Hydrocephalus Canada Kidz & Youth Book Club

Connect with the Hydrocephalus Canada community and receive new resources periodically, as they become available including featuring stories and resources created for kids and youth living with hydrocephalus and spina bifida.

Families raising children with hydrocephalus and/or spina bifida often search for books where their child feels seen, understood, and empowered. The Hydrocephalus Canada Kidz & Youth Book Club offers carefully curated books and resources designed specifically for children and youth living with hydrocephalus and/or spina bifida.

Our book selections help children understand their experiences, build confidence, and connect with characters facing similar journeys while giving parents, caregivers, educators, and healthcare professionals tools to support meaningful conversations.

How to Sign Up

1. Tell us about your child

Fill out a 2 minute form to share a bit about your child and your family. This helps us choose the perfect books.
Find the form HERE.

2. Enjoy Your First Book.

Your child’s first handpicked book will be mailed and carefully chosen to celebrate and reflect their unique journey with hydrocephalus or spina bifida.

3. Love It? Become a Member!

If your child enjoys their first book we hope you will consider joining our spina bifida and hydrocephalus community.

Spend 60 seconds and complete the form here

Why Representation Matters

Children living with hydrocephalus or spina bifida may experience hospital visits, surgeries, mobility differences, learning challenges, or social questions from peers. Seeing these realities reflected in books helps children:

• Feel less alone
• Build self-confidence and resilience
• Understand their medical journey
• Develop social and emotional skills
• Connect with peers and communities

Books Created for Kids Like Yours

Our Kidz & Youth Book Club highlights books that include:

Stories featuring children living with hydrocephalus or spina bifida
Books about medical journeys and hospital experiences
Stories promoting disability inclusion and accessibility
Confidence-building and mental wellness themes
Educational resources for families and classrooms
Canadian and international stories supporting diverse experiences

Each title is selected with families in mind, helping children see that their differences are strengths.

Who Is This Book Club For?

Our curated book collection is designed for:

• Children ages 3–14
• Youth living with hydrocephalus
• Youth living with spina bifida
• Families seeking disability-positive books
• Educators teaching inclusion and accessibility
• Canadian families seeking community resources

Youth Ages 15 and Up

We can send curated recourses that reflects the changes, questions, and challenges that come with growing up like identity, friendships, and independence.

Our Transition Kit explores themes like self-discovery, transition, independence, and belonging. Resources that reflect your journey into adulthood.

Contact Hydrocephalus Canada for specific youth and adult resources at info@hydrocephalus.ca or 1-800-387-1575

Helping Kids and Youth Build Confidence Through Storytelling Stories give children language to describe their experiences and help them build confidence when navigating school, friendships, and healthcare settings. Reading together can open conversations about:

Medical differences
Self-advocacy
Accessibility needs
Mental wellness
Building friendships
Confidence and resilience

Together, we can do more. By joining Hydrocephalus Canada, you strengthen our voice in advocacy, expand our support programs, and help us reach every Canadian impacted by these conditions. Become a member today.

As a member of Hydrocephalus Canada you become part of a supportive and understanding community, helping your child access empowering stories while also supporting programs that benefit families nationwide.

Where Your Membership Support Goes

Your membership helps Hydrocephalus Canada continue delivering vital programs and services for Canadians living with hydrocephalus and spina bifida, including:

• Family and caregiver support groups
• One-on-one support and navigation assistance
• Education and awareness initiatives across Canada
• Research advocacy and community programs
• Resources and supports for children, youth, and families at every stage of their journey

Together, we are building stronger support networks and brighter futures for families across Canada.

Strength in community. Become a member, Champion Change

A Message From Our Director, Shauna Beaudoin impacted by Spina Bifida.

We hope that you take advantage of our programs and services, such as community support networks, educational webinars and information, health and well-being program, social media platforms, one-to-one support and much more.

Reach out to us anytime for information and support,

Shauna