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    <title>&amp;quot;Now more than ever&amp;quot; by Kathrin Wersing</title>
    <description>How can we succeed - despite the life-changing diagnosis of Parkinson's disease - in making life positive, worth living and colorful? In my podcast I talk to people who live positively with Parkinson's in many different ways. A podcast that is meant to encourage, from people with PD for people with PD, relatives and everyone who is looking for a positive approach to the topic of Parkinson's.</description>
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    <itunes:subtitle>Living positively with Parkinson's disease</itunes:subtitle>
    <itunes:summary>How can we succeed - despite the life-changing diagnosis of Parkinson's disease - in making life positive, worth living and colorful? In my podcast I talk to people who live positively with Parkinson's in many different ways. A podcast that is meant to encourage, from people with PD for people with PD, relatives and everyone who is looking for a positive approach to the topic of Parkinson's.</itunes:summary>
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      <title>episode 9 - We are one Parkinson&amp;#039;s family with Hannington Kabugo at the WPC2023</title>
      <description><![CDATA[<p>Welcome to my podcast "Now more than ever - Living positively with Parkinson's disease."</p>
<p>My name is Kathrin Wersing and today I am sharing with you another short episode with impressions from the World Parkinson's Congress. The Congress took place in Barcelona from 4-7 July this year. The four days in Barcelona were colourful, diverse, loud and lively but most of all they were a wonderful opportunity to meet people I knew so far only from online meetings and social media. I was especially looking forward to meeting Hannington Kabugo, a truely inspiring man from Uganda.</p>
<p>Unfortunately, my audio recordings from the WPC turned out very poorly and so I have been struggling for a long time whether to publish more episodes from the conference or not. But now I've finally decided that I'm just going to put up with this poor sound quality because I really wanted to give you an update on Hannington's story.</p>
<p>Hannington Kabugo from Uganda was a guest on my podcast in April 2022, if you haven't heard that episode I absolutely recommend you listen to it.</p>
<p>Here you can find the episode on spotify:</p>
<p><a href="https://open.spotify.com/episode/6uj8uJptnFSWHmGDy7K1yI?si=PWLe9AAkQEihONGw0u1eAw" rel="noopener noreferrer nofollow">https://open.spotify.com/episode/6uj8uJptnFSWHmGDy7K1yI?si=PWLe9AAkQEihONGw0u1eAw</a></p>
<p>Hannington is a person who shows that no matter how hopeless a situation seems, we always have the power to make changes for the better. Hannington's mother had Parkinson's disease. In Uganda, one of the poorest countries in the world, the disease was long considered a curse. Anyone who had Parkinson's symptoms was considered bewitched, they were treated like outcasts and no one was allowed to even come close to these people because Parkinson's was believed to be contagious. Hannington experienced his mother's suffering first hand and after her death decided that never again should a person with Parkinson's suffer so much in Uganda. He founded Parkinson's si Buko, an organisation that today ensures that villages and communities in Uganda are educated about the true background of Parkinson's. With the help of supporters in the USA, Hannington has been able to make an incredible difference. This great commitment was recognised at the World Parkinson's Congress, where Hannington received a very special award.</p>
<p>Links to this episode:</p>
<ul><li><p>Homepage of the partner organization in the USA: <a href="https://parkinsonssibuko.org/" rel="noopener noreferrer nofollow">https://parkinsonssibuko.org/</a> There you can also find a direct link to donate via PayPal in favor of Parkinson's si Buko USA. All employees work on a voluntary basis and all donations go directly to Uganda.</p>
</li></ul><ul><li><p>Contact Hannington Kabugo</p>
<ul><li><p>via facebook: <a href="https://www.facebook.com/kabugo.hannington.330" rel="noopener noreferrer nofollow">https://www.facebook.com/kabugo.hannington.330</a></p>
</li><li><p>via E-Mail: <a href="mailto:hannyug@hotmail.com" rel="noopener noreferrer nofollow">hannyug@hotmail.com</a></p>
</li></ul></li></ul><ul><li><p>Information about Parkinson's Africa: <a href="https://www.parkinsonsafrica.org/" rel="noopener noreferrer nofollow">https://www.parkinsonsafrica.org/</a></p>
</li></ul><p>Thank you very much for your donation and support</p>
<p>I look forward to your feedback on this podcast episode. Feel free to write to me: kontakt@jetzt-erst-recht.info</p>
]]></description>
      <pubDate>Fri, 03 Nov 2023 06:00:00 +0100</pubDate>
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      <content:encoded><![CDATA[<p>Welcome to my podcast "Now more than ever - Living positively with Parkinson's disease."</p>
<p>My name is Kathrin Wersing and today I am sharing with you another short episode with impressions from the World Parkinson's Congress. The Congress took place in Barcelona from 4-7 July this year. The four days in Barcelona were colourful, diverse, loud and lively but most of all they were a wonderful opportunity to meet people I knew so far only from online meetings and social media. I was especially looking forward to meeting Hannington Kabugo, a truely inspiring man from Uganda.</p>
<p>Unfortunately, my audio recordings from the WPC turned out very poorly and so I have been struggling for a long time whether to publish more episodes from the conference or not. But now I've finally decided that I'm just going to put up with this poor sound quality because I really wanted to give you an update on Hannington's story.</p>
<p>Hannington Kabugo from Uganda was a guest on my podcast in April 2022, if you haven't heard that episode I absolutely recommend you listen to it.</p>
<p>Here you can find the episode on spotify:</p>
<p><a href="https://open.spotify.com/episode/6uj8uJptnFSWHmGDy7K1yI?si=PWLe9AAkQEihONGw0u1eAw" rel="noopener noreferrer nofollow">https://open.spotify.com/episode/6uj8uJptnFSWHmGDy7K1yI?si=PWLe9AAkQEihONGw0u1eAw</a></p>
<p>Hannington is a person who shows that no matter how hopeless a situation seems, we always have the power to make changes for the better. Hannington's mother had Parkinson's disease. In Uganda, one of the poorest countries in the world, the disease was long considered a curse. Anyone who had Parkinson's symptoms was considered bewitched, they were treated like outcasts and no one was allowed to even come close to these people because Parkinson's was believed to be contagious. Hannington experienced his mother's suffering first hand and after her death decided that never again should a person with Parkinson's suffer so much in Uganda. He founded Parkinson's si Buko, an organisation that today ensures that villages and communities in Uganda are educated about the true background of Parkinson's. With the help of supporters in the USA, Hannington has been able to make an incredible difference. This great commitment was recognised at the World Parkinson's Congress, where Hannington received a very special award.</p>
<p>Links to this episode:</p>
<ul><li><p>Homepage of the partner organization in the USA: <a href="https://parkinsonssibuko.org/" rel="noopener noreferrer nofollow">https://parkinsonssibuko.org/</a> There you can also find a direct link to donate via PayPal in favor of Parkinson's si Buko USA. All employees work on a voluntary basis and all donations go directly to Uganda.</p>
</li></ul><ul><li><p>Contact Hannington Kabugo</p>
<ul><li><p>via facebook: <a href="https://www.facebook.com/kabugo.hannington.330" rel="noopener noreferrer nofollow">https://www.facebook.com/kabugo.hannington.330</a></p>
</li><li><p>via E-Mail: <a href="mailto:hannyug@hotmail.com" rel="noopener noreferrer nofollow">hannyug@hotmail.com</a></p>
</li></ul></li></ul><ul><li><p>Information about Parkinson's Africa: <a href="https://www.parkinsonsafrica.org/" rel="noopener noreferrer nofollow">https://www.parkinsonsafrica.org/</a></p>
</li></ul><p>Thank you very much for your donation and support</p>
<p>I look forward to your feedback on this podcast episode. Feel free to write to me: kontakt@jetzt-erst-recht.info</p>
]]></content:encoded>
      <slash:comments>0</slash:comments>
      <itunes:author>Kathrin Wersing</itunes:author>
      <itunes:duration>00:13:04</itunes:duration>
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      <itunes:title>episode 9 - We are one Parkinson&amp;#039;s family</itunes:title>
      <itunes:subtitle>with Hannington Kabugo at the WPC2023</itunes:subtitle>
      <itunes:summary>Welcome to my podcast "Now more than ever - Living positively with Parkinson's disease."

My name is Kathrin Wersing and today I am sharing with you another short episode with impressions from the World Parkinson's Congress. The Congress took place in Barcelona from 4-7 July this year. The four days in Barcelona were colourful, diverse, loud and lively but most of all they were a wonderful opportunity to meet people I knew so far only from online meetings and social media. I was especially looking forward to meeting Hannington Kabugo, a truely inspiring man from Uganda.

Unfortunately, my audio recordings from the WPC turned out very poorly and so I have been struggling for a long time whether to publish more episodes from the conference or not. But now I've finally decided that I'm just going to put up with this poor sound quality because I really wanted to give you an update on Hannington's story.

Hannington Kabugo from Uganda was a guest on my podcast in April 2022, if you haven't heard that episode I absolutely recommend you listen to it.

