Spewing Mummy's Books
Suffering hyperemesis gravidarum can be such a lonely and terrifying experience. It is my hope with these books that women will know that they are not alone and there there is help and support available. My approach is proactive and positive and I hope that shines through in my books...
Hyperemesis Gravidarum - The Definitive Guide
- By Caitlin Dean, RGN and Amanda Shortman
For the last year I have been working with my friend and colleague Amanda Shortman to write a great big book all about hyperemesis gravidarum. It's now finished and ready for you to buy via mainstream online retailers.
It was launched for pre-order on 1st October and by the following morning had reached #3 on Amazon's best seller list for Pregnancy and Childbirth.
Covering everything from treatment options to coping strategies, the emotional impact to planning another baby, this book is filled to the brim with information based on the latest research and the personal experiences of thousands of survivors. Proactive and inspiring, it is the definitive guide to hyperemesis gravidarum for sufferers, their partners and the healthcare professionals caring for them. The four part book, comprising 14 chapters, is devised to make the information you need as accessible as possible.
Part one covers definitions of hyperemesis gravidarum, theories into it's causes, information on treatments and management plans. Aimed more at the healthcare professionals it covers in depth the current research and care plans yet is accessible and essential for the sufferer too.
Part two is the essential survival guide for sufferers, their partners and family and friends. Covering coping strategies for the numerous symptoms of hyperemesis gravidarum, from excessive saliva and oral hygiene to the emotional impact and people who just “don't get it”, this section won't cure you but it will make the nightmare nine months that little bit easier.
Part three approaches life after hyperemesis gravidarum including recovering from the trauma, mental health issues and preparing for another. Alternatives to pregnancy, such as adoption and single child family structures are gently discussed and the book is rounded up with a positive pro-active approach to coping with hyperemesis as part of your life experience.
Part four provides a range of useful information, links, contacts, tables and charts to help you survive your journey with HG.
Buy The Book
You can now order the book in all major high street book shops and online retailers.
I'd love it most if you bought it directly from me though as it helps me to cover the cost of running this blog and providing a free specialist HG nurse advisory service to sufferers. Please click here or on the picture to buy via my Shopify shop:
If you prefer to buy through Amazon then here are the Amazon links for the UK, these are affiliate links so I get paid a little if you buy through it at no extra cost to you (although it's still loads better to buy direct from me)!
Charts, Tables and Care Plans From the Book
If you've read the book and are looking for the accompanying downloads, such as the cheat sheet, treatment ladder and fluid balance chart then click here.
Despite discussions with agents and publishers both here and in America we decided to go down the independent publishing route for two main reasons. Firstly and most importantly was control over content. We both feel that unless the editor happened to have been a sufferer themselves they were highly unlikely to understand the importance of much of the book's content, particularly the emotional aspects of hyperemesis support and care. We didn't want, what we consider to be, the most important aspects of the book to be stripped out or toned down by an editor who has never suffered. Secondly, there is a pretty niche market for hyperemesis gravidarum literature as it's not a hugely common condition, so quite frankly, we'll make more money, much of which will be ploughed back into the HG charities, by publishing independently!
Hyperemesis gravidarum is not a "popular" condition to donate money to and the two main international charities, Pregnancy Sickness Support and The Hyperemesis Education and Research Foundation both struggle to get the funds to continue their crucial work. Both the authors currently provide significant financial and practical support not just the UK charity but the Hyperemesis Improvement Movement happening around the world – We need to make that more sustainable. If we published through a traditional publishing house it would be years before we saw a penny for our work, if ever. This way a significant proportion of every book sale will come straight back to the authors (as long as you buy from us) and therefore further the work of the International Hyperemesis Improvement Movement by funding their work. Not only will a minimum of 10% of the profit from the book go direct to hyperemesis charities but the remainder will allow the authors to continue dedicating so much time and energy to raising awareness and supporting women.
How to be an HG Hero!
Helping children understand Hyperemesis Gravidarum
- By Caitlin Dean, illustrated by Paul Colledge
How to be an HG Hero – helping children understand Hyperemesis Gravidarum, does what it says on the tin… aimed at pre-school to junior school aged children the book enables them to understand what is happening in their world and how they can take a proactive approach as a member of the family “team”.
Following a little child and his mum through an HG pregnancy it offers explanations of what is happening, enables discussion of concerns and worries and makes positive suggestions for children (and relatives) to help the situation.
Author, Caitlin Dean, believes that if you give a child the opportunity to be part of the team, to help mummy when she is ill and an understanding of what is happening in the family, then the impact of HG in their lives can actually be a positive one.
The book contains two "HG Hero Certificates" to cut out and present to your HG Heroes.
In conjunction with Pregnancy Sickness Support and Plymouth University I am looking for women who have been treated for HG in the last 2 years in the UK to take part in a research survey. Please click here to find out more.
I am mother of three beautiful children and wife to a fantastic and supportive husband. I am a nurse, a farmer and a trustee for Pregnancy Sickness Support. I love working hard and spending time with my kids.
About this blog
Information and support for pregnancy sickness and hyperemesis gravidarum. Views are my own and do not represent those of any other organisation. Information provided here should not be a substitute for medical advice. My aim is to raise awareness and encourage sufferers to know they are not alone.
Explore past posts:2017May 2017 (1)February 2017 (1)January 2017 (5)2016November 2016 (1)October 2016 (1)September 2016 (4)August 2016 (1)July 2016 (1)June 2016 (3)April 2016 (2)February 2016 (2)January 2016 (1)2015December 2015 (2)November 2015 (1)October 2015 (1)September 2015 (1)August 2015 (1)July 2015 (3)June 2015 (5)May 2015 (3)April 2015 (3)March 2015 (3)February 2015 (5)January 2015 (3)2014December 2014 (1)November 2014 (4)October 2014 (4)September 2014 (3)August 2014 (4)July 2014 (3)June 2014 (2)May 2014 (5)April 2014 (5)March 2014 (5)February 2014 (4)January 2014 (5)2013December 2013 (6)November 2013 (6)October 2013 (10)September 2013 (5)July 2013 (1)June 2013 (1)April 2013 (1)March 2013 (2)February 2013 (1)2012December 2012 (1)June 2012 (1)February 2012 (1)2011December 2011 (1)November 2011 (1)October 2011 (1)September 2011 (1)July 2011 (2)June 2011 (1)May 2011 (6)April 2011 (1)