Cathy Bowen's guest appearances

Cathy Bowen

Staying Connected

PodChatLive - Live Podiatry Discussion

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In this episode we were joined by Prof Cathy Bowen (Lead of the Foot &amp; Ankle Research programme at Southampton University, Chair of the Research Committee for the Royal College of Podiatry, and Editor-in-Chief for JFAR) to talk about the timeline of a journal article, from the moment you think you have an idea for one, until the moment you are reading it in black and white. How do you choose what journal to submit to? What's the deal with ethical approval? How can you maximise your chances of not getting rejected? What does the peer review process look like? All this information and more.

In this episode we were joined by Prof Cathy Bowen (Lead of the Foot &amp; Ankle Research programme at Southampton University, Chair of the Research Committee for the Royal College of Podiatry, and Editor-in-Chief for JFAR) to talk about the timeline of a journal article, from the moment you think you have an idea for one, until the moment you are reading it in black and white. How do you choose what journal to submit to? What's the deal with ethical approval? How can you maximise your chances of not getting rejected? What does the peer review process look like? All this information and more.

PodChatLive Episode 98 with Cathy Bowen [Getting Published in a Journal]

Cathy Bowen tells us about her son, David Daniel Bowen III, and the colostomy reversal that ultimately took his life in 1996 at the age of 14, due to medical mismanagement and the hospital’s lack of knowledge about Vascular Ehlers-Danlos Syndrome (VEDS). Dave’s death left Cathy an empty shell, and she dealt with his loss by putting the love she had for her son towards others with VEDS. She had also made Dave a promise, that this would be her lifelong mission. Shortly after his death, she started advocating for people with VEDS with other mothers. She worked with the EDS National Foundation (now known as the EDS Society) and opened a local branch in New Jersey.  A few years later she co-founded EDS Today, which began as a newsletter for people in the EDS community sharing news and publications about all types of EDS. She was also a member of the original VEDS yahoo email support group back in 1996, which is now the VEDS Facebook group. Read more about Dave and Cathy’s story, and the Bowen story, here: http://edstoday.org/david-daniel-bowen-iii/ You can also read Dave’s poem, which was read on this podcast, here: https://fibromusculardysplasia.blogspot.com/2013/12/today-i-want-to-share-with-you.html  Find more information about the VEDS Collaborative Natural History Study and enroll at https://redcap.iths.org/surveys/?s=LTWWDAC3XJ  If you would like to share your story with VEDS on this podcast, visit https://translucentone.blog/contact/. I look forward to hearing from you! Find more information about VEDS, including support groups and medical webinars, at TheVEDSMovement.org. This podcast is not associated with The VEDS Movement or The Marfan Foundation. Find the full disclaimer at translucentone.blog. 

Cathy Bowen tells us about her son, David Daniel Bowen III, and the colostomy reversal that ultimately took his life in 1996 at the age of 14, due to medical mismanagement and the hospital’s lack of knowledge about Vascular Ehlers-Danlos Syndrome (VEDS). Dave’s death left Cathy an empty shell, and she dealt with his loss by putting the love she had for her son towards others with VEDS. She had also made Dave a promise, that this would be her lifelong mission. Shortly after his death, she started advocating for people with VEDS with other mothers. She worked with the EDS National Foundation (now known as the EDS Society) and opened a local branch in New Jersey.  A few years later she co-founded EDS Today, which began as a newsletter for people in the EDS community sharing news and publications about all types of EDS. She was also a member of the original VEDS yahoo email support group back in 1996, which is now the VEDS Facebook group. Read more about Dave and Cathy’s story, and the Bowen story, here: <a href="http://edstoday.org/david-daniel-bowen-iii/" rel="nofollow" target="_blank">http://edstoday.org/david-daniel-bowen-iii/</a> You can also read Dave’s poem, which was read on this podcast, here: <a href="https://fibromusculardysplasia.blogspot.com/2013/12/today-i-want-to-share-with-you.html" rel="nofollow" target="_blank">https://fibromusculardysplasia.blogspot.com/2013/12/today-i-want-to-share-with-you.html</a> Find more information about the VEDS Collaborative Natural History Study and enroll at<a href="https://redcap.iths.org/surveys/?s=LTWWDAC3XJ" rel="nofollow" target="_blank"> https://redcap.iths.org/surveys/?s=LTWWDAC3XJ</a> If you would like to share your story with VEDS on this podcast, visit <a href="https://translucentone.blog/contact/" rel="nofollow" target="_blank">https://translucentone.blog/contact/</a>. I look forward to hearing from you! Find more information about VEDS, including support groups and medical webinars, at <a href="http://TheVEDSMovement.org" rel="nofollow" target="_blank">TheVEDSMovement.org</a>. This podcast is not associated with The VEDS Movement or The Marfan Foundation. Find the full disclaimer at translucentone.blog.