Here you can find the episode on spotify:

https://open.spotify.com/episode/6uj8uJptnFSWHmGDy7K1yI?si=PWLe9AAkQEihONGw0u1eAw

Hannington is a person who shows that no matter how hopeless a situation seems, we always have the power to make changes for the better. Hannington's mother had Parkinson's disease. In Uganda, one of the poorest countries in the world, the disease was long considered a curse. Anyone who had Parkinson's symptoms was considered bewitched, they were treated like outcasts and no one was allowed to even come close to these people because Parkinson's was believed to be contagious. Hannington experienced his mother's suffering first hand and after her death decided that never again should a person with Parkinson's suffer so much in Uganda. He founded Parkinson's si Buko, an organisation that today ensures that villages and communities in Uganda are educated about the true background of Parkinson's. With the help of supporters in the USA, Hannington has been able to make an incredible difference. This great commitment was recognised at the World Parkinson's Congress, where Hannington received a very special award.

Links to this episode:

Homepage of the partner organization in the USA: https://parkinsonssibuko.org/ There you can also find a direct link to donate via PayPal in favor of Parkinson's si Buko USA. All employees work on a voluntary basis and all donations go directly to Uganda.

Contact Hannington Kabugo

via facebook: https://www.facebook.com/kabugo.hannington.330

via E-Mail: hannyug@hotmail.com

Information about Parkinson's Africa: https://www.parkinsonsafrica.org/

Thank you very much for your donation and support

I look forward to your feedback on this podcast episode. Feel free to write to me: kontakt@jetzt-erst-recht.info

</itunes:summary>
      <itunes:episode>9</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
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      <title>episode 8 - World peace is possible, now! Interview with Nenad Bach at the WPC2023 (17.09.2023)</title>
      <description><![CDATA[<p>Welcome to my podcast “Jetzt erst recht – Positiv leben mit Parkinson”. My name is Kathrin Wersing, I am 44 years old and I live in Germany. 4 years ago I was diagnosed with Parkinson’s myself. One year later I started this podcast which is about life-affirming positive inspirations from people living with Parkinson’s disease. II am convinced that – no matter if we live with Parkinson’s or not – WE are in control of our own lives and that the way we look into the future has a huge impact on our own quality of life.</p>
<p>A few weeks ago in July, I visited the World Parkinson’s Congress in Barcelona. Those 4 days in Barcelona were not only hot in terms of temperature, but also hot in terms of topics. But what was most important for me during these days: to absorb the spirit of this event. There were so many interesting, committed and absolutely impressive people related to Parkinson’s gathered in one place, as I have never experienced before. More than 2600 people from 73 countries, including over 900 doctors and therapists, 450 people from the caring and therapeutic professions, 685 people with Parkinson’s and 260 relatives.</p>
<p>During those days in Barcelona, I had many conversations, I took a lot of photos and audio recordings. Finally, I was faced with the overwhelming task of how to pack all this into just ONE podcast episode. So I decided to publish several short episodes with people and topics that touched ME the most at this World Parkinson’s Congress. Today I’ll start with an interview with a unique man whom I had the pleasure of meeting again at the World Parkinson’s Congress: Nenad Bach is not only a wonderful musician and composer but also the founder of the worldwide movement PingPongParkinson, which has spread like wildfire from NewYork all over the world since 2017. The idea of PingPongParkinson is quite simple: People with Parkinson’s play table tennis together in regional sports clubs in their hometown. The sport helps those affected to stay active in social life and to delay the progression of the Parkinson‘s. I experienced it myself: PingPongParkinson helps a lot of people to improve their quality of life. Nenad Bach is a man of many talents – but above all he is a visionary and an inspiring peace activist. In this interview, he tells us what keeps him moving regarding PingPongParkinson and what table tennis and peace have in common.</p>
<p>Links to this episode:</p>
<ul><li><p>Link to Nenad Bachs artice “World peace in 1 hour” in the united Nations Chronicle <a href="https://www.un.org/en/un-chronicle/world-peace-one-hour" rel="noopener noreferrer nofollow">https://www.un.org/en/un-chronicle/world-peace-one-hour</a></p>
</li><li><p>Link to PingPingParkinson worldwide: <a href="https://www.pingpongparkinson.org/" rel="noopener noreferrer nofollow">https://www.pingpongparkinson.org/</a></p>
</li><li><p>Link to PingPongParkinson Germany: <a href="https://www.pingpongparkinson.de/" rel="noopener noreferrer nofollow">https://www.pingpongparkinson.de/</a></p>
</li></ul><p>I appreciate your feedback on this podcast episode. Feel free to send me an email: <a href="mailto:kontakt@jetzt-erst-recht.info" rel="noopener noreferrer nofollow">kontakt@jetzt-erst-recht.info</a></p>
]]></description>
      <pubDate>Mon, 18 Sep 2023 15:29:00 +0200</pubDate>
      <link>https://cyehry.podcaster.de/download/episode_75_-_World_peace_is_possible-_now-_Interview_with_Nenad_Bach_on_the_WPC2023(2).mp3?origin=feed</link>
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      <dc:creator>Kathrin Wersing</dc:creator>
      <content:encoded><![CDATA[<p>Welcome to my podcast “Jetzt erst recht – Positiv leben mit Parkinson”. My name is Kathrin Wersing, I am 44 years old and I live in Germany. 4 years ago I was diagnosed with Parkinson’s myself. One year later I started this podcast which is about life-affirming positive inspirations from people living with Parkinson’s disease. II am convinced that – no matter if we live with Parkinson’s or not – WE are in control of our own lives and that the way we look into the future has a huge impact on our own quality of life.</p>
<p>A few weeks ago in July, I visited the World Parkinson’s Congress in Barcelona. Those 4 days in Barcelona were not only hot in terms of temperature, but also hot in terms of topics. But what was most important for me during these days: to absorb the spirit of this event. There were so many interesting, committed and absolutely impressive people related to Parkinson’s gathered in one place, as I have never experienced before. More than 2600 people from 73 countries, including over 900 doctors and therapists, 450 people from the caring and therapeutic professions, 685 people with Parkinson’s and 260 relatives.</p>
<p>During those days in Barcelona, I had many conversations, I took a lot of photos and audio recordings. Finally, I was faced with the overwhelming task of how to pack all this into just ONE podcast episode. So I decided to publish several short episodes with people and topics that touched ME the most at this World Parkinson’s Congress. Today I’ll start with an interview with a unique man whom I had the pleasure of meeting again at the World Parkinson’s Congress: Nenad Bach is not only a wonderful musician and composer but also the founder of the worldwide movement PingPongParkinson, which has spread like wildfire from NewYork all over the world since 2017. The idea of PingPongParkinson is quite simple: People with Parkinson’s play table tennis together in regional sports clubs in their hometown. The sport helps those affected to stay active in social life and to delay the progression of the Parkinson‘s. I experienced it myself: PingPongParkinson helps a lot of people to improve their quality of life. Nenad Bach is a man of many talents – but above all he is a visionary and an inspiring peace activist. In this interview, he tells us what keeps him moving regarding PingPongParkinson and what table tennis and peace have in common.</p>
<p>Links to this episode:</p>
<ul><li><p>Link to Nenad Bachs artice “World peace in 1 hour” in the united Nations Chronicle <a href="https://www.un.org/en/un-chronicle/world-peace-one-hour" rel="noopener noreferrer nofollow">https://www.un.org/en/un-chronicle/world-peace-one-hour</a></p>
</li><li><p>Link to PingPingParkinson worldwide: <a href="https://www.pingpongparkinson.org/" rel="noopener noreferrer nofollow">https://www.pingpongparkinson.org/</a></p>
</li><li><p>Link to PingPongParkinson Germany: <a href="https://www.pingpongparkinson.de/" rel="noopener noreferrer nofollow">https://www.pingpongparkinson.de/</a></p>
</li></ul><p>I appreciate your feedback on this podcast episode. Feel free to send me an email: <a href="mailto:kontakt@jetzt-erst-recht.info" rel="noopener noreferrer nofollow">kontakt@jetzt-erst-recht.info</a></p>
]]></content:encoded>
      <slash:comments>0</slash:comments>
      <itunes:author>Kathrin Wersing</itunes:author>
      <itunes:duration>00:17:08</itunes:duration>
      <itunes:image href="https://files.pdcstrcdn.de/s/i/de1d695e-855f-4f23-a4bc-77bdebf28ce0/Folge_75_WPC2023_-_---World_peace_is_possible---_interview_with_Nenad_Bach.jpg"/>
      <itunes:title>episode 8 - World peace is possible, now!</itunes:title>
      <itunes:subtitle>Interview with Nenad Bach at the WPC2023 (17.09.2023)</itunes:subtitle>
      <itunes:summary>Welcome to my podcast “Jetzt erst recht – Positiv leben mit Parkinson”. My name is Kathrin Wersing, I am 44 years old and I live in Germany. 4 years ago I was diagnosed with Parkinson’s myself. One year later I started this podcast which is about life-affirming positive inspirations from people living with Parkinson’s disease. II am convinced that – no matter if we live with Parkinson’s or not – WE are in control of our own lives and that the way we look into the future has a huge impact on our own quality of life.

A few weeks ago in July, I visited the World Parkinson’s Congress in Barcelona. Those 4 days in Barcelona were not only hot in terms of temperature, but also hot in terms of topics. But what was most important for me during these days: to absorb the spirit of this event. There were so many interesting, committed and absolutely impressive people related to Parkinson’s gathered in one place, as I have never experienced before. More than 2600 people from 73 countries, including over 900 doctors and therapists, 450 people from the caring and therapeutic professions, 685 people with Parkinson’s and 260 relatives.

