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Free NDIS condition guide

Fragile X Syndrome and the NDIS

Fragile X syndrome (FXS) is a genetic condition caused by a change (called a full mutation) in the FMR1 gene on the X chromosome.

Download the guide

32 pages, free, and we do not ask for your email address. The last four pages are a workbook you fill in and take to your planning meeting.

Download in EnglishPDF, 1.7 MB
Pages
32
Version
2.0
Reviewed

Other languages

  • EnglishEnglish1.7 MB
  • فارسیFarsiComing soon
  • اردوUrduComing soon
  • हिन्दीHindiComing soon
  • ਪੰਜਾਬੀPunjabiComing soon
  • العربيةArabicComing soon
  • 中文ChineseComing soon
  • Tiếng ViệtVietnameseComing soon
  • TürkçeTurkishComing soon
  • EspañolSpanishComing soon
  • TagalogTagalogComing soon

Interpreters are free at every NDIS meeting. Call TIS National on 131 450 and ask for your language, or ask us to arrange one.

What is in this guide

6 sections, written around fragile x syndrome rather than the NDIS in general.

  1. 01page 04

    About Fragile X Syndrome

  2. 02page 08

    The NDIS basics

  3. 03page 15

    Your supports

  4. 04page 19

    Why InLife

  5. 05page 22

    Resources & next steps

  6. 06page 27

    Your workbook

Who this guide is for

  • People recently diagnosed with fragile x syndrome, or told they may qualify for the NDIS.
  • Families and carers supporting someone living with it, who need the scheme explained once, clearly.
  • Health professionals helping a person put an access request together.
  • Support coordinators looking for something plain to hand a new participant.

This guide is general information, not clinical or legal advice. Funding decisions are made by the NDIA, and no provider can influence them.

Talk it through with someone

Reading about the NDIS and getting a plan built are different problems. We are a registered NDIS provider working across Victoria, and we are happy to answer questions whether or not you ever become a participant with us.