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I think this is a great post - really helpful and informative.

This post highlights everything that is wrong with the support available for the partners/carers of people with mental health issues. The advice from the Mental Health Foundation is too generalised and patronising. In my experience, the GP has been unwilling to listen to the partner (me), the sufferer (him) does not want to do "normal" things like exercise, join a group or even participate in something online because of their sense of ill worth and failure. There is such a lack of assistance and advice available for the carer/partner and even if you dig deep (and believe me, I've spent the last 10 years digging) the only help available is a few ill-written leaflets and the advice of people who haven't actually been in your situation.

These comments are in no way a slur on the "Breaking The Silence" admin, after all, you are only posting the information available and the article was originally written for another publication.

Hi Nickie, yes I think there were similar comments when this was originally posted on the NHS website. I think the advice is well meaning and a general starting point for people who find themselves in this situation and the aim of the piece was to help carers recognise that they also need a break and not feel bad about that but as you say if you have a loved one and need specific, practical and effective help, it doesn't go anywhere near covering it. We don't take negative or constructive feedback about articles posted personally and consider that a blog is an excellent place to publish such experiences, we hope we can continue to inspire the trust in readers to be able to share their experiences away from the well-meaning - but very general - advice of senior professionals.
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Most NHS Mental Health Trusts have dedicated carer support workers (I know ours do) who in my experience are very good. However these may only be available if the person with mental health issues is involved in secondry services (i.e. has a CPN or a consultant psychatrist).

GPs may not even know about them - it's worth ringing the community mental health team and asking. You will probably need to be refereed though.

These workers can give advice about what support networks are available, as well as eduction about the mental illness and ways in which to deal with that person (not that carers don't already know that of course).

They can also act as advocates in dealing with the MH system.

This is what happens in the trust i work in anyhow, other trusts may vary.

Thanks Dan for your very valued input.

Hi again Linda. I always feel very negative when I talk about the support (or lack thereof) that we've had regarding my partner's MH and I know that there are some wonderful services out there. We've been living in limbo for so long because I can support so well (seemingly - most of the time that's not the case).

This blog is going to be a great source of information/experience for many people, including myself.

Your high quality articles are so great, and can we buy some ads from you? If you agree, just emial me the ad type and fee per month. If you own some other high quality related blogs, selling ads would be welcomed.

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