About 48 channels for "Dwarfism"

We are a Very unique family. Cristian,Camila & Mateo all have a type of dwarfism (achondroplasia). We love being different and want to raise awareness💚 P.O BOX 4561 CARSON, CA 90749

Interviews that are intended to create a more inclusive world. SBSK started when I was a teacher for students with disabilities. Originally intended to be a book written by my students, SBSK soon grew to be video interviews of disabled people of all ages and diagnoses. Since our beginning in 2015, I have interviewed hundreds of people across the world while providing over $1,300,000 to those featured on this channel through a combination of grants and fundraising. Starting in 2016, SBSK is now a 501(c)3 organization that seeks to normalize the diversity of the human condition under the pillars of honesty, respect, mindfulness, positivity and collaboration. This multi-media movement supports the acceptance and inclusion of all members of the neurodiverse/disability community regardless of diagnosis, age, race, religion, income, sexual orientation, gender or gender expression. -Chris

What's up Mama Maniacs?! You may know me from being the star and Executive Producer of Lifetime Channel's hit TV Shows, "Little Women: LA" and "Terra's Little Family". This channel is a passion project of mine, where you can find awesome videos about my family life, challenges, DIYs and vlogs! I love to respond to all of my fans so please leave comments and questions under any video you view! Subscribe and don't forget to give a thumbs up if you like the video! Mail Terra Jole: PO Box 487 La Habra, CA 90633

Just a BIG person trying to make it in this Little World! #Normalizedwarfism #Areyouastallasme

Welcome to my YouTube channel! A few years ago, I stopped playing the piano publicly, and so I thought a YouTube channel would be a great place for you all to continue to hear me play. Since I'm an audio snob, I didn't just want to record these anywhere. All of my cover videos are shot @ Bates Brothers Recording Studio (batesbrothersrecording.com) on their amazing Yamaha 6' G3 Piano. In addition to cover videos, I also have a few documentaries and concerts, where you can hear a little more about my life. You can also check me out on Instagram (@jmopiano) and FaceBook. Some of my cover songs have sheet music, which can be purchased on MusicNotes website (https://www.musicnotes.com/sheet-music/artist/jon-michael-ogletree). If you enjoy my videos, please subscribe and share with your friends and family!

My name is Elena Gant! And I am here to share with you my love for family, friends, beauty and much more... I hope you'll enjoy watching my videos! Xoxo Instagram - @gantelena

Nick Smith is one of the most unique gifts in this world. He has MOPD type 2 Microcephalic osteodysplastic primordial dwarfism type II (MOPDII) is a condition characterized by short stature (dwarfism) with other skeletal abnormalities (osteodysplasia) and an unusually small head size (microcephaly). He is one of the most fun loving guys you will ever meet & he will steal your heart! https://m.youtube.com/watch?v=4cVXLwKS4S0 documentary on his life filmed several years ago. He lives in Jefferson Ga with family and friends all around him. His mom Shelly and close friend Patti-aka Patticake watch over him and make sure everyone who meets Nick is touched somehow by his story. In life...”the noblest art is that of making others happy” PT Barnum FOLLOW ON FACEBOOK! At NickSmith@nicksmithfanpage

What's up everybody my name is Caden Teneycke, I'm a 19-year-old University student and current full time content creator that stands at only 3.5 ft tall!

BlackPaperWings’ Motto: "Just another day, just another game." I like to live like the gamers do: game on, game off, a little something in between, and repeat. This channel will feature monster-related genres, which include Monster Hunter, Pokémon, Hogwarts Legacy, and other Mon-associated games. You can follow my other channel @LittleRicky, where I talk about dwarfism and discuss how I’ve been able to manage the malicious wonders of the world. You can also find me on Twitch via @BlackPaperWings. https://koji.to/BlackPaperWings I’m always ready to game!

Hiya, I am Tanyalee Davis. I'm a Comedian, Storyteller, Motivational Speaker and Actor. Guinness World record holder for the shortest comedian at 3'3" tall . I don’t have a victim mentality. If u feel sorry for me, that’s a YOU problem. I ve lived my life believing I can do whatever I set my mind to. That’s what being an UnstoppableMe attitude is about. I have done 2 #TEDxTalks ... #TEDxLiverpool #TEDXUNic in #Cyprus both on Ted.com I go LIVE on TikTok daily. My tour schedule https://beacons.page/tanyaleedavis My motto in life is being an #UnstoppableMe

Real Families features documentaries and TV series about modern family life, with the challenges and successes that all moms and dads experience at some point. Our stories are seen through the eyes of parents and children, and sometimes with guidance and advice from parenting experts. More than being a spectator, the viewer dives into people’s lives and stories to discover the journeys of families becoming … Real Families. Real Families is part of the Little Dot Studios Network. To get in touch please email owned-enquiries@littledotstudios.com.

