Kudos to Deer Creek & the Dave Matthews Band

Last Saturday Irena and I had the pleasure of attending the Dave Matthews Band concert at Deer Creek (Ruoff Music Center…but I’m from the time when it was called Deer Creek, as is Dave Matthews, and I’m pretty sure we both refuse to call it anything corporate) with our close friends Scott & Phoenix. A few months ago I reserved our tickets over the live nation app on my phone. While selecting lawn “seats” I didn’t see any option for selecting wheelchair accessible lawn seating, and though there was no mention of rules regarding accessible parking, I opted not to purchase the “premium parking” with our tickets…assuming our disability parking tag would get us as close to the front as possible.

As always, whenever going to a venue like Deer Creek, I called ahead to be sure I understood all of the options. A very knowledgeable customer service person answered all of my questions.

Yes, there was wheelchair accessible seating in the lawn. Two “concrete pads” were set up for people with disabilities. We should have been able to reserve space on them when we reserved our tickets, but because I used an app on my phone I didn’t see all of the options that I would have seen on my laptop…lesson learned.

No, the fact that I didn’t reserve wheelchair accessible lawn seats for our tickets wasn’t an issue. get there early and try to be near the front of the line when the gates open and we should be able to get seats in the wheelchair accessible area…you can reserve seats in those sections, but they’re mostly first come, first serve…sure, if my family and friends want to lay on a blanket near the accessible seating they can, but they should be able to fit all four of my companions on the “pad” with me. They didn’t mention that there would be folding chairs for companions and people with disabilities who don’t need wheelchairs, already available in the accessible section, but that was a nice surprise! It was really more of an extension of the seated pavilion sections than part of the lawn. Scott has his own disability that impacts his mobility too, though he needs a cane rather than a chair, but being in this ramped section at the front of the lawn was a huge benefit to accommodate his experience as well!

No, I didn’t need to purchase premium parking. My accessible parking tag would get us all the way up to the parking closest to the facility. The only issue was that they didn’t tell me to be sure to park on the front side of Deer Creek. There is a back entrance that goes directly into the top area of the lawn. Due to where we pulled in, we were directed to the accessible parking on the back side. When we got out of the vehicle someone from the parking team told us that they had called for a large golf cart to come pick us up. That person moved on as quickly as they spoke to us, back to directing the parking lot. The sloped que for the line on that side wasn’t too far away, though it would still require going a short distance on a gravel road to get there. After waiting for a little bit and watching the line start to grow, we decided to walk/roll to the line without waiting any longer for the cart. By the time we claimed our spots in line we were only a short distance from the gates. We sat in the sun and chatted for about 40 minutes and then the line started to move. At that point a member of the staff, Erica, spotted me in the wheelchair and stopped us from proceeding. Apparently on this side there were stairs inside the gates, and I didn’t have my prosthetics; we would need to move around to the main entrance, where the line had been forming for some time, and the gates wouldn’t open for another 20 minutes or so.

Erica was very clear that she would return momentarily with a cart large enough for the five of us to drive us around to the other side. I was using my rigid frame chair, which doesn’t fold in the normal “flattening” way that folding frame chairs do. My chair didn’t exactly fit in the cart, so Irena and Phoenix sat on the back and held my chair up off the ground as we were chauffeured to the front of the facility…I just want to point out that the wives of men with disabilities prove their equality, and sometimes superiority (yes, I said it, and I mean it) on a daily basis. We moved at a quick pace through parts of Deer Creek that I had never seen before; the areas where the tour busses park, press areas, staff areas, etc. As we came around the north side of the facility and the main entrance came into view I was distraught at the sight of the growing sea of people. There was no way for Erica to get us through them, not even to deposit us at the end of the line.

We parked in front of what Erica referred to as the VIP gate, off to the side of the main gates, where no one appeared to be waiting to enter, and no staff appeared to be ready to open. Erica radioed the staff working that area and explained our situation, to which they replied with instruction and a commitment to take responsibility for helping us from there. From a professional customer service perspective, Scott and I were both impressed when we heard Erica reply “what I heard is that you want me to leave them at the VIP gate and you’ll take responsibility for letting them in when the gates open and help them from there, is that correct?” We waited for a while, watching as different lines of ticket holders with special status were let in, which had me concerned, as there was no place for anyone else to sit while we waited and I knew Scott’s disability causes it’s own unique brand of fatigue, but he’s stronger than he knows and fought through it. Ultimately, as the main gates were opened a staff person whom we believe was named Abby approached, personally did our security check, and then sent us into the throng of people searching for the perfect spot to enjoy the concert.

