Jimmy  Darts

SB Mowing

Pattie Gonia

Little Miss Flint

Kalina Silverman / @makebigtalk on Instagram

Samuel Weidenhofer

Patriotic Kenny Foundation

Ben Saunders - Flawless Cleaning

The Dogist

Peter Bond

Amy Jandrisevits

Ask Uncle Jack

That Good News Girl

Tess Bohne

FowlMouthFarmer

Latonja and Taylor Richardson

Officer Richard Craig

Flavor Flav

John Wolfe

Khloe

<div>✨ <strong>Que se abran puertas y caminos: Ayúdanos a llegar a EULAR 2025 </strong>✨
</div>
<div>Somos Laura (investigadora y persona con lupus diagnosticada en el año 2000) y Efrén (editor y compañero de vida de Laura). Creemos que otras realidades son posibles. Por eso, tejemos un proyecto que une ciencia, amor y comunidad: el Centro de Estudios Transdisciplinarios Athié-Calleja por los Derechos de las Personas con Lupus (Cetlu A.C.).
</div>
<div><br />
</div>
<div>Este 2025, tres trabajos nacidos desde nuestra experiencia, nuestras investigaciones y el activismo colectivo, han sido seleccionados para presentarse en el Congreso Europeo de Reumatología (EULAR), el más importante del mundo en su tipo, que se celebrará del 11 al 14 de junio en Barcelona, España. <strong>¡Por segunda ocasión fuimos seleccionados con tres trabajos! Estamos muy orgullosos y agradecidos con la vida.</strong>
</div>
<div><br />
</div>
<div>Con alegría profunda y compromiso, llevaremos nuestras voces hasta allá, en nombre de todas las personas que viven con lupus en México. Pero para lograrlo, necesitamos tu ayuda.
</div>
<div><br />
</div>
<div> Meta de recaudación: $47,000 MXN
</div>
<div>Este monto cubrirá:
</div>
<div><br />
</div>
<ul>
<li>Vuelos de ida y vuelta desde Ciudad de México
</li>
<li>Traslados y alimentación durante el congreso en Barcelona
</li>
</ul>
<div><br />
</div>
<div><strong>¿Por qué es importante?</strong>
</div>
<div>Porque estas presentaciones visibilizan lo que muchas veces no se ve:
</div>
<div>– Que el lupus también se piensa desde la infancia y la adolescencia
</div>
<div>– Que hay saberes que nacen desde quienes viven con la enfermedad
</div>
<div>– Que el derecho a una vida digna no debe ser privilegio, sino garantía
</div>
<div><br />
</div>
<div><strong>Nuestras ponencias aceptadas son:</strong>
</div>
<div><br />
</div>
<div> POS1437. Discursive Memory and Perception of Lupus in Children, Adolescents, and Young People
</div>
<div> Presenta: Dra. Laura Athié – Sábado 14 de junio, 10:15–11:45 CEST
</div>
<div><br />
</div>
<div> POS1014-PARE. Agency for Recognizing the Disease: Lúpica as a Tool for (Self-)Learning for Doctors and People with Lupus
</div>
<div> Presenta: Dr. Efrén Calleja Macedo – Jueves 13 de junio, 12:00 CEST
</div>
<div><br />
</div>
<div> ABS1251-PARE. In Search of a Law for the Rights of People with Lupus in Mexico
</div>
<div> Aceptado para publicación – Coautoría de Laura Athié y Efrén Calleja
</div>
<div><br />
</div>
<div><strong> ¿Quiénes somos?</strong>
</div>