During those days in Barcelona, I had many conversations, I took a lot of photos and audio recordings. Finally, I was faced with the overwhelming task of how to pack all this into just ONE podcast episode. So I decided to publish several short episodes with people and topics that touched ME the most at this World Parkinson’s Congress. Today I’ll start with an interview with a unique man whom I had the pleasure of meeting again at the World Parkinson’s Congress: Nenad Bach is not only a wonderful musician and composer but also the founder of the worldwide movement PingPongParkinson, which has spread like wildfire from NewYork all over the world since 2017. The idea of PingPongParkinson is quite simple: People with Parkinson’s play table tennis together in regional sports clubs in their hometown. The sport helps those affected to stay active in social life and to delay the progression of the Parkinson‘s. I experienced it myself: PingPongParkinson helps a lot of people to improve their quality of life. Nenad Bach is a man of many talents – but above all he is a visionary and an inspiring peace activist. In this interview, he tells us what keeps him moving regarding PingPongParkinson and what table tennis and peace have in common.

Links to this episode:

Link to Nenad Bachs artice “World peace in 1 hour” in the united Nations Chronicle https://www.un.org/en/un-chronicle/world-peace-one-hour

Link to PingPingParkinson worldwide: https://www.pingpongparkinson.org/

Link to PingPongParkinson Germany: https://www.pingpongparkinson.de/

I appreciate your feedback on this podcast episode. Feel free to send me an email: kontakt@jetzt-erst-recht.info

</itunes:summary>
      <itunes:episode>8</itunes:episode>
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      <title>episode 6 - Let&amp;#039;s talk about women&amp;#039;s issues with Dr. Annelien Oosterbaan (22.01.2023)</title>
      <description><![CDATA[<p>Hello  and welcome to my podcast. My name is Kathrin Wersing and I live in Germany. Two and a half years ago I started this podcast after I was  diagnosed with Parkinson’s. I wanted to find out how to live a positive  and inspiring life despite the disease. Most of my interviews so far  were in German language but last year I also started talking to people  from all over the world in English. In my special series Parkinson’s  around the world I want to continue to find out how parkinson’s is seen  and treated in other countries.</p>
<p>My guest today is Annelien  Oosterbaan from the Netherlands. She was diagnosed at the age of 33. As a  mother of 3 children, she was just about to start her career as a  doctor when the diagnosis hit her cold. But Annelien is an impressive  fighter and in the last 5 years she has not only thrown herself into  Parkinson’s research with great enthusiasm but has also had a fourth  child. I can promise you, this woman will impress you! I hope you enjoy  this interview!</p>
<p>Links to this episode:</p>
<ul><li><p><a href="https://jetzt-erst-recht.info/wp-content/uploads/2023/01/Movement-Disorders-2022-Subramanian-Unmet-Needs-of-Women-Living-with-Parkinson-s-Disease-Gaps-and-Controversies.pdf" rel="noopener noreferrer nofollow">Article  in the Journal for Movement Disorders 2022 Subramanian “Unmet needs of  women living with Parkinson’ disease. Gaps and controversies.”</a></p>
</li><li><p>Website for the women’s survey, Michael J. Fox Foundation: <a href="https://foxinsight.michaeljfox.org" rel="noopener noreferrer nofollow">https://foxinsight.michaeljfox.org</a></p>
</li><li><p>The pregnancy registry <a href="https://www.pregspark.com/" rel="noopener noreferrer nofollow">https://www.pregspark.com/</a> (The links doesn’t work until the expected kick off medio 2023)</p>
</li><li><p>Advice to register: <a href="https://www.mymovesmatter.com/" rel="noopener noreferrer nofollow">https://www.mymovesmatter.com/</a></p>
</li><li><p>Get in touch with Annelien:</p>
<ul><li><p>Twitter: @pdwomen_nl &nbsp;/ @OosterbaanA</p>
</li><li><p>Instagram: @annelienoosterbaan</p>
</li></ul></li><li><p>Sponsor link to support Annelien’s research: <a href="https://radboudumc.voorradboudfonds.nl/project/vrouw-en-parkinson" rel="noopener noreferrer nofollow">https://radboudumc.voorradboudfonds.nl/project/vrouw-en-parkinson</a></p>
</li></ul><p>I appreciate your feedback on this podcast episode. Feel free to send me an email: kontakt@jetzt-erst-recht.info</p>
]]></description>
      <pubDate>Mon, 18 Sep 2023 15:22:00 +0200</pubDate>
      <link>https://cyehry.podcaster.de/download/episode_62_-_let-s_talk_about_women-s_issues_with_Dr-_Annelien_Oosterbaan-ENGLISH(1).mp3?origin=feed</link>
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      <dc:creator>Kathrin Wersing</dc:creator>
      <content:encoded><![CDATA[<p>Hello  and welcome to my podcast. My name is Kathrin Wersing and I live in Germany. Two and a half years ago I started this podcast after I was  diagnosed with Parkinson’s. I wanted to find out how to live a positive  and inspiring life despite the disease. Most of my interviews so far  were in German language but last year I also started talking to people  from all over the world in English. In my special series Parkinson’s  around the world I want to continue to find out how parkinson’s is seen  and treated in other countries.</p>
<p>My guest today is Annelien  Oosterbaan from the Netherlands. She was diagnosed at the age of 33. As a  mother of 3 children, she was just about to start her career as a  doctor when the diagnosis hit her cold. But Annelien is an impressive  fighter and in the last 5 years she has not only thrown herself into  Parkinson’s research with great enthusiasm but has also had a fourth  child. I can promise you, this woman will impress you! I hope you enjoy  this interview!</p>
<p>Links to this episode:</p>
<ul><li><p><a href="https://jetzt-erst-recht.info/wp-content/uploads/2023/01/Movement-Disorders-2022-Subramanian-Unmet-Needs-of-Women-Living-with-Parkinson-s-Disease-Gaps-and-Controversies.pdf" rel="noopener noreferrer nofollow">Article  in the Journal for Movement Disorders 2022 Subramanian “Unmet needs of  women living with Parkinson’ disease. Gaps and controversies.”</a></p>
</li><li><p>Website for the women’s survey, Michael J. Fox Foundation: <a href="https://foxinsight.michaeljfox.org" rel="noopener noreferrer nofollow">https://foxinsight.michaeljfox.org</a></p>
</li><li><p>The pregnancy registry <a href="https://www.pregspark.com/" rel="noopener noreferrer nofollow">https://www.pregspark.com/</a> (The links doesn’t work until the expected kick off medio 2023)</p>
</li><li><p>Advice to register: <a href="https://www.mymovesmatter.com/" rel="noopener noreferrer nofollow">https://www.mymovesmatter.com/</a></p>
</li><li><p>Get in touch with Annelien:</p>
<ul><li><p>Twitter: @pdwomen_nl &nbsp;/ @OosterbaanA</p>
</li><li><p>Instagram: @annelienoosterbaan</p>
</li></ul></li><li><p>Sponsor link to support Annelien’s research: <a href="https://radboudumc.voorradboudfonds.nl/project/vrouw-en-parkinson" rel="noopener noreferrer nofollow">https://radboudumc.voorradboudfonds.nl/project/vrouw-en-parkinson</a></p>
</li></ul><p>I appreciate your feedback on this podcast episode. Feel free to send me an email: kontakt@jetzt-erst-recht.info</p>
]]></content:encoded>
      <slash:comments>0</slash:comments>
      <itunes:author>Kathrin Wersing</itunes:author>
      <itunes:duration>00:28:38</itunes:duration>
      <itunes:image href="https://files.pdcstrcdn.de/s/i/230b0e46-49cc-4f85-bd56-490e50e8cb58/Podcast_Titelbilder%287%29.jpg"/>
      <itunes:title>episode 6 - Let&amp;#039;s talk about women&amp;#039;s issues</itunes:title>
      <itunes:subtitle>with Dr. Annelien Oosterbaan (22.01.2023)</itunes:subtitle>
      <itunes:summary>Hello  and welcome to my podcast. My name is Kathrin Wersing and I live in Germany. Two and a half years ago I started this podcast after I was  diagnosed with Parkinson’s. I wanted to find out how to live a positive  and inspiring life despite the disease. Most of my interviews so far  were in German language but last year I also started talking to people  from all over the world in English. In my special series Parkinson’s  around the world I want to continue to find out how parkinson’s is seen  and treated in other countries.

My guest today is Annelien  Oosterbaan from the Netherlands. She was diagnosed at the age of 33. As a  mother of 3 children, she was just about to start her career as a  doctor when the diagnosis hit her cold. But Annelien is an impressive  fighter and in the last 5 years she has not only thrown herself into  Parkinson’s research with great enthusiasm but has also had a fourth  child. I can promise you, this woman will impress you! I hope you enjoy  this interview!

Links to this episode:

Article  in the Journal for Movement Disorders 2022 Subramanian “Unmet needs of  women living with Parkinson’ disease. Gaps and controversies.”

