Non-profit multiple sclerosis organisation MS Society SA & NT in voluntary administration

Non-profit organisation Multiple Sclerosis SA & NT has gone into voluntary administration.

In an email to donors, supporters and partners, the organisation — which supports almost 3,000 clients living with multiple sclerosis — said that the "difficult decision" included its disability employment arm, Multiple Solutions.


"This difficult decision follows a period of significant challenges, including changes to the NDIS, the outcome of the recent Inclusive Employment Australia tender, and a decline in lottery sales which have long helped fund our services," the email said.

"We are currently working with administrators from Heard Phillips Lieberenz who are continuing to trade the organisation while they explore every possible option to retain vital support services for people in South Australia and the Northern Territory living with multiple sclerosis."


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MS Society SA & NT has sent an email to its donors and supporters saying it has gone into voluntary administration. (ABC News: Daniel Taylor)


The email also thanked supporters and said further updates would be provided in the future.

According to the MS Society SA & NT annual report for 2023-2024 the organisation had 2,985 clients, which was 150 more clients than the previous financial year.

The move comes as disability support service and employer Bedford announced in July that it was planning to go into voluntary administration, before the South Australian government stepped in with a $15 million lifeline.

Last week, Federal Minister for Health, Ageing and Disability Mark Butler said he was "not blasé about the depths of the financial challenge" facing Bedford, while Premier Peter Malinauskas said "the financial position of Bedford was even more dire than what we expected".


Multiple sclerosis is a degenerative disease that progressively damages nerves, making it increasingly difficult for the brain and the body to communicate.

There is no known single cause of MS and there is no cure.


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MS Society SA & NT has about 3,000 clients living with multiple sclerosis. (ABC News: Daniel Taylor)


'Tough year financially'​

The MS Society SA & NT 2023-24 annual report noted the organisation had a "tough year financially" during that period, due to factors including the loss of its home lottery program.

"The cost-of-living crisis has impacted our other fundraising programs and lowered the financial performance of Multiple Solutions' program," the report said.

In the report, then chief executive Janine Jackson — who left the organisation at the end of last year — said Multiple Solutions had "faced market pressure, including tighter conditions, increased competition, changes in government funding and rising costs".


"Despite these challenges, we are committed to securing new opportunities to adapt to the current market," she said in the report.

A spokesperson from the federal Department of Social Services said the tender process for the new Inclusive Employment Australia (IEA) model contracts was conducted at "arms length from government" and acknowledged that "changeovers can be difficult".


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Multiple sclerosis is a degenerative disease which has no cure. (ABC News: Daniel Taylor)


"The tender documents were consulted on extensively with the sector, and the tender was overseen by independent procurement and probity experts," the spokesperson said.

In a separate statement, a federal health spokesperson said MS Society SA & NT was "well known to many in the SA community, especially through their lottery sales".

"This is the first the government has heard of them going into voluntary administration," the spokesperson said.


"The Department of Health, Disability and Ageing will engage with MS SA and NT for further information."

The ABC has made attempts to contact the organisation, while SA Minister for Human Services Nat Cook was not available for comment.
 

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That's sad news. Pity the SA Minister Nat Cook wasn't available for comment.
 
My beautiful daughter has MS, and it’s really hard to see her struggling. 2 daughters, aged 9 and 10 to manage. Thank goodness her husband is a saint. The NDIS is a pathetic joke. She gets nothing, except a disability parking permit, and no assistance whatsoever with house cleaning. Sometimes she gets 6 Physio visits a year. Big deal! My husband donates a lot of money to MS QLD. There’s a lot of scammers out there, who abuse the system, and the really needy get a pittance. It’s a joke. Because she is only 35 years old, she gets abused by selfish old cows, for taking up disabled parking spaces. It’s abusive insulting and disrespectful to say the least. Grocery shopping consists of a trolley supporting her, so she has a bit of mobility. There’s no cure, but medication attacks the immune system, but at least it minimises spinal lesions. Some people are totally ignorant and don’t realise how blessed they are. Gezzabel.
 