On this channel you will experience our daily lives as people leaving with dwarfism, Fun, mother and daughter conversations and outings sometimes will add a pinch of spices where we add Dad and Grandmother. Basically this is a channel where you will get to ask questions about dwarfism and get answers from the horses mouth not the hearsay and get to see that we are just as normal as everyone just a little bit shorter than you ☺️ Hope to give you the content you deserve and collaborations😍 to more heeey welcome to our YouTube channel 🍩🥂😘😂 Love Gabi and Hlelo ❤️

My name is Luisa i'm 33 and i was born in Scotland but i live in Italy ,i was born with metatropic dwarfism i always loved to sing, i have never been trained and my biggest dream would be to become a singer, and i'd love to be an inspiration to others and show them that no matter what you can make your dreams come true =)

Hello Guys....Welcome to CelebrityStatus Channel... This Channel All About News and Gossips Celebrity in The World... Dont Forget Like & Subscribe...

This page was started over 6 years ago. My son Christian, was born with a rare from of dwarfisim. Thanatophoric dysplasia type 1. He lived to be 3 1/2 years old. He beat may odds and lived for much longer than the drs said he would. Please refrain from leaving hate comments. I have had to delete and report many people already. I would like to say thank you though, to those that have left very heartfelt comments. your compassion means very much. I miss my son so much. He was full of love and happiness. If you have questions about TDT1 or about Christian, please feel free to ask. However, I will not reply to any repulsive comments. I will delete, report and block them. We have decided to start adding more content to this page. Christian's spirit is still with us. We want to share our family and our love we have for him. We want to share how life can continue after such a traumatic loss of a loved one can still go on.

My name is Gareth Mason and I created Walking Tall with G-MAN to inspire, motivate and encourage people to achieve their dreams and to never give up in life. I have a disability which is Dwarfism however I never let that affect me as I see it as a blessing because it has made me the person I am today. In this channel, I will share my personal stories and challenges as well as create motivational videos to help inspire people to reach for the stars and achieve their goals in life. I want to show the world that anything is possible as long as you believe in yourself and have faith in everything that you do. No matter what the challenges are whether it’s physical or mental you can do anything. I will also do sporting video's chatting about recent sporting events as well as any other interesting topics that are being spoken about around the world. Please subscribe to Walking Tall with G-MAN and join me on this journey, I promise you won't regret it. Stay Safe and Never Give Up

I am a real-life, damn near Snow f*cking White (super pale AND gifted at dwarf wrangling) from the Midwest who blogs semi-regularly about everything from my kids’ antics to my husband’s sketchy facial hair to me shitting myself. When I'm not cleaning up random bodily fluids (from the kids, ya' pervs!), taking care of my girlies, & studying up on random, unsolved medical issues, I find time to share about my unique life being married to a stud glassblower and raising three amazing kiddos, two of whom happen to have neuro-metabolic, genetic superpowers. Primary life goals: Find joy daily. Love the hell out of the life I was given. Celebrate everything. Optimize, optimize, optimize, babyyyy. xo Show me some love at -- gwen@thehartleyhooligans.com

Welcome to the "Love a Little Podcast"! Join us as we follow the Garcia family's remarkable journey, where love and laughter thrive. Meet Cristian and Jenn Garcia, the heart of our podcast. Cristian, a proud husband and father with dwarfism, stands tall in spirit alongside his wife, Jenn, whose love knows no limits. Together, they navigate life as a family of four, with their two children sharing Cristian's condition. Through candid conversations, heartfelt stories, and moments of pure joy, they offer a refreshing perspective on embracing diversity and the power of love. Tune in for inspiration and laughter with the Garcia family!

Hi! I'm Lil Gabi D, your Friendly Internet Little Person! I am a Toronto-based content creator who happens to have Dwarfism. I love showcasing my life at 3 feet 11 inches tall! I share my daily adventures and struggles in a world not built for me. My goal is to show people that little people are just like everyone else, just shorter!

Aubrey Smalls is a filmmaker with dwarfism. Born in Louisiana, Smalls begin his career in the circus world, before transitioning to film and television. Currently, Smalls is focused on telling original fiction and non-fiction stories that highlight artists with dwarfism.