lifestyle

 
All images: Sophia L. Smith www.makingofmemories.com | Art work: Deborah Shedrick www.deborahshedrick.com

All images: Sophia L. Smith www.makingofmemories.com | Art work: Deborah Shedrick www.deborahshedrick.com

 

The Haute is “Corporate Gents” series spotlights successful businessmen who are hidden within the fast-paced executive suites, corporate boardrooms, corner offices and the serial entrepreneur’s glass ceilings.

 

Ovell r.Barbee

Haute’s Corporate Gent

By Jennifer Ginger | Contributing Feature Writer & LaVonne Trent | Lifestyle Editor

Our summer issue pays homage to a Corporate Gent who exemplifies excellence in business, and lives a cultured and fashionable lifestyle.  Once a professional model (with a billboard to prove it), he masterfully incorporates his debonair style within and beyond the casual business attire during workdays — fashionably standing on his own terms whether he’s at a speaking engagement, traveling the world or serving on the Men’s Ministry Committee at Messiah Baptist church.

Barbee accepting the Grand Rapids Community College’s Walter Coe Public Service Award.

Ovell Barbee is a modern-day renaissance man.  As Senior Vice President of Human Resources and Diversity Officer at Spectrum Health, Barbee is a leading figure in his Grand Rapids community. Known for his confidence, candor and understated swag — he wore a plaid suit and ascot tie to receive Grand Rapids Community College’s Walter Coe Public Service Award — Barbee actively mentors young professionals and contributes to the organizations that supported him as he pursued an education. Each year he sponsors a local student and covers their text books and school supplies. But his first and most impactful investment was in himself. 

From an early age, Barbee’s family instilled the importance of obtaining an education, and they emphasized how professional contributions led to more life choices and options. Craving financial independence and the freedoms it affords, Barbee started his first job as a newspaper carrier at 12. He bought his own clothes and later a moped then a car. He aspired to replace news reporter Geraldo Rivera on 20/20, but as he neared completion of his communications degree, he pivoted to social work. His new career path seemed like a better fit of his skills and interests, though he didn’t think he should be compensated for wanting to help people. He found his niche when he took a personnel management class related to social work in the workplace. He later completed a second Masters in Labor Relations and Human Resources at Michigan State University. 


Never too far from work Ovell utilizes his home office.

“I realize that a very important component of being a leader at this level is relationships. Early on in an individual’s career people spend a lot of time being the best performer, hoping that their performance can l (5).png

After transitioning to human resources, Barbee was propelled to and flourished in a range of leadership positions that allowed him to help shape and thrive at several Fortune 500 companies. He was helping people. And he was a direct reflection of what years of focus, dedication and determination can bring: results. 

Barbee credits his involvement with professional African American organizations with exposing him to other professionals with similar backgrounds and stories — people who understood how to navigate corporate work environments and the importance of outreach and expansive networking.  

“Usually in most corporate environments it's rare to have an opportunity to network with individuals who look like you,” said Barbee, who has decades-long involvement with Alpha Phi Alpha fraternity, the Society of Human Resource Managers and the National Black MBA Association, which named him one of the top 50 executives in the country. “I realize that a very important component of being a leader at this level is relationships. Early on in an individual's career people spend a lot of time being the best performer, hoping that their performance can lead to career advancement if it is of interest. And what happens, over time, as you continue to advance, relationships become increasingly more important.” 

Though aware of the soft spotlight cast upon him as he navigates the mostly white and male C-suite, Barbee doesn’t assimilate or contort himself to fit other’s expectations — he is unapologetically himself. He walks into a room and greets everyone he encounters. He expresses his opinions. He respectfully challenges ideas. 

An avid runner Ovell often competes in marathons.

“It’s never been a goal or objective of mine to prove my self-worth. I validate myself,” said Barbee. Instead, he leads with authenticity and action, not his accomplishments. And on occasions when things don’t go as he intended, he takes pride in being able to look himself in the eye and know that he made the right decision because he was true to himself. 

And while it can often seem like a radical act to be black, confident and self-aware in America, Barbee’s personal and professional aspirations aim to directly address and help remedy the socially determining categories (healthcare, education, transportation, housing) that contribute to the often-fraught outcomes experienced by underrepresented groups. Through his actions, Barbee shows that by investing in ourselves and our local communities, we can implement policies and practices that help us thrive. 

Haute is salutes our quintessential Corporate Gent, Ovell Barbee, who reflects compassionate leadership, excellence, and philanthropy to help shape a diverse, vibrant and meaningful community and corporate world. 


