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**29802

**?xml version="1.0" encoding="UTF-8"?> feed xmlns:yt="http://www.youtube.com/xml/schemas/2015" xmlns:media="http://search.yahoo.com/mrss/" xmlns="http://www.w3.org/2005/Atom"> link rel="self" href="http://www.youtube.com/feeds/videos.xml?channel_id=UCiDkfLrwkQyRur8pXZbJWiQ"/> id>yt:channel:iDkfLrwkQyRur8pXZbJWiQ/id> yt:channelId>iDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>stepscharity/title> link rel="alternate" href="https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2010-02-02T13:48:05+00:00/published> entry> id>yt:video:Xmhh17Cx5rE/id> yt:videoId>Xmhh17Cx5rE/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Adults who have, or do, experience symptoms associated with their childhood Clubfoot./title> link rel="alternate" href="https://www.youtube.com/watch?v=Xmhh17Cx5rE"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2024-08-21T13:38:15+00:00/published> updated>2024-09-25T05:11:12+00:00/updated> media:group> media:title>Adults who have, or do, experience symptoms associated with their childhood Clubfoot./media:title> media:content url="https://www.youtube.com/v/Xmhh17Cx5rE?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i1.ytimg.com/vi/Xmhh17Cx5rE/hqdefault.jpg" width="480" height="360"/> media:description>Clubfoot, also known as congenital talipes equinovarus (CTEV), is a condition present at birth where one or both feet are turned, often inward and downward. While it is primarily seen as a childhood condition, many adults who were treated in childhood may experience signs and symptoms as they grow older. These changes can present challenges, particularly in finding the right support and resources. In this insightful webinar, we bring together three adults with lived experiences of clubfoot and clinical expert Nat Pahiar. Our panel discusses the most common questions and concerns about the impact of clubfoot into adulthood. Watch the recorded webinar to gain valuable insights and share it with others who may benefit. For additional support, visit the Steps website at www.stepsworldwide.org./media:description> media:community> media:starRating count="10" average="5.00" min="1" max="5"/> media:statistics views="262"/> /media:community> /media:group> /entry> entry> id>yt:video:Rf3h7IjXB5g/id> yt:videoId>Rf3h7IjXB5g/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Developmental Dysplasia of the Hip an introduction/title> link rel="alternate" href="https://www.youtube.com/watch?v=Rf3h7IjXB5g"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2024-06-06T19:12:21+00:00/published> updated>2024-10-28T21:11:08+00:00/updated> media:group> media:title>Developmental Dysplasia of the Hip an introduction/media:title> media:content url="https://www.youtube.com/v/Rf3h7IjXB5g?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i3.ytimg.com/vi/Rf3h7IjXB5g/hqdefault.jpg" width="480" height="360"/> media:description>Developmental Dysplasia of the Hip (DDH) has many names; Clicky Hip, congenital dislocation of the hip (CDH), Hip dysplasia and more. It is a spectrum of abnormalities that affect the hip joint, ranging from immature hip development, through to complete hip dislocation. Treatments focus on, where possible, getting the ball back into the cup (the head of the femur bone into the hip acetabulum), often through the use of a Pavlik harness, or a Spica cast. Understanding the different types of DDH, how it is diagnosed and treated, and what current research is underway at the University of Liverpool, can help you better understand your child's diagnosis. In this informative webinar, our esteemed speaker, Joanna Craven, an orthopaedic registrar (doctor) who is currently undertaking a PhD with the University of Liverpool and Alder Hey Children's Hospital, shares her knowledge of the topic. Watch the recorded webinar to gain insights from our speaker and feel free to share it with others who may benefit from this knowledge. Also, use the QR code at the end to sign up and support Joanna's research going forward. If you would like to sign up to participate in her research please follow this link: https://docs.google.com/forms/d/1duH7hJw5AtZUEYTbWetVGancZisBP2aegKRgHsOTUnk/edit If you want to know more, Subscribe to the YouTube Channel or come and visit us at https://www.stepsworldwide.org/media:description> media:community> media:starRating count="2" average="5.00" min="1" max="5"/> media:statistics views="103"/> /media:community> /media:group> /entry> entry> id>yt:video:s-c0jjeHCkY/id> yt:videoId>s-c0jjeHCkY/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Perthes Disease - The Journey into Adulthood/title> link rel="alternate" href="https://www.youtube.com/watch?v=s-c0jjeHCkY"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2023-11-11T21:21:51+00:00/published> updated>2024-08-22T11:17:44+00:00/updated> media:group> media:title>Perthes Disease - The Journey into Adulthood/media:title> media:content url="https://www.youtube.com/v/s-c0jjeHCkY?