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Our Mom is Sick- Really, Really Sick, But She Rocks!

Our Mom is Sick- Really, Really Sick, But She Rocks!

Told through the perspective of Angela Parker-Brown’s twin twelve-year-old daughters, this slim volume offers children and young adults the tools to navigate a parent’s serious medical diagnosis. For Angela Parker-Brown, that diagnosis was ALS, Amyotrophic Lateral Sclerosis, a debilitating disease for which there is no cure. From the early signs of the illness to the later stages, Paris and Parker openly talk about their journey with their mother. They discuss their fear and confusion, as well as their sense of unfairness that this should happen to their wonderful mom, who took such good care of them and continued to do so as her condition deteriorated.

Guided by a helpful book, Real Kids Talk About ALS, Feeling Normal Sad and Different, and by their mother, Parker and Paris learned about the disease and how to cope with their emotions. Although they are twins, each daughter responded to their new situation differently. Parker delved into research, finding out additional details about ALS, which scared her so much she didn’t tell her sister. Angela impressed on her girls how important it is to have the right information, and Parker says how glad she was that their mother didn’t try to hide the truth from them. “I liked that our mom trusted us enough to tell us the truth,” she said. “It’s way scarier when you don’t know what’s going on, but you know something is going on, but nobody is telling you.”

As the disease progressed, Paris and Parker learned that they were still able to do normal things like watching TV together, having friends to visit and especially making memories with their mother. Through all the changes in their mother’s condition, the girls learned how important it is to acknowledge their feelings, to ask for help, and to always know their mom is still their mom – and that she rocks!

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average rating is 4 out of 5

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A Heartfelt Read

This book is told through the perspective of 12-year-old Nova Scotian twin girls, Paris and Parker, whose mom suffered from a deadly disease called Amyotrophic Lateral Sclerosis (ALS). It’s somewhat of a memoir of their courageous journey and how each twin handled loss differently - from the initial discovery of the symptoms until its later stages. Readers come along on the girls’ journey of navigating the landscape of their new reality.

This read was a short yet pretty complex one. It illustrated the complicated feelings the twins experienced as their mom’s health declined as well as explored the questions they had about her condition. As a twin myself, I loved that the twins’ individuality was highlighted throughout the book. Unfortunately, I found it extremely short and too fast-paced for a book that spans several years. I would have loved to see this as a full-length memoir instead.

I can see how readers may find that the simple diction, used to represent tweens, juxtaposed with the difficulties they endured, creates enough tension to maintain a balance. Unfortunately, it just wasn’t my favourite writing style. Nevertheless, I admire the way both girls handle their hardships with grace and determination. Their family’s outlook on life is very positive. I also loved the way that different places in Nova Scotia were casually mentioned such as Salmon River, the Grand Enfield Lake, and Wolfville’s Farmers’ Market etc. Their fondness of Truro and the memories they have there were wonderfully captured. It made me want to visit Nova Scotia again!

Paris and Parker honoured their mother’s legacy in a beautiful way. This book paints a genuine story of the power of love. It was a gentle reminder to count your blessings and to remember that you never know what someone is going through. I believe this is a helpful resource for other tweens experiencing similar things. I recommend this book to anyone looking for a short, heart-wrenching, yet inspiring read.

I rate this book 🌟 3.5 / 5 stars 🌟

I recommend this book.

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