Originally posted by Ellie
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Quote away Music man's wife πππβDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user.
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Music man's wife I think that sounds the right course of action Court of Protection & Human Rights Act. CCG need to know this is being taken taken further....they may then play ball to prevent further action?Initial diagnosis 7-4-2021 'suspected MND' confirmed by 2nd opinion 4th June 2021 ALS. Began with R foot limp and lots of falls. NIV overnight. Generally weak. Mostly terrified.ββββββ
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Originally posted by LindaB View PostCCG need to know this is being taken taken further....they may then play ball to prevent further action?
βDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user.
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https://twitter.com/cascaidr/status/...GdaCaS77w&s=19
belinda schwehr is as sharp as they come & her legal expertise regarding CCG and the legal framework is 2nd to none.Last edited by LindaB; 4 February 2022, 17:57.Initial diagnosis 7-4-2021 'suspected MND' confirmed by 2nd opinion 4th June 2021 ALS. Began with R foot limp and lots of falls. NIV overnight. Generally weak. Mostly terrified.ββββββ
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Music man's wife
I am so sorry you both are going through this.
CCG seem different in each region and I know there was a court case and a person was legally left in soiled adult nappies over night (not MND related).
But others are getting over night care at home.
I hope you get joy from the lawyer.
Can you connect to your local MP about the situation?
I have had great support from my mum's MP regarding dementia care. I would definately alert them to the situation.
I have just emailed my MP about a minor petition but from his automatic reply, it is obvious that he advocates for his consituents (asking for DWP references etc)
From my reading it is a total post code lottery, please keep fighting.
I would also connect the MND association because I believe they have helped others
Best wishes to you bothDonna
Carer for husband Thomas, diagnosed with MND of Fail Arm Type in July 2020.
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So a bit of an update. CHC agreed to fund care for 12 hours a day. I'm the 24 hour carer with 12 hours per day of support. Chris came home nearly two weeks ago. Have to say it's been a tremendous struggle.
The good news is he goes back in the hospice one week in four.
Chris is happy to be home though it's frustrating for him as he can't do all the things he enjoys. He misses the security of the hospice where sometimes 4 staff got him up. He knows I struggle as do his other carers. It can easily take over 2 hours to get him up.
We had to sign a risk assessment basically saying if this didn't work it's the General hospital or the care home in Newcastle, possibly included other things but we were so sick of the whole carry on, we signed and left.
Anyhow that's us, take care everyone.
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Originally posted by Music man's wife View PostSo a bit of an update. CHC agreed to fund care for 12 hours a day. I'm the 24 hour carer with 12 hours per day of support. Chris came home nearly two weeks ago.Diagnosed 18th May 2021 with sporadic ALS. Limb onset. Terrified of not being able to breathe easily.
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Originally posted by Music man's wife View PostCHC agreed to fund care for 12 hours a day. I'm the 24 hour carer with 12 hours per day of support.
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We had to sign a risk assessment basically saying if this didn't work it's the General hospital or the care home in Newcastle
There is zero logic in that - seems that someone (vindictive) has made up their mind and will not back down, no matter who suffers π I don't blame you for throwing in the towel, it's too hurtful...
It's good for you both that Chris gets to go back to the hospice 1 week in 4. ππβDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user.
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Music man's wife how about asking the hospice to record exactly what support they give to Chris in a 24hr period. This to be replicated at home.Initial diagnosis 7-4-2021 'suspected MND' confirmed by 2nd opinion 4th June 2021 ALS. Began with R foot limp and lots of falls. NIV overnight. Generally weak. Mostly terrified.ββββββ
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Originally posted by Ellie View Post
That's such a contradiction in terms Music man's wife it must stick in your throat - we'll give you 12hrs of help per day to care for Chris and if you cannot cope, we'll send him off to a place where he'll get 24hr care because that's what he needs. It's like they're almost setting you up to 'fail'.
There is zero logic in that - seems that someone (vindictive) has made up their mind and will not back down, no matter who suffers π I don't blame you for throwing in the towel, it's too hurtful...
It's good for you both that Chris gets to go back to the hospice 1 week in 4. ππ
However things have settled down, we have got into a routine and things are working well.
I just hope some people can sleep at night.
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Originally posted by LindaB View PostMusic man's wife how about asking the hospice to record exactly what support they give to Chris in a 24hr period. This to be replicated at home.
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Originally posted by Music man's wife View PostI just hope some people can sleep at night.βDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user.
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