So. even after a $15mil bail out they still went under.
There is more not being reported I suspect.
As one already commented here that The NDIS is a joke that needed a big shake up ages ago.
If fact, 6 years ago I was doing a TAFE Cert IV course in Community Services and even they said avoid anything to do with NDIS, even back then they can see the writing on the wall.
I never entered the industry for a few reasons. The main one being Mandatory Reporting and policies and procedures really didn't cover the worker, only the Company.
Another reason was the amount of paperwork.
 
Funny how the over paid pollies, are never available for comment, when the going gets tough! It all goes into the “too hard basket”. I’m sure she was shampooing her hair that day! Gezzabel.
 
The Minister is not available??? What could possibly be more important? The Premier should be making her face the media. Its her portfolio and one should expect her to front up with some explanations and plans to assist the people the MS Society are meant to help. Disgraceful Government!
 
My beautiful daughter has MS, and it’s really hard to see her struggling. 2 daughters, aged 9 and 10 to manage. Thank goodness her husband is a saint. The NDIS is a pathetic joke. She gets nothing, except a disability parking permit, and no assistance whatsoever with house cleaning. Sometimes she gets 6 Physio visits a year. Big deal! My husband donates a lot of money to MS QLD. There’s a lot of scammers out there, who abuse the system, and the really needy get a pittance. It’s a joke. Because she is only 35 years old, she gets abused by selfish old cows, for taking up disabled parking spaces. It’s abusive insulting and disrespectful to say the least. Grocery shopping consists of a trolley supporting her, so she has a bit of mobility. There’s no cure, but medication attacks the immune system, but at least it minimises spinal lesions. Some people are totally ignorant and don’t realise how blessed they are. Gezzabel.
 
Why is it that the not for profits get looked over by the government who backs and helps so many for profit organisations. Priorities need to be realigned and NDIS taken back in control of the government not by for profit organisations.
 
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I Friend who worked with me in Age Care, (Community) has MS. We also had a Client with MS. It was hard for my Friend to get help. Went to the NDIS, and yes given the run around. It was when NDIS first started. She ended up going to them, and said I will not move from here until I receive some help. Our Company, had advised her that her best bet would be NDIS, as they at the time hadn`t applied to be an NDIS Provider. After a lot of hassling, she eventually got help, as at the time she really only required a ramp at the back door, the Shower made more accessible. She now has Home Help, housework, help with showering, and help making the evening meal. Also goes monthly to the local Hospital for a transfusion, to help slow down the MS. I live interstate now, but visit when down in the area I lived and worked. But she had to fight for everything she needed. It helped that she worked in Age Care and knew a lot of the procedures that one has to jump through.
 
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Medical associations (including research) such as this do NOT get Govt. funding even if they apply.
They have to rely on donations and pay Govt. taxes etc out of them.
By law they also have to have their accounting system etc audited which they have to pay for even if a certified accountant gives them a discount
 
The Minister is not available??? What could possibly be more important? The Premier should be making her face the media. Its her portfolio and one should expect her to front up with some explanations and plans to assist the people the MS Society are meant to help. Disgraceful Government!
She probably went to lunch.
 
Medical associations (including research) such as this do NOT get Govt. funding even if they apply.
They have to rely on donations and pay Govt. taxes etc out of them.
By law they also have to have their accounting system etc audited which they have to pay for even if a certified accountant gives them a discount
My daughter is a Doctor of Medical Sciences who does a lot of research work .....she is fully funded by the university she works for, but has to also put in the hours as a Senior Anatomy Lecturer.
 
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My beautiful daughter has MS, and it’s really hard to see her struggling. 2 daughters, aged 9 and 10 to manage. Thank goodness her husband is a saint. The NDIS is a pathetic joke. She gets nothing, except a disability parking permit, and no assistance whatsoever with house cleaning. Sometimes she gets 6 Physio visits a year. Big deal! My husband donates a lot of money to MS QLD. There’s a lot of scammers out there, who abuse the system, and the really needy get a pittance. It’s a joke. Because she is only 35 years old, she gets abused by selfish old cows, for taking up disabled parking spaces. It’s abusive insulting and disrespectful to say the least. Grocery shopping consists of a trolley supporting her, so she has a bit of mobility. There’s no cure, but medication attacks the immune system, but at least it minimises spinal lesions. Some people are totally ignorant and don’t realise how blessed they are. Gezzabel.
So sorry to hear that your girl has this terrible affliction, Jezzebel.
 
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