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i4.ytimg.com/vi/s-c0jjeHCkY/hqdefault.jpg" width="480" height="360"/> media:description>Perthes Disease (Legg-Calve-Perthes Disease) manifests in childhood, and this is the primary focus of treatment. However, for some sufferers, the shape in which the joint heals and the consequences of having had Perthes Disease linger into adulthood. Understanding the impact of treatment in childhood and how that may be linked to causes of discomfort and changes in movement becomes crucial to support interventions beyond the childhood years. In this informative webinar, journey through the intricacies of orthopaedics with our esteemed speaker, Nigel Kiely, a trailblazer in understanding Perthes Disease. Graduating from Nottingham University Medical School in 1991, Nigel dedicated his career to delivering comprehensive care. Nigel Kiely is a Consultant at the Robert Jones and Agnes Hunt Orthopaedic Hospital since January 2004, specialising in both Childrenâ€™s and Adult Orthopaedics. From weekly general clinics to specialized sessions, Nigel offers invaluable insights across a spectrum of conditions, making this video a valuable resource for anyone seeking a deeper understanding of this condition. Watch the recorded webinar to gain insights from these esteemed speakers and feel free to share it with others who may benefit from this knowledge. If you want to know more, Subscribe to the YouTube Channel or come and visit us at https://www.stepsworldwide.org/media:description> media:community> media:starRating count="12" average="5.00" min="1" max="5"/> media:statistics views="744"/> /media:community> /media:group> /entry> entry> id>yt:video:lCqSRAtkkAI/id> yt:videoId>lCqSRAtkkAI/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Perthes Disease in Childhood - An Introduction/title> link rel="alternate" href="https://www.youtube.com/watch?v=lCqSRAtkkAI"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2023-11-08T09:48:43+00:00/published> updated>2024-09-16T10:41:07+00:00/updated> media:group> media:title>Perthes Disease in Childhood - An Introduction/media:title> media:content url="https://www.youtube.com/v/lCqSRAtkkAI?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i1.ytimg.com/vi/lCqSRAtkkAI/hqdefault.jpg" width="480" height="360"/> media:description>Perthes Disease, also known as Legg-Calve-Perthes Disease, is a rare childhood condition that affects the hip joint. It occurs when the blood supply to the femoral head, the "ball" part of the hip joint, is disrupted, leading to a temporary interruption of blood flow. This, in turn, causes a lack of oxygen and nutrients to reach the bone, resulting in the death of bone cells and the gradual degeneration of the hip joint. Over time, the body attempts to repair the damage by forming new bone, but during this healing process, the hip may become deformed, leading to pain, a limp, and a limited range of motion. Perthes Disease typically affects children between the ages of 4 and 8, with a higher incidence in boys than girls. In this informative webinar, we were fortunate to have two distinguished experts sharing their expertise and some exciting news about the research happening right now in the UK. Dr. Daniel Perry, a Consultant Children's Orthopaedic Surgeon at Alder Hey Childrenâ€™s Hospital in Liverpool, is known for his groundbreaking research in children's trauma and orthopaedics. He discussed key aspects of Perthes Disease, making this video an invaluable resource. We were also joined by Adam Galloway, a Physiotherapist with a specialist interest in Children's Orthopaedics. Adam has been working in Leeds since 2013 and is currently a clinical academic. At time of recording he is completing a HEE/NIHR Pre-Doctoral Clinical Academic