
Looms4Lupus
@looms4lupus
Looms For Lupus-501c3 provides bilingual resources & support to minority families affected by Lupus,Fibromyalgia,mentalhealth linktr.ee/looms4lupus
ID: 1045553383430488065
http://looms4lupus.org 28-09-2018 05:58:46
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We had the pleasure of attending a luncheon hosted by Autoimmune Association , featuring Dr. Victoria Shanmugam, Director of the Office of Autoimmune Disease Research. We are excited about all the emerging developments & future progress in autoimmune research.



We are incredibly proud of Alexandra Blumhorst for her inspiring presentation on "Support Groups & Chronic Illnesses" at #ACR24. We are honored to have sponsored her poster, Looms4Lupus believes support groups are key to making a difference in the lives of patients & caregivers




Hola! Acompañenos hoy a las 5PM PST para la "Platica Con Las Hermanas Mata" Unase con las hermanas Mata Blanca estela mata y Juany Mata para platicar en Español sobre familia, alla salud, salud mental, celebraciones me scales y mucho mas!!! #matasisters #HmnasMata #Looms4lupus

Hola! Acompañenos hoy a las 5PM PST para la "Platica Con Las Hermanas Mata" Unase con las hermanas Mata Blanca estela mata y Juany Mata para platicar en Español sobre familia, alla salud, salud mental, celebraciones me scales y mucho mas!!! #matasisters #HmnasMata #Looms4lupus


We’re excited to share the video recap of our Community Educational Symposium on Dec 14, 2024. The hybrid event covered medical expense management, financial assistance info, & #FinancialLiteracy insights. Thanks to Gloria Garcia Cisneros, BMO City of Baldwin Park, CA Aurinia Pharmaceuticals Inc.

#MCEDAct is still not in the EOY package. Senator Marco Rubio: Archived Rep. Vern Buchanan Congresswoman Sheila Cherfilus-McCormick Congressman Greg Steube Rep. John Rutherford U.S. Senator Bill Cassidy, M.D. Congresswoman Julia Letlow Rep. Clay Higgins Congressman Troy A. Carter Congressman Drew Ferguson Rep. Lucy McBath Nikema Williams, pass the #MCEDAct now.


We're thrilled to announce that International Pain Foundation® iPain Living Magazine's Winter 2025 edition features our co-founders, JuanaMata & Estela Mata, the #MataSisters! Their dedication to the #Lupus community & community as a whole is truly inspiring! ipain.com


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




On 2/25/2025 Looms4Lupus participated in California Life Sciences (CLS) Rare Disease Lobby Day in Sacramento. Together, we aim to make a difference and reshape the future of healthcare. #RareDiseaseDay California Life Sciences (CLS) #Healthcare #PolicyChange #Looms4Lupus


We're proud that our president, Blanca estela mata, serves as a Measure BP SOC member. Congrats to Baldwin Park City Soccer Club for earning the Community Empowerment Grant to support youth! ¡Felicitaciones por este logro increíble! 📸: City of Baldwin Park, CA


#L4LWellnessDay2i025 us on May 24, 2025, 9AM–3PM, for the Looms4Lupus 5th Annual Wellness Day. FREE In-person & live-streamed at City of Baldwin Park, CA Arts & Rec Center. Honoring Lupus, Fibromyalgia & Mental Health Awareness Month. In English & Español! #L4LWellnessDay2025