Website for the women’s survey, Michael J. Fox Foundation: https://foxinsight.michaeljfox.org

The pregnancy registry https://www.pregspark.com/ (The links doesn’t work until the expected kick off medio 2023)

Advice to register: https://www.mymovesmatter.com/

Get in touch with Annelien:

Twitter: @pdwomen_nl  / @OosterbaanA

Instagram: @annelienoosterbaan

Sponsor link to support Annelien’s research: https://radboudumc.voorradboudfonds.nl/project/vrouw-en-parkinson

I appreciate your feedback on this podcast episode. Feel free to send me an email: kontakt@jetzt-erst-recht.info

</itunes:summary>
      <itunes:episode>6</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
    </item>
    <item>
      <title>episode 7 - Poets with Parkinson&amp;#039;s with Nigel Smith (05.03.2023)</title>
      <description><![CDATA[<p>Welcome  to my podcast. My name is Kathrin Wersing and I live in Germany. I  started this podcast over 2 years ago because I was looking for people  who live a positive life despite having Parkinson’s disease. When I was  diagnosed with Parkinson’s at the age of 40, I read and heard only  frightening stories everywhere. I was determined to change that. Today I  know that there are so many wonderful people out there who live  exciting and inspiring lives despite PD. One of them is Nigel Smith from  England. Nigel is a poet, he is one of the founders of poets with  Parkinson’s. We talk about many topics in this interview. Nigel has gone  through particlarly rough times in recent years which he talks about  honestly. But his story is also about how writing poetry has brought him  back to life and how important it is that we recognise our own worth  and value. However there is also a lot of humour and laughter in our  conversation. So you see, there is lots to say about Nigel, but he tells  us better in his own voice, which by the way is really beautiful  storyteller’s voice. So I hope you’ll enjoy this interview.</p>
<p>Links to this episode:</p>
<ul><li><p>Homepage poets wall: <a href="https://www.poetswall.com/" rel="noopener noreferrer nofollow">https://www.poetswall.com/</a></p>
</li><li><p>YouTube channel: <a href="https://www.youtube.com/@TheWall-PoetswithParkinsons111" rel="noopener noreferrer nofollow">https://www.youtube.com/@TheWall-PoetswithParkinsons111</a></p>
</li><li><p>Get in touch with Nigel: <a href="mailto:nigel@poetswithparkinsons.com" rel="noopener noreferrer nofollow">nigel@poetswithparkinsons.com</a></p>
</li><li><p>Invitation to online “poets with Parkinson’s” events:</p>
<ul><li><p>“Away in La La Land” – A 30 min Rock n Rhyme True Tale: <a href="https://www.poetswall.com/event-details-registration/away-in-la-la-land-a-30-min-rock-n-rhyme-true-tale" rel="noopener noreferrer nofollow">https://www.poetswall.com/event-details-registration/away-in-la-la-land-a-30-min-rock-n-rhyme-true-tale</a></p>
</li><li><p>First ever GERMAN Open Mic Poetry: <a href="https://www.poetswall.com/event-details-registration/1-poesie-trifft-parkinson-abend-first-ever-german-open-mic-poetry" rel="noopener noreferrer nofollow">https://www.poetswall.com/event-details-registration/1-poesie-trifft-parkinson-abend-first-ever-german-open-mic-poetry</a></p>
</li></ul></li></ul><p>I appreciate your feedback on this podcast episode.</p>
<p>Feel free to send me an email: <a href="mailto:kontakt@jetzt-erst-recht.info" rel="noopener noreferrer nofollow">kontakt@jetzt-erst-recht.info</a></p>
]]></description>
      <pubDate>Mon, 18 Sep 2023 15:22:00 +0200</pubDate>
      <link>https://cyehry.podcaster.de/download/episode_65_-_poets_with_Parkinson-s_with_Nigel_Smith_-_ENGLISH.mp3?origin=feed</link>
      <guid isPermaLink="false">pod-ba0e4f8773fba898df628dcda8e</guid>
      <author>kontakt@jetzt-erst-recht.info (Kathrin Wersing)</author>
      <enclosure type="audio/mpeg" length="50220635" url="https://cyehry.podcaster.de/now-more-than-ever-by-kathrin-wersing/media/episode_65_-_poets_with_Parkinson-s_with_Nigel_Smith_-_ENGLISH.mp3?origin=feed"/>
      <dc:creator>Kathrin Wersing</dc:creator>
      <content:encoded><![CDATA[<p>Welcome  to my podcast. My name is Kathrin Wersing and I live in Germany. I  started this podcast over 2 years ago because I was looking for people  who live a positive life despite having Parkinson’s disease. When I was  diagnosed with Parkinson’s at the age of 40, I read and heard only  frightening stories everywhere. I was determined to change that. Today I  know that there are so many wonderful people out there who live  exciting and inspiring lives despite PD. One of them is Nigel Smith from  England. Nigel is a poet, he is one of the founders of poets with  Parkinson’s. We talk about many topics in this interview. Nigel has gone  through particlarly rough times in recent years which he talks about  honestly. But his story is also about how writing poetry has brought him  back to life and how important it is that we recognise our own worth  and value. However there is also a lot of humour and laughter in our  conversation. So you see, there is lots to say about Nigel, but he tells  us better in his own voice, which by the way is really beautiful  storyteller’s voice. So I hope you’ll enjoy this interview.</p>
<p>Links to this episode:</p>
<ul><li><p>Homepage poets wall: <a href="https://www.poetswall.com/" rel="noopener noreferrer nofollow">https://www.poetswall.com/</a></p>
</li><li><p>YouTube channel: <a href="https://www.youtube.com/@TheWall-PoetswithParkinsons111" rel="noopener noreferrer nofollow">https://www.youtube.com/@TheWall-PoetswithParkinsons111</a></p>
</li><li><p>Get in touch with Nigel: <a href="mailto:nigel@poetswithparkinsons.com" rel="noopener noreferrer nofollow">nigel@poetswithparkinsons.com</a></p>
</li><li><p>Invitation to online “poets with Parkinson’s” events:</p>
<ul><li><p>“Away in La La Land” – A 30 min Rock n Rhyme True Tale: <a href="https://www.poetswall.com/event-details-registration/away-in-la-la-land-a-30-min-rock-n-rhyme-true-tale" rel="noopener noreferrer nofollow">https://www.poetswall.com/event-details-registration/away-in-la-la-land-a-30-min-rock-n-rhyme-true-tale</a></p>
</li><li><p>First ever GERMAN Open Mic Poetry: <a href="https://www.poetswall.com/event-details-registration/1-poesie-trifft-parkinson-abend-first-ever-german-open-mic-poetry" rel="noopener noreferrer nofollow">https://www.poetswall.com/event-details-registration/1-poesie-trifft-parkinson-abend-first-ever-german-open-mic-poetry</a></p>
</li></ul></li></ul><p>I appreciate your feedback on this podcast episode.</p>
<p>Feel free to send me an email: <a href="mailto:kontakt@jetzt-erst-recht.info" rel="noopener noreferrer nofollow">kontakt@jetzt-erst-recht.info</a></p>
]]></content:encoded>
      <slash:comments>0</slash:comments>
      <itunes:author>Kathrin Wersing</itunes:author>
      <itunes:duration>00:35:20</itunes:duration>
      <itunes:image href="https://files.pdcstrcdn.de/s/i/123a5ffd-9f8f-4407-bba1-aad51c77aa3d/Podcast_Titelbilder%288%29.jpg"/>
      <itunes:title>episode 7 - Poets with Parkinson&amp;#039;s</itunes:title>
      <itunes:subtitle>with Nigel Smith (05.03.2023)</itunes:subtitle>
      <itunes:summary>Welcome  to my podcast. My name is Kathrin Wersing and I live in Germany. I  started this podcast over 2 years ago because I was looking for people  who live a positive life despite having Parkinson’s disease. When I was  diagnosed with Parkinson’s at the age of 40, I read and heard only  frightening stories everywhere. I was determined to change that. Today I  know that there are so many wonderful people out there who live  exciting and inspiring lives despite PD. One of them is Nigel Smith from  England. Nigel is a poet, he is one of the founders of poets with  Parkinson’s. We talk about many topics in this interview. Nigel has gone  through particlarly rough times in recent years which he talks about  honestly. But his story is also about how writing poetry has brought him  back to life and how important it is that we recognise our own worth  and value. However there is also a lot of humour and laughter in our  conversation. So you see, there is lots to say about Nigel, but he tells  us better in his own voice, which by the way is really beautiful  storyteller’s voice. So I hope you’ll enjoy this interview.

Links to this episode:

Homepage poets wall: https://www.poetswall.com/

YouTube channel: https://www.youtube.com/@TheWall-PoetswithParkinsons111

Get in touch with Nigel: nigel@poetswithparkinsons.com

Invitation to online “poets with Parkinson’s” events:

“Away in La La Land” – A 30 min Rock n Rhyme True Tale: https://www.poetswall.com/event-details-registration/away-in-la-la-land-a-30-min-rock-n-rhyme-true-tale

First ever GERMAN Open Mic Poetry: https://www.poetswall.com/event-details-registration/1-poesie-trifft-parkinson-abend-first-ever-german-open-mic-poetry

I appreciate your feedback on this podcast episode.

