People You Should Know Podcast:
People You Should Know is a weekly podcast that will feature guests from a wide array of backgrounds. These people are either leading philanthropic organizations, raising awareness for a cause they are passionate about, inventing devices that will change the future, creating art or passionately dedicating their time to a unique hobby/subject matter.
Guests of the podcast will share their stories, the inception of their mission/idea and their hope for the future of the industry, cause or topic in which they devote their lives.
Episode 8: Jonny Imerman - Imerman Angels (Cancer Support)
After beating cancer, Jonny Imerman realized there needed to be a network for cancer fighters to connect with cancer survivors, so he founded Imerman Angels. Jonny and Bill discuss the creation of Imerman Angels, the speed in which the foundation has grown, and then Jonny provides current cancer fighters with a word of advice.
About Imerman Angels:
Imerman Angels provides free, personalized, one-on-one cancer support for cancer fighters, survivors and caregivers across the globe. To learn more, visit imermanangels.org.
Episode 7: Julie & Cheryl Gistenson - Blindness
Two sisters. Same condition. Both blind.
Both Julie and Cheryl Gistenson lost their vision due to Axenfeld-Rieger Syndrome. The sisters discuss growing up as one another's supports and what they learned from their father, who is also blind. Bill and the sisters then play a game called "Ask A Blind Person" in which Bill asks questions about blindness that sighted individuals may feel too uncomfortable to ask.
About Axenfeld-Rieger Syndrome (ARS):
ARS is a condition that causes abnormalities within the eye, particularly in the frontal region near the pupil. Individuals impacted by ARS tend to develop Glaucoma, a condition that creates pressure and subsequent pain behind the eye.
Episode 6: Stacey Skrysak - Triple Heart Foundation
In 2013, after undergoing months of fertility treatment, Stacey Skrysak’s three children, Peyton, Parker and Abby, were born prematurely. Tragically, both Parker and Abby passed away in the hospital. After returning home with their surviving triplet, Stacey and her husband, Ryan, created the Triple Heart Foundation to honor the memory of Abby and Parker.
Bill and Stacey discuss her journey with infertility treatment, the day she delivered her children and the families Triple Heart Foundation has touched since its inception.
About Triple Heart Foundation:
Triple Heart Foundations sends care packages and books to families in Nicu nurseries who find themselves in a similar situation as Stacey and Ryan. The hope is to provide not only support, but books for parents to read to their children.
Episode 5: Natalie Hayden - Crohn's Disease
Natalie was diagnosed with Crohn’s Disease in July 2005. After several hospitalizations, countless medications and flare ups she underwent her first surgery in August 2015. Since recovering from the surgery, Natalie has become an advocate for Crohn's patients via her blog, Lights, Camera, Crohn's: An Unobstructed View, where she provides readers with weekly insight about what life is like living with a chronic, invisible disease.
About Crohn's Disease:
Crohn's Disease is a category of Inflammatory Bowel Disease (IBD). Individuals with the condition experience chronic inflammation of their gastrointestinal tract, which results in abdominal pain, fever, and loss of appetite, among many other life-altering symptoms.
Episode 4: Janey Lowes - WECare Worldwide
In 2014, after backpacking in Sri Lanka, Janey Lowes learned of a large population of dogs living in poor health and under terrible conditions on the island. Being a trained veterinarian, she returned home to the United Kingdom, where she formed the nonprofit organization, WECare Worldwide. She returned to the island shortly thereafter and has made it her life’s mission to care for the dogs in Sri Lanka.
About WECare Worldwide:
WECare Worldwide is an organization that provides free veterinary care to animals in need worldwide. Ultimately, WECare Worldwide plans to extend veterinary services around the globe but, right now, they are concentrating on tackling the issues with the street dog population in Sri Lanka. It is estimated that there are up to 3 million street dogs in Sri Lanka. WECare Worldwide is in the process of carrying out a 5 year plan, in which they will look to help eliminate rabies in the country and also humanely reduce the number of unwanted street dogs.
Episode 3: Jay Austin - Minimalism
This week's guest is Jay Austin. Bill and Jay discuss the Minimalist lifestyle, how he purged much of what he owned, moved into a tiny house and how he is now living off the grid for the next several years! Jay is currently biking around the world with his girlfriend as he strives to achieve a life of Minimalism and happiness.
Minimalism is a lifestyle in which an individual removes unnecessary items from their life in an attempt to better themselves and focus on what truly matters to them.
Episode 2: Erin Gianaras - 27 Year-Old Stroke Survivor
Bill sits down with Erin Gianaras, who at age twenty-seven suffered a life-altering stroke while running errands on a hot summer day. Erin shares intimate details of that day and how she spent the past year recovering and rebuilding her life.
A stroke can happen to anyone at any age. A stroke occurs when blood flow to any part of the brain is cut off. Each year, nearly 800,000 people experience a new or reoccurring stroke, making strokes the fifth leading cause of death and the leading cause of disability in the United States.
Episode 1: Megan King - Ehlers-Danlos Syndrome
The debut episode of People You Should Know Podcast! Bill describes the vision for the podcast and then speaks with Megan King, who shares her experiences as an individual with Ehlers-Danlos Syndrome (EDS).
Ehlers-Danlos Syndrome is a connective tissue disorder, which causes skin hyperextensibility (skin that can be stretched further than normal), joint hypermobility (joints that stretch further than normal) and tissue fragility. According to the Ehlers-Danlos Society, research statistics of EDS show the prevalence as 1 in 2,500 to 1 in 5,000 people.