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I write because it's fun and it's a daily practice like yoga or meditation.I write to get clarity and to go deeper. I write because writing itself is action. I write as a way to take a small step in repairing the world.

SAMARRAH FINE CLAYMAN

“Where is my loud, silly brother?” Lyla asks. Lyla is seven, and her three-year old brother, Jax, has a brain tumor—a marble-sized lump in his head that has to be removed with surgery. Jax is in the hospital. Lyla is hoping he will be home for Thanksgiving and the family can all be together.

 

Any family that has had a sick child will recognize the feelings of uncertainty and anxiety that Lyla expresses. With this story, Samarrah hopes to help other children and their parents through challenging times, emphasizing the importance of love and hope.

In 2017, Samarrah’s 23-month-old son was diagnosed with a ependymoma—a rare brain tumor. Samarrah wrote this book for her family and other families faced with illness. The story is about a child’s worries about and growing understanding of her brother’s illness. It is also about gratitude and a celebration of life–no matter what.

 

All profits from the sale of this book will support pediatric brain tumor research.

 

After, her son’s diagnosis, she and her husband created The Ependymoma Research Foundation, to support research for pediatric brain tumors, with the goal of a cure.

You can learn more at: www.ependymomaresearchfoundation.org

If you are looking for a book for siblings of childhood cancer patients, this is a good one to explain what could happen with family dynamics. Given a scary environment filled with changes and uncertainty, Clayman’s child-friendly language and Preveza’s bright colors make for an optimistic, hopeful read.

Further, Clayman writes with authority on the subject, as she pulls from her own experience. In 2017, her 23-month-old son was diagnosed with an ependymoma, a rare brain tumor found mainly in young children. While the treatment involves surgery and radiation, the tumor can often reoccur, and there is no cure. For this reason, she and her husband created The Ependymoma Research Foundation, and all profits from the sale of this book will be donated there.
 

Pamela Brunskill, Literary Coach and Writer

Book Review Blog 

 

 

The book is incredible!!!

It is so touching and brought tears to my eyes.  It will no doubt be so helpful for other families facing these terrifying moments. Samarrah captured the poignancy of the effects on family and how to weave it into life as time marches on.  What an incredible and wonderful book.

 

Dr. Torunn Yock

Director, Pediatric Radiation Oncology, Massachusetts General Hospital

COMING IN 2020

Samarrah is writing a children's yoga book, which will be released in 2020.

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© 2020 by Samarrah Fine Clayman. Designed by Stephanie Gerber Wilson

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