Info
Spinal Muscular Atrophy (SMA) is a rare genetic muscle wasting disease that is the childhood version of motor neurone disease. If you are newly diagnosed, or have just come across...
show more
Spinal Muscular Atrophy (SMA) is a rare genetic muscle wasting disease that is the childhood version of motor neurone disease.
If you are newly diagnosed, or have just come across our page for the first time, we urge you to get involved, within the SMA community here in Australia. We would love to hear from you and are happy to support you on your journey.
We acknowledge that each person is different, and we endeavour to assist you and your requirements.
show less
If you are newly diagnosed, or have just come across our page for the first time, we urge you to get involved, within the SMA community here in Australia. We would love to hear from you and are happy to support you on your journey.
We acknowledge that each person is different, and we endeavour to assist you and your requirements.
SMA Australia
SMA Australia
The Benefits of Intensive Therapy (Webinar)
23 MAY 2022
What About Me? Accessing Treatments for Adults
10 OCT 2021 · We know the non-recommendation of both Nusinursen (Spinraza) and Evrysdi (Risdiplam) for the adult community has left many feeling deflated. We want to acknowledge this and also reassure you; we haven’t stopped in our quest to work with the relevant stakeholders to ensure that future submissions to the PBAC are the best representation of our adult community – but we can’t do this without YOU!
So we are hosting this follow-up webinar with Dr. Lauren Saunders, from St Vincent’s Hospital in Melbourne, and Jo Watson, the Deputy Chair and Consumer Rep for the PBAC.
We want to respond to your questions that you have regarding not being able to access treatment. Dr. Lauren will be answering any clinical questions, and Jo Watson, any questions you may have for the PBAC.
SMA Webinar Series Number 9: What about me? Accessing treatments for adults
We are asking YOU to submit questions to SMA ahead of the meeting so that we can address them on the Zoom call with everyone.
We also want to plan for the next steps and how you can be involved.This is really important moving forward – as the united voice of the community, with regards to access to treatment is vital right now.
We invite and encourage you to attend. These meetings have been organised to keep you in the loop and inform you what is needed moving forward.
Please feel free to share amongst the community for those we may not be in touch with, the greater the conversation we can have around this issue, the better we can help you to gain access to medicines.
Newborn Screening Advocacy Next Steps (Webinar)
19 AUG 2021 · Now that Newborn Screening (NBS) has been recommended, we turn our focus to the Australian states and territories, as this is where NBS gains funding. Each state has to allocate in their budget to pay for testing.
Some states are actively looking at funding NBS, whilst in other states it’s not even on their radar for funding, so we together as a team need to campaign as a team to highlight the need for NBS in each state.
As we have previously stated, a person’s postcode shouldn’t determine if they get screened at birth for SMA.
Why do I need to see an adult Neurologist
28 JUN 2021 · Why do I need to see an adult Neurologist with Lauren Sanders
Q&A with Jo Watson
27 MAY 2021
The Importance of a patient registry and why to participate
5 MAY 2021 · The Importance of a patient registry and why to participate
Guest: Robin Forbes
Visit http://smaaustralia.org.au for more information
Getting involved in sports with a disability
21 APR 2021 · In this episode, we speak to Australian Paralympian Champion, Daniel Michel about getting involved in sports with a disability.
Self Managing your NDIS
22 FEB 2021
Adult working group and next steps
26 JAN 2021
Spinal Muscular Atrophy (SMA) is a rare genetic muscle wasting disease that is the childhood version of motor neurone disease. If you are newly diagnosed, or have just come across...
show more
Spinal Muscular Atrophy (SMA) is a rare genetic muscle wasting disease that is the childhood version of motor neurone disease.
If you are newly diagnosed, or have just come across our page for the first time, we urge you to get involved, within the SMA community here in Australia. We would love to hear from you and are happy to support you on your journey.
We acknowledge that each person is different, and we endeavour to assist you and your requirements.
show less
If you are newly diagnosed, or have just come across our page for the first time, we urge you to get involved, within the SMA community here in Australia. We would love to hear from you and are happy to support you on your journey.
We acknowledge that each person is different, and we endeavour to assist you and your requirements.
Information
| Author | Alba Prime |
| Organization | Alba Prime |
| Categories | News |
| Website | - |
| - |
Copyright 2024 - Spreaker Inc. an iHeartMedia Company