Feel free to send me an email: kontakt@jetzt-erst-recht.info

</itunes:summary>
      <itunes:episode>7</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
    </item>
    <item>
      <title>episode 5 - Stay present in the present with Elisabeth Ildal (30.10.2022)</title>
      <description><![CDATA[<p>Welcome to my podcast which I started 2  years ago because I was diagnosed with Parkinson’s at the age of 40.  Since then I have been looking out for people with positive stories.  Isn’t it strange that we remember negative stories easily while positive  ones seem hard to find? But actually there are so many encouraging and  positive stories out there that show us how people cope with life  despite Parkinson’s. And these wonderful stories I did not only find in  German speaking countries but also in many other places around theworld.  Today in my special series “Parkinson’s around the world“ I virtually  traveled to Denmark &nbsp;and met Elisabeth Ildal. You’ll hear it right away –  we had an incredible amount of fun during our interview and laughed a  lot, but we also focused on serious facts of Parkinson’s. Elisabeth has  been living with PD for almost 10 years and has overcome many challenges  during that time. In the beginning she hid the disease from nearly  everyone but later she spoke frankly from one day to the next and since  then she has been tirelessly involved in helping people with  Parkinson’s. She is a courageous, strong but above all fun-loving woman  and I am very happy that I can share her story with you today. Our  English is colorful and not perfect but that’s how I think life should  be! I hope you enjoy this interview.</p>
<p>If you want to learn more about Elisabeths numerous activities have a look at the following links:</p>
<ul><li><p><a href="https://www.ittffoundation.org/news/details/if-you-can-dream-it-you-can-do-it-elisabeth-ildal" rel="noopener noreferrer nofollow">https://www.ittffoundation.org/news/details/if-you-can-dream-it-you-can-do-it-elisabeth-ildal</a></p>
</li><li><p><a href="https://www.tv2bornholm.dk/artikel/parkinsonpatienter-spiller-bordtennis-paa-bornholm" rel="noopener noreferrer nofollow">https://www.tv2bornholm.dk/artikel/parkinsonpatienter-spiller-bordtennis-paa-bornholm</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=U25VRK7X-fM" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=U25VRK7X-fM</a></p>
</li><li><p><a href="https://tv2bornholm.dk/artikel/bordtennis-hjaelper-paa-parkinsons-sygdom" rel="noopener noreferrer nofollow">https://tv2bornholm.dk/artikel/bordtennis-hjaelper-paa-parkinsons-sygdom</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=zIjcoMgjqs4" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=zIjcoMgjqs4</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=GeWE0oJjT9w" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=GeWE0oJjT9w</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=6Qda0Z9JLXA" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=6Qda0Z9JLXA</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=0dg7ioNzC_U&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=0dg7ioNzC_U&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=_FYrf1LRXwo&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=2" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=_FYrf1LRXwo&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=2</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=cBqv5t5hPrc&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=4" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=cBqv5t5hPrc&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=4</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=ooUTFtYkAls&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=7" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=ooUTFtYkAls&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=7</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=DpjDQe0Fs9A" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=DpjDQe0Fs9A</a></p>
</li></ul>]]></description>
      <pubDate>Mon, 18 Sep 2023 15:15:00 +0200</pubDate>
      <link>https://cyehry.podcaster.de/download/episode_57_-_Stay_present_in_the_present_with_Elisabeth_Ildal(2).mp3?origin=feed</link>
      <guid isPermaLink="false">pod-83c2ec52e21d99bcb7423590e88</guid>
      <author>kontakt@jetzt-erst-recht.info (Kathrin Wersing)</author>
      <enclosure type="audio/mpeg" length="47415489" url="https://cyehry.podcaster.de/now-more-than-ever-by-kathrin-wersing/media/episode_57_-_Stay_present_in_the_present_with_Elisabeth_Ildal(2).mp3?origin=feed"/>
      <dc:creator>Kathrin Wersing</dc:creator>
      <content:encoded><![CDATA[<p>Welcome to my podcast which I started 2  years ago because I was diagnosed with Parkinson’s at the age of 40.  Since then I have been looking out for people with positive stories.  Isn’t it strange that we remember negative stories easily while positive  ones seem hard to find? But actually there are so many encouraging and  positive stories out there that show us how people cope with life  despite Parkinson’s. And these wonderful stories I did not only find in  German speaking countries but also in many other places around theworld.  Today in my special series “Parkinson’s around the world“ I virtually  traveled to Denmark &nbsp;and met Elisabeth Ildal. You’ll hear it right away –  we had an incredible amount of fun during our interview and laughed a  lot, but we also focused on serious facts of Parkinson’s. Elisabeth has  been living with PD for almost 10 years and has overcome many challenges  during that time. In the beginning she hid the disease from nearly  everyone but later she spoke frankly from one day to the next and since  then she has been tirelessly involved in helping people with  Parkinson’s. She is a courageous, strong but above all fun-loving woman  and I am very happy that I can share her story with you today. Our  English is colorful and not perfect but that’s how I think life should  be! I hope you enjoy this interview.</p>
<p>If you want to learn more about Elisabeths numerous activities have a look at the following links:</p>
<ul><li><p><a href="https://www.ittffoundation.org/news/details/if-you-can-dream-it-you-can-do-it-elisabeth-ildal" rel="noopener noreferrer nofollow">https://www.ittffoundation.org/news/details/if-you-can-dream-it-you-can-do-it-elisabeth-ildal</a></p>
</li><li><p><a href="https://www.tv2bornholm.dk/artikel/parkinsonpatienter-spiller-bordtennis-paa-bornholm" rel="noopener noreferrer nofollow">https://www.tv2bornholm.dk/artikel/parkinsonpatienter-spiller-bordtennis-paa-bornholm</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=U25VRK7X-fM" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=U25VRK7X-fM</a></p>
</li><li><p><a href="https://tv2bornholm.dk/artikel/bordtennis-hjaelper-paa-parkinsons-sygdom" rel="noopener noreferrer nofollow">https://tv2bornholm.dk/artikel/bordtennis-hjaelper-paa-parkinsons-sygdom</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=zIjcoMgjqs4" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=zIjcoMgjqs4</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=GeWE0oJjT9w" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=GeWE0oJjT9w</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=6Qda0Z9JLXA" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=6Qda0Z9JLXA</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=0dg7ioNzC_U&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=0dg7ioNzC_U&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=_FYrf1LRXwo&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=2" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=_FYrf1LRXwo&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=2</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=cBqv5t5hPrc&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=4" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=cBqv5t5hPrc&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=4</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=ooUTFtYkAls&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=7" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=ooUTFtYkAls&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=7</a></p>
</li><li><p><a href="https://www.youtube.com/watch?v=DpjDQe0Fs9A" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=DpjDQe0Fs9A</a></p>
</li></ul>]]></content:encoded>
      <slash:comments>0</slash:comments>
      <itunes:author>Kathrin Wersing</itunes:author>
      <itunes:duration>00:36:23</itunes:duration>
      <itunes:image href="https://files.pdcstrcdn.de/s/i/c916b9e3-5991-4ad5-b751-ed4d55cab085/Podcast_Titelbilder%286%29.jpg"/>
      <itunes:title>episode 5 - Stay present in the present</itunes:title>
      <itunes:subtitle>with Elisabeth Ildal (30.10.2022)</itunes:subtitle>
      <itunes:summary>Welcome to my podcast which I started 2  years ago because I was diagnosed with Parkinson’s at the age of 40.  Since then I have been looking out for people with positive stories.  Isn’t it strange that we remember negative stories easily while positive  ones seem hard to find? But actually there are so many encouraging and  positive stories out there that show us how people cope with life  despite Parkinson’s. And these wonderful stories I did not only find in  German speaking countries but also in many other places around theworld.  Today in my special series “Parkinson’s around the world“ I virtually  traveled to Denmark  and met Elisabeth Ildal. You’ll hear it right away –  we had an incredible amount of fun during our interview and laughed a  lot, but we also focused on serious facts of Parkinson’s. Elisabeth has  been living with PD for almost 10 years and has overcome many challenges  during that time. In the beginning she hid the disease from nearly  everyone but later she spoke frankly from one day to the next and since  then she has been tirelessly involved in helping people with  Parkinson’s. She is a courageous, strong but above all fun-loving woman  and I am very happy that I can share her story with you today. Our  English is colorful and not perfect but that’s how I think life should  be! I hope you enjoy this interview.

