<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>

Francisco Sandoval Alarcon

Dulce Corina  Martinez Castelan

MARIA INES CAMARENA DE OBESO

Pilar Martínez

Elsa Medina Castro

Landy De la Parra

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Daniela ALò

Gabriele Schuster-Klackl

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Anonymous

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Claudia Reyes

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

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