Ellie Simmonds has joined the line-up of Strictly Come Dancing 2022. She is making history on the programme as she's the first star born with dwarfism to step out on the iconic ballroom
Dwarfism is a genetic or medical condition that causes short stature. Learn about the causes, types, diagnoses, and treatments for dwarfism in children here.
Allison Warrell was born with Achondroplasia Dwarfism and is only 3'11", but she has never let dwarfism keep her from achieving her goals.
They are giving their community a voice.
Meet Caitlin Hellyer, the fashion blogger with dwarfism who has been an inspiration to others. Meet Caitlin Hellyer, the fashion blogger with dwarfism who has been an inspiration to others; Dwarfism is short stature that results from a genetic or medical condition. Dwarfism is generally defined as an adult height of 4 feet 10 inches (147 […]
"As soon as the word came out of her mouth, it stung."
Very short stature of 4 feet 10 inches or less that results from a genetic or medical condition is considered dwarfism. Learn about causes and treatment.
“Dwarves are still the butt of jokes. It’s one of the last bastions of acceptable prejudice,” said “Game of Thrones” actor Peter Dinklage. Catcalls, mocking, gawking, strangers taking photos are only a few of the daily challenges associated with having dwarfism.
These are just a handful of the athletes who will tonight pick up the sporting mantle as they get ready to take part in the Paralympic Games.
Sofiya Cheyenne talks about her type of dwarfism.
It is a bit surreal to think that while we can’t physically experience history because we’re born in a particular place and time, the power of technology has empowered us to see it, understand it, and make conclusions from it.
Kenadie is one of the world's smallest vital human beings who, at age 3, weighs only 10 pounds. Kenadie is a primordial dwarf and one of the sweetest children you could ever hope to meet. Kenadie is like a fairy princess...
October is Dwarfism Awareness Month! Just as I have done previously with Infertility Awareness Week, I am using my Facebook feed to try to raise awareness about dwarfism by posting interesting info and links. I've gotten some good feedback so far, lots of interest and quite a few people thanking me saying they're learning a lot. That's exactly what I'm going for :-) Below are the posts I have made thus far. I'll add to this periodically as I post more. If you'd like to also help raise awareness about dwarfism feel free to copy and paste any of the below info you like! Very few people know anything about dwarfism so the more awareness that can be raised, the better! ------------------------------------ October is awareness month for two causes that are near and dear to my heart: Pregnancy and Infant Loss Awareness, and Dwarfism Awareness. I'll be posting about both this month because neither are as well understood as they should be and my hope is that I may be able to provide you, my friends, with some information about them. [Hubs] and I never thought we'd have to say goodbye to our first child and we never thought our second would be born with Achondroplasia, the most common form of dwarfism. We miss our angel every day and we are thankful every day for the amazing son we hold in our arms. I hope you'll take a minute to read my posts this month! Learn some facts about dwarfism! Did you know that the majority of children born with dwarfism (80%) have average-sized parents? Dwarfism is caused by a spontaneous gene mutation at conception. What prompts a gene to change is not yet clearly understood. It is seemingly random and unpreventable, and can occur in any pregnancy. That means you too could one day have a child with dwarfism! Did you know that there is over 200 different types of dwarfism? Jack's form is called Achondroplasia, which is the most common form. It is characterized by a large head, average sized trunk and shorter arms and legs (think: Peter Dinklage aka badass Tyrion Lannister from G.O.T.). We are grateful to have a diagnosis as it helps us and Jack's doctors know what to expect and what to watch out for. Many babies with dwarfism won't have a diagnosis confirmed for many months, even years, and some never officially receive a diagnosis at all. Most types of dwarfism have medical complications, some more severe than others. Some common ones associated with Achondroplasia (the type Jack has) are sleep apnea, hydrocephalus ("water on the brain"), spinal compression, chronic ear infections, and orthopedic issues. We are always on the lookout for signs of each of these problems and see specialists regularly. Now that Jack is 6 months old we are beginning to notice some of the expected delays in motor skill development due to his Achon. Most kiddos with Achon will experience motor delays with things like controlling the movements of the head, sitting up, crawling, and