If you want to learn more about Elisabeths numerous activities have a look at the following links:

https://www.ittffoundation.org/news/details/if-you-can-dream-it-you-can-do-it-elisabeth-ildal

https://www.tv2bornholm.dk/artikel/parkinsonpatienter-spiller-bordtennis-paa-bornholm

https://www.youtube.com/watch?v=U25VRK7X-fM

https://tv2bornholm.dk/artikel/bordtennis-hjaelper-paa-parkinsons-sygdom

https://www.youtube.com/watch?v=zIjcoMgjqs4

https://www.youtube.com/watch?v=GeWE0oJjT9w

https://www.youtube.com/watch?v=6Qda0Z9JLXA

https://www.youtube.com/watch?v=0dg7ioNzC_U&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1

https://www.youtube.com/watch?v=_FYrf1LRXwo&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=2

https://www.youtube.com/watch?v=cBqv5t5hPrc&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=4

https://www.youtube.com/watch?v=ooUTFtYkAls&amp;list=PL5L2xv6Yv4xV2Fqxd6-I08A45HhksRFV1&amp;index=7

https://www.youtube.com/watch?v=DpjDQe0Fs9A

</itunes:summary>
      <itunes:episode>5</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
    </item>
    <item>
      <title>episode 3 - Tomorrow is a new day with Margie Alley (05.06.2022)</title>
      <description><![CDATA[<p>Welcome to my podcast. My name is Kathrin Wersing, I am 43 years old and I live in Germany. I started this podcast nearly 2 years ago because I was diagnosed with Parkinson’s and since then I have been collecting stories of people with PD who manage to live their life in a positive way and also stories of people who help those living with the disease. After I was able to talk to 40 inspiring people from Germany, Austria and Switzerland last year, my focus this year is on how Parkinson’s is seen and treated in other countries around the world. Though Parkinson’s is a serious disease and we all know the challenges, worries and fears on bad days, each of us also has strategies, resources, and helpful thoughts that we can pass on to others as a way to help. In my “Parkinson’s around the world” series, I’ve already spoken with people from Iceland and Uganda. Today, I’m traveling to the U.S. to meet Margie Alley, a great and inspiring woman who I had the pleasure to meet in person at a table tennis tournament in Germany a year ago.&nbsp; So I hope you enjoy this interview.</p>
<p>Links to this episode:</p>
<ul><li><p>Margie’s documentary GOTTA KEEP MOVING: <a href="https://www.youtube.com/watch?v=sYFMarC6tHc" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=sYFMarC6tHc</a></p>
</li><li><p>PingPongParkinson USA: <a href="https://www.pingpongparkinson.org/" rel="noopener noreferrer nofollow">https://www.pingpongparkinson.org/</a></p>
</li></ul><p>I appreciate your feedback on this podcast episode. Feel free to write to me: <a href="mailto:kontakt@jetzt-erst-recht.info" rel="noopener noreferrer nofollow">kontakt@jetzt-erst-recht.info</a></p>
]]></description>
      <pubDate>Sun, 17 Sep 2023 22:36:00 +0200</pubDate>
      <link>https://cyehry.podcaster.de/download/Folge_48_-_Tomorrow_is_a_new_day_with_Margie_Alley(1).mp3?origin=feed</link>
      <guid isPermaLink="false">pod-0a0fd40ae959488bfc62e19d07a8</guid>
      <author>kontakt@jetzt-erst-recht.info (Kathrin Wersing)</author>
      <enclosure type="audio/mpeg" length="82320461" url="https://cyehry.podcaster.de/now-more-than-ever-by-kathrin-wersing/media/Folge_48_-_Tomorrow_is_a_new_day_with_Margie_Alley(1).mp3?origin=feed"/>
      <dc:creator>Kathrin Wersing</dc:creator>
      <content:encoded><![CDATA[<p>Welcome to my podcast. My name is Kathrin Wersing, I am 43 years old and I live in Germany. I started this podcast nearly 2 years ago because I was diagnosed with Parkinson’s and since then I have been collecting stories of people with PD who manage to live their life in a positive way and also stories of people who help those living with the disease. After I was able to talk to 40 inspiring people from Germany, Austria and Switzerland last year, my focus this year is on how Parkinson’s is seen and treated in other countries around the world. Though Parkinson’s is a serious disease and we all know the challenges, worries and fears on bad days, each of us also has strategies, resources, and helpful thoughts that we can pass on to others as a way to help. In my “Parkinson’s around the world” series, I’ve already spoken with people from Iceland and Uganda. Today, I’m traveling to the U.S. to meet Margie Alley, a great and inspiring woman who I had the pleasure to meet in person at a table tennis tournament in Germany a year ago.&nbsp; So I hope you enjoy this interview.</p>
<p>Links to this episode:</p>
<ul><li><p>Margie’s documentary GOTTA KEEP MOVING: <a href="https://www.youtube.com/watch?v=sYFMarC6tHc" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=sYFMarC6tHc</a></p>
</li><li><p>PingPongParkinson USA: <a href="https://www.pingpongparkinson.org/" rel="noopener noreferrer nofollow">https://www.pingpongparkinson.org/</a></p>
</li></ul><p>I appreciate your feedback on this podcast episode. Feel free to write to me: <a href="mailto:kontakt@jetzt-erst-recht.info" rel="noopener noreferrer nofollow">kontakt@jetzt-erst-recht.info</a></p>
]]></content:encoded>
      <slash:comments>0</slash:comments>
      <itunes:author>Kathrin Wersing</itunes:author>
      <itunes:duration>00:34:17</itunes:duration>
      <itunes:image href="https://files.pdcstrcdn.de/s/i/3080c9fc-00e1-41d6-9351-b053536d02bb/Podcast_Titel%281%29.jpg"/>
      <itunes:title>episode 3 - Tomorrow is a new day</itunes:title>
      <itunes:subtitle>with Margie Alley (05.06.2022)</itunes:subtitle>
      <itunes:summary>Welcome to my podcast. My name is Kathrin Wersing, I am 43 years old and I live in Germany. I started this podcast nearly 2 years ago because I was diagnosed with Parkinson’s and since then I have been collecting stories of people with PD who manage to live their life in a positive way and also stories of people who help those living with the disease. After I was able to talk to 40 inspiring people from Germany, Austria and Switzerland last year, my focus this year is on how Parkinson’s is seen and treated in other countries around the world. Though Parkinson’s is a serious disease and we all know the challenges, worries and fears on bad days, each of us also has strategies, resources, and helpful thoughts that we can pass on to others as a way to help. In my “Parkinson’s around the world” series, I’ve already spoken with people from Iceland and Uganda. Today, I’m traveling to the U.S. to meet Margie Alley, a great and inspiring woman who I had the pleasure to meet in person at a table tennis tournament in Germany a year ago.  So I hope you enjoy this interview.

Links to this episode:

Margie’s documentary GOTTA KEEP MOVING: https://www.youtube.com/watch?v=sYFMarC6tHc

PingPongParkinson USA: https://www.pingpongparkinson.org/

I appreciate your feedback on this podcast episode. Feel free to write to me: kontakt@jetzt-erst-recht.info

