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Content provided by Nele von Horsten (née Handwerker) and Nele Handwerker. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Nele von Horsten (née Handwerker) and Nele Handwerker or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.
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#123: Living with MS & Making a Difference. Claudia’s Journey of Fundraising, Resilience, and Hope

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Manage episode 496042562 series 3562061
Content provided by Nele von Horsten (née Handwerker) and Nele Handwerker. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Nele von Horsten (née Handwerker) and Nele Handwerker or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.
👤 About this episode

In this episode, Claudia Dieckmann shares her personal journey of living with multiple sclerosis (MS) and how she transformed her diagnosis into a driving force for community action and purpose-driven fundraising. Based in Cape Town, South Africa, Claudia is not only an MS advocate but also a creative event organizer behind campaigns like Swim4MS and Quiz4MS, supporting the work of Multiple Sclerosis South Africa (NPO 003-275).

Claudia speaks openly about her diagnosis, treatment changes, symptom management, and the emotional side of adjusting to a “new normal.” She also reflects on the importance of community, mindset, and creating fun, inclusive spaces that raise awareness and funds for MS.

🧭 What you’ll learn:
  • How Claudia experienced her MS diagnosis and what helped her move forward

  • Why self-empowerment and community are key pillars in her life

  • Her personal routines and what “motion is lotion” means to her

  • Insights into organizing MS fundraising events in South Africa

  • Her hopes for the future of MS treatment and awareness

🔗 Resources & Links: 💬 Claudia’s message to others living with MS:

“Mindset is everything. You are not alone—and you don’t have to do it all on your own.”

Best place to keep up to date is via the MSSA website and social media platforms.

---

Thank you Claudia for all your fundraising efforts.

See you soon and try to make the best out of your life, Nele

For more information and positive thoughts, subscribe to my newsletter for free.

Click here for an overview of all podcast episodes published so far.

  continue reading

123 episodes

Artwork
iconShare
 
Manage episode 496042562 series 3562061
Content provided by Nele von Horsten (née Handwerker) and Nele Handwerker. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Nele von Horsten (née Handwerker) and Nele Handwerker or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://podcastplayer.com/legal.
👤 About this episode

In this episode, Claudia Dieckmann shares her personal journey of living with multiple sclerosis (MS) and how she transformed her diagnosis into a driving force for community action and purpose-driven fundraising. Based in Cape Town, South Africa, Claudia is not only an MS advocate but also a creative event organizer behind campaigns like Swim4MS and Quiz4MS, supporting the work of Multiple Sclerosis South Africa (NPO 003-275).

Claudia speaks openly about her diagnosis, treatment changes, symptom management, and the emotional side of adjusting to a “new normal.” She also reflects on the importance of community, mindset, and creating fun, inclusive spaces that raise awareness and funds for MS.

🧭 What you’ll learn:
  • How Claudia experienced her MS diagnosis and what helped her move forward

  • Why self-empowerment and community are key pillars in her life

  • Her personal routines and what “motion is lotion” means to her

  • Insights into organizing MS fundraising events in South Africa

  • Her hopes for the future of MS treatment and awareness

🔗 Resources & Links: 💬 Claudia’s message to others living with MS:

“Mindset is everything. You are not alone—and you don’t have to do it all on your own.”

Best place to keep up to date is via the MSSA website and social media platforms.

---

Thank you Claudia for all your fundraising efforts.

See you soon and try to make the best out of your life, Nele

For more information and positive thoughts, subscribe to my newsletter for free.

Click here for an overview of all podcast episodes published so far.

  continue reading

123 episodes

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