We aim to support people affected by genetic haemochromatosis, educate, raise awareness and encourage research. The Haemochromatosis UK is patient organisation and charity. We aim to support people affected, educate and raise awareness, and encourage research.
* Disclaimer *
We facilitate discussion in this forum in good faith but without any warranty of any kind, express or implied, as to the
accuracy or validity of the information provided by any contributor, whether an officer of the charity or not. HUK shall not be liable for any loss, damage, or other consequences arising from the use of the forum or attributed to any inaccuracies or omissions therein. Specifically, information provided about haemochromatosis and associated physiology or treatment does not constitute individual medical advice and must not be regarded as such. Users must consult their own doctor or consultant. Do not rely on information on the site to manage your or your family's health. The charity accepts no liability and will not entertain any form of claim in this regard.