</itunes:summary>
      <itunes:episode>3</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
    </item>
    <item>
      <title>episode 4 -  Find your superpower with Larry Gifford (07.08.2022)</title>
      <description><![CDATA[<p>Welcome to my podcast which is about living positively with Parkinson‘s disease. My name is Kathrin Wersing, I live in Germany and I started this podcast about 2 years ago because I was diagnosed with Parkinson’s disease at the age of 40 and I was looking for positive stories about PD. In my podcast I talk to experts: people who actually live with PD and their family members. I started with 50 inspiring people in Germany, Austria and Switzerland. This year, I am happy to welcome guests from all over the world to my podcast, so there are now some episodes in English language as well. And this is one of them! For today’s podcast interview, I virtually traveled to Canada and met the wonderful Larry Gifford. Larry is a professional talk radio director, passionate podcaster, and dedicated advocate for people with Parkinson’s. But most of all, he is a wonderful person with a lot of charm, humor and a big heart. So join me and meet Larry Gifford. I promise you won’t forget this interview!</p>
<p>Links to this episode:</p>
<ul><li><p>Website PD Avengers: <a href="https://www.pdavengers.com/" rel="noopener noreferrer nofollow">https://www.pdavengers.com/</a></p>
</li><li><p>Larrys Podcast “When life gives your Parkinson’s”: <a href="https://podcasts.apple.com/us/podcast/when-life-gives-you-parkinsons/id1404983468" rel="noopener noreferrer nofollow">https://podcasts.apple.com/us/podcast/when-life-gives-you-parkinsons/id1404983468</a></p>
</li><li><p>Film “The long road to hope”: <a href="https://www.youtube.com/watch?v=A6tbHSPTEUM" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=A6tbHSPTEUM</a></p>
</li><li><p>World-Parkinson-Congress:</p>
<ul><li><p>Main Website: <a href="https://wpc2023.org/" rel="noopener noreferrer nofollow">https://wpc2023.org/</a></p>
</li><li><p>Information about travel grants: <a href="https://wpc2023.org/page/TravelGrants" rel="noopener noreferrer nofollow">https://wpc2023.org/page/TravelGrants</a></p>
</li></ul></li><li><p>Book “Ending Parkinson’s disease”: <a href="https://www.amazon.com/Ending-Parkinsons-Disease-Prescription-Action/dp/1541724526" rel="noopener noreferrer nofollow">https://www.amazon.com/Ending-Parkinsons-Disease-Prescription-Action/dp/1541724526</a></p>
</li></ul><p>I appreciate your feedback on this podcast episode. Feel free to write to me: <a href="mailto:kontakt@jetzt-erst-recht.info" rel="noopener noreferrer nofollow">kontakt@jetzt-erst-recht.info</a></p>
]]></description>
      <pubDate>Sun, 17 Sep 2023 22:36:00 +0200</pubDate>
      <link>https://cyehry.podcaster.de/download/Special_episode_52_-Find_your_superpower_with_Larry_Gifford(1).mp3?origin=feed</link>
      <guid isPermaLink="false">pod-ed35608f1decbe9c5d18f8d6348</guid>
      <author>kontakt@jetzt-erst-recht.info (Kathrin Wersing)</author>
      <enclosure type="audio/mpeg" length="90074647" url="https://cyehry.podcaster.de/now-more-than-ever-by-kathrin-wersing/media/Special_episode_52_-Find_your_superpower_with_Larry_Gifford(1).mp3?origin=feed"/>
      <dc:creator>Kathrin Wersing</dc:creator>
      <content:encoded><![CDATA[<p>Welcome to my podcast which is about living positively with Parkinson‘s disease. My name is Kathrin Wersing, I live in Germany and I started this podcast about 2 years ago because I was diagnosed with Parkinson’s disease at the age of 40 and I was looking for positive stories about PD. In my podcast I talk to experts: people who actually live with PD and their family members. I started with 50 inspiring people in Germany, Austria and Switzerland. This year, I am happy to welcome guests from all over the world to my podcast, so there are now some episodes in English language as well. And this is one of them! For today’s podcast interview, I virtually traveled to Canada and met the wonderful Larry Gifford. Larry is a professional talk radio director, passionate podcaster, and dedicated advocate for people with Parkinson’s. But most of all, he is a wonderful person with a lot of charm, humor and a big heart. So join me and meet Larry Gifford. I promise you won’t forget this interview!</p>
<p>Links to this episode:</p>
<ul><li><p>Website PD Avengers: <a href="https://www.pdavengers.com/" rel="noopener noreferrer nofollow">https://www.pdavengers.com/</a></p>
</li><li><p>Larrys Podcast “When life gives your Parkinson’s”: <a href="https://podcasts.apple.com/us/podcast/when-life-gives-you-parkinsons/id1404983468" rel="noopener noreferrer nofollow">https://podcasts.apple.com/us/podcast/when-life-gives-you-parkinsons/id1404983468</a></p>
</li><li><p>Film “The long road to hope”: <a href="https://www.youtube.com/watch?v=A6tbHSPTEUM" rel="noopener noreferrer nofollow">https://www.youtube.com/watch?v=A6tbHSPTEUM</a></p>
</li><li><p>World-Parkinson-Congress:</p>
<ul><li><p>Main Website: <a href="https://wpc2023.org/" rel="noopener noreferrer nofollow">https://wpc2023.org/</a></p>
</li><li><p>Information about travel grants: <a href="https://wpc2023.org/page/TravelGrants" rel="noopener noreferrer nofollow">https://wpc2023.org/page/TravelGrants</a></p>
</li></ul></li><li><p>Book “Ending Parkinson’s disease”: <a href="https://www.amazon.com/Ending-Parkinsons-Disease-Prescription-Action/dp/1541724526" rel="noopener noreferrer nofollow">https://www.amazon.com/Ending-Parkinsons-Disease-Prescription-Action/dp/1541724526</a></p>
</li></ul><p>I appreciate your feedback on this podcast episode. Feel free to write to me: <a href="mailto:kontakt@jetzt-erst-recht.info" rel="noopener noreferrer nofollow">kontakt@jetzt-erst-recht.info</a></p>
]]></content:encoded>
      <slash:comments>0</slash:comments>
      <itunes:author>Kathrin Wersing</itunes:author>
      <itunes:duration>00:37:31</itunes:duration>
      <itunes:image href="https://files.pdcstrcdn.de/s/i/c3cd0ae6-1472-433e-af13-8311da938caf/Podcast_Titelbilder%285%29.jpg"/>
      <itunes:title>episode 4 -  Find your superpower</itunes:title>
      <itunes:subtitle>with Larry Gifford (07.08.2022)</itunes:subtitle>
      <itunes:summary>Welcome to my podcast which is about living positively with Parkinson‘s disease. My name is Kathrin Wersing, I live in Germany and I started this podcast about 2 years ago because I was diagnosed with Parkinson’s disease at the age of 40 and I was looking for positive stories about PD. In my podcast I talk to experts: people who actually live with PD and their family members. I started with 50 inspiring people in Germany, Austria and Switzerland. This year, I am happy to welcome guests from all over the world to my podcast, so there are now some episodes in English language as well. And this is one of them! For today’s podcast interview, I virtually traveled to Canada and met the wonderful Larry Gifford. Larry is a professional talk radio director, passionate podcaster, and dedicated advocate for people with Parkinson’s. But most of all, he is a wonderful person with a lot of charm, humor and a big heart. So join me and meet Larry Gifford. I promise you won’t forget this interview!

Links to this episode:

Website PD Avengers: https://www.pdavengers.com/

Larrys Podcast “When life gives your Parkinson’s”: https://podcasts.apple.com/us/podcast/when-life-gives-you-parkinsons/id1404983468

Film “The long road to hope”: https://www.youtube.com/watch?v=A6tbHSPTEUM

World-Parkinson-Congress:

Main Website: https://wpc2023.org/

Information about travel grants: https://wpc2023.org/page/TravelGrants

Book “Ending Parkinson’s disease”: https://www.amazon.com/Ending-Parkinsons-Disease-Prescription-Action/dp/1541724526

I appreciate your feedback on this podcast episode. Feel free to write to me: kontakt@jetzt-erst-recht.info

</itunes:summary>
      <itunes:episode>4</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
    </item>
    <item>
      <title>episode 2 - Parkinson&amp;#039;s si Buko with Hannington Kabugo (03.04.2022)</title>
      <description><![CDATA[<p>Welcome to a new special episode of "Parkinson's around the world". In this series, my focus is on how Parkinson's is seen and treated in other countries around the world. This episode, I have to be honest, has touched me the most of all so far: Imagine you have Parkinson's, imagine you live in one of the poorest countries on earth, imagine people around you think you are jinxed if you have Parkinson's and they dare not go near you and banish you. I met Hannington Kabugo from Uganda. He told me the story of his mother, who had Parkinson's disease. Her painful fate led Hannington to found an organization in Uganda that cares for people with Parkinson's disease. Travel with me to Uganda in this podcast and meet a truly remarkable man.</p>
<p>Links to this episode:</p>
<ul><li><p>Homepage of Sherryl Klinglhofer's partner organization in the USA: <a href="https://parkinsonssibuko.org/" rel="noopener noreferrer nofollow">https://parkinsonssibuko.org/</a> There you can also find a direct link to donate via PayPal in favor of Parkinson's si Buko USA. All employees work on a voluntary basis and all donations go directly to Uganda.</p>
</li><li><p>Contact Hannington Kabugo</p>
<ul><li><p>via facebook: <a href="https://www.facebook.com/kabugo.hannington.330" rel="noopener noreferrer nofollow">https://www.facebook.com/kabugo.hannington.330</a></p>
</li><li><p>via E-Mail: <a href="mailto:hannyug@hotmail.com" rel="noopener noreferrer nofollow">hannyug@hotmail.com</a></p>
</li></ul></li></ul><p>Thank you very much for your donation and support</p>
]]></description>
      <pubDate>Sun, 17 Sep 2023 21:37:00 +0200</pubDate>
      <link>https://cyehry.podcaster.de/download/episode_45_-_Parkinson-s_si_Buko_(ENGLISH)_-_with_Hannington_Kabugo(1).mp3?origin=feed</link>
      <guid isPermaLink="false">pod-1057a91b524a98967618bff5a68</guid>
      <author>kontakt@jetzt-erst-recht.info (Kathrin Wersing)</author>
      <enclosure type="audio/mpeg" length="102891298" url="https://cyehry.podcaster.de/now-more-than-ever-by-kathrin-wersing/media/episode_45_-_Parkinson-s_si_Buko_(ENGLISH)_-_with_Hannington_Kabugo(1).mp3?origin=feed"/>
      <dc:creator>Kathrin Wersing</dc:creator>
      <content:encoded><![CDATA[<p>Welcome to a new special episode of "Parkinson's around the world". In this series, my focus is on how Parkinson's is seen and treated in other countries around the world. This episode, I have to be honest, has touched me the most of all so far: Imagine you have Parkinson's, imagine you live in one of the poorest countries on earth, imagine people around you think you are jinxed if you have Parkinson's and they dare not go near you and banish you. I met Hannington Kabugo from Uganda. He told me the story of his mother, who had Parkinson's disease. Her painful fate led Hannington to found an organization in Uganda that cares for people with Parkinson's disease. Travel with me to Uganda in this podcast and meet a truly remarkable man.</p>
<p>Links to this episode:</p>
<ul><li><p>Homepage of Sherryl Klinglhofer's partner organization in the USA: <a href="https://parkinsonssibuko.org/" rel="noopener noreferrer nofollow">https://parkinsonssibuko.org/</a> There you can also find a direct link to donate via PayPal in favor of Parkinson's si Buko USA. All employees work on a voluntary basis and all donations go directly to Uganda.</p>
</li><li><p>Contact Hannington Kabugo</p>
<ul><li><p>via facebook: <a href="https://www.facebook.com/kabugo.hannington.330" rel="noopener noreferrer nofollow">https://www.facebook.com/kabugo.hannington.330</a></p>
</li><li><p>via E-Mail: <a href="mailto:hannyug@hotmail.com" rel="noopener noreferrer nofollow">hannyug@hotmail.com</a></p>
</li></ul></li></ul><p>Thank you very much for your donation and support</p>
]]></content:encoded>
      <slash:comments>0</slash:comments>
      <itunes:author>Kathrin Wersing</itunes:author>
      <itunes:duration>00:42:52</itunes:duration>
      <itunes:image href="https://files.pdcstrcdn.de/s/i/8da36fbe-6545-4ba9-bd61-000381192d9c/Podcast_Titel.jpg"/>
      <itunes:title>episode 2 - Parkinson&amp;#039;s si Buko</itunes:title>
      <itunes:subtitle>with Hannington Kabugo (03.04.2022)</itunes:subtitle>
      <itunes:summary>Welcome to a new special episode of "Parkinson's around the world". In this series, my focus is on how Parkinson's is seen and treated in other countries around the world. This episode, I have to be honest, has touched me the most of all so far: Imagine you have Parkinson's, imagine you live in one of the poorest countries on earth, imagine people around you think you are jinxed if you have Parkinson's and they dare not go near you and banish you. I met Hannington Kabugo from Uganda. He told me the story of his mother, who had Parkinson's disease. Her painful fate led Hannington to found an organization in Uganda that cares for people with Parkinson's disease. Travel with me to Uganda in this podcast and meet a truly remarkable man.