<div>Laura vive con lupus desde hace 24 años. Su cuerpo, su lucha y su voz han sido el origen de investigaciones que hoy abren caminos en la ciencia social del lupus. Efrén es su compañero, editor y cofundador de este sueño compartido, ha apoyado este camino de la manera más amorosa. Ambos, impulsamos:
</div>
<div><br />
</div>
<ul>
<li>La iniciativa de ley por los derechos de las personas con lupus y otras enfermedades autoinmunes en México
</li>
<li>La revista Lúpica, la primera en su tipo en América Latina
</li>
<li>La brazada por los derechos de las personas con lupus en México
</li>
<li>El libro Nos esforzamos y somos valientes. Memorias de nuestras batallas con el lupus
</li>
<li>La Red de Investigadoras con Lupus (RILU)
</li>
<li>Y el Congreso Internacional Potencia Lupus
</li>
</ul>
<div><br />
</div>
<div>Desde Cetlu A.C. creemos en el poder de la comunidad, de la organización y del conocimiento compartido.
</div>
<div><br />
</div>
<div><strong> ¿Cómo puedes ayudar?</strong>
</div>
<div>Con tu apoyo —sea cual sea— podemos llegar a Barcelona.
</div>
<div>Puedes donar, compartir esta campaña o simplemente enviarnos tu buena energía.
</div>
<div><br />
</div>
<div>Gracias por estar. Por ser parte de esta historia.
</div>
<div>Gracias por creer que la ciencia, el arte y el amor pueden caminar juntos.
</div>
<div><br />
</div>
<div>Un abrazo con dos corazones 
</div>
<div>Que se abran puertas y caminos.
</div>
<div><br />
</div>
<div><strong>Laura Athié y Efrén Calleja Macedo</strong>
</div>
<div><strong>Presidenta y Director de Cetlu A.C.</strong>
</div>
<div>Con nuestras perras Paz, Transa y Volován, nuestras plantas y muchos sueños floreciendo 
</div>
<div><br />
</div>
<div>✨ <strong>May Doors and Paths Open: Help Us Reach EULAR 2025</strong> ✨
</div>
<div>We are Laura (researcher and person diagnosed with lupus in 2000) and Efrén (editor and Laura’s life partner). We believe that other realities are possible. That’s why we’ve woven together a project that unites science, love, and community: the Athié-Calleja Transdisciplinary Center for the Rights of People with Lupus (Cetlu A.C.).
</div>
<div><br />
</div>
<div>In 2025, three works born from our lived experience, research, and collective activism have been selected for presentation at the European Congress of Rheumatology (EULAR) — the most important congress of its kind in the world — to be held June 11–14 in Barcelona, Spain.
</div>
<div><strong>For the second time, three of our works have been selected!</strong>
</div>
<div>We are filled with pride and deep gratitude.
</div>
<div><br />
</div>
<div>With heartfelt joy and commitment, we will raise our voices there on behalf of all the people living with lupus in Mexico.
</div>
<div>But to get there, we need your support.
</div>
<div><br />
</div>
<div><strong> Fundraising Goal:</strong> $2,500 USD (approx. $47,000 MXN)
</div>
<div>This amount will cover:
</div>
<div><br />
</div>
<ul>
<li>Round-trip flights from Mexico City
</li>
<li>Transportation and meals during the congress in Barcelona
