Quite a
few years ago I did a stint as a charity fundraiser (yes I was a Chugger for a
short while) and during that time I was raising funds for a dementia charity.
It was during that period I had one of the most memorable yet heart wrenching
conversations that has stayed with me until this day.
On the
streets of Sittingbourne in Kent I met a man who told me about his father who
had dementia. His father lived with him and his family but had been
deteriorating rapidly and the man was faced with the decision of whether or not
to ‘put’ his father into care.
It was
obvious that on health grounds the decision was logical but it was clear that
the man felt a sense of failure about not being able to look after his father
and the option of sending him to a home was an option of last resort that was
accompanied by a huge sense of guilt and the pressure of having that decision was
tearing the man apart.
On a more
personal level my own Grandfather developed dementia, my uncle cared for him
but had to work to and it was when he returned from work one day to find my
Grandad had tried to microwave some food in metallic dishes that managed to
blow the microwave, but luckily not cause a wider fire, that the family
seriously had to consider whether a care home might be the most appropriate
option.
Dementia
is a disease that affects the individual but one that also has a serious impact
on the families of sufferers and with the predicted rise in numbers of people
with dementia even more families will feel the impact of having to make such
decisions along with the feelings of guilt and failure.
The news
of increased funding into the research dementia is welcome there it cannot
simply be research on treatments and cures. Whilst the application of medical
research is the best approach in the long term cures and treatments can often
take decades to come to fruition. In the meantime we need to tackle the social
impact of the disease, provide more help and guidance to families and raise public
awareness of all the issues on which dementia impacts.
It would
be good to see greater research on how we can improve social care to meet the
needs of those with dementia. There is, currently, a lot of good work going on
in this area and we need to make certain that this reaches a wider number of
care providers and becomes a standard for dementia care.
Today’s announcement
is a starting point, one that will hopefully be extended in the social care
White Paper due shortly. The amount
promised for research stills pales compared with research spending on other
issues yet it is a start in recognising such an important issue. But we also
need funding to support the care of people with dementia and funding for
support services for the families who have to come to terms with the impact of
dementia on their lives.
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