Interview with a woman with Invisible Disabilities as the result of a spinal injury

Meet Brooke

Brooke is an International Award-winning Entrepreneur, Host, Stage/TV Actor and Fortune 500 Spokesperson. Extremely social, she used to be out at events and on red carpets on a regular basis, averaging 12-15 events/week for years. She’s well known in the live-streaming community for her positive attitude – always moving forward in life.

Interview with An Inspiring Woman With An Invisible Disability

Meet Lauren Rowe

Lauren Rowe has battled Cystic Fibrosis since birth. When she was 19 she had less than 2 weeks left to live and received a double lung transplant. Although this transplant added years to her life, Lauren has been living off of 30% lung capacity.

Lauren created a not-for-profit organization in Australia called, “Gifted Life” to provide support for other transplant recipients. Lauren’s work was

Women who has a disability & chronic pain from POTS & EDS Syndromes

Meet Alexa Chronister

Alexa Chronister is not your stereotypical college student. She doesn’t spend the weekend tailgating before football games or playing beer pong at fraternity parties. Alexa suffers from Postural Orthostatic Tachycardia Syndrome (POTS) and Ehlers-Danlos Syndrome (EDS); two chronic, painful and often debilitating conditions. As a college freshman, Alexa felt isolated as she struggled to manage the symptoms of her chronic illnesses

Q & A with EDS Ehlers Danlos syndrome warrior Lara Bloom about Life, Style & Disability.

Meet Lara Bloom

Lara Bloom is the international Executive Director of the Ehlers-Danlos Society where she is responsible for raising awareness of rare and invisible diseases, including Ehlers-Danlos.
She works to raise funds for research and speaks at conferences all over the world, lecturing medical students and professionals, and supporting specialists in the EDS field by offering her experience as a leading patient expert.

Stylish Woman who has MS, an Invisible Disability does an interview

Meet Ardra Shephard

Ardra Shephard is a devastating illness expert, having lived with multiple sclerosis for more than 15 years. Her blog Tripping On Air is the irreverent, insider-scoop about MS that manages to inspire without ever being saccharine. It’s frank, it’s funny, it’s what you’d want your best friend to tell you about what it’s like to live with chronic illness. Ardra was named one of the Top 50 MS bloggers “in the universe” by feedspot.com, one of the Top 25 MS bloggers by healthlabs.com, and was featured on Sickboy Podcast (October 2017).

Woman with CMT Charcot Marie Tooth Disorder Inspires others with Fitness Tips

Tara Lyn Emerson Q&A

Tara has been in athletics her whole life. She is a certified trainer, spinning, and TRX instructor, and she was named one of Los Angeles’ best instructors by Class Pass.

Movement is important to Tara because she lives with Charcot Marie Tooth Disease (CMT). This disease has caused progressive atrophy in her lower legs, limiting her balance and strength.

Woman with a nerve disorder & physical disability from an accident inspires

AMBERLY LAGO

Meet Amberly Lago! Amberly is a motivational speaker, and author of True Grit And Grace: Turning Tragedy Into Triumph. She started her speaking career after her life was deeply altered and her world was completely changed in May 2010. While riding her motorcycle in Woodland Hills, CA, she was hit by a SUV and thrown…

Girl with neuromuscular disorder called CMT interviewed about her life with a disability

REBECCA ETCHBERGER

Meet Rebecca, a perfectly imperfect woman who inspires! She has Charcot Marie Tooth Disorder, a slowly progressive neuromuscular disorder that affects the peripheral nerves. Rebecca is 33 and works as a television producer living in Los Angeles. She grew up in Hershey, PA where her family still resides. After graduating from the University of California,…