Talking With Your Family & Friends – Spanish
Hablar sobre su afección y diagnóstico de poliquistosis renal autosómica dominante, o ADPKD por sus siglas en inglés, es su decisión. Read More
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At Risk for ADPKD: A Guide for Talking About ADPKD – Spanish
La poliquistosis renal autosómica dominante, o ADPKD por sus siglas en inglés, representa la mayor parte de los casosde riñón poliquístico (9 de 10). Algunas personas con ADPKD están en… Read MoreSupporting Your Loved One With ADPKD – Spanish
Hablar sobre la ADPKD es una decisión personal y puede ser difícil para su ser querido que enfrenta esta afección. Read MoreWhere Can I Find Help for ADPKD – Spanish
Hay muchas organizaciones y recursos disponibles en la comunidad sobre la enfermedad renal poliquística, o PKD por sus siglas en inglés, para ayudarlo a usted y a su ser querido… Read MoreTalking With Your Employer – Spanish
Hablar sobre su afección y diagnóstico de poliquistosis renal autosómica dominante, o ADPKD por sus siglas en inglés, es su decisión. Read MoreWorking With Your Healthcare Provider to Help Manage ADPKD – Spanish
La poliquistosis renal autosómica dominante, o ADPKD por sus siglas en inglés, representa la mayor parte de los casos de riñón poliquístico (9 de 10). La ADPKD puede progresar rápidamente… Read MoreVoices From The Community Episode 19 – Conversation with Mariah: Healthcare Challenges in the Transgender Community
Learn about gender affirming care and the various challenges faced by the transgender community in this podcast. Read MoreAnxiety: A Significant Mental Health Issue For Kidney Disease Patients
This article brings attention to the effects of mental health on patients with chronic kidney disease, specifically anxiety. Read MoreCaring for Yourself While Caring for a Loved One With ADPKD
When you are caring for someone with autosomal dominant polycystic kidney disease (ADPKD), it may be difficult to focus on your needs as well as those of your loved one. Read MoreTalking With Your Family & Friends
Because ADPKD is genetic, meaning it runs in families, it can affect the family as a whole. This is one reason you may find it essential to talk with family… Read MoreNephU is supported by Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) and Otsuka America Pharmaceutical, Inc. (OAPI) - committed supporters of the Kidney Health Community. The information provided through NephU is intended for the educational benefit of health care professionals and others who support care for those with kidney disease and other related conditions. It is not intended as, nor is it a substitute for, medical care, advice, or professional diagnosis. Health care professionals should use their independent medical judgement when reviewing NephU’s educational resources. Users seeking medical advice should consult with a health care professional. No CME or CEU credits are available through any of the resources provided by NephU. Some of the contributors may be paid consultants of OPDC and/or OAPI.©2024 Otsuka Pharmaceutical Development & Commercialization, Inc. All rights reserved. - IgAN
