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Hyperemesis Gravidarum Research

After experinencing hyperemesis gravidarum, a severe and debilitating pregnancy complication, three times I have dedicated my working life to improving care and treatment for others with the condition. I write extensively on the subject for the medical and lay press and my blog offers hope and inspiration to those going through it now. I am also the chair person for the UK charity Pregnancy Sickness Support (PSS) and established the nation wide support network. In this voluntary role I advise NHS trusts on service development and provide education to healthcare professionals as well as overseeing the day to day running of this life saving, yet tiny and underfunded charity. I do not claim expenses.

Having informaly conducted research surveys over the last few years which have made headlines around the world and raised a huge amount of awareness about the babies lost to hyperemesis gravidarum, I am now undertaking an MSc in Clinical Research and hope to start a PhD in September. This is formalising my research role and all of my research relates to Hyperemesis Gravidarum. 

Currently I self fund all of my hyperemesis awareness activity. I do not earn money through my blog, my charity work or even really though the books I have written. 

I need support from the families I am helping to carry on this work and fund my research. 

PSS is a tiny charity and receives no formal funding yet so I can't claim expenses when I travel around the UK to give teaching sessions or present at conferences. 

It would mean so much to me for the hyperemesis community I am supporting to support me too. I have ambitions to break down the stigma of HG and ensure every woman in the UK receives top notch, compassionate care by 2020. For this to happen a huge amount of research needs to be conducted and disseminated into mainstream healthcare in the next few years. I can do it but not alone. I need your help.

"Go Fund Me" wants me to write how thankfully I would be... the truth is words can not express how thankfully I would be. And it would just be me. An entire generation of sufferers, their daughters and granddaughters would thank you too. 

Please, make this research happen!

Organizer

Caitlin Dean
Organizer

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