Ruth Wilson

Mom/Wife/Lupus Warrior/Lupus Advocate/Science Lover/Nerd at heart

"It is during our darkest moments that we must focus to see the light" -Aristotle

[Ruth Wilson @ruthyr0cks]

Check out this piece by @AP bringing awareness to Lupus and the struggles of living with Autoimmune disease https://t.co/sGqnXzq0mg

[Ruth Wilson @ruthyr0cks]

Remote patient monitoring system in development to improve care for people with lupus https://t.co/OI1gKPRYFj
Very excited to collaborate with this group as a patient investigator and bring this to patients for improved clinical care.

[Lupus Research @LupusResearch]

A new powerful @AboutTheAP feature spotlights the journey of advocate Ruth Wilson — and the scientific breakthroughs redefining how we understand autoimmunity.

From CAR T cell therapies to initiatives like the Lupus Landmark Study led by the Lupus Research Alliance, researchers are working to uncover the root causes of lupus and related autoimmune diseases.

The Lupus Research Alliance is proud to work with incredible lupus advocates, researchers, clinicians, and industry partners who lend their voices and pave the way toward more precise, personalized breakthroughs.

Read more: https://t.co/0Fyc0l4rMy

#LupusResearch #Autoimmunity #ScienceNews #LupusAwareness

[Lupus Research @LupusResearch]

Thank you, NYC, Virtual, and Dallas! It was incredible coming together with our walkers, sponsors, and the entire lupus community for the Walk with Us to Cure Lupus! ✨

We're so inspired by the way this community unites around one shared goal: advancing lupus research that will unravel the complexity of this disease and bring us closer to personalized treatments and, one day, a cure. 👟

#WalkWithUs #ManyOneCan

[Lupus Research @LupusResearch]

Continuing our series highlighting the unique experiences of individuals in the lupus community, we introduce you to Ruth Wilson. Diagnosed with Systemic Lupus Erythematosus (SLE) and Lupus Nephritis (LN) when she was 30 years old, Ruth shares this inspiring message about living with lupus, in English and Spanish.

Lupus is a challenging disease that often requires adjustments to daily life. It’s crucial to advocate for yourself, seek support from others who understand, and remain persistent in managing your health to maintain a high quality of life.

__________

El lupus es una enfermedad desafiante que a menudo requiere ajustes en la vida diaria. Es fundamental abogar por uno mismo, buscar apoyo de quienes entienden la enfermedad y ser persistente en el manejo de la salud para mantener una alta calidad de vida.

#MyLupus #Lupusespañol #HispanicHeritageMonth

[Ruth Wilson @ruthyr0cks]

Check out Young Leaders Board's team fundraising page - https://t.co/9EvbNkqO2a

[UMass Lupus @UMassLupus]

Hi all! The UMass Lupus Center has partnered with Ruth Wilson to create the LupUS Support Group🤍 Please join us every 2nd Wednesday of the month to have lively discussions and connect with other local lupus patients. Register here: https://t.co/2R0fjfD4V2

[Trisha @TrishaReads8]

@UMassLupus SUPERSTARS on hand at today’s symposium! @racaricchiomd & @ruthwilson 💜💁🏻‍♀️🦋

[Ruth Wilson @ruthyr0cks]

Please join us as a volunteer, walker or donor at the ManyOne Can Walk to Cure Lupus. Every dollar collected goes directly to fund research to help us find a cure.

[UMass Chan Medical School @UMassChan]

Today is #WorldLupusDay. @UMassChan and Lupus Foundation New England hosted the 2024 Lupus Medical and Educational Symposium on Thursday, which included a session on lupus support groups and a presentation on cell therapies for #Lupus patients. @UMassLupus @LupusNE @ruthyr0cks

[Trisha @TrishaReads8]

@ruthyr0cks - Thank you! 🦋 #LupusAwarenessMonth

[UMass Lupus @UMassLupus]

@ruthyr0cks @ruthyr0cks shares her personal story about #lupus 💜
She emphasizes the importance of a social support network 👥💕

[UMass Lupus @UMassLupus]

Up next, @ruthyr0cks will speak about #lupus support groups! 💜

[Ruth Wilson @ruthyr0cks]

Check out Young Leaders Board's team fundraising page - https://t.co/9EvbNkrlRI any amount helps! Thank you 💜

[Ruth Wilson @ruthyr0cks]

Please join me as a volunteer, walker or donor at the ManyOne Can walk to cure lupus happening October 21, 2023! All funds go directly to te research that is so desperately needed! 💜

[Nia | The Chronic Notebook @chronicnotebook]

With chronic illness, you normalise so many things most people won't ever feel. You normalise high levels of pain, being exhausted, medical procedures and trauma, needing to rest after a shower. People see you surviving with an illness, but not all you had to normalise to do so.

[Lupus Research @LupusResearch]

Today is the first day of the #Fall season, and if you’re looking for events to participate in, here is our schedule for LRA’s 2022 Fall Walks around the country. 🍁

[Lupus Research @LupusResearch]

In our latest #ManyOneCan - Make a Difference video, LRA Young Leader Martin Lewis talks about how sharing his personal story helps him gain and give support to others with lupus.

[Lupus Research @LupusResearch]

We’re 2 weeks away! There is so much excitement for the 2022 #ManyOneCan Mid-Atlantic Walk with Us to Cure Lupus on 10/1 at The National Harbor, MD.

Here are a few ways to help you prepare for the Walk. Get more information and register at: https://t.co/c7amDpJAme

[Lupus Research @LupusResearch]

LRA announces the appointment of Albert Roy to President & Chief Executive Officer effective 9/6. Currently, serves as Executive Director of Lupus Therapeutics, the clinical trial affiliate of the LRA. He will succeed Ken Farber who is continuing as President-Emeritus till 12/31.