New to HD
 
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New to HD

If you, a family member or a friend are learning about or dealing with HD for the first time, this is a place for you to learn and share your story, what you are going through or raise any concerns you may have. Perhaps you are at risk of HD and are thinking about getting tested. Maybe you are considering whether to tell others about your gene status. Maybe you are considering the future and how HD may impact on it and your decisions.

Or maybe you have just found out a family member or friend is diagnosed or at risk of HD. Remember you can also contact the HV Information service to discuss and receive support about your individual situation.

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HCC is not a crisis service so if you require immediate support and/or feel in danger or unsafe, we recommend that you please contact 000 or one of the following crisis support services.