Skip navigation
Journey into the world of hyperemesis gravidarum...
27Apr 13

Two years on...

On 30th April it will be 2 years since I started this blog and first got in touch with Pregnancy Sickness Support (crazy; that's flown by!). In that time the charity and profile of hyperemesis gravidarum has obviously grown exponentially and I now work harder than ever, immersed deeply in the world of HG! My original purpose of the blog was to document my journey with HG for the third time and in particular the pre-emptive treatment I had. This has proved to be of particular interest to so many women and I now spend vast amounts of time talking to women about how they can prepare for the challenges of such a horrendous pregnancy. To that end I have recently produced some documents for the PSS Website including a care plan based on the one that I devised for my own pregnancy with my wonderful GP Dr Harriet Tullberg. She and I are now collaborating to develop further GP education in the region as well as guidelines for Acute Care at Home teams to be able to treat HG sufferers with IV fluids in their own home... Standard practice in America!

I've also recently had an article published in a nursing journal, Nursing in Practice... Wow, I'm literally beaming from ear to ear about that!

The Charity is also involved in developing Greentop guidelines for the NHS, which is really exciting and our online research surveys are going to be closed soon so that we can start trawling and analysing the results to then present at our own conference in September as well as various others throughout the Autumn. The increasingly frequent emails from consultants looking to develop guidelines for their hospitals is thoroughly encouraging too.

One of the key factors that made my third pregnancy so much more bearable and less traumatic was the amazing support I received from woman across the UK via the supporters network we developed 18 months ago. We now have 86 women involved in the network and are hosting another national conference in Birmingham in July for our supporters. I really love meeting the other women who are all working so hard for the cause. Lots of women (now friends) who have holidayed in Cornwall have stopped in to see me and it really is great to meet them, their husbands/partners and their kids. HG seems to create a bond between women which makes us almost automatically friends!

All in all it's a very exciting time for the charity and I can't help but sit back now and then and feel a deep sense of pride with what has been achieved in the last two years by the hard work of a few dedicated people.

I am currently sat in the beautiful home of one of my PSS colleagues, and friend, waiting for the quarterly trustee meeting to start when the others arrive and thinking about how lucky I am to be involved in such a fantastic organisation with such fantastic people.

Thank you everyone who has made the last two years of my life two of the most incredible ones!

Share with...


The Book

Hyperemesis Gravidarum - The Definitive Guide by Caitlin Dean

The Kids Book

Hoe to be an HG Hero by Caitlin Dean

About Me

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.

Previous award nominations

MAD Blog Awards UK 2015