As I said, the accessible seating for the lawn at Deer Creek is really more like an extension of the seated pavilion, just at the front of the lawn off to either side of the stage, instead of under the pavilion roof. It’s ramped up so that you’re not sitting right on the pavement in the main walkway, which gives you a pretty much unobstructed view of the action on stage as well as a conveniently positioned big view screen…and a great place to watch the crowd! There was a constant dance obstacle course to cross the main path just to our left and below us; so much fun to watch! They also positioned a beverage vending station right on the opposite side of the walk from the front of the ramp and had more than one vendor walking around selling pizzas, cotton candy, etc…you just needed to get their attention to get them to come up into the section.

My only issue with this section, which is separated from the rest of the lawn by metal fencing, is that the obvious intended openings to access the lawn from the accessible section were closed off with sections of metal fence zip-tied over the openings…cutting people with physical disabilities off from the rest of the lawn. I know that this was done to prevent people in the lawn who didn’t need to take up space in the accessible area from abusing that space, but it was also disappointing to not be able to access the lawn if I would rather lay on a blanket in the grass instead of sitting in my wheelchair. I should note that we did see a group of people with no obvious physical impairments among them take up a lot of seats in the accessible section before the concert started. After a while a member of the security staff approached them, spoke with them discreetly, and then they left.

All things considered, it was a great concert experience! We had a wonderful time with beautiful weather and a great night with our dear friends! The Dave Matthews band was performing at a level and intensity that I’ve never seen before, and I’ve been to more than one of his concerts going all the way back to when Ruoff Music Center was simply Deer Creek! Scott is a bigger fan than I am and he was blown away by the musical master class that we were lucky enough to witness. He said it was the best concert he’d ever attended! Kudos to Deer Creek and the Dave Matthews band for ensuring a great accessible entertainment opportunity for all people of all abilities! #DMB #RuoffMusicCenter #DeerCreek

Walking Spirit Blog – Historical Posts

I invite you to read my journey here: Walking Spirit. Through the archives you can begin with the earliest blog posts, written by my sister to keep our community of family, friends, and supporters updated on my condition while I was in a medically induced coma and in the early days of my recovery. You can then read along as I share highlights of my journey through the years adapting to an ever changing life as a person with disabilities.

Survival Day #15 – Year of the Pandemic

What has happened to our world? (Part of me just wants to leave it there, that question, unanswered, and go back to bed). Fifteen years ago an almost 6 week medically induced coma was a wonderful way to escape from reality. Though not my intent when I climbed into my Jeep after a long day of work at the Walden Inn on DePauw University’s campus in Greencastle Indiana to start my hour long commute back to Indy, the long nap that followed allowed me to kick the habit of smoking cigarettes and it brought my loved ones together in ways that only traumatic events can. It also sent me into a dream world that maybe, just maybe, you’ll all get to read about soon. (Please understand that “soon” is a relative and somewhat aspirational word…at least in this case).

In many ways we’ve all been living through one long traumatic event that has dominated 2020. That dream world, which was full of nightmare experiences interspersed with beautiful imagery, thrilling moments, and awe inspiring revelations seems far more inviting now than at any point in the past fifteen years. If I could just go to sleep for a while…for a long while…maybe when I wake up all the madness will be over and my family and friends will all be able to gather together once more and hold each other in loving embrace without fear of unseen, potentially lethal, viral infection. But, alas, I have not voted yet, so no such restorative nap is imminent. For truly, now more than ever, our collective votes may be the only chance we have of flipping the script and putting an end to all of this absurdity…so I will stay awake.

The year has been strange and challenging for all of us. While in a strange way the conditions of the pandemic has led to improved health for me, I also had to stand witness as my wife, step-children, brother & sister’s-in-law, and all of their family suffered through the loss of my father-in-law. He was an amazing man who led a long and fantastic life. Alzheimer’s afflicted him before I ever really had the chance to know him, but I have fond memories of him as I came to know his family and love his daughter & grandchildren. In the years that he was a part of my life, we had one day where we were together throughout the entire day and he was surprisingly lucid all day long. He shared personal stories with me about himself, the love of his life (my wife’s mother), and his family history. I will treasure that day and his stories always. Sadly, he was among the first in his nursing home to contract Covid-19 from an asymptomatic nurse who didn’t wear a mask when she entered his room. (In all fairness to the nurse, this was early on when our nation’s leadership had not embraced the concept of such simple protective measures…though it was months after they knew better and were still hiding many truths from us). He fought the virus longer than most, for nearly two months, as we all came to terms with what this really looked like, and in the end he showed us how to leave this earth with a legacy of family and history and the impact of all of his many good acts in life.

