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Journey into the world of hyperemesis gravidarum...

Help Fund the Hyperemesis Improvement Movement

I already put my money where my mouth is and both donate and fundraise a lot of money for Pregnancy Sickness Support. I also give my time, as a trustee and spokesperson, I run the PSS office and it's day-to-day affairs as well as organise it's national conferences and liaise with the media and help further it's research goals... 

Now it's your turn to help where you can. 

If you are in the UK then please consider a one off or monthly donation to Pregnancy Sickness Support:

Click here to support Pregnancy Sickness Support

 

If you live outside the UK then please support the HER Foundation who are based in the USA but provide international support around the world.

Click here to support the HER Foundation

By funding these organisations we can work to make sure that our daughters and granddaughters won't suffer as we did. They may still get HG because as yet a cure is not in sight. But by increasing awareness and ensuring support is easily available we can reduce the isolation, misery and so much of the suffering. Together we can make sure that all women have access to the most up-to-date evidenced based treatments WITHOUT a fight! 

These organisations are massively underfunded and rely entirely on donations rather than funding from the lottery or other sources. It's vital that the women who suffered and their families give as generously as they can... if the women who have suffered don't donate then why will anyone else?

Fund Hyperemesis Research

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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.

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MAD Blog Awards UK 2015

 

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