The effects of the Covid-19 pandemic have transformed daily life for everyone, with the impact on many bereaved people being even more severe due to their isolation in lockdown and a sudden loss of face-to-face support from family, friends or counsellors. In such a difficult time, Sue Ryder's Online Bereavement Support services have provided a vital lifeline.
Sue Ryder survey reveals almost half of people experience poor mental health following the death of a loved one
In response to the survey commissioned by Sue Ryder, we are launching our #JustSaySomething campaign in a bid to encourage everyone to open up about grief and bereavement, enabling a more honest, supportive grieving process for those affected and people supporting them.
This week sees the UK’s first ever National Grief Awareness Week, encouraging us all to #OpenUpToGrief and break the taboo around death and bereavement, for a more open discussion of a subject which affects us all at some time in our lives.
Today, on Carers Rights Day, our Human Rights Lead Jacqui Graves highlights the rights of carers looking after people with life-limiting conditions and how they can ensure their rights are respected and protected.
After Richard Littledale lost his beloved wife Fiona back in 2017, he decided to chronicle his experience of bereavement in the hope of comforting others. They have been turned into a book Postcards from the Land of Grief, published today, and 100% of the royalties will go directly towards Sue Ryder's expert and compassionate care.
Whilst Brits know how they would spend their last days on earth, few are preparing for them, our new survey has revealed. As a result of this, we are calling on the nation to start talking about death.
Yesterday’s Daily Telegraph reported that, according to NHS nurses, too many patients are being subjected to Do Not Attempt Resuscitation (DNAR) orders without families being told. Our Human Rights Lead Jacqui Graves provides the important clinical context behind the headlines.
"People who have lost a limb sometimes experience the presence of the limb long after it has gone – as if the nervous system refuses to accept this new, altered reality. Just recently, I experienced a similar thing with my grief on two occasions." Blogger Richard Littledale opens up about times when he has turned to his late wife Fiona, only to find her no longer there.
People with neurological conditions in England are being let down by the very health and care systems that are supposed to be supporting them – that’s the finding of our new report Time to get it right, writes our Policy and Public Affairs Manager (England) Duncan Lugton.
After seeing the difference that his wife makes every day as a palliative care nurse, Mike decided to cycle 400 kilometres from Vietnam to Cambodia to raise money for our Sue Ryder Leckhampton Court Hospice. Here he talks about his trip of a lifetime.