</li>
</ul>
<div><br />
</div>
<div><strong>Why is this important?</strong>
</div>
<div>Because these presentations shine a light on what is often left in the shadows:
</div>
<div>– That lupus affects children and adolescents, and they must be heard
</div>
<div>– That knowledge is born from those who live with the disease
</div>
<div>– That the right to a dignified life must not be a privilege, but a guarantee
</div>
<div><br />
</div>
<div><strong>Our accepted presentations:</strong>
</div>
<div> POS1437. Discursive Memory and Perception of Lupus in Children, Adolescents, and Young People
</div>
<div> Presenter: Dr. Laura Athié – Saturday, June 14, 10:15–11:45 CEST
</div>
<div><br />
</div>
<div> POS1014-PARE. Agency for Recognizing the Disease: Lúpica as a Tool for (Self-)Learning for Doctors and People with Lupus
</div>
<div> Presenter: Dr. Efrén Calleja Macedo – Thursday, June 13, 12:00 CEST
</div>
<div><br />
</div>
<div> ABS1251-PARE. In Search of a Law for the Rights of People with Lupus in Mexico
</div>
<div> Accepted for publication – Co-authored by Laura Athié and Efrén Calleja
</div>
<div><br />
</div>
<div> <strong>Who Are We?</strong>
</div>
<div>Laura has lived with lupus for 24 years. Her body, her voice, and her struggle have become the foundation for research that now opens new pathways in the social sciences of lupus. Efrén is her partner, editor, and co-founder of this shared dream — and has supported this journey with unwavering love.
</div>
<div><br />
</div>
<div><strong>Together, we have led:</strong>
</div>
<div><br />
</div>
<ul>
<li>A legislative initiative to secure the rights of people with lupus and other autoimmune diseases in Mexico
</li>
<li>The creation of Lúpica, the first magazine of its kind in Latin America
</li>
<li>The Brazada for the Rights of People with Lupus (swimming awareness event)
</li>
<li>The book We Strive and Are Brave: Memoirs of Our Battles with Lupus
</li>
<li>The founding of the Network of Women Researchers with Lupus (RILU)
</li>
<li>And the International Potencia Lupus Congress
</li>
</ul>
<div><br />
</div>
<div>At Cetlu A.C., we believe in the power of community, of organized care, and of shared knowledge.
</div>
<div><br />
</div>
<div><strong>How Can You Help?</strong>
</div>
<div>With your support — whatever the amount — we can make it to Barcelona.
</div>
<div>You can donate, share this campaign, or simply send us your positive energy.
</div>
<div><br />
</div>
<div>Thank you for being here. Thank you for being part of this story.
</div>
<div>Thank you for believing that science, art, and love can walk together.
</div>
<div><br />
</div>
<div>A hug from two hearts 
</div>
<div>May doors and paths open.
</div>
<div><br />
</div>
<div><strong>Laura Athié &amp; Efrén Calleja Macedo</strong>
</div>
<div><strong>President and Director of Cetlu A.C.</strong>
</div>
<div>With our dogs Paz, Transa, and Volován, our beloved plants, and many blooming dreams 
</div>

