{"id":825,"date":"2016-03-22T12:29:34","date_gmt":"2016-03-22T12:29:34","guid":{"rendered":"https:\/\/chistaging.wordpress.com\/?page_id=825"},"modified":"2021-06-28T19:37:53","modified_gmt":"2021-06-28T19:37:53","slug":"chi-trustees","status":"publish","type":"page","link":"https:\/\/childhealthinternational.org\/staging\/chi-trustees\/","title":{"rendered":"Meet the team"},"content":{"rendered":"\n
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Child Health International is run entirely by volunteers and medical professionals who give their time and expertise to ensure children and young adults living cystic fibrosis receive the best possible care, no matter where they live. Find out more about our team below. <\/p>\n\n\n\n

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Dr Chris Rolles <\/strong>
President<\/strong><\/p>\n\n\n\n

\"\"<\/figure><\/div>\n\n\n\n

Dr.\u00a0Chris\u00a0Rolles\u00a0is a retired paediatric specialist in Cystic Fibrosis who led the medical team from University Hospital Southampton in CHI\u2019s first major project (1993 \u2013 1996). This had a large impact on the treatment of CF in Russia, and has provided a framework for CHI’s future work. Chris is married with 4 sons and lives in lives in Southampton.<\/p>\n<\/div><\/div>\n<\/div>\n\n\n\n

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David Wilford<\/strong>
Chairman<\/strong><\/p>\n\n\n\n

\"David<\/figure><\/div>\n\n\n\n

David is a retired consultant with >45 years\u2019 experience in banking focusing on implementation and compliance with PRA, FCA and European regulatory requirements, governance frameworks and credit and legal risk management systems and procedures. He is married with two children (one with CF) and enjoys scuba diving.<\/p>\n<\/div>\n\n\n\n

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Dr Julian Legg<\/strong>
Trustee<\/strong> and Medical Consultant<\/strong><\/p>\n\n\n\n

\"\"<\/figure><\/div>\n\n\n\n

Julian qualified from Cambridge University in 1990, and has subsequently worked and trained across Birmingham Children’s hospital, St George’s University Hospital, Great Ormond Street Hospital, Southampton University. and the Children’s Hospital in Perth, West Australia. He now works as a consultant at Southampton.<\/p>\n<\/div>\n<\/div>\n\n\n\n

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Michael Ridgway<\/strong> <\/strong>
Trustee<\/strong><\/p>\n\n\n\n

\"Michael<\/figure><\/div>\n\n\n\n

Son of the founders of the charity, Roy and Dorothea Ridgway, Michael has been a trustee for many years. He is a one-time actor and self-employed carpenter. He has 4 grown-up children and lives in London. In 2005 he completed a sponsored cycle for CHI from Lands End to John O\u2019Groats and in 2019 cycled from Southampton to Paris!<\/p>\n<\/div><\/div>\n<\/div>\n\n\n\n

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Dr Mary Carroll<\/strong><\/strong>
Trustee<\/strong> and Medical Advisor<\/strong><\/p>\n\n\n\n

\"\"<\/figure><\/div>\n\n\n\n

Mary is a consultant in respiratory medicine at Southampton University Hospital, where she heads the Adult CF service. She is involved in testing new treatments for people with CF. Her work has contributed to the development of nasal ventilation techniques and an increased understanding of the role of nebulised heparin in thinning sputum for easier expulsion. <\/p>\n<\/div>\n\n\n\n

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Kerry Rait<\/strong>
Trustee<\/strong> and Communications<\/strong> Lead<\/strong><\/p>\n\n\n\n

\"\"<\/figure><\/div>\n\n\n\n

Kerry has a background in biogeochemical research, published under her maiden name, Dr Kerry Dinsmore, and now works as a chemical pollution expert for environmental charity, Fidra. She joined CHI in 2020, motivated by the loss of her son, Finn, who died from complications resulting from cystic fibrosis. Kerry is now Director of Communications for CHI.<\/p>\n<\/div><\/div>\n<\/div>\n<\/div>\n\n\n\n

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Judi Maddison<\/strong><\/strong>
Trustee<\/strong><\/p>\n\n\n\n

\"Judi<\/figure>\n\n\n\n

Judi is a Paediatric Cystic Fibrosis Nurse Specialist, working at Southampton’s Children’s Hospital. She trained at Great Ormond\u00a0Street Hospital and Charing Cross Hospital, moving to Southampton shortly after. Judi became interested in working with children with CF whilst working\u00a0on a medical unit and it has remained a passion ever since.\u00a0<\/p>\n<\/div>\n\n\n\n

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Tracey Daniels<\/strong><\/strong>
Trustee<\/strong><\/p>\n\n\n\n

\"Tracey<\/figure><\/div>\n\n\n\n

Tracey is a physiotherapist and research fellow at the York and Hull adult CF centre.  Tracey has worked with adults and children with CF for around the last 20 years in a number of UK CF centres.  Within CHI, Tracey provides a link to the allied health professions such as physiotherapists in order to best support our partnership working model.<\/p>\n<\/div>\n\n\n\n

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Tony Wolstenholme<\/strong>
Project Manager<\/strong><\/strong><\/strong><\/p>\n\n\n\n

\"\"<\/figure><\/div>\n\n\n\n

Tony is a retired naval officer and diplomat, and is a fluent Russian speaker. Tony is a previous trustee and ex-chairman of Child Health International and has rejoined the charity to lead CHI’s work in Russia.\u00a0<\/p>\n<\/div>\n<\/div>\n\n\n\n

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Child Health International is also proud to work with volunteer medical professionals from:<\/h2>\n\n\n\n

The Royal Brompton Hospital Adult Cystic Fibrosis Centre<\/a>
The University Hospital Southampton <\/a>
Birmingham Children\u2019s Hospital<\/a><\/p>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

Child Health International is run entirely by volunteers and medical professionals who give their time and expertise to ensure children and young adults living cystic fibrosis receive the best possible care, no matter where they live. Find out more about our team below. Dr Chris Rolles President Dr.\u00a0Chris\u00a0Rolles\u00a0is a retired paediatric specialist in Cystic Fibrosis who led the medical team … <\/p>\n","protected":false},"author":3,"featured_media":1492,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_mi_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"yoast_head":"\nMeet the team - Child Health International<\/title>\n<meta name=\"description\" content=\"Child Health International is run entirely by volunteers and medical professionals who give their time and expertise to ensure children and young adults living cystic fibrosis receive the best possible care, no matter where they live. 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