents.’ I am proud to be a CHANGE AGENT, sharing my story, empowering, supporting, connecting, & making a difference one day at a time!

Thank you Senator Lena Gonzalez for authoring #SB 1016 Latino & Indigenous Health Disparities Reduction Act. We all need to be seen,we all deserve better healthcare outcomes!! Thank you Gavin Newsom! This is more than just a post it is a celebration!! 🍾 🪅

We have been working with Lupus LA since 2012, offering the bilingual support group & #Spanish support group. It's always great to see Dr. Daniel J. Wallace and hear about the latest in Lupus treatments.

Today, I met Norma Roque Univision journalist I’ve admired for years. She’s delivered news to our community for over 30 years. Meeting her reminded me of the power of representation. Norma, a seasoned journalist at Univision Noticias has won 11 Emmy Awards and 3 Golden Mic Awards. 💖

I attended the celebration of #SB537 at LA Plaza de Cultura y Artes commemorating the 1930s Mexican Repatriation Acts. Attendees included Mayor Karen Bass, Senator Josh Becker, Senator María Elena Durazo @SenGonzalez_33, Cabrera Financial Capital Claudia Romo Edelman The bill funds a memorial for deported Mexican Americans.

Grateful to have been part of this event! We connected with the Spanish speaking community. We learned, laughed, cried & provided resources. Families came to support their loved ones, from sisters supporting sisters to parents supporting their daughters, husbands & friends. 💜

I am proud to have worked alongside Aracely Campa De Ramirez California Life Sciences (CLS) to host a community event including all stakeholders not only identifying barriers but also finding solutions to ensure equitable healthcare access for all. "Together we are Knitting a Community of Hope."

We deeply understand the significance of #grassroot engagement with the community. Looms4Lupus is present where the community gathers, so we can bring valuable resources and actively engage. This hands-on approach helps us identify how we can best support & make a difference.

It was a pleasure to join a panelist of amazing woman leaders for the "Appointments Workshop" hosted by Assemblywoman Rubio & CA Women Lead. The attendees left with knowledge, tools, & insights into the appointment process, ready to make a difference in their communities.

Glad to see Take a Pain Check Foundation "Lupie" the LLama exploring DC! Looking forward to having having both Amanda G & Lupie the Llama join us in 2025 for some of the Looms4Lupus #Autoimmune, #Lupus & #Mentalhealth annual events! #ACR24

Wishing everyone a Happy New Year 2025!! The best is yet to come!! #Looms4Lupus #MataSisters Estela Mata Mata Advocacy And Support (MAS) JuanaMata

We Support Rare Disease Day! 1 in 10 Americans live with a rare disease. Over 95% of rare diseases have no approved treatment. ¡Apoyamos el Día de las Enfermedades Raras! 1 de cada 10 estadounidenses vive con una enfermedad rara. #RareDiseaseDay #LoomsForLupus

Today is #RareDiseaseDay! 1 out of 10 Americans live with a rare disease. Together, we aim to make a difference and reshape the future of healthcare. Thanks to California Life Sciences (CLS) for organizing Rare Advocacy Day.

Both my sister JuanaMata and I support & empower #lupus patients, their loved ones to get the resources they need, get the best treatments possible to manage lupus symptoms, through support groups, information #ClinicalTrials & hope! CreakyJoints.org lupushealthcenter.org

Do you have #LUPUS and #BrainFog? Help us develop the Lupus Brain Fog Severity Scale—a validated questionnaire to measure brain fog severity in lupus. Your input is essential. Please participate today & RT to share. More info ⬇️⬇️

Today, on World Lupus Day, we honor everyone affected by lupus. If you're living with lupus or supporting someone who is, the Lupus Help Center offers trusted information, expert videos, and real patient stories — all to help you understand clinical trials and take the next step