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Struthers girl with Williams syndrome shows no diagnosis is bigger than heart

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This touching video is a short, two and a half minute clip from a news platform, WKBN. It tells the story of a girl with Williams syndrome, and discusses how it affects her everyday life. What I thought was interesting was the connection to music the kids diagnosed with this syndrome have. For example, Emily likes to beatbox and sing. The main focus of the video is on how friendly people with Williams syndrome are, and how kids with this condition should be defined as that.

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This video goes over the basics of Williams syndrome- how it originates and what it does. It also goes more into depth on the actual structure of the chromosomes and how the problem occurs. Williams syndrome is caused by a deletion on the seventh chromosome. The full name of the syndrome is Williams-Beuren Syndrome, and it causes physical and developmental problems.

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Williams' Syndrome - CRASH! Medical Review Series

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This was the 35 minute video I chose to watch. It was very informative- instead of giving personal stories, it was more the back story behind the science itself and advice to parents on what types of doctors to consult and what tests to get (Calcium level test, for example). Some interesting things I learned included features of the syndrome including prenatal growth delays, 'elfin faces', hypertension, and joint hypermobility. The video focused on the medical side, and it even showed pictures of the pregnancy before the baby is born. There is a link between it to the size of the Aorta, and all motor skills are typically delayed. Interestingly, people with Williams syndrome are very good at memorizing words to meaning, but have trouble applying that meaning to a subject. It has also been noticed that these children love to talk to and meet strangers, which can pose as a danger to them and is something parents have to handle and teach their kids. It is possible for children with Williams syndrome to go to high school and get a college degree, but it is not common.

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Williams Syndrome: Extraordinary Gifts, Unique Challenges

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This video focuses on the idea that there are challenges but also gifts to having this condition. It affects roughly between 10,000 to 20,000 people in the US- it is very rare. It is the deletion of 26 genes on the 7th chromosome. Interestingly, children with this syndrome can experience hypersensitive hearing. Something that is shocking to me is how many challenges there are that come with having this syndrome. The positives focus on the connections they are able to make with other people.

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I learned a lot while completing this project. Watching all the videos was a very bittersweet experience- it is beautiful to see such happy, pure people persevering in their lives, but the amount of challenges they face is staggering and devastating. I had never heard about this syndrome before, but I am so glad I chose this one to research. It offered me a new perspective to look at and was a reminder of how many health complications some people have, and to be grateful for good health.

Something I thought was really interesting was the connection to music and other auditory sounds- their sensitivity to hearing and an unexplainable connection to music. Something else I thought that was interesting was another common pattern between children with Williams syndrome and how they all are drawn to speaking with strangers. Overall, this was such an interesting topic.

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Skye's Life with Williams Syndrome (The "Happy" Syndrome)

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Something about these interview videos really hook you. I found myself watching a half an hour of different interviews with people with Williams syndrome in addition to the ones I am using for my project- they are all so happy. In this video a young girl answers interview questions, and it is evident she is happy all the time, and has love for everybody. A main thing that has showed up in other videos in addition to this one is that kids with Williams Syndrome struggle with stranger danger, because they love and trust everybody. Additionally, the girl being interviewed struggled with basic math skills, like 1 plus 1, or 2 + 2, but she was clearly trying despite that.

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Rare but Real: The Importance of Research for Williams syndrome

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Williams Syndrome, Causes, Signs and Symptoms, Diagnosis and Treatment.

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I think the music paired with the words was a really good way to portray the story of this baby girl. It definitely touches your heart and informs the viewer while telling a story. For example, she had GI problems, which is common for children with this condition. Despite this, seeing her glowing smile is truly amazing.

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This video went more in depth on certain parts of the science behind it, and had many nifty drawings and animations that were helpful to understanding it. The deletion occurs during the formation of the egg or sperm. If someone who has Williams syndrome has children, the likelihood they will pass it down to their children is 50%.

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This video was interesting because it was designed to educate and help parents that have Williams syndrome. Learning, planning, problem solving, and spatial awareness are all things that are potentially affected. They love to be around people and are very friendly. A tip to help children focus is when they become distracted with another topic, focusing on that topic instead will help them. Or, tapping an object they should be focusing on can help too.

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Your Classmate Has Williams Syndrome - Boy

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It has been difficult to find videos about William syndrome that focus on the school aspect. I think because there are so many other issues to deal with school is very important but not the main thing kids struggle with. The focus was on the hypothetical that if you had a classmate with Williams syndrome, and it brought awareness to the differences that may be between the viewer of the video and of a child who has Williams syndrome.

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This video was definitely emotional- I found myself heavily invested in the stories of these children who go through so much at a young age- it's heartbreaking. At the end of the video, the women speaking in it tied it back into raising awareness of Williams syndrome and of their goal to fundraise for more research, because not much has been done, and government funding is decreasing.