Fellowship, which focuses on a rare hip disease in children called Perthes. The combined expertise of Dr. Perry and Adam Galloway during the webinar provided comprehensive insights into Perthes Disease, making this video a valuable resource for anyone seeking a deeper understanding of this condition. Watch the recorded webinar to gain insights from these esteemed speakers and feel free to share it with others who may benefit from this knowledge. If you want to know more, Subscribe to the YouTube Channel or come and visit us at https://www.stepsworldwide.org/media:description> media:community> media:starRating count="10" average="5.00" min="1" max="5"/> media:statistics views="691"/> /media:community> /media:group> /entry> entry> id>yt:video:aLjsnpqH0_k/id> yt:videoId>aLjsnpqH0_k/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>StepIn Camps - for children with lower limb conditions and their families/title> link rel="alternate" href="https://www.youtube.com/watch?v=aLjsnpqH0_k"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2022-03-21T12:59:57+00:00/published> updated>2024-08-23T08:02:48+00:00/updated> media:group> media:title>StepIn Camps - for children with lower limb conditions and their families/media:title> media:content url="https://www.youtube.com/v/aLjsnpqH0_k?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i2.ytimg.com/vi/aLjsnpqH0_k/hqdefault.jpg" width="480" height="360"/> media:description>"StepIn" Camps offer an invaluable weekend experience where families with children affected by a lower limb condition come together to meet, discuss and share their experiences of living with that condition. This may well be the first-time children will meet others sharing their condition therefore the weekend is designed to offer activities and workshops where the entire family can â€œstep-inâ€ and share medical, social and emotional experiences that will be of use and some comfort to the families involved. The weekend also promises to offer lots of fun through the many activities available! With qualified professionals, volunteers and other dedicated staff on hand, we hope to provide some time and space for families to make lasting friendships. To see more about our â€œStep Inâ€ Camps, please visit https://www.stepsworldwide.org/get-involved/step-in-camps/ Donate to help more families benefit from the "StepIn" Camp experience: https://www.justgiving.com/campaign/stepincamps/media:description> media:community> media:starRating count="9" average="5.00" min="1" max="5"/> media:statistics views="657"/> /media:community> /media:group> /entry> entry> id>yt:video:znvph6qU-M4/id> yt:videoId>znvph6qU-M4/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Perthes Disease Research Update - webinar/title> link rel="alternate" href="https://www.youtube.com/watch?v=znvph6qU-M4"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2022-01-20T18:25:54+00:00/published> updated>2024-08-29T06:35:40+00:00/updated> media:group> media:title>Perthes Disease Research Update - webinar/media:title> media:content url="https://www.youtube.com/v/znvph6qU-M4?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i3.ytimg.com/vi/znvph6qU-M4/hqdefault.jpg" width="480" height="360"/> media:description>Adam Galloway, Senior Children's Physiotherapist and NIHR Pre-doctoral Clinical Academic Fellow provides an update on progress with the research he is undertaking in which he aims to assess the effectiveness of non-surgical intervention for patients with Perthes disease when compared with surgical management. You can watch the original research briefing webinar here: https://youtu.be/RMRTkAoJREQ Research is essential to establish which treatments work better for patients. Without research, it is difficult to discover new treatments or ensure that the ones we currently use are the best ones. Research is key to finding answers to questions that currently have â€˜no answerâ€™. It fills gaps in knowledge and changes the way that healthcare professionals work. Steps charity worldwide strongly believes that continuous research and clinical trials are a must and should be part of every national healthcare system. People around the world benefit from past research and continue to benefit from research that is currently being carried out. Panelist: Adam Galloway, Senior Children's Physiotherapist and NIHR Pre-doctoral Clinical Academic Fellow. Adam is a Physiotherapist