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having a folder with all the relevant information is a must |
How many agree......
When originally
looking for supports, regarding the right direction for accessing assistance or
sourcing specialised services, and so on, the information you found was so
overwhelming, swamping you with conflicting so-called well-meaning suggestions
and ideas on what to do and where to start, that you were more confused than
before you began looking?
I definitely agree -
'YES' I did fit that category.
When I stepped onto
the ASD pathway looking for help, research, understanding and intervention,
especially when A.J. began to crash-and-burn needing that all important
assistance I still had no idea where to look or even if such services existed
in our local area.
Being the 'Nan' to
my adorable grandchild, addressing autism was very difficult to face and was
hindered by so many additional variables and hurdles we had to overcome or
justify before anyone would listen to my concerns that something else was
wrong.
As a parent
"you" know your child better than anyone else, you view the everyday
actions and behaviours that professionals miss or have limited time to
completely view and assess, making educated textbook guesses instead of
correlating long-term factual evidence.
Now as I fast
forward to today taking the first steps with A.J. through the NDIS pathway,
setting up his personal plan,
I realise and
acknowledge how important any additional support can be.
I also realise the
struggles some families may have sourcing the correct type of help.
Due to this I am
helping others by sharing the information I have gained, helping to connect
with service providers, giving a general over-view and personal perspective on
what you may go through, regarding the correct order, realistic expectations,
and the official process, etc.
Helping to make it
just a little easier to understand.
To begin, take a
breath and sit down, while I take you through each step in layman's term...
The first thing you
need to know, is, this process isn't going to happen over night.
There are specific
steps and stages we have to go through, and sometimes if there are a lot of
applications pending it may delay your process a little.
Knowing this, the
sooner you can gain the go-ahead to register, the sooner the process begins and
you can gain supports.
The first steps.....
What is the NDIA? -
National Disability Insurance Agency
This is the
organisation, a group of people assigned to process and approve all applicants
registering for inclusion.
What is the NDIS? -
National Disability Insurance Scheme is the actual program set up to initiate
funding to provide the specific personalised services necessary to support each
individual applicant.
Pre-Application Preparation - before
we get to the application stage, it will make the process much easier if you
have already organised and arranged all relevant documentation and evidence to
prove the necessity for specific services.
Arrange any letters
from different medical professionals, paediatrician, psychologist, OT,
physiotherapist, speech therapist, etc,
etc.
Also the number one
priority is to document your own personal experience and journey, how the
family etc relates to any process, and what you personally feel will benefit
the participant. Another great idea, with the use of modern technology, to
assisting when attending services, is recording any unusual behaviour or
concerning mannerisms, as evidence of their disability.
I myself have always
documented A.J.'s daily process for many different reasons, making it easier to
continue when we began on the ASD processing path.
Applying for Registration
- contacting the NDIA - a phone contact is the quickest easiest process to gain
first contact and make it known you wish to apply to the NDIS program.
To call the NDIA -
phone - 1800 800 110
You will reach a
person who will ask you a few simple questions regarding the disability, etc,
as a confirmation, with personal contact details etc, then they will forward a
few lengthy forms, one part you will fill out, the other part filled out by an
appropriate medical professional.
In my case...
A.J.'s paediatrician
filled out the forms and provided an additional in-depth review of his needs
and requirements.
We also gained
documentation from A.J.'s psychologist regarding his anxiety, sensory
sensitivities, early history trauma, etc.
This altogether gave
a very clear picture of all the concerning areas and issues he was trying to
deal with.
Once all that is
gathered together we mailed it back in the appropriate envelope and waited for
the next step.
****note****
always remember to keep copies of ALL documentation.
To give an
indication of a possible time frame you may be looking at....
Our phone call was
made at the end of August, papers received mid/end September (after awe had the
appointment with the paediatrician to fill out his forms), we had everything
ready to return-post early October.
A letter of
confirmation our application arrived was sent at the end October.
Another letter early
December to confirm we were granted access to the NDIS and we would receive a
letter confirmation for the next step.
A phone-call was
made in January confirming another letter will be sent providing all the
details regarding A.J.'s NDIS plan and appointments.
A pre-plan
appointment was held with a Community connector mid January, where they will
help you understand the Plan Ready requirements.
Then the official
Plan Ready meeting was booked for the end of February.
Plan Ready meeting - everything is set out regarding appropriate
supports and services.
A.J.'s plan was
arranged for approved Physio, speech therapy, psychology, and O.T.
appointments.
Although they work
on long term goals, they will break it down into 12 month intervals with annual
assessments to assure everything is going on track. Remembering if there are
any hurdles or concerns regarding additional assistance or adjustments early assessments
can be arranged to re-organise the plan package.
Arranging the payment process - there
are three options for payments of services
1/ NDIA makes
payments directly to service providers
-with
this option the service MUST be registered with the NDIA
2/Registered Plan
Management Provider, this is an individual or organisation that manages the
funding on your behalf
3/ Self-Managing
where you control the payments and personally choose the services you access.
-this
option gives you a broader access to services that aren't registered with the
NDIA
A participant can
decide to use any single option or a variation of the above options, although
with self-managing they must maintain all paperwork and online registration of
services.
Each type will be
explained and you can decide which option you will be more comfortable working
with.
With all options you
will gain access to the online participation portal to monitor all activities.
By this point you
are fully registered and ready to begin booking services, set up Service
Agreements with each provider, and on your way to physically accessing
assistance.
Lithgow Nanna's
Touch ASD Support can also help to guide you through any process stage with
personal support and assistance, while helping you to maintain family
stability.
Anyone wishing to
register for self-management, although concerned about how you may cope, we
will be holding Self-Management workshops to help you through each step and
assist to maintain paperwork, on-line management and additional assistance, as
required.
Booking information
will be posted shortly when venue and date availability is known
- interim dates -
for April/May 2016.
For further details
contact Sue on 0409765601
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