hi, I’m chandler

advocate. public speaker. communications professional. social media savvy. beau’s human. diet coke drinker. swiftie. pure barre & core power yoga obsessed. sophisticated & sarcastic.

Hi, I’m Chandler – founder and curator of chandlercrews.com, not necessarily a lifestyle blog, but a virtual kaleidoscope where anyone who visits, gets a colorful glimpse at every single version of myself – fragments of my life through broken pieces (literally) and multiple metamorphoses. 🦋 Ever since I was 16, I have been showing the universe all facets of myself in full transparency. 🪩 Millions have watched me grow, evolve and transform – personally, physically, and professionally into the woman + social butterfly I am today. 👩🏼‍💻 This is my creative outlet where I can better connect with my audience. 🫶🏻 Here, I am candidly and unapologetically Chandler…so, if you see a grammatical error, typo, or one damn too many ‘shit’ and ‘fuck’s…no you didn’t 😉 (but if you did, my mom already bugged me about it)

Most of my content spans from my own life and is targeted to those who are seeking their own personal, physical, and professional growth or who are looking for new opportunities and advancements when it comes to treatment(s) for achondroplasia and other forms of skeletal dysplasia. When it comes to personal and physical growth, I am not an expert in any way, shape, or form other than my own personal experiences. If you would like to know more about my personal experience(s), contact me here – my inbox and comment sections are always open. However, if you are looking for a Communications Professional specialized in social media management, content creation, event + conference planning, and public speaking – let’s work together!

I’m best known for breaking my bones…well, having them broken for me. It all started when I was 16 years old and documented my journey through limb lengthening on Facebook. While growing (literally), I developed a passion for advocating and bringing awareness to unapologetically changing your body, mind, and lifestyle. Being the first person with achondroplasia to document their journey through the treatment every leg of the way in real time through blood, sweat, and tears, my content and controversy became viral.

I spend most of my days developing content, engaging with communities, and networking with industries to create a better social world between advocates, leaders, and organizations within patient populations, healthcare and biotech industries (while also being an expert on all things pop culture).

When I’m not online, you’ll either find me in barre or yoga or in front of the TV with Beau binge-watching Olivia Benson take on heinous crimes in NYC or the BAU traveling on their private jet to catch their latest unsub (I love TV).

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@friends in press + media:

Chandler Crews is an advocate and public speaker. Since 2010, she has been candid about her personal experience living with the most common form of dwarfism, achondroplasia, and undergoing limb lengthening treatment. At 16 years old and 3 feet 10 inches tall, Chandler became the first person with achondroplasia to actively document their journey through the process in real-time through daily entries gaining her a major online presence. She documented her journey not only for herself, but to debunk all of the rumors and misconceptions surrounding limb lengthening for dwarfism which is very controversial. After three limb lengthening procedures, Chandler stands today at 4 feet 11 inches tall and with longer arms.

Over the years, Chandler has been interviewed and featured in numerous news and media outlets around the world – BBC, SBS, The Baltimore Sun, and NBC. She has also been a guest blogger on Love What Matters and other outlets and has served as a co-author on numerous research articles and posters.

In 2018, she founded The Chandler Project (TCP) a nonprofit organization that provides those affected with achondroplasia, and other forms of dwarfism and skeletal dysplasia with the latest in pharmaceutical research and surgical advancements. TCP provides advocacy, awareness, support, and hope for. Since 2019, TCP has hosted the annual Achondroplasia Research Conference – the only conference in North America that brings together patients, caregivers, researchers, physicians, and biotech/pharmaceutical companies to connect and build a strong and trustworthy community to learn about the latest breakthroughs in achondroplasia research.

To connect with Chandler, follow her on Instagram and Twitter @chancrews or on her website, www.chandlercrews.com

disclaimer: chandlercrews.com does not provide medical advice. the information, including but not limited to, text, graphics, images and other material contained on this website are for informational purposes only. No material on this site is intended to be a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of your physician or other qualified health care provider with any questions you may have regarding a medical condition or treatment and before undertaking a new health care regimen, and never disregard professional medical advice or delay in seeking it because of something you have read on this website.