Links to this episode:

Homepage of Sherryl Klinglhofer's partner organization in the USA: https://parkinsonssibuko.org/ There you can also find a direct link to donate via PayPal in favor of Parkinson's si Buko USA. All employees work on a voluntary basis and all donations go directly to Uganda.

Contact Hannington Kabugo

via facebook: https://www.facebook.com/kabugo.hannington.330

via E-Mail: hannyug@hotmail.com

Thank you very much for your donation and support

</itunes:summary>
      <itunes:episode>2</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
    </item>
    <item>
      <title>episode 1 - All you need is Ping Pong, Special from the PPP German Open (18.09.2021)​</title>
      <description><![CDATA[<p>Welcome to my Podcast and to this special  English episode. In my podcast I want to share positive stories about  life with Parkinson’s Disease and so I talk to many inspiring people  with exciting life stories who manage to enjoy their lives – despite  Parkinson’s. Usually this podcast is in German language but today there  is a special episode for my English speaking friends who I had the  pleasure to meet at the PingPongParkinson German Open in Nordhorn in  early September this year. People from 12 nations took part in the  tournament and despite Parkinson’s, they were fantastic table tennis  players and spread a lot of passion, joy and enthusiasm. This episode is  about PingPongParkinson – a worldwide movement that offers table tennis  for people with Parkinson’s disease. Playing table tennis can help  improving symptoms and slow down progression. But most of all – it’s  fun! So, join me and meet some great people from all over the world who  share the same dream – they all love to play table tennis. Believe me,  after listening to this episode you will want to play table tennis too.  Here are some links to find a group in your country (I would be  delighted to add more countries – please get in touch when you have  further information)</p>
<ul><li><p>USA: <a href="https://www.pingpongparkinson.org" rel="noopener noreferrer nofollow">www.pingpongparkinson.org</a></p>
</li><li><p>Germany: <a href="https://www.pingpongparkinson.de" rel="noopener noreferrer nofollow">www.pingpongparkinson.de</a></p>
</li><li><p>UK: Parkinson Table Tennis UK <a href="https://goneactive.co.uk/tt" rel="noopener noreferrer nofollow">https://goneactive.co.uk/tt</a></p>
</li></ul><p>Watch these inspiring videos:</p>
<ul><li><p><a href="https://youtu.be/sYFMarC6tHc" rel="noopener noreferrer nofollow">Margie Alley: https://youtu.be/sYFMarC6tHc</a></p>
</li><li><p>Nenad Bach: <a href="https://vimeo.com/422138964" rel="noopener noreferrer nofollow">https://vimeo.com/422138964</a>, <a href="https://vimeo.com/309645164" rel="noopener noreferrer nofollow">https://vimeo.com/309645164</a></p>
</li></ul><p>Thanks for listening. I would love to hear from you: <a href="mailto:kontakt@jetzt-erst-recht.info" rel="noopener noreferrer nofollow">kontakt@jetzt-erst-recht.info</a></p>
<p>My website: <a href="https://www.jetzt-erst-recht.info" rel="noopener noreferrer nofollow">www.jetzt-erst-recht.info</a></p>
]]></description>
      <pubDate>Sun, 17 Sep 2023 21:23:00 +0200</pubDate>
      <link>https://cyehry.podcaster.de/download/Special_English_Episode_No-30_-_All_you_need_is_PingPong(1).mp3?origin=feed</link>
      <guid isPermaLink="false">pod-809fcbbbf62e98bc5171c536083</guid>
      <author>kontakt@jetzt-erst-recht.info (Kathrin Wersing)</author>
      <enclosure type="audio/mpeg" length="29148613" url="https://cyehry.podcaster.de/now-more-than-ever-by-kathrin-wersing/media/Special_English_Episode_No-30_-_All_you_need_is_PingPong(1).mp3?origin=feed"/>
      <dc:creator>Kathrin Wersing</dc:creator>
      <content:encoded><![CDATA[<p>Welcome to my Podcast and to this special  English episode. In my podcast I want to share positive stories about  life with Parkinson’s Disease and so I talk to many inspiring people  with exciting life stories who manage to enjoy their lives – despite  Parkinson’s. Usually this podcast is in German language but today there  is a special episode for my English speaking friends who I had the  pleasure to meet at the PingPongParkinson German Open in Nordhorn in  early September this year. People from 12 nations took part in the  tournament and despite Parkinson’s, they were fantastic table tennis  players and spread a lot of passion, joy and enthusiasm. This episode is  about PingPongParkinson – a worldwide movement that offers table tennis  for people with Parkinson’s disease. Playing table tennis can help  improving symptoms and slow down progression. But most of all – it’s  fun! So, join me and meet some great people from all over the world who  share the same dream – they all love to play table tennis. Believe me,  after listening to this episode you will want to play table tennis too.  Here are some links to find a group in your country (I would be  delighted to add more countries – please get in touch when you have  further information)</p>
<ul><li><p>USA: <a href="https://www.pingpongparkinson.org" rel="noopener noreferrer nofollow">www.pingpongparkinson.org</a></p>
</li><li><p>Germany: <a href="https://www.pingpongparkinson.de" rel="noopener noreferrer nofollow">www.pingpongparkinson.de</a></p>
</li><li><p>UK: Parkinson Table Tennis UK <a href="https://goneactive.co.uk/tt" rel="noopener noreferrer nofollow">https://goneactive.co.uk/tt</a></p>
</li></ul><p>Watch these inspiring videos:</p>
<ul><li><p><a href="https://youtu.be/sYFMarC6tHc" rel="noopener noreferrer nofollow">Margie Alley: https://youtu.be/sYFMarC6tHc</a></p>
</li><li><p>Nenad Bach: <a href="https://vimeo.com/422138964" rel="noopener noreferrer nofollow">https://vimeo.com/422138964</a>, <a href="https://vimeo.com/309645164" rel="noopener noreferrer nofollow">https://vimeo.com/309645164</a></p>
</li></ul><p>Thanks for listening. I would love to hear from you: <a href="mailto:kontakt@jetzt-erst-recht.info" rel="noopener noreferrer nofollow">kontakt@jetzt-erst-recht.info</a></p>
<p>My website: <a href="https://www.jetzt-erst-recht.info" rel="noopener noreferrer nofollow">www.jetzt-erst-recht.info</a></p>
]]></content:encoded>
      <slash:comments>0</slash:comments>
      <itunes:author>Kathrin Wersing</itunes:author>
      <itunes:duration>00:21:50</itunes:duration>
      <itunes:image href="https://files.pdcstrcdn.de/s/i/368cb18b-29f0-42ec-a2cb-b817837cb46c/IMG_9473%281%29.jpg"/>
      <itunes:title>episode 1 - All you need is Ping Pong</itunes:title>
      <itunes:subtitle>Special from the PPP German Open (18.09.2021)​</itunes:subtitle>
      <itunes:summary>Welcome to my Podcast and to this special  English episode. In my podcast I want to share positive stories about  life with Parkinson’s Disease and so I talk to many inspiring people  with exciting life stories who manage to enjoy their lives – despite  Parkinson’s. Usually this podcast is in German language but today there  is a special episode for my English speaking friends who I had the  pleasure to meet at the PingPongParkinson German Open in Nordhorn in  early September this year. People from 12 nations took part in the  tournament and despite Parkinson’s, they were fantastic table tennis  players and spread a lot of passion, joy and enthusiasm. This episode is  about PingPongParkinson – a worldwide movement that offers table tennis  for people with Parkinson’s disease. Playing table tennis can help  improving symptoms and slow down progression. But most of all – it’s  fun! So, join me and meet some great people from all over the world who  share the same dream – they all love to play table tennis. Believe me,  after listening to this episode you will want to play table tennis too.  Here are some links to find a group in your country (I would be  delighted to add more countries – please get in touch when you have  further information)

USA: www.pingpongparkinson.org

Germany: www.pingpongparkinson.de

UK: Parkinson Table Tennis UK https://goneactive.co.uk/tt

Watch these inspiring videos:

Margie Alley: https://youtu.be/sYFMarC6tHc

Nenad Bach: https://vimeo.com/422138964, https://vimeo.com/309645164

Thanks for listening. I would love to hear from you: kontakt@jetzt-erst-recht.info

My website: www.jetzt-erst-recht.info

</itunes:summary>
      <itunes:episode>1</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:season>1</itunes:season>
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