"Disability is Not a Dirty Word.  Say it. Celebrate it. Share it" campaign logo.

#DisabilityPride

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Thank you to all those who have shared your stories with us.

Discover the stories that were submitted here at our website below.

Visit our influencer story page to see the stories that have been shared by our influencer partners.

Want to see your story here? Simply fill out the form below and upload your image or video to share your Disability Pride with us.

#DisabilityPride

Jimmy

I am a man in my 50’s with a rare birth defect called spina bifida. The doctors told my parents that I wasn’t supposed to live past a year old, and here I am, 50-some years later (knock on wood). I had a challenging childhood that continued into adulthood, but with the help of family and friends, this journey overall has been great. I have been to places like London and Paris and places within the United States. Some of the travel has been hard, BUT my philosophy is 'life is what you make it.'

Nicole

As someone who was always ashamed of having anxiety, ADHD, and trichotillomania for the past 20 years, I am forever grateful to have found an organization that takes pride in disability and helps others embrace who they are! I am slowly but surely opening up to others about this and I am so thankful to have friends and colleagues who love and accept me for who I am, as I'm still learning to love myself just how I am along the way.

Juan Carlos

Uso muletas para movilizarme desde hace 39 años asta el momento soy feliz tengo una hija de 15 años i pues disfruto la vida.

Vince

I’m a 74-year-old power-chair user and the Admin/Publicist for the Facebook page TRAINED ACTORS with REAL DISABILITIES for FILM & TV. I previously spent 32 years as a Disability Rights Advocate, ADA Consultant, and Podcast Producer.

Robyn

I was born disabled. On the evening of December 30th, 2015, I had my VERY first seizure. And then on January 15, 2016, I got diagnosed with epilepsy. We did genetic testing, to see if there was a connection. And there was. They found out that I have Smith-Magenis Syndrome, which is a rare chromosome disorder. It affects different parts of the body. So for me, my left kidney is smaller and has scar tissue and a benign heart condition. I’ve also got ADD.

Mike

My name is Mike D. My friends call me Money Mike. I live in Los Angeles. I love to surf. I like to make tie dye shirts. I even teach people to tie dye. I work at a resale shop because I love books and DVDs.

Anna

I believe we all share the same heart and should love one another.

Working at Easterseals has only deepened this belief, and I’m grateful to be a part of it.

Cynthia

I'm 40 years old, and I was in a vehicle accident 15 years and four months ago. My left arm ended up crushed and paralyzed, basically known as a dead limb. After 14 years and 6 months of procrastinating on whether or not to have it amputated, I decided to take my doctor's advice and I finally amputated my arm. It was a hard decision, especially with some family members being so against it that they decided to stop speaking with me. At times it hurts and it's a constant reminder of whether I made the right decision, but I know it's been done and there's nothing I can change other than to move forward. Especially with my husband and daughters' support.

Ajai

My Journey with Dialysis and Disability.

Hello, I’m Ajai, 36, living in California. For the past few years, I’ve been navigating life with chronic kidney disease, requiring dialysis four times a week. It’s been a tough journey, but I take it one day at a time. Dialysis has become a major part of my life, both physically and emotionally, and I rely on disability benefits for support while focusing on my health.

This experience has taught me patience and gratitude, helping me appreciate the small joys like time with family or a good movie. I’ve also learned the value of community—whether through healthcare professionals or others facing similar challenges.

Though the journey is difficult, advances in medicine, support from loved ones, and my own determination keep me going. I share my story not for sympathy but to inspire others struggling with chronic illness or disability. Life may be hard, but it’s still worth fighting for.

To anyone facing similar challenges: you are not alone. Together, we find strength.

Stevie

Stevie was two years old when she was diagnosed with Sotos syndrome (a very rare genetic disorder). She is doing great, working hard, and always has a smile on her face. She loves to sing and is known for giving the best hugs.

Nik

Hi! My name is Nik Sanchez and I am Awesomely Autistic! 😎💙 I didn't always think I was awesome, though. With my autism, I also have ADHD and Tourette's Syndrome. I used to be bullied a lot and I wanted to be "normal" so bad. I never wanted to talk about my disabilities, but the more I tried to hide them and everything that makes me me, the more lost I felt. I finally learned to embrace it all and be proud of what makes me, me, because there is only one Me. Different does not have to mean "wrong" or "bad". Different can be cool and unique and AWESOME! I am the only Awesomely Autistic Nik and I am proud of that. 😀 We are all one of a kind and should love everything about ourselves as much as possible.

Shivani

Francisco

Hi, my names is Shivani and I am living and thriving with Ataxia-telangiectasia (AT). As someone with a disability, I have personally experienced the challenges as well as the fruitful outcomes. Learning how to overcome the obstacles that come with a disability have shaped me and my personality to what I am today. I have many people in my life that I wouldn't know if it weren't for my disability as well as so many incredible life experiences. I've accomplished so much: receiving my AA from Grossmont College with honors, and my BA from SDSU, also with honors. I'm currently working on writing my memoir to inspire people with or without disabilities. Disability is definitely NOT a dirty word!

