Life With Livy Videos

Life With Livy Videos


Living with and raising a child with disabilities takes determination, patience, perseverance, knowledge and a whole lot of love. Our lives have been forever changed because of the new world in which we live. We have often heard from our family, friends and even complete strangers, "I don't know how you do it." So many of you have helped us along the way that we thought it was time you got to meet the real Olivia, to see the obstacles she faces as well as the challenges and great joy we share as a family. We also want to show you what Livy has inspired us to create and how age doesn't matter when wanting to make a difference. Livy is a constant reminder for us to never give up hope. In the spirit of our endeavor, we will be adding videos of our experiences to this page on a regular basis so you have a better understanding of Life With Livy.

Episode 32: 7/26/2016 - The Scheinman Family and Lemonade for Livy

Episode 31: 5/9/2016 - President and CEO of the Epilepsy Foundation Kids Crew

Episode 30: 4/14/2016 - Trip to the National Walk for Epilepsy in 2015

Episode 29: 3/14/2016 - Presenting at the Epilepsy Foundation of Indiana Roaring Toward A Cure Gala 2016

Episode 28: 2/15/2016 - Livy Using Tobii Eye Gaze

Episode 27: 1/13/2016 - Livy Opening Tobii Eye Gaze

Episode 26: 6/17/2015 - A Father's Promise: Making A Stand Against Epilepsy

Episode 25: 4/30/2015 - Hospice Gala 2015 Presentation

Episode 24: 11/15/2014 - The Epilepsy Lip Sync Challenge

Episode 23: 6/26/2014 - A Family's Stand Against Epilepsy

Episode 22: 3/31/2014 - Don't Give Up. Give Back.

Episode 21: 3/22/2014 - Opening Minds And Hearts Award 2014

Episode 20: 10/18/2013 - Imagine A Cure

Episode 19: 5/30/2013 - Livy's Hope For A Cure

Episode 18: 3/21/2013 - And The Award Goes To...

Episode 17: 2/25/2013 - Rock Star For A Day

Episode 16: 1/1/2013 - What Is Your Message?

Episode 15: 12/13/2012 - Giving Back 

Episode 14: 10/19/2012 - A Sister's True Talent

Episode 13: 7/31/2012 - My Olympic Dream

Episode 12: 7/22/2012 - From The Beginning

Episode 11: 6/18/2012 - I Am Livy

Episode 10: 6/11/2012 - Bath Time For Livy

Episode 9: 6/4/2012 - Hailey And Livy On Bay News 9

Episode 8: 5/29/2012 - Road Trip To The Project Store

Episode 7: 5/8/2012 - Visiting Winter The Dolphin

Episode 6: 4/30/2012 - Easter 2012

Episode 5: 2/27/2012 - Young Hero

Episode 4: 11/19/2011 - Changing Livy's Mic-Key Button

Episode 3: 10/28/2011 - Olivia Standing In Her TeeKoz

Episode 2: 6/17/2011 - Olivia's Daily Food And Medication Routine

Episode 1: 6/8/2011 - The First Six Years


Episode 22: 3/31/2014 - Don't Give Up. Give Back.

Most of us will face a traumatic experience at least once in our lives. Where we feel we can no longer keep going. Where every day seems like it is a fight just to get through. We wish our days away hoping for an answer. Am I on the right path? Am I strong enough to make it? How will I keep going? We have been in that very same position with Livy a number of times. For years, we didn't know how we could function in a normal capacity ever again. We were angry. We were heartbroken. We were devastated, confused and lost all at the same time. And most of all, we were so sad for Livy and all she went through.

Our last major hospital stay due to uncontrolled seizures was in April of 2010. It had been a year since Livy’s hemispherectomy operation. We were gradually starting to see her seizures get worse. We asked ourselves, “What are we going to do this time? She can’t have any more surgeries?” Allison called me from the pediatrician’s office since we always follow protocol to make sure nothing else is going on. Shortly after the doctor assessed her, he said, “Get her to the hospital now,” and off we went.

We were admitted and over the next several days, Livy got worse and worse. The seizures came at a violent pace. With arms outstretched, her little face contorted and eyes blinked rapidly. She held her breath and I watched her stomach collapse in on itself. When finally she was able to take a gasp of air, she let out a defeated whimper and would lay there lifeless. I didn't think it was possible for someone’s heart to shatter so frequently but with every new round of seizures, I ached for her and was crushed.

This went on for several weeks. During this visit, we were asked for the second time in six years if we wanted to sign a DNR (Do Not Resuscitate). We met in a board room with the entire team of doctors, nurses and psychology staff to discuss our options. We were told that this could potentially be Livy’s life for as long as she lived. To me, that was not a very good option.

After our meeting, Allison and I went back to Livy’s room, kissed her on the forehead and embraced each other. We collapsed onto the couch in tears and sobs. Was it really the end? Would Livy not come back this time? Over the next several days, Allison was told by the doctors that she needed to go home. She had become so distraught that they feared for her health. I took over and tried to separate the intense emotions I was feeling from the job I had to do which was to make sure everything was done for Livy that needed to be done.

