Today is an interview with, well, me. When I interviewed Stephen way back when I started the podcast, we got off the recording he offered that if I ever wanted to be interviewed myself then he would be honoured to do that. So I reached out to him for my 12 month anniversary of starting the podcast to interview me.

In today's episode we talk about how the podcast has gone over the 12 months and tips that I've learnt from others while doing the podcast, how I feel about famous people getting diagnosed with MS, how having funding from the NDIS has changed my life and some highlights from my plans, as well as the best thing to come from my diagnosis and what I would tell people to make MS more understood.

Before we get into the interview I just want to say a huge thank you to Stephen for taking the time to interview me, I want to say thank you to anyone who has listened to even one episode, thank you to my parents and friends who listened to my idea before I was ready to dive in, thank you to anyone who has volunteered their time to be a guest on the show, obviously this podcast wouldn't exist without you and thank you to anyone who has listened to an episode and taken the time to send me a message, the podcast is still going because of you!

I'm really excited for the next 12 months of MS Understood, I'm mixing things up a little bit. I have some incredible interviews coming for you from an MS Physiotherapist, from someone who use to work at the NDIS, occupational therapists and someone who is all to close with grief, as well as incredible and inspiring episode from people from all over the world who live with MS.

Constant Pain and Multiple Sclerosis with Stephen Papadopolous

Multiple Sclerosis, the Great Wake Up Call with Jillian Kingsford Smith