Informations about rare kidney disease

Rare kidney conditions are, by definition, ones most families have never heard of before the diagnosis. The organisations below publish reliable information and, in many cases, connect families facing the same condition.

Information written for one country may not match how a condition is investigated, treated or funded in Canada. Bring anything you read here to your child’s nephrologist, who can tell you what applies to your situation.

Where to start

  • IPNA patient education

    Material collected by the International Pediatric Nephrology Association, searchable by disease, language and country of origin, in more than a dozen languages. The best first stop for a specific diagnosis.

  • AboutKidsHealth

    Paediatric health information written and reviewed by clinicians at The Hospital for Sick Children, in plain language and several languages.

Nephrotic syndrome and FSGS

  • NephCure

    Focused on nephrotic syndrome and FSGS, with material for families as well as for adults living with the condition, and a research and clinical trial section.

Haemolytic uraemic syndrome and complement disorders

  • aHUS Canada

    A Canadian patient organisation for atypical haemolytic uraemic syndrome, run by families affected by it.

Metabolic and inherited conditions

Systemic conditions affecting the kidney

  • Lupus Canada

    National organisation for people living with lupus, which can involve the kidneys as lupus nephritis.

  • Kidney Cancer Canada

    Patient-led organisation for kidney cancer, including the rare forms that occur in childhood.

Is your child’s condition missing from this page? Tell us at contact@capneph.ca and we will look for a reliable source to add.