Con lupus y esperanza hasta Barcelona: ¡Ayúdanos a llegar!

Laura Isabel Athié Juárez

<div>✨ <strong>Que se abran puertas y caminos: Ayúdanos a llegar a EULAR 2025 </strong>
</div>
<div>Somos <strong>Laura</strong> (investigadora y persona con lupus diagnosticada en el año 2000) y <strong>Efrén </strong>(editor y compañero de vida de Laura). Creemos que otras realidades son posibles. Por eso, tejemos un proyecto que une ciencia, amor y comunidad: el Centro de Estudios Transdisciplinarios Athié-Calleja por los Derechos de las Personas con Lupus (<strong>Cetlu A.C.</strong>).
</div>
<div><br />
</div>
<div>Este 2025, tres trabajos nacidos desde nuestra experiencia, nuestras investigaciones y el activismo colectivo, han sido seleccionados para presentarse en el Congreso Europeo de Reumatología (EULAR), el más importante del mundo en su tipo, que se celebrará en Barcelona, España. <strong>¡Por segunda ocasión fuimos seleccionados con tres trabajos! </strong>Estamos muy orgullosos y agradecidos con la vida.
</div>
<div><br />
</div>
<div>Con alegría profunda y compromiso, llevaremos nuestras voces hasta allá, en nombre de todas las personas que viven con lupus en México. Pero para lograrlo, necesitamos tu ayuda.
</div>
<div><br />
</div>
<div><strong>Meta de recaudación:</strong> $50,000 MXN
</div>
<div>Este monto cubrirá:
</div>
<ul>
<li>Vuelos de ida y vuelta desde Puebla-Ciudad de México-Puebla
</li>
<li>Traslados y alimentación durante el congreso en Barcelona
</li>
<li>El costo de dos noches de hotel (Ya hemos costeado el resto)
</li>
<li>La impresión de nuestros carteles en gran formato
</li>
</ul>
<div><br />
</div>
<div><strong>¿Por qué es importante?</strong>
</div>
<div>Porque estas presentaciones visibilizan lo que muchas veces no se ve:
</div>
<div>– Que el lupus también se piensa desde la infancia y la adolescencia
</div>
<div>– Que hay saberes que nacen desde quienes viven con la enfermedad
</div>
<div>– Que el derecho a una vida digna no debe ser privilegio, sino garantía
</div>
<div><br />
</div>
<div><strong>Nuestras ponencias aceptadas son:</strong>
</div>
<div>POS1437. Discursive Memory and Perception of Lupus in Children, Adolescents, and Young People
</div>
<div>Presenta: Dra. Laura Athié
</div>
<div><br />
</div>
<div>POS1014-PARE. Agency for Recognizing the Disease: Lúpica as a Tool for (Self-)Learning for Doctors and People with Lupus
</div>
<div>Presenta: Dr. Efrén Calleja Macedo
</div>
<div><br />
</div>
<div>ABS1251-PARE. In Search of a Law for the Rights of People with Lupus in Mexico
</div>
<div>Aceptado para publicación – Coautoría de Laura Athié y Efrén Calleja
</div>
<div><br />
</div>
<div><strong>¿Quiénes somos?</strong>
</div>
<div>Laura vive con lupus desde hace 24 años. Su cuerpo, su lucha y su voz han sido el origen de investigaciones que hoy abren caminos en la ciencia social del lupus. Efrén es su compañero, editor y cofundador de este sueño compartido, ha apoyado este camino de la manera más amorosa. Ambos, impulsamos:
</div>
<ul>
<li>La iniciativa de ley por los derechos de las personas con lupus y otras enfermedades autoinmunes en México
</li>
<li>La revista Lúpica, la primera en su tipo en América Latina
</li>
<li>La brazada por los derechos de las personas con lupus en México
</li>
<li>El libro Nos esforzamos y somos valientes. Memorias de nuestras batallas con el lupus
</li>
<li>La Red de Investigadoras con Lupus (RILU)
</li>
<li>Y el Congreso Internacional Potencia Lupus
</li>
</ul>
<div><br />
</div>
<div>Desde Cetlu A.C. creemos en el poder de la comunidad, de la organización y del conocimiento compartido.
</div>
<div><br />
</div>
<div><strong>¿Cómo puedes ayudar?</strong>
</div>
<div>Con tu apoyo —sea cual sea— podemos llegar a Barcelona.
</div>
<div>Puedes donar, compartir esta campaña o simplemente enviarnos tu buena energía.
</div>
<div><br />
</div>
<div>Gracias por estar. Por ser parte de esta historia.
</div>
<div>Gracias por creer que la ciencia, el arte y el amor pueden caminar juntos.
</div>
<div><br />
</div>
<div>Un abrazo con dos corazones
</div>
<div><br />
</div>
<div><strong>Laura Athié y Efrén Calleja Macedo</strong>
</div>
<div><strong>Presidenta y Director de Cetlu A.C.﻿</strong>
