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Parkinson's / Huntingdon's Disease ? What Happens When A LA Cuts the Support Package ! - Carers UK Forum

Parkinson's / Huntingdon's Disease ? What Happens When A LA Cuts the Support Package !

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Milton Keynes Council : Man " Struggled to feed himself after care cut. "

A man with Huntington's disease was treated " Worse than an animal " after his care package was cut by a council, his family has said.



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Milton Keynes Council cut Roy Baker's care from 35 to 23.5 hours a week after an officer said the authority no longer funded "shopping and domestic support".

However, an investigation by the Local Government and Social Care Ombudsman found the council was "at fault".

The authority has apologised for its "mistake".

Huntington's Disease is a rare inherited disorder that damages certain nerve cells in the brain. Symptoms can include involuntary movements, personality changes and altered behaviour.

When Mr Baker's care and support needs were reviewed by the council in April 2017 it was noted he was "unable to get drinks and food on bad days" and needed help "managing and maintaining nutrition".

However, an assessment officer told Mr Baker his direct payments would be reduced because the council "no longer funded shopping, domestic and meal preparation".

The ombudsman said the cut meant Mr Baker's care package "was not sufficient" - he lost help for basic needs such as showering and eating - and both he and his ex-wife Sarah suffered "significant injustice" as a result.

Ms Baker said: "Our two boys were affected. They would worry what condition they'd find their father in."

During one week when his care was cut, Mr Baker allegedly only ate one meal while his carer was on holiday.

"I actually said to the council, the week the carer was off that they wouldn't treat an animal the way he has been taken care of by Milton Keynes Council," Ms Baker said.

The authority reassessed Mr Baker in January and increased his care package to 52.5 hours a week.

However, the ombudsman concluded the council's assessments were "inadequate" as it had not considered alternative ways to meet his needs.

The authority said: "We have apologised for this mistake and are sorry to have got it wrong."

It added it had reviewed 734 service users and changed the level of support in 127 cases, mostly to increase support.

Mr Baker's care is now funded by the NHS. ( CHC / NHS Continuing Healthcare ? )



Just how many more Roy Baker's are there out there ?

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This is exactly my problem the council are cutting everything and only giving basic care.

Cleaning you can pay for a cleaner, the council won't pay for cleaning anymore.
Shopping you can do that on the internet, who puts it all away, who prepares the meals, does the washing up? and the general housekeeping.

The council are just not thinking about all the needs just leaving people to manage except they can't.
Londonbound wrote:
Thu Oct 17, 2019 4:29 pm
This is exactly my problem the council are cutting everything and only giving basic care.

Cleaning you can pay for a cleaner, the council won't pay for cleaning anymore.
Shopping you can do that on the internet, who puts it all away, who prepares the meals, does the washing up? and the general housekeeping.

The council are just not thinking about all the needs just leaving people to manage except they can't.
I have had the same issue too. When my son was really small, we contacted NHS wheelchair services to ask about wheelchairs. They could not help us so we had to lokk at other more expensive sources of funding for aids and equipment. Even his water based physical therapy sessions were private due to lack of skill etc. My family also have been impacted by disability cuts to crucial services etc. Not so much as other families but we still feel the after effects.

Every time I take him to a restaurant (like I did last night) or a library, I automatically find myself methodically trying to measure doorways and ceilings. I also think that we are wasting money on silly things that don't really help us either. Parking fines, anyone? Whenever I have to read a boring and depressing article on funding cuts, I feel stressed and upset. I honestly think that the money that often gets wasted could be used to improve things in this country. Seriously.
I've known many people with PD, not HD. It's simply appalling what is happening. Do we have to glue a loved one to a train to get heard?