Tired All the Time - Book Review
- Kirstin Maltby
- 6 days ago
- 3 min read
There are several books that we have listed here on our website about Ehlers-Danlos Syndrome (EDS) and common related conditions. The problem is you can't always tell how helpful they will be until you get them. So we are working through our own library of books and getting some reviews up.
Our forthcoming book review is authored by another Australian physician, focusing once again on Dysautonomia. This book, published in early 2025 by Brisbane, QLD Specialists, is written by Dr. Brendan Hanrahan. Dr. Hanrahan, a General Physician/Internist, specialises in managing complex disorders. In this book, Dr. Hanrahan shares his personal journey of treating Dysautonomia, which began around 2012. I will leave the details of his story for readers to discover.
This book serves as a comprehensive guide for managing and living with Dysautonomia. It is an excellent reference resource for both patients and healthcare professionals, providing valuable insights that warrant a place in any medical library. As a reference book, it allows readers to navigate through sections as needed, without the necessity of reading it cover to cover.
The content includes diagnosis, treatment options, medication guides, references, printable templates, and sample documents, with a website link for downloading these resources. The author acknowledges the evolving nature of medical science and plans to update the resources section and publish updated editions as new information becomes available. Further to the content aimed at POTS patients, there is an inclusion of information related to Ehlers-Danlos/Hypermobility and Mast Cell Activation Syndrome.
Noteworthy aspects of the book include the use of a dyslexia-friendly font to enhance readability, and clear medication guides that detail the what, why, and how much. The book is expected to be a valuable reference for general practitioners and similar health professionals, offering guidance on initiating the testing and treatment of patients with suspected POTS. It is emphasised that this book should not replace professional medical advice, nor is it for patients with complex issues.
Reviewing this book posed a challenge for me, as I am already familiar with much of the content due to having consulted with the author. As the book is designed to evolve with ongoing advancements, it is understood that any perceived gaps may be addressed in future editions and on their referenced website
I would have appreciated more detailed information on the various types of Dysautonomia and POTS (neurogenic, hyperadrenergic, hypovolemic, etc.) in the introductory sections to provide clarity on this complex topic. Additionally, a discussion on the impact of sleep on Dysautonomia, complementing the health pillars of diet and exercise, would be beneficial. Some guidance on NDIS would also be valuable, although including every possible piece of information would transform this from a concise reference into an extensive volume.
Primarily focused on Postural Orthostatic Tachycardia Syndrome (POTS), this book is an excellent resource for new patients and healthcare professionals. While those with years of experience managing POTS may still find it useful, it is mainly intended as an introductory guide for POTS patients. Individuals with rare forms of Dysautonomia may find it less applicable.
This book is well priced at $16.95AUD + delivery (which, if you are an Amazon member is free) and available on Amazon
This book was purchased privately, and all views are those of the author only. This review is done just to give a general exposure of the contents to help people decide if this is worth purchasing/reading for them.
If you have your own review of this book or other EDS books you wish to have published on the blog, please email us at ehlersdanlosaus@gmail.com
For more general info on POTS, check out the Australian POTS Foundation.
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