Support for parents of

Clubfoot Cuties

 

Clubfoot Parents are in a special club of their own

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Are you a new clubfoot parent? Sign up for your Welcome Letter to hear more about my journey and my TOP 5 must do items before your clubfoot cutie is born!

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Hey there!

I am Maureen Hoff, a clubfoot cutie mom, who understands the challenge of having a child born with a medical difference because I am living it.

I know the impact of having a child born with a birth defect can have on your personal life and your surrounding family unit. I am here to support, listen, validate and encourage you during your most challenging moments.

Parenting is hard, exhausting, and also amazingly beautiful. If it isn’t the definition of a beautiful challenge, I don’t know what is!

Clubfoot Chronicles: Tips for Helping Your Clubfoot Cutie During Treatment

Written by a clubfoot parent for other clubfoot parents, this book is filled with resources, tips, and personal experiences to help you feel seen and supported on your clubfoot treatment journey. It’s unique blend of memoir and resource guide provides an in depth look at the first year of clubfoot treatment from a parent who has lived it, and suggestions to help during the most challenging times.

Parent Education & Support

I am passionate about parent’s ability to educate themselves about their child’s diagnosis and treatment. The more you know, the more empowered you will feel to make decisions regarding your child’s care.

I focus on creating resources for parents to utilize on their journey. I strive to create a variety of resources on different platforms, so that parents can find something that finds their needs.

It started with the book, Clubfoot Chronicles, as I have always retained information through books. I expanded to the podcast, A Clubfoot Mom, as an auditory option and a way to create more connections through the clubfoot community. I created the Baby Sparks class, as a visual alternative, which gives the parents perspective in clubfoot treatment.

I partner with We Are Brave Together, to start the virtual support group for Moms of Clubfoot Cuties, to focus on how shared experiences can help support us on our treatment journey’s.

Support is not a one sizes fits all situation, parents need something that fits within their life to feel confident and empowered on their treatment journey. If you want more information on any of the resources or have any questions, click below to contact me.

Clubfoot Speaking & Consulting Engagements

We need to bridge the gap between medical advice and parent experience to create a better support system for the clubfoot community.

I often partner with MD Orthopaedics to create educational events that includes the parent experience of clubfoot treatment. Majority of clubfoot treatment is done at home by the caregivers and in order to achieve successful outcomes parents need to be educated and supported on their role.

If you are interested in hearing more about the speaking or consulting engagements, click below to contact me.