with a specialist interest in Children's Orthopaedics. He has worked in Leeds since 2013 after graduating at Leeds Metropolitan [Beckett] University. Adam is currently completing a HEE/NIHR Pre-Doctoral Clinical Academic Fellowship which secured 2 years of funding to spend 50% of his time developing a doctoral fellowship project and application. Prior to entering the world of Children's physiotherapy Adam worked with adults and as part of his HEE/NIHR funded MSc Clinical Research Methods he completed a research study to evaluate the reliability of an outcome measure in patients who had recently undergone brain surgery. His interest in this matter laid within the unknown usefulness/effectiveness of pre-existing measures in populations that have no current 'gold-standard'. This, in essence, led him to his current research area focus in which he aims to assess the effectiveness of non-surgical intervention for patients with Perthes' disease when compared with surgical management, for which there is currently no standardised treatment course or indeed outcome measure./media:description> media:community> media:starRating count="12" average="5.00" min="1" max="5"/> media:statistics views="1513"/> /media:community> /media:group> /entry> entry> id>yt:video:IMlcIDDziAs/id> yt:videoId>IMlcIDDziAs/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Sarah's journey with Developmental Dysplasia of the Hip/title> link rel="alternate" href="https://www.youtube.com/watch?v=IMlcIDDziAs"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2021-12-01T19:13:51+00:00/published> updated>2024-08-26T19:28:12+00:00/updated> media:group> media:title>Sarah's journey with Developmental Dysplasia of the Hip/media:title> media:content url="https://www.youtube.com/v/IMlcIDDziAs?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i2.ytimg.com/vi/IMlcIDDziAs/hqdefault.jpg" width="480" height="360"/> media:description>Developmental dysplasia of the hip (DDH) is when the ball shaped part of the end of the thighbone and the socket do not fit correctly together. There are varying levels of hip dysplasia, from mild to severe. If the ball (femoral head) is not held correctly in place, the socket (acetabulum) may be more shallow than usual. Sometimes this makes the joint less stable and the ball may slide in and out of the socket. This is called a dislocatable or â€˜subluxatableâ€™ hip. If the ball loses contact with the socket and stays outside the joint it is called a dislocated hip. One or both hips may be affected. Sarahâ€™s Hip Dysplasia never fully recovered after treatment during her childhood. Unfortunately, many adolescents with hip dysplasia that was treated in childhood often have abnormalities of the socket and the ball â€” the acetabulum and the femoral head. When symptomatic or when getting worse, this generally requires surgery to correct both the acetabulum and the femoral head abnormalities./media:description> media:community> media:starRating count="3" average="5.00" min="1" max="5"/> media:statistics views="558"/> /media:community> /media:group> /entry> entry> id>yt:video:1oGY396seYw/id> yt:videoId>1oGY396seYw/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Run Free 2030/title> link rel="alternate" href="https://www.youtube.com/watch?v=1oGY396seYw"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2021-10-16T18:03:49+00:00/published> updated>2024-08-23T22:34:20+00:00/updated> media:group> media:title>Run Free 2030/media:title> media:content url="https://www.youtube.com/v/1oGY396seYw?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i2.ytimg.com/vi/1oGY396seYw/hqdefault.jpg" width="480" height="360"/> media:description>We want a world where every child born with clubfoot / talipes can run free from disability by 2030. As part of the Global Clubfoot Initiative, we partner with national healthcare systems around the world to provide quality training and the materials they need. Help us raise awareness by sharing this video./media:description> media:community> media:starRating count="6" average="5.00" min="1" max="5"/> media:statistics views="355"/> /media:community> /media:group> /entry> entry> id>yt:video:FDrlA3d7Bjo/id> yt:videoId>FDrlA3d7Bjo/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Medical Negligence Teenagers in and Adults/title> link rel="alternate" href="https://www.youtube.com/watch?v=FDrlA3d7Bjo"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2021-09-28T20:14:24+00:00/published> updated>2024-08-24T08:49:39+00:00/updated> media:group> media:title>Medical Negligence Teenagers in and Adults/media:title> media:content url="https://www.youtube.com/v/FDrlA3d7Bjo?