As I sat at Livy’s bed side and watched her get a moment of sleep after being given extra medication to stop her seizures, I searched my mind for what I could do. With a lack of sleep and emotions raw, the brain tends to wonder in escape. Only for me, this moment led me to the idea of what Livy’s Hope could be. For years I had helplessly watched Livy and many of her friends and classmates wither under the weight of epilepsy. But then they miraculously recovered and their brilliant, pure smiles returned. I believe this was possible because they never gave up and neither did their families. Never giving up hope has been incredibly powerful for us and the only way we have made it through when all seemed lost. Creating an organization based on hope that is able to inspire others and to give back was what I envisioned. I desperately wanted to regain a sense of control that had been lost because of epilepsy and I wanted the means to help Livy and others like her.

Livy did recover from that hospital stay and she has never given up since. She has fought every day through the 1,000’s of seizures. She has endured broken bones, falls and a permanently dislocated hip which constantly causes her pain. She cannot speak or feed herself or tell us what hurts. But she can smile, show emotion and love. She has taught us all how precious life is and that every person has purpose. She is the reason for Livy’s Hope and she is the spirit that lifts our hearts to new levels. She has given us a new direction; one that is filled with inspiration and a desire to help others.

Hailey’s life has also been changed because of Livy. As twins, I would expect there to be a special bond. But I never expected there to be the amazing relationship that has developed. Hailey always includes Livy in what she is doing. She sees, in Livy, a sister, a friend and a hero. Hailey admires Livy for what she has endured and is the first one to comfort her when needed. It is because of that love that Hailey has the ability to help others and to recognize the community’s need for hope and inspiration. She spreads her happiness from person to person and teaches us that we can all make a difference. She helped to create Livy’s Hope and it started with the sale of her first painting on eBay. As you will see in the video, Hailey is as much a part of Livy’s Hope as Allison, Livy and I are.

As Livy’s Hope has evolved, we realize more each day the strength that comes from bringing people together. Some we have met have similar stories. Some are inspired by our story and want to get involved. But all have one thing in common. They want to help others. Our mission is to support children with medical needs and their families and to motivate as many as we can to do the same. Winston Churchill once said, “We make a living by what we get. We make a life by what we give.” We want to make amazing lives for us and all those who become a part of Livy’s Hope.

So if you ever find yourself in a situation where all appears lost or you don’t think you can take any more or your emotions overwhelm you, remember, “Don’t Give Up.” Instead, turn to helping others and making a difference. Do everything you can to “Give Back.” Your life will be changed forever.


Episode 24: 11/15/2014 - The Epilepsy Lip Sync Challenge

Presenting our #lipsync4epilepsyLip Sync Video! Help us support epilepsy research with the Epilepsy Lip Sync challenge.

We challenge The Livy's Hope Kids Crew, Jayde Donovan from Tampa's Hot 101.5 and singer Katy Perry to a sing off as we join together to search for a cure with the Epilepsy Foundation of America at

Please share the campaign with your family and friends. If you would like to participate, just make a lip sync video to your favorite song alone or with a group. The more creative the better. Before you start the music, make sure you tell people why you made the video, challenge three of your friends and let people know what you will be singing. Then post the video to the web using this verbiage, "Help me support epilepsy research with the #lipsync4epilepsy challenge! I challenge X Y Z (tag your friends here) to a sing off as we join together to search for a cure with the @EpilepsyFoundationofAmerica at". You can also suggest that people make a donation to the campaign when going to


Episode 23: 6/26/2014 - A Family's Stand Against Epilepsy

We have no idea what life for our family would be like if Livy hadn't been born with epilepsy. From the moment she took her first breath, she was destined to change what we perceived to be our path in this world. We never knew what epilepsy could do to someone or to a family. A seizure was something we saw in shows like ER or House when people were in accidents or had brain tumors. We didn't know the statistics such as 1 in 26 people will develop epilepsy or that there are 3 million people in the United States and 65 million people worldwide that have epilepsy or that two thirds of people with epilepsy don’t even know the cause. We didn't know that an estimated 50,000 people in the United States die each year from status epilepticus (prolonged seizures), Sudden Unexpected Death in Epilepsy (SUDEP), and other seizure-related causes such as drowning and other accidents. We didn't know.

We are now deeply intimate with all that epilepsy is and the devastating effects it can have on individuals and families. When we hear stories of our friends or those outside of our circle whose children are in the hospital because of uncontrolled seizures, our hearts break because we have been there and are all too familiar with the intense feelings of helplessness and isolation. There are many different levels of severity in epilepsy and we have seen the worst.

We have no idea what is like to have twins that run and jump, ride bikes or play dress up together. We're not sure how it feels to go to Disney or a restaurant or a movie as a family without worrying if it is too loud or if we brought the right medications. The last time the four of us flew on a plane as a family was nine years ago when we traveled back from Boston Children’s Hospital. The girls were five months old and Livy had already been to three hospitals. Life is full of surprises and we suppose that when each of us gets up in the morning, we never really know how our lives will change.

What we do know is that we were given an incredible gift that has inspired our family to do something special and that we will not let epilepsy beat us. What we do know is if people across the country work as one, if we speak with a unified voice, we can make significant progress toward finding a cure. What we do know is that we will fight for the millions of epilepsy warriors and their families who desperately need relief from the disorder. What we do know is that our family is ready to make a stand and show that hope is stronger than epilepsy.


Episode 25: 4/30/2015 - Hospice Gala 2015 Presentation

In 2005, Livy spent 5 months at the Woodside Hospice House in Pinellas Park, FL. The hospice team was an unending source of support and we are grateful for all they did for our family. We were honored to speak at the Suncoast Hospice Gala in February 2015 to share our story.


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