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Living with Multiple Sclerosis (MS) can feel overwhelming, especially after a new diagnosis. Fatigue, brain fog, uncertainty, and fear can make it difficult to imagine a hopeful future. But today's conversation is about why hope still matters and why there has never been a better time to live with MS.
In this episode of On My Nerves: MS Unfiltered, Michelle (MSchelleRx) and Tim share what keeps them moving forward through the hardest days of Multiple Sclerosis. They discuss faith, resilience, mindset, and why hope is something we intentionally practice rather than simply wait to feel.
Michelle also offers a unique perspective as both a pharmacist and someone diagnosed with MS in 2001. She explains how dramatically MS treatments have improved over the past two decades and why today's therapies are giving people opportunities that simply didn't exist years ago.
In this episode, we discuss:
✔ What keeps us going on the hardest MS days
✔ Why hope is an action, not just a feeling
✔ Faith and living with Multiple Sclerosis
✔ How MS treatments have changed over the last 25 years
✔ Why mindset matters with chronic illness
✔ The importance of movement and exercise with MS
✔ Finding encouragement after a new diagnosis
✔ How to reframe negative thinking without denying reality
✔ Living well with MS between appointments
We hope this conversation reminds you that while Multiple Sclerosis is hard, it does not have to define your future.
🧡 THANK YOU FOR BEING HERE
Living with MS can feel lonely sometimes, but you don't have to navigate it alone.
JOIN THE ON MY NERVES COMMUNITY
Substack:
On My Nerves Podcast | Substack
🎙️ LISTEN TO THE PODCAST
YouTube Playlist:
Podcast
Apple Podcasts:
https://podcasts.apple.com/us/podcast/on-my-nerves-ms-unfiltered/id1889080445
Spotify:
https://open.spotify.com/show/1xkjDPzAKJBePHNcoDuaWw
📱 FOLLOW US
TikTok @OnMyNervesPodcast
Instagram: @on_my_nerves_podcast
BUSINESS & SPEAKING INQUIRIES
Email:[email protected]
💬 If this video helped you, leave a comment and tell us where you're watching from.
We read every comment and love hearing your MS story.
By Tim Conway and Michelle (MSChelleRx)Living with Multiple Sclerosis (MS) can feel overwhelming, especially after a new diagnosis. Fatigue, brain fog, uncertainty, and fear can make it difficult to imagine a hopeful future. But today's conversation is about why hope still matters and why there has never been a better time to live with MS.
In this episode of On My Nerves: MS Unfiltered, Michelle (MSchelleRx) and Tim share what keeps them moving forward through the hardest days of Multiple Sclerosis. They discuss faith, resilience, mindset, and why hope is something we intentionally practice rather than simply wait to feel.
Michelle also offers a unique perspective as both a pharmacist and someone diagnosed with MS in 2001. She explains how dramatically MS treatments have improved over the past two decades and why today's therapies are giving people opportunities that simply didn't exist years ago.
In this episode, we discuss:
✔ What keeps us going on the hardest MS days
✔ Why hope is an action, not just a feeling
✔ Faith and living with Multiple Sclerosis
✔ How MS treatments have changed over the last 25 years
✔ Why mindset matters with chronic illness
✔ The importance of movement and exercise with MS
✔ Finding encouragement after a new diagnosis
✔ How to reframe negative thinking without denying reality
✔ Living well with MS between appointments
We hope this conversation reminds you that while Multiple Sclerosis is hard, it does not have to define your future.
🧡 THANK YOU FOR BEING HERE
Living with MS can feel lonely sometimes, but you don't have to navigate it alone.
JOIN THE ON MY NERVES COMMUNITY
Substack:
On My Nerves Podcast | Substack
🎙️ LISTEN TO THE PODCAST
YouTube Playlist:
Podcast
Apple Podcasts:
https://podcasts.apple.com/us/podcast/on-my-nerves-ms-unfiltered/id1889080445
Spotify:
https://open.spotify.com/show/1xkjDPzAKJBePHNcoDuaWw
📱 FOLLOW US
TikTok @OnMyNervesPodcast
Instagram: @on_my_nerves_podcast
BUSINESS & SPEAKING INQUIRIES
Email:[email protected]
💬 If this video helped you, leave a comment and tell us where you're watching from.
We read every comment and love hearing your MS story.