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i3.ytimg.com/vi/FDrlA3d7Bjo/hqdefault.jpg" width="480" height="360"/> media:description>Medical Negligence and Hip Dysplasia in teenagers and young adults â€“ what can we learn from it? This recorded webinar aims to answer some of the key questions raised by parents, carers and young adults affected by hip dysplasia. Panellist Will Jones is a solicitor in the Medical Negligence Department at Fieldfisher. He acts for a number of patients who have suffered as a result of a late diagnosis of developmental dysplasia of hip. Will works closely with NHS independent medical experts who ultimately determine whether the medical professional is responsible for negligence./media:description> media:community> media:starRating count="0" average="0.00" min="1" max="5"/> media:statistics views="336"/> /media:community> /media:group> /entry> entry> id>yt:video:7VzaB6-hwQ8/id> yt:videoId>7VzaB6-hwQ8/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Gwen's family raising awareness of PFFD in Malta/title> link rel="alternate" href="https://www.youtube.com/watch?v=7VzaB6-hwQ8"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2021-09-19T10:23:32+00:00/published> updated>2024-09-24T07:35:19+00:00/updated> media:group> media:title>Gwen's family raising awareness of PFFD in Malta/media:title> media:content url="https://www.youtube.com/v/7VzaB6-hwQ8?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i4.ytimg.com/vi/7VzaB6-hwQ8/hqdefault.jpg" width="480" height="360"/> media:description>Gwen, who lives in Malta with her parents and brother, was born with Proximal Femoral Focal Deficiency (PFFD). Dad Matt explains how Gwen and the family have been raising awareness of the condition locally by working with Gwen's school. Gwen gave classmates amputee Barbie dolls, donated by @Mattel, to help generate conversations at home with parents and siblings. PFFD is a condition where the end of the thigh bone closest to the hip is too short or not completely developed. In most cases, the hip joint is also not well developed. You can find out more about PFFD and access Steps' guides and factsheets here: https://www.stepsworldwide.org/conditions/pffd//media:description> media:community> media:starRating count="14" average="5.00" min="1" max="5"/> media:statistics views="2162"/> /media:community> /media:group> /entry> entry> id>yt:video:djDSI3i5pzE/id> yt:videoId>djDSI3i5pzE/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Declan's doing it for Perthes!/title> link rel="alternate" href="https://www.youtube.com/watch?v=djDSI3i5pzE"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2021-09-19T09:50:57+00:00/published> updated>2024-09-24T01:20:13+00:00/updated> media:group> media:title>Declan's doing it for Perthes!/media:title> media:content url="https://www.youtube.com/v/djDSI3i5pzE?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i1.ytimg.com/vi/djDSI3i5pzE/hqdefault.jpg" width="480" height="360"/> media:description>Sheffield Wednesday footballer Declan Thompson is going to score 100 goals for Perthes Awareness Month this October. What will you do? https://www.stepsworldwide.org/ways-to-give/awareness-campaigns/perthes-awareness-month//media:description> media:community> media:starRating count="13" average="5.00" min="1" max="5"/> media:statistics views="427"/> /media:community> /media:group> /entry> entry> id>yt:video:1vCGHZ1h-KQ/id> yt:videoId>1vCGHZ1h-KQ/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Limb Lengthening webinar/title> link rel="alternate" href="https://www.youtube.com/watch?v=1vCGHZ1h-KQ"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2021-07-18T11:48:08+00:00/published> updated>2024-08-29T12:05:27+00:00/updated> media:group> media:title>Limb Lengthening webinar/media:title> media:content url="https://www.youtube.com/v/1vCGHZ1h-KQ?