We all know that MS is a misunderstood disease that shows up differently for each of us. Each week an episode will be released that'll share the highs and lows of this unpredictable disease. My hope is that these episodes will shed some light for those who are newly diagnosed and those of us who have been living with it for years. Each week we will chat with someone who has been effected by Multiple Sclerosis, whether that be someone who lives with it, a family member, spouse, nurse or friend.
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We all know that MS is a misunderstood disease that shows up differently for each of us. Each week an episode will be released that'll share the highs and lows of this unpredictable disease. My hope is that these episodes will shed some light for those who are newly diagnosed and those of us who have been living with it for years. Each week we will chat with someone who has been effected by Multiple Sclerosis, whether that be someone who lives with it, a family member, spouse, nurse or friend.
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Today on MS Understood we chat with public speaker, resilience coach, artist and medical advocate Justine Martin. We talk about how her life has done a complete 180 since diagnosis, we speak about how art has changed her life, and so much more. I seriously loved her answer to my "what's been the best thing to happen to you because of your MS?', so make sure to stick around to the end of the episode to hear that.
Thank you so much for listening to today's episode of MS Understood. You can find Justine on Facebook at JUZT art Justine Martin Artist, and you can find her Australian MS Support Facebook Group at Supporting Each Other With MS in Australia. You can find me on Instagram @Clare.Reilly The best thing you can do to support this podcast is click follow on Spotify, Subscribe on your other podcast listening platforms and leave a review, this helps others find the podcast.
I'm always looking for new guests for the MS Understood podcast, if this is you or someone you know, please send me a message via either of my instagram accounts. In an effort to make sure to have representation I'd love to hear from any members of the lGBTQI+ community, our Black and BIPOC community or any men willing to share their stories of living with Multiple Sclerosis.
Thanks again for listening and please share this episode with someone you think it might help
MS Understood
We all know that MS is a misunderstood disease that shows up differently for each of us. Each week an episode will be released that'll share the highs and lows of this unpredictable disease. My hope is that these episodes will shed some light for those who are newly diagnosed and those of us who have been living with it for years. Each week we will chat with someone who has been effected by Multiple Sclerosis, whether that be someone who lives with it, a family member, spouse, nurse or friend.