For me, the growing reality of the pandemic began on my 45th birthday. I had broken my tailbone during a bad fall the week before and was laying in a reclined position on our bed with an ice-pack under my butt, watching the news as lockdowns were being reported all across our state and the horrors of overwhelmed healthcare systems were being reported from New York and countries abroad. Irena was working in the living room…day one of what has now been an eight month continuing exile from her office. Colleen was in her room sleeping after we had made her get up early for a school bus that never came (our bad for not checking our emails before we went to bed on March 12th). After several days of watching the world shut down I couldn’t sit on my bruised rear-end in front of the tv any longer. So, I put an inflatable donut pillow in my wheelchair (not easy to balance on with no legs, but it probably did wonders for my core strength) and headed outside to begin building a garden for Irena and her sister to maintain.

I dismantled the sections of a privacy fence we had removed from the middle of our yard on day one of our ownership of this property. For over a year it had leaned against the back of our storage shed and now, due to the pandemic, I had motivation and inspiration to put the lumber to good use as raised garden beds. I went a little overboard, had several arguments with Irena about how big she wanted the garden to be and the number of cedar bushes I would have to remove to make space for it (fyi, for all the married people out there, we weren’t arguing about the garden or the shrubs, we were stressed and hurting and didn’t know how to deal), and ultimately had a summer and fall with a lot of zucchini, tomatoes, cucumbers, and some mystery vegetables & herbs that we don’t remember planting on the menu.

When the garden was done I threw myself into whatever outside projects I could find. While my tailbone continued to heal I built a new ramp for the storage shed (which also doubles as a new roof with attic space for a warren of chipmunks that I couldn’t bring myself to kill). I started swimming laps three days a week again, and laid a new patio with bricks that a neighbor was kind enough to donate, in an effort to improve my mobility outside. As the outdoor projects dwindled I began to recognize the need to stay active and so began looking for work. I also dusted off the half completed manuscript of a book that I walked away from four years ago and started the editing process on the only completed portion of it. With Irena’s support we created an outdoor office space where I can focus without being a distraction for her while she works in the living room turned office space, or disturbing Cade or Colleen while they work in their respective home spaces turned classrooms.

Conversations with old friends and mentors ultimately led to a new relationship with an old organization from my past. I began doing outreach for a non-profit that helps people with disabilities live as independently as they want. This introduced me to the world of Zoom and other virtual meeting platforms…a challenge for a semi-robotic luddite, but I’m learning. Beginning this work has also reconnected me with peers from the disability community whom I had not communicated with in years. I’m actually now going in to an office one day a week, which gives me a reason to regularly use my prosthetics again. During the pandemic I have actually improved my health and expanded my circles of influence…a five year plan is beginning to take shape.

While there is still a great deal of uncertainty in the world…including our personal world…there is also a lot of positivity. We have been lucky, and every day I’m reminded to count our blessings. Irena has been able to adapt her job to work from home and has only become more valuable to her operation. She had major surgery on her hip in the middle of all of this and has safely recovered with more energy and mobility than before. While many are laid-off or furloughed I have been able to find work that is both rewarding and purposeful. Our children have stayed healthy and have been able to maintain a semblance of a social life, while also continuing their education.

In the middle of all of the sickness, economic instability, racially & socially driven violence, and death that has dominated our past year it is easy to feel the hate, anger, and uncertainty in the world and let it take control through depression or intimidate you to hide from it all by going to sleep for as long as possible. If you’re struggling with that, take a step back, meditate or pray if need be, but focus that meditation and prayer on allowing your eyes to open to the good things in your life, the blessings…your blessings, and the hope that is still very much alive in our world. If you still struggle to see it, then I would encourage you to take a long hard look at what you don’t like or what obstacles are in your path and then take action to change your situation. Maybe it’s placing a call to a friend, a doctor, or an organization that is there to help. Or, if the challenges that confront you are more global and less personal, then vote to change our leadership across the board and give the world around you a new chance to improve and evolve. If you’re not satisfied with your current situation, or the state of our world, change is the only way to bring about improvement. It can be scary, but change doesn’t have to be bad, especially if you take an active role in it.

Friends Pitch In For Indy Man’s High-Tech Legs

A life changing car accident nine years ago left Indianapolis’ Jeremy Warriner a double amputee. Warriner’s friends are helping him fundraise for his third set of prosthetic legs that carry a combined price tag of over $100,000.

Chrysler Bankruptcy Impacts Consumer Lawsuits, Pension Plans

Walking with hydraulic prosthetics, Jeremy Warriner can appreciate good engineering and design. He’s on his third set of legs in three years. He lost his birth pair in a fiery crash in October 2005 and believes a highly flammable plastic brake fluid container in his Jeep Wrangler is to blame. Now he wants the right to face Chrysler in court.