If there’s one thing that can damage Labour's brand, it’s misspending public money on vanity projects and unnecessary PR campaigns instead of funding things that really matter to everyday Kiwis. The opposition knows this, and often attempts to exploit a perception that Labour isn’t able to properly allocate taxpayer dollars in a way that truly benefits the entire country.
However, unlike the opposition, the vast majority of voters are thankfully a lot more reasonable, particularly in terms of the Government’s funding allocations. This is especially the case when you consider the considerable amounts of money being generated for the Government through our hard work and an export sector that is incredibly profitable.
Obviously we should all share in our mutually generated wealth, and one of the best ways to do that is by ensuring our infrastructure is functioning properly and everyone’s basic needs are being adequately met. However, the current Government unfortunately appears to have lost the high ground and has already become arrogant about where they allocate vast sums of public money. Not yet into their third-termitis, the Labour led Government's disconnect between what should and what is being funded appears to be getting worse, and therefore needs to be highlighted.
While MBIE is busy spending hundreds of thousands of taxpayers dollars on flashy new PR videos about climate change, that try to place responsibility for man-kinds biggest existential threat onto us mere individuals, inflation has all but wiped out any wage increases for low to middle income earners, ensuring that most will be without the financial means necessary to adapt to the serious consequences of climate change.
While the Minister of Energy and Resources, Megan Woods, is busy making excuses for another badly produced video that cost taxpayers $600,000, students are having to take the Government to court to try and halt new oil and gas exploration…polluting enterprises that will ensure New Zealand has already failed to meet our COP26 obligations before the ink has even dried.
While Minister Carmel Sepuloni is busy promoting a new so-called Ministry for the Disabled, which will be run by the same old dysfunctional Ministry of Social Development, she's also splashing $500,000 worth of public money on a badly designed book website, which has little to no value for most hard working Kiwis. Meanwhile, the re-allocated support for people who’re struggling to survive is almost non-existent.
Obviously the Government’s current incrementalist approach to beneficial social change isn’t going to fix the entrenched inequality that creates adverse effects throughout Aotearoa, whereby one in five Kiwi kids continues to go without adequate food or proper housing.
In fact the Labour led Government has decided, somewhat under the cover of Covid-19, to even start hassling disabled WINZ clients again, in order to make cuts to their welfare payments. Surely not I hear you say? But here’s a small sample of tweets from a recent online discussion by and for the New Zealand disability community, which clearly shows the Government isn’t being very kind at all, not even to our most isolated and vulnerable citizens:
Someone close to me had Spina Bifida (she passed away in 2019) & every year MSD/WINZ demanded a medical certificate from her to prove her condition had not miraculously "gone away"!?
— Frank,Socialist Hermit Kingdom,sez get vaccinated (@fmacskasy) November 4, 2021
I cannot over state the vileness of this cruel practice.
Have been doing this for my autistic son for 17 years.
— Jo politically homeless (@JoGillett4) November 4, 2021
Dr signed for 5 years and I had to asked her to change it to 2 as anything over that gets either declined/questioned etc. Plain &simple stupid.
My mum's cerebral palsy finally didn't need a Drs cert by the time she was 53!
My friend had to keep giving evidence that her son's arm hadn't grown back.
— Mrs W - vaxxed for Aotearoa (@teresanz68) November 4, 2021
My son has albinism. We go through this regularly as well. Like you don't grow out of Down Syndrome, albinism....or a host of other disabilities. I think they should have a list of disabilities that don't go away, but that would be too easy. My GP gets really mad
— Charlotte French ๐ณ๐ฟ She/Her ๐ณ️๐ ๐ณ️⚧️ (@lottiefrench45) November 4, 2021
Oh for... @CarmelSepuloni this needs to be fixed!! One, dangerous to take a baby into a clinic RN, and two, most of the issues in this thread are permanent. Why WINZ needs to make people jump hoops is beyond me. Cruel, like waterboarding.
— scan, then stitch all the things BMLSc ✝️ (@paulainauckland) November 5, 2021
My grandmother who broke her spine in several places in a car accident in the 70s or 80s also had to suffer through this ordeal, wheeling herself in her MNUAL WHEELCHAIR the 10km to the local WINZ office to prove she hadn't suddenly decided to start walking again...made me irate!
— ๐๐ธ๐ผ๐ฑ ๐๐พ๐ฌ๐ช๐ผ ✌๐ป (@giosuelucas) November 5, 2021
I see nothing has changed since my daughter received CDA 20 years ago…nope her congenital scoliosis has not fixed itself, yes we are holding out for a miracle but they seem to be in short supply… like PICU beds…
— Jussi ๐๐ (@justjussi) November 4, 2021
Omg I gotta do my two yearly to, for my ASD boy and yup still there . 2 years later my boy is still himself but nope gotta do this stupid form again just in case he got cured from being himself lol
— T (@AnyaNaraya6) November 4, 2021
No different for me being autistic and having to explain that "no, my brain wiring hasn't changed"
— Katz (@CaelKatzi) November 4, 2021
My mother, who has been blind for 50 years, is going through this now with her disability allowance. I can totally empathize with your patients.
— Hayley ☀️ (@LadyHayley_) November 4, 2021
It’s the same for T1 Diabetes. Maybe they know something we don’t about a cure. pic.twitter.com/XWD095qq8A
— Haupแดua Muษนu (@hpm_1) November 4, 2021
Yes it is so depressing, parents HATE doing it. Can my brain damaged child feed herself these days ? No. Can she walk? No can she talk? No. It is cruel.
— Anne Keith (@as_wk) November 4, 2021
This stuff is just heartbreaking.
— DebNZ Vaxxed x2 (@DebNZ4) November 4, 2021
My son fronts up every two years. No, his back isn't better, yes it has deteriorated further since he last was checked.
Inhumane, degrading BS.
Frankly, I thought a Labour government would put a stop to this dehumanising practice. Guess not๐ข
So dumb. My cousins son has Williams Sydrome that they had to affirm constantly for ORS I think. No he hasn’t grown his chromosome back again this year ๐.
— JDF Hockey (@JulesFDF) November 4, 2021
My friend was tetraplegic, could not even move his head. When he told them he couldn't do the jobs they suggested, they then said - well what about this other job, how do you feel about climbing ladders?
— AliS (@AliS63206825) November 4, 2021
!!!!!!!!!!!
We were promised that this stupidity would stop several years ago but no.. Try this 1. My son had his benefit stopped because he didn't respond to a letter WINZ didn't send asking to prove his genetic syndrome hadnt suddely gone away.
— Broken (@Head_Weasel) November 4, 2021
Same for friend with multiple sclerosis. Ridiculous and time consuming and an unnecessary cost to provide medical certificates
— Satsuma (@Satsuma04523379) November 4, 2021