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Just Diagnosed with Down Syndrome in Quebec

You're not behind. There's no timeline. Start wherever you're ready and go at your own pace. Everything on this page is free.

Right Now

You're not alone. Whatever you're feeling right now is normal.

Congratulations on your baby. Take a breath. Your baby needs the same thing every baby needs right now — you. Everything else can wait.

Who to call today

Canadian Down Syndrome Society: 1-800-883-5608

Ask about the 21 Welcomes program — they'll send a welcome basket and connect you with a parent mentor.

Medical note

Has a cardiac screening (echocardiogram) been done? Heart defects are common with Down syndrome and should be checked early. If not yet done, ask your pediatrician.

A note about late-night Googling

We've all done it. At 2am you'll find yourself reading something terrifying written in 1997 that doesn't reflect where things are today. If you're spiraling, close the laptop and come back here tomorrow. The information on this page is current, Canadian, and reviewed. You're going to be okay.

When You're Ready — The Important Stuff

These programs have waitlists — some are months long. Applying now means you'll be closer to the front when you need them. None of this is urgent today. But when you have the energy, start here.

Disability Tax Credit (DTC)

Opens the door to $200/month in child benefits, $90,000 in RDSP grants, and several other tax credits.

How to apply:Ask your child's doctor to fill out form T2201. That's it.

Read the full DTC guide

Quebec provincial programs

Supplement for Handicapped Children

$236/month (2025)

Monthly supplement paid to families of children with disabilities requiring exceptional care.

Official website

Assistive Technology Program (RAMQ)

Covers cost of assistive devices, wheelchairs, and orthotics through the Regie de l'assurance maladie du Quebec.

Official website

About waitlists

Apply for everything on this list even if you're not ready to use the services yet. You can always decline when your name comes up, but you can't get back the time you spent not on the list. Think of it as holding your place in line.

The Paperwork

Nobody tells you that a disability diagnosis comes with a mountain of paperwork. Here's what you need and where to keep it. Get a folder (physical or digital). Label it. Everything goes in there.

Documents to gather

  • 1Get a copy of the genetic test results (karyotype) confirming diagnosis
  • 2Request documentation from the pediatrician or geneticist
  • 3Ask for referrals to early intervention programs immediately
  • 4Request cardiac and thyroid screening results (common co-occurring conditions)
  • 5Start a health journal tracking developmental milestones

Always have copies of

  • Child's health card
  • Social Insurance Number (SIN) — apply if you don't have one
  • Birth certificate
  • All therapy reports and progress notes
  • School records and IEP documents
  • Receipts for all medical expenses, therapy, equipment, travel

Track your expenses

Starting today, keep every receipt for anything related to your child's condition: therapy sessions, medications, equipment, mileage to appointments, parking at the hospital. These are claimable on your taxes.

View Tax Calendar

Building Your Team

Raising a child with Down Syndromeisn't something you do alone. Here are the people and organizations who can help.

National organizations

Canadian Down Syndrome Society (CDSS)

Founded in 1987 and based in Calgary, CDSS is Canada's national voice for Down syndrome. Offers a toll-free support line, resources including 21 Welcomes (prenatal), Today and Tomorrow (aging), and 3.21 Magazine (quarterly). The Inployable initiative advocates for inclusive employment, highlighting that over 50% of people with Down syndrome cannot find paying jobs.

NationalWebsite

Organizations in Quebec

LE REGROUPEMENT POUR LA TRISOMIE 21

Registered Canadian charity providing disability-related services. CRA Registration: 119008902RR0001

Regroupement pour la Trisomie 21

Quebec provincial organization for Down syndrome (Trisomie 21) providing support, information, and advocacy in French and English.

Recommended therapies

Here are the therapies typically recommended for Down Syndrome:

  • Occupational therapy
  • Speech-language pathology
  • Physiotherapy
View full therapy plan

Specialists to request

  • Pediatric cardiologist (heart defects are common)
  • Endocrinologist for thyroid screening
  • Speech-language pathologist (early intervention is critical)
  • Occupational therapist and physiotherapist
  • Developmental pediatrician
  • Audiologist (hearing issues are common)

You are the expert on your child. The doctors are consultants. Don't be afraid to ask questions, disagree, or get a second opinion.

Looking Ahead

You don't need to think about any of this today. Bookmark this section and come back when you're ready — whether that's next month or next year.

RDSP (Registered Disability Savings Plan)

The government will give your child up to $90,000 over their lifetime — but only if you open this account. You need the DTC first. Once approved, open an RDSP even if you can't contribute. The government deposits bonds for low-income families automatically.

RDSP Guide

Henson Trust

If your child will receive provincial disability support as an adult, a regular inheritance could disqualify them. A Henson Trust protects the inheritance without affecting benefits. You don't need to set this up now — but when you write your will, make sure your lawyer knows about Henson Trusts.

Education rights in Quebec

Quebec uses Individualized Education Plans (Plans d'intervention) for students with special needs. The Ministry of Education provides grants to school boards for students requiring additional services. Services are available in both French and English school systems.

Your Rights guide

Turning 18

Children's services end at age 18 (19 in BC). Adult disability programs have separate applications and often long waitlists. This feels far away. It comes faster than you think. But you don't need to worry about it now — just know it's covered in our guide.

Turning 18 Guide

Tax planning

Most families of children with disabilities leave $10,000+ per year in unclaimed benefits.

You're Not Alone

Thousands of Canadian families navigate this path every year. Connecting with others who understand can make all the difference.

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Know of a service we should list?

This directory grows because people in the community help us find what we've missed. Let us know about organizations, programs, or services across Canada.