Senate of… by Ellana Rose Thornton-Wheybrew [PDF/iPad/Kindle]
Senate of Blood
Senate of Blood
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Senate of Blood

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Completed on 2015-09-09

About the Book

I had everything - I had a university education, a wife, children, loving parents, and I was close to becoming the United States President.

I lost everything. I lost my sanity. In its place, I found her.

~

Part novel, part short story collection, and part psychotic ramblings, Senate of Blood tells the story of one man and his fall from grace.

During a public appearance as a part of his campaign, an assassin attempts to take the life of Presidential candidate Robert Weaver. His body survives, but his mind begins to fail, turning him from the envy of all, to America’s Most Wanted. He is declared brain dead, despite there being no medical reason for it. Weaver continues to write, confusing the medical staff further.

Soon the scenes he describes come true, and the bodies start to pile up...

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About the Author

Ellana Rose Thornton-Wheybrew
Ellana Rose Thornton-Wheybrew

Ellana Thornton-Wheybrew was born in London, UK, and from an early age showed an interest in literature and writing. By the time she had entered her teenage years, she already had a large catalogue of poetry and short stories. Her love of literature is not just a passion; it has become quite a large part of her life and education.

Ellana can be found on Twitter via @EllanaRose_ and her page on Facebook, Ellana Rose Thornton-Wheybrew.

All of her books will remain free, with any money readers wish to pay going to charity. Ellana makes no money from her writing.

Causes Supported

Brittle Bone Society

http://www.brittlebone.org/

The Brittle Bone Society is the only charity working with people who live with Osteogenesis Imperfecta(OI) and supports over 820 members and their families across the UK and the Republic of Ireland. Our work involves addressing isolation and facilitating networking opportunities.

The Brittle Bone Society is the only charity working with people who live with Osteogenesis Imperfecta(OI) and supports over 820 members and their families across the UK and the Republic of Ireland. Our work involves addressing isolation and facilitating networking opportunities. We provide support, signposting, advocacy, factual information, obtain funds towards purchase of specialised wheelchairs and equipment and provide subsidised access to our conference events. We also provide access to the best medical and healthcare professionals in the UK specialising in metabolic bone health disorders. When a parent learns their new baby has the condition it is vital they connect with our Support Worker. We fund specialised wheelchairs (costing £3k-£16k) not available from the NHS that help with mobility and independence. Our latest project – our new Volunteer Support Group Programme helps provide a sense of community to OI families, to help combat isolation, promote living successfully with OI and help families connect with Brittle Bone Society services and resources.

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