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‘I couldn’t believe it when I found out that there was a charity that deals with HG. I actually broke down, at last what I had seemed valid.’ - a hyperemesis gravidarum sufferer

Support is Vital

"The support I received over the past 6 weeks helped get me through what has been the toughest time of my life. Having someone who really who really understood the condition give advice helped us through and crucially, at times, gave me really useful information I didn't get from my own medical practitioners. In my experience, HG is such a debilitating and lonely struggle, the more support you get the better chance you have of surviving it" - Lisa, from London.

History

Dr Barnie-Adshead first became interested in pregnancy sickness and hyperemesis gravidarum in the 1960's as a GP and did some research trying to find the cause. When Dr Gadsby joined the practice in 1979, he became involved in developing the research. It was clear that the condition was generally under-researched and not fully appreciated & that the natural history of the condition was not well described. Funding was obtained to do a prospective community study, describing the features of pregnancy sickness in 363 women, each of whom delivered a healthy baby. This study was published in 1993 and it has become widely quoted. The work has been described in a number of newspaper articles and Dr Gadsby has spoken on the BBC radio 4 programme "You and Yours" on two occasions and he was "referee" for the BMJ, Breath of Learning article, Treatments for nausea and vomiting Oct 2004.

In 1998, Dr Gadsby was invited to talk about this research at the first International Conference on Nausea & Vomiting in Pregnancy held in Toronto. There he met people from "motherisk" based at the Hospital for Sick Children in Toronto, who run a telephone support line for women experiencing pregnancy sickness and hyperemesis. He thought it would be wonderful to be able to provide a similar service here in the UK. Since then Dr Barnie-Adshead and Dr Gadsby have been raising funds and as a result, Pregnancy Sickness Support was registered as a Charitable Trust in 2002.

Following the 2011 conference, PSS has seen the introduction of new trustees to the Pregnancy Sickness Support Trust and an increase in fund raising activity and volunteer recruitment. Projects are now under way to get a National Supporters Network up and running as well as the development of fresh and up to date printed information leaflets for sufferers. We are working on raising the National Profile of the condition and it's treatment with Health Care Professionals, the public and the media.