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C3G Awareness Day 2025 

On September 25th, NephCure is proud to recognize C3G Awareness Day, a day dedicated to shining a light on Glomerulopatía del complemento 3 (C3G), a rare chronic kidney disease that damages the glomeruli, the tiny filtering units in the kidneys that help remove toxins from the blood and can ultimately lead to kidney failure. 

For the first time ever, there are FDA-approved treatments, FABHALTA y EMPAVELI, that may help preserve kidney function y prevent the need for dialysis or transplant.

The time to be proactive is now. Join NephCure on September 25th and share your story, repost one of our posts, or create your own post using the hashtag #C3GAwarenessDay y help us spread awareness.

Living with C3G: What You Need to Know

If you or a loved one has been diagnosed with C3G, you may have questions about what comes next. Rare kidney diseases can be difficult to manage—but there is hope.

Watch this educational session to hear from kidney experts, patient advocates, and real patients as they share:

  • What C3G is and how they affect the kidneys
  • Current treatment options and their limits
  • The value of clinical trials
  • Patient experiences and practical advice for talking with your doctor

What is Glomerulopatía del complemento 3 (C3G)?

Complement 3 Glomerulopathy (C3G) is a kidney condition where excessive activation of the complement system damages the filtering units (glomeruli), impairing kidney function. It affects individuals differently and can progress without noticeable symptoms—making early awareness and diagnosis vital.

Aprende más

Involucrarse

Spread the word about C3G Awareness Day! Share our downloadable graphics on your social media and use your voice to raise awareness. Be sure to check out the C3G Awareness Day Toolkit—it’s packed with templates and tips to make posting easy and impactful. Don’t forget to use #C3GAwarenessDay and tag @NephCure in your posts!

Download toolkit

How You Can Help

Raising awareness for C3G starts with simple actions that anyone can take—every post, conversation, and shared resource brings us closer to better understanding, treatment, and support.

  • Post on Social Media: Use #C3GAwarenessDay y #RareTogether and tag @NephCure to share your support and help more people learn about this rare disease.
  • Download the Awareness Toolkit: Access ready-to-share graphics, fact sheets, and suggested captions.
  • Share Your Story: Your voice matters—personal experiences help others feel less alone and spread understanding.

Breakthrough Treatment Options Are Here

Research into C3G is moving faster than ever before. New therapies and treatment approaches are emerging that offer hope for slowing disease progression, protecting kidney function, and improving quality of life. These advancements include recently approved FABHALTA y EMPAVELI, and open the door to more targeted and personalized care for people living with C3G.

Opciones de tratamiento

C3G Handbook Interest Form

We’re currently developing a comprehensive handbook designed to educate and empower the C3G community. This resource will include important information about Opciones de tratamientosupport tools, y educational materials to help you navigate your rare kidney disease journey with confidence.

If you’re interested in receiving a copy once it’s available, please complete the form below.

Comparte tu historia

Tu historia tiene el poder de inspirar esperanza e impulsar el cambio. Al compartir tu experiencia, puedes generar conciencia, conectarte con otras personas y abogar por una mejor atención. ¡Tu historia importa!

C3G Patient Stories and Resources

Glomerulopatía C3 (C3G)

Chase G.

En 2009, a Chase Gallagher, a la edad de 8 años, le diagnosticaron MPGN tipo III, ahora conocida como C3G. El pediatra principal de Chase originalmente lo diagnosticó erróneamente, diciendo que sus ojos hinchados eran...

Hoja de hechos

Glomerulopatía C3 (C3G)

Descripción general de C3G: C3G significa glomerulopatía del complemento 3, una enfermedad crónica muy rara que hace que los riñones no funcionen correctamente. El C3 hace referencia a una sangre clave…

Glomerulopatía C3 (C3G)

Lindsey F.

Lindsey Fuller tiene una forma rara de C3G hereditaria. Su abuelo murió de insuficiencia renal y su padre tuvo cuatro trasplantes en el transcurso de 20 años...

Video

NephCure U: Seminario web de actualización de C3G

Este seminario web de NephCure U, organizado por la Dra. Carla Nester, nos brinda información actualizada sobre C3G (un nombre colectivo para un grupo de enfermedades renales raras que involucran una parte específica de su sistema inmunológico).

Documentos informativos

Hable con su médico sobre la salud de sus riñones

A menudo, los síntomas de la enfermedad renal son invisibles o no obvios. Es importante conocer los síntomas a los que debe prestar atención y las preguntas que debe hacerle a su médico para que simple...

Thank you to the following partners who are working to help improve the lives of C3G patients and families

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