walking, but intellectual development is normal. Did you know that the word “midget” is considered highly offensive to those with dwarfism? This dates back to "freak show" times when little people were only seen as here for others' entertainment and not as people in their own right. Acceptable words to use are: dwarf, little person, person with dwarfism, or short-statured. But most people with dwarfism just prefer to be called by their name rather than by their condition. Please click on the below link to learn 5 things you should never say to a little person and to get a glimpse of what daily life is like for many short-statured individuals. http://www.foxnews.com/health/2014/08/26/5-things-should-never-say-to-little-person/ As the parent of a little person this is hard for me to read but it just reaffirms why we need dwarfism awareness. https://lovebecxo.wordpress.com/2015/10/02/6/ There is no single treatment for dwarfism and most people with this condition and their families do not feel it is something to be "fixed". Instead, individualized accommodations such as specialized furniture, stools, long grabbers/sticks, etc., are used by people with dwarfism throughout their lives. Individuals with short stature can do just about everything an average-height person can, sometimes just in a different way. Their height does not keep them from leading fulfilled lives, achieving higher levels of education, or accomplishing career and personal ambitions. Dwarfism is not a disease and though opinions vary within the little people community about whether dwarfism is a disability, it is a recognized condition under the Americans with Disabilities Act. When [Hubs] and I found out at 36 weeks pregnant that our child had dwarfism we had no idea what to do or what to think. We knew almost nothing about dwarfism and didn't even know that we, as two average height people with no other little people (LPs) in our families, could even conceive a child with dwarfism! We were lucky to quickly find some LP groups on facebook and were welcomed by some wonderful people into this new family with open arms. We were offered all kinds of guidance, resources, and support for which we will be forever grateful. It was hard to wrap our brains around what was happening and that our child (and in fact our future) would be very different from what we had always pictured. One of the things that helped us come to terms with that is the following essay we were given called "Welcome to Holland": http://www.our-kids.org/archives/Holland.html
In a heartbreaking video filmed by his mother Yarraka Bayles, 9-year-old Quaden cries and says he wants to take his own life because he gets bullied over having Dwarfism every single day. The video spurred some celebrities to lend Quaden a helping hand, including comedian Brad Williams.
News, information, random musings, and occasional Deep Thoughts about Diana Gabaldon's books and the OUTLANDER TV series.
An Indigenous Australian boy who had been bullied for his dwarfism was cast in the upcoming prequel to 2015's "Mad Max: Fury Road."
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Since 2009, LPA has been recognizing October as Dwarfism Awareness Month? The intention is to raise positive awareness around dwarfism, addressing common mi
Doctors told this mother that her baby would only last a few days. We're so happy they were wrong.
And he made a documentary all about it.
It is an old-standing theory in evolutionary ecology: animal species on islands have the tendency to become either giants or dwarfs in comparison to mainland relatives. Since its formulation in the 1960s, however, the 'island rule' has been severely debated by scientists. In a new publication in Nature Ecology and Evolution on April 15, researchers solved this debate by analyzing thousands of vertebrate species. They show that the island rule effects are widespread in mammals, birds and reptiles
Adult German Shepherds diagnosed with Dwarfism: It's possible that they were born with defective DNA that hampered their capacity to grow muscles and the skeleton.
The pet's owner said he "loves jumping around and playing with his ball and squeaky toys"
His accent makes it even better.
The before and after pictures are nothing short of incredible.
Adult German Shepherds diagnosed with Dwarfism: It's possible that they were born with defective DNA that hampered their capacity to grow muscles and the skeleton.
Nobody wants their clothes to age them
Most people have heard about dwarfism and seen characters with dwarfism in fairy tales and films. However, most people have never met someone like me and thus I, and others with dwarfism, are often treated in a way which is reflective of these representations. As a university lecturer with dwarfism, whose research explores the cultural and social aspects of living with dwarfism, I want to try and dispel some myths.
