What a Chiari diagnosis means, what happens next, and the questions worth asking.
Print it and bring it. Write on it — the margins are wide on purpose. The questions on the last pages are the part clinicians tell us patients most often forget to ask, so tick the ones you want answered before you go in.
This page is first because it matters most. If any of these is happening, contact your care team, an urgent care line, or emergency services — do not wait for a scheduled appointment.
These are the guides most people read first. Each one is written to be understood without a medical background, and none of them assumes you already know the vocabulary.
Newly diagnosed with Chiari malformation? Learn what Chiari means, what low-lying cerebellar tonsils mean, common symptoms, MRI findings, syrinx, CSF flow…
Learn the different types of Chiari malformation, including Chiari type I, type II, rare types III and IV, Chiari 0, Chiari 1.5, acquired Chiari, and…
Learn what Chiari type I malformation means, common symptoms, MRI findings, syrinx, CSF flow, when monitoring is enough, and when surgery may be considered.
Learn what Chiari type II means for babies and children with spina bifida, including myelomeningocele, hydrocephalus, symptoms, shunts, fetal surgery…
Learn about rare Chiari malformation types III and IV, including prenatal diagnosis, encephalocele, cerebellar hypoplasia, symptoms, prognosis, surgery…
Learn what Chiari 0, borderline Chiari, low-lying cerebellar tonsils, and tonsillar ectopia mean, including symptoms, syrinx, CSF flow, MRI findings…
Eighteen of the 265 terms in the full dictionary — the ones most likely to appear on a report or be said in a consultation.
Tick what you want answered. Appointments move fast — a written list is the difference between leaving with answers and leaving with new worries.
Independent organisations that support people with this condition. AURORA is not affiliated with any of them and does not receive anything for listing them.
Directory pending verification. Contact details and scope are being confirmed with each organisation before this booklet is published. Names are listed without links until that is done.
Patient education, research funding and a directory of clinicians who see Chiari regularly.
Support networks, clinical centre listings and patient conferences.
Information for people living with a syrinx alongside Chiari.
Condition summaries and financial assistance signposting.
This booklet is patient education. It describes groups of people, not you. It cannot examine you, read your scan, or know your history — and reading it creates no clinician–patient relationship. Every decision about your care belongs to you and a qualified clinician who knows your case.