</div>
<div>Con nuestras perras Paz, Transa y Volován, nuestras plantas y muchos sueños floreciendo
</div>
<div><br />
</div>
<div>✨ <strong>May Doors and Paths Open: Help Us Reach EULAR 2025</strong> ✨
</div>
<div>We are Laura (researcher and person living with lupus) and Efrén (editor and Laura’s life partner). We believe other realities are possible. That’s why, years ago, we created a project that unites science, love, and community: the Athié-Calleja Transdisciplinary Center for the Rights of People with Lupus (Cetlu A.C.).
</div>
<div><br />
</div>
<div>In 2025, three of our research-based and deeply lived proposals have been selected to be presented at the European Congress of Rheumatology (EULAR) — the most important international forum on rheumatology — taking place from June 11 to 14 in Barcelona, Spain.
</div>
<div><br />
</div>
<div>We’re honored and overjoyed. But to make this trip a reality, we need your help.
</div>
<div><br />
</div>
<div>Goal: $2,500 USD (approx. $47,000 MXN)
</div>
<div>This amount will cover:
</div>
<ul>
<li>Round-trip flights from Puebla-Mexico City-Puebla
</li>
<li>Local transportation and meals during the congress in Barcelona
</li>
<li>2 night of hotel stay
</li>
<li>Large-format printing of our posters
</li>
</ul>
<div><br />
</div>
<div><strong>Why is this important?</strong>
</div>
<div>Because these presentations share what is often unheard and unseen:
</div>
<div>– That lupus affects children and young people too
</div>
<div>– That people living with lupus hold valid, necessary knowledge
</div>
<div>– That dignity and rights should not be a privilege, but a promise
</div>
<div><br />
</div>
<div><strong>Our accepted presentations:</strong>
</div>
<div>POS1437. Discursive Memory and Perception of Lupus in Children, Adolescents, and Young People
</div>
<div>Presenter: Dr. Laura Athié
</div>
<div><br />
</div>
<div>POS1014-PARE. Agency for Recognizing the Disease: Lúpica as a Tool for (Self-)Learning for Doctors and People with Lupus
</div>
<div>Presenter: Dr. Efrén Calleja Macedo
</div>
<div><br />
</div>
<div>ABS1251-PARE. In Search of a Law for the Rights of People with Lupus in Mexico
</div>
<div>Accepted for publication – Co-authored by Laura Athié and Efrén Calleja
</div>
<div><br />
</div>
<div><strong> Who Are We?</strong>
</div>
<div>Laura has lived with lupus for 24 years. Her body, her resilience, and her voice have shaped research that is now transforming how lupus is understood in Latin America. Efrén is her partner, an editor, and co-creator of this shared dream.
</div>
<div><br />
</div>
<div><strong>Together, we’ve led:</strong>
</div>
<div><br />
</div>
<ul>
<li>The creation of Lúpica, the first magazine dedicated to lupus in Latin America
</li>
<li>The first walk and swim for lupus rights in Mexico
</li>
<li>The book We Strive and Are Brave: Memoirs of Our Battles with Lupus
</li>
<li>The Network of Women Researchers with Lupus (RILU)
</li>
<li>And the International Potencia Lupus Congress
</li>
<li>Through Cetlu A.C., we believe in community care, gentle resistance, and shared knowledge.
</li>
</ul>
<div><br />
</div>
<div><strong>How Can You Help?</strong>
</div>
<div>With your support — big or small — we can take this step forward.
</div>
<div>You can donate, share this campaign, or simply send us your love.
</div>
<div><br />
</div>
<div>Thank you for believing that science, art, and love can walk together.
</div>
<div>Thank you for helping voices with lupus be heard on a global stage.
</div>
<div>Thank you for being part of this journey.
</div>
<div><br />
</div>
<div>A big hug from both of our hearts.
</div>
<div>May doors and paths open.
</div>
<div><br />
</div>
<div><strong>Laura Athié &amp; Efrén Calleja Macedo</strong>
</div>
<div><strong>President and Director of Cetlu A.C.</strong>
</div>
<div>Along with our dogs Paz, Transa, and Volován, a forest of plants, and many, many dreams
</div>
<div><br />
</div>

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Laura Isabel Athié Juárez

Laura Isabel Athié Juárez

What they care about

Featured causes

Con lupus y esperanza hasta Barcelona: ¡Ayúdanos a llegar!

Con lupus y esperanza hasta Barcelona: ¡Ayúdanos a llegar!

About me