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i2.ytimg.com/vi/1vCGHZ1h-KQ/hqdefault.jpg" width="480" height="360"/> media:description>When a childhood condition affecting the legs leads to a leg length difference, operations or internal nails/rod may be used to help 'equalise' the legs or, in some cases, amputation of the foot and part of the leg may be required. This webinar aims to address some of the key questions raised by parents of children with leg length conditions and focuses on leg lengthening./media:description> media:community> media:starRating count="5" average="5.00" min="1" max="5"/> media:statistics views="1800"/> /media:community> /media:group> /entry> entry> id>yt:video:5y2sqAGCan4/id> yt:videoId>5y2sqAGCan4/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Family Support Days - Steps Christmas Party/title> link rel="alternate" href="https://www.youtube.com/watch?v=5y2sqAGCan4"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2021-06-28T12:39:15+00:00/published> updated>2024-08-21T13:13:07+00:00/updated> media:group> media:title>Family Support Days - Steps Christmas Party/media:title> media:content url="https://www.youtube.com/v/5y2sqAGCan4?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i2.ytimg.com/vi/5y2sqAGCan4/hqdefault.jpg" width="480" height="360"/> media:description>Throughout the year, including a very special event at Christmas, Steps organises a series of Family Support Days in a relaxed and safe environment. Families or carers of children with lower limb conditions have the opportunity to meet and discuss their journeys. It is also a chance for families or carers to meet with the Steps team and share ideas, concerns or simply to say 'hi'! In this video, attendees of our 2019 Christmas party in Winchester talk about why this is such a special day. For more information on the latest events please visit: https://www.stepsworldwide.org/get-help/family-and-peer-support//media:description> media:community> media:starRating count="1" average="5.00" min="1" max="5"/> media:statistics views="300"/> /media:community> /media:group> /entry> entry> id>yt:video:4FY9d2kdYb8/id> yt:videoId>4FY9d2kdYb8/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Hip Health Awareness Month - help us spread the word!/title> link rel="alternate" href="https://www.youtube.com/watch?v=4FY9d2kdYb8"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2021-06-21T14:44:27+00:00/published> updated>2024-08-24T07:16:51+00:00/updated> media:group> media:title>Hip Health Awareness Month - help us spread the word!/media:title> media:content url="https://www.youtube.com/v/4FY9d2kdYb8?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i1.ytimg.com/vi/4FY9d2kdYb8/hqdefault.jpg" width="480" height="360"/> media:description>March is Hip Health awareness month. As many as 15% of babies worldwide are born with some form of neonatal hip instability, many of which remain undiagnosed or untreated. Help us raise awareness and reach more families who need help./media:description> media:community> media:starRating count="0" average="0.00" min="1" max="5"/> media:statistics views="551"/> /media:community> /media:group> /entry> entry> id>yt:video:TI06NMzHQLk/id> yt:videoId>TI06NMzHQLk/yt:videoId> yt:channelId>UCiDkfLrwkQyRur8pXZbJWiQ/yt:channelId> title>Steps Hip Dip sponsored swim/title> link rel="alternate" href="https://www.youtube.com/watch?v=TI06NMzHQLk"/> author> name>stepscharity/name> uri>https://www.youtube.com/channel/UCiDkfLrwkQyRur8pXZbJWiQ/uri> /author> published>2021-06-15T17:41:45+00:00/published> updated>2024-08-21T07:57:28+00:00/updated> media:group> media:title>Steps Hip Dip sponsored swim/media:title> media:content url="https://www.youtube.com/v/TI06NMzHQLk?version=3" type="application/x-shockwave-flash" width="640" height="390"/> media:thumbnail url="https://i1.ytimg.com/vi/TI06NMzHQLk/hqdefault.jpg" width="480" height="360"/> media:description>Hip Dip is a sponsored swim with a distance to suit all abilities - the main aim is to have fun! Swimming is particularly good for those born with hip conditions as it emphasises upper body activities while the body weight is supported, thus avoiding any load on the hip joint. You can choose whether to swim 400m, 1.5k, 2.5k, 5k or triple 5k as an individual, or 1.5k or 5k as part of a team â€“ you decide! Then get people to sponsor you. To find out more go to https://www.stepsworldwide.org/ways-to-give/awareness-campaigns/hip-health-awareness-month//media:description> media:community> media:starRating count="0" average="0.00" min="1" max="5"/> media:statistics views="127"/> /media:community> /media:group> /entry> /feed>

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