Jared

Breyton

I was diagnosed with autism and ADHD when I was two years old. A neurologist told my parents that I would never go to college, much less finish high school. She also said that I would have to be taken care of for the rest of my life. However, in 2018, I graduated with my master's degree in accounting, and I live independently in a one-bedroom apartment in Los Angeles. I’m a saxophonist, rapper, and singer by the name of B. Able. Through my music career, I want to inspire those with disabilities not to let anything or anyone define who they are or what they can do.

I’m 29 and have autism. I love playing video games and take a video animation class every week. I’d enjoy meeting and spending time with others.

We are so proud of the work we do here at Easterseals Southern California Behavioral Provider Network. We dedicate our lives to make the world a better place. We can all do it TOGETHER.

Susanna

My name is Susana, aka Susie or Q. I am 41 years old and was born with cerebral palsy. I’ve faced plenty of obstacles and challenges throughout my life, but I’ve tried to make the best of it. I have an A.A. and A.S. in early childhood development. I have been an educator for the past fifteen years, and I have enjoyed it to the fullest. My dream is to write a book to inspire children and people with disabilities, showing them that they can do anything they set their mind to, no matter how challenging it may be. 'Where there's a will, there's a way.' If I can do it with all the adversity and obstacles, anyone can.

Tuve un accidente en mi trabajo y me quebre la espina dorsal y ahora uso silla de rueda

Amanda

Hello, I was born with a heart condition called AVSD and have undergone four open-heart surgeries—three before I turned 5 and one when I was 26. I was in special education classes throughout my life. After high school, I worked here and there, but never had many opportunities to work growing up because my mom was very protective of me. Now, at 34 years old, I’ve finally got a job, and I absolutely love it!

Vadim

Hello everyone!

My name is Vadim, I'm 54 years old, and I’m originally from Russia. I do everything with my right hand 🦾. After an injury, I had to rebuild my life from scratch. I have three wonderful sons, lead a healthy lifestyle, and have been living in LA for the past two years, working 12–14 hours a day in delivery.

My dream is to become a U.S. citizen and start a production line for equipment designed specifically for people with disabilities. There is nothing like it in the U.S., and this business would provide job opportunities for many individuals with disabilities.

I’m truly grateful for everything I have and wish peace and kindness to everyone. Love and hugs to all!

Maria

I’ve had brain tumors that, after surgery, impaired my memory and thinking. Even though I look "normal" on the outside, things are not that normal on the inside. When I tell people I’m on disability or show my handicap placard, I often get a "why" look, as if a disability should only be associated with someone in a wheelchair. I struggle with what I should look like as a disabled person, since I seem "normal" to others. Sometimes, I choose not to park in handicap spaces to avoid stares from those around me. I feel like the world needs to be aware that disabilities come in many different forms.

Dayane

Katiyana

Katiyana is a vibrant and creative individual with a passion for self-expression and connection. Living with visual impairment and cerebral palsy, she embraces life with curiosity and determination. She loves drawing, dancing, and diving into research on topics that spark her interest. Set to begin community college next year, Katiyana is excited to expand her horizons both academically and personally. Her experience as an extra on the show "This Is Us" ignited a newfound passion for acting, inspiring her to explore the performing arts further. With a strong desire to build meaningful connections, Katiyana hopes to make friends within the disability community, sharing experiences and learning about different disabilities to foster understanding and support.

Lorraine

This is a great place to work, as it has allowed me to support individuals and change the way I view disability. Thank you, Easterseals, for giving me the opportunity to grow and develop while getting to know the individuals I support throughout my time with the organization.

Kathy

My name is Kathy, and my disability is not visible, but it limits what I can do. It’s called Trigeminal Neuralgia, also known as Suicide Disease. I experience intense pain on the left side of my face, which feels like burning, stabbing, and an electrifying sensation all the time. What triggers it? Sunlight, cold breeze, touching my face, and many other things—too many to list. As you can see, it’s something hard to live with, but I don’t let it bring me down because I am not my disorder, and it’s not me. We work together to achieve my goals. It may take a little longer than for others, but I get there.

Mario

My name is Mario, and I was born with a processing disability. But I don’t let that stop me from achieving my goals. Ever since I was seven, I knew I had the potential to accomplish great things. Now, as a young man, I work for the Boys and Girls Club as a Youth Development Professional, and I’m also attending CSUN. It’s amazing to prove to myself and others that, despite having a learning disability, nothing is impossible.

Eriko

I grew up with autism. At the age of 7 years old I was diagnosed by my elementary teacher. I was offered medication, but my parents refused. I went through all the treatments. I went to speech therapy during my elementary years because of my lack of speaking because of my disability. I was not good in school because of my learning disability. During my whole schooling years, I had to have a psychologist every day. I went through bullying for the way I looked different from everyone. Now as an adult, I look different from when I grew up and I want to continue to advocate my disability story.

Miracle

Miracle Pelayo is an actor based in Los Angeles with Cerebral Palsy. Growing up in a family with a strong acting background, she was drawn to the camera at a young age, creating stories with her family’s home video camera when she was just four. At twelve, after seeing a production of The Miracle Worker, she became determined to pursue acting, and the theater ignited her passion for performing.

Join us as we celebrate 

DISABILITY PRIDE

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