This resource was developed in collaboration with people who have a diagnosis of MS and their family and friends.
It has been created for people who are going through the challenging and often emotional time that happens when a person they know is diagnosed with MS.
Having a diagnosis of MS can be life-changing for both the person and for those who care about them. This resource is designed to empower you with the knowledge and strategies to help support you and your person with MS.
We hope you find this resource useful. If you'd like more information on any of the topics covered, you can call MS Plus on 1800 042 138 or email: [email protected]
You can access more resources in our Carers, Family & Friends Toolkit
What is MS? How is MS diagnosed and who gets it? Join MS Nurse advisor, Jane Bridgman as she unpacks the basics and discusses symptoms and treatments. This is suited to those recently diagnosed while also being a great refresher for those who have been living with the disease for some time.
In this episode of the MS Boost, we talk to Nicola Palfrey, clinical psychologist at headspace National about the parenting challenge of talking to your teenagers about chronic illness. Nicola shares her expert insights into approaching these difficult conversations sensitively and efficacy. We also explore the important topic of knowing what are the signs that your teen may need some mental health support and how to navigate access. If you are a parent with teenagers, this is an episode you will really appreciate.
We all want the best for those we care about. But knowing how to best support someone after a diagnosis of MS can be difficult. Join MS Plus Nurse Advisor, Jane Gilliland as she provides insights into the role you can play, and the helpful and not so helpful things you can do following the diagnosis.
