One of the most important things we do is facilitate meetings of people who are affected by genetic haemochromatosis (GH). Meeting and talking to other patients is often the best way to learn about haemochromatosis and how to deal with it.
In some areas independent volunteer groups in several cities also arrange regular meetings for GH patients and their families. Often these will include refreshments and speakers, the opportunity to ask questions of medical experts, and a chance to share experiences with other patients and families.
GH North-West Support Group
The GH North West Support Group (GHNWSG) is affiliated to The Haemochromatosis Society. As well as arranging patient meetings the group works hard to raise awareness in the North-West of England. The group is run by hard working volunteers who are all affected or have family members who are affected. You can learn more about the group, check their next meeting dates and make contact by visiting their website at northwest.haemochromatosis.org.uk/.
Blackpool, Fylde and Wyre GH Support Group
The Blackpool, Fylde and Wyre GH Support Group is also affiliated to the society. For further details of this group and their events you can contact Marguerite Smith on 07768 042802, by email at email@example.com, or at their website which you can find at blackpool.haemochromatosis.org.uk. The group meets quarterly in Blackpool.
Wales GH Social and Support Group
This group have emerged following a successful patient meeting in Cardiff in early 2017. If you would like to learn more or get involved in helping please make contact through the group’s Facebook Group at https://www.facebook.com/groups/373045636411063 or email our trustee Lisa Flude at firstname.lastname@example.org.
Keeping you informed
You can ensure you have advance notice of patient meetings by becoming a member of the society. As a member you will receive our regular magazine and email bulletins. At meetings we always welcome non-members; you will find the meeting especially helpful if you have been newly or recently diagnosed.
Patient Information Days
The Haemochromatosis Society as a national organisation organises conferences and patient information days throughout the year.
Please visit our events page for news of our main events planned over the next few months.