 Health & wellness


Epilepsy - My Story

By Angie May | Haute Is Contributing Writer

Angie May | Mom | Cheerleader | Epilepsy Cure Crusader.

Angie May | Mom | Cheerleader | Epilepsy Cure Crusader.

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Life works in very mysterious ways. You could be leading a very typical, happy life until one day when something completely unexpected happens and in that moment everything changes and a brand new chapter of your life begins. In 2011 life was wonderful. Our daughter Madison was a very happy, healthy and busy two year old little girl. I was working for an experiential marketing firm in a career I absolutely loved. My husband John and I both traveled for our jobs but loved spending time together and with Madison, our idyllic family life. One night in October 2011 we put Madison to bed like every night prior and we went to bed ourselves. Since she was still so little and at the time we were living in a bungalow style home we had a video monitor in her bedroom. Little did we know this video monitor would be the most valuable item in our home, because that night it saved Madison’s life? In the middle of the night we heard a strange noise on the monitor and looked to see Madison face down in her bed shaking. We ran to her room to find her completely unresponsive, jaw clenched, eyes unfocused and her little body jerking, what was happening to our baby? We immediately called 911 and in minutes the police and paramedics were in our living room saying the word “seizure”, “she’s having a seizure”. We were completely dumbfounded, she was healthy, normal birth, perfect development, in fact she was an advanced learner, how could this happen to her? Little did we know anyone can have a seizure at any point in their life for a number of different reasons but also for no reason at all. This is where our epilepsy journey began.

 
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Epilepsy is the general term for a variety of neurological conditions characterized by recurrent unprovoked seizures. A seizure is a brief disturbance in the electrical activity of the brain that causes temporary changes in movement, awareness, feelings, behavior, or other bodily functions. Epilepsy is the fourth most common neurological disorder in the United States after migraine, stroke, and Alzheimer’s disease. About one percent of Americans have some form of epilepsy, and nearly four percent (1 in 26) will develop epilepsy at some point in their lives. The number of Americans who have epilepsy is greater than the numbers who have multiple sclerosis, Parkinson’s disease, and cerebral palsy combined. 10% of Americans will have at least one seizure at some point in their lives. Epilepsy is prevalent among other disability groups such as autism (25.5%), cerebral palsy (13%), Down syndrome (13.6%), and intellectual disability (25.5%). For people with both cerebral palsy and intellectual disability the prevalence of epilepsy is 40%. Anyone can develop epilepsy at any time. Incidence is highest among the very young and the very old.

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Epilepsy is the fourth most common neurological disorder in the United States after migraine, stroke, and Alzheimer’s disease.

After Madison’s first seizure she started medication and was treated by a neurologist. She went on to have a few more Tonic Clonic seizures called “break through” seizures before we had her medication dosed correctly for her to be controlled. A Tonic Clonic seizure formally called Grand Mal is the type of seizure people typically think of when they think of epilepsy as it can be very intense with body jerking movements and many physical changes and usually lasts just a few minutes before the person returns to normal consciousness. There are about 30 different types of seizures and over 60 different types of epilepsy. In fact people often go undiagnosed for many years because they do not realize that they are experiencing seizures. In our case it was very clear what was happening to our daughter and we were committed to get answers.

Shortly after Madison was diagnosed with Epilepsy we were desperate for more information and to learn about what was in store for Madison and our family. We attended an “open house” event at the Epilepsy Foundation of Michigan offices in Southfield, MI and we were immediately embraced by their staff and others in the epilepsy community who were experiencing exactly what we had been going through. The connection to the Epilepsy Foundation of Michigan is where this new journey took a positive turn. We quickly learned that Madison was on the wrong medication and through the help if the foundation we found an Epileptologist, a doctor who specializes in epilepsy and things started to feel somewhat manageable. We began to get involved with the programs and events hosted by the foundation and we started a team for the annual Metro Detroit Summer Stroll for Epilepsy.

 
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In 2012 our youngest daughter Ashlyn was born and our life felt complete. We were back to all activities, family vacations, life as normal for many years. Then in 2016 our life once again took a turn when at the age of just 3 years old Ashlyn suffered from a life threatening seizure that felt like a reoccurring nightmare. Now our fight against this horrible disease of epilepsy became twice as strong. The main positive factor at this point was that we knew what to do this time, we were prepared for this diagnosis and we had many more resources and more information in order to help her live with epilepsy

Having more than one person in a family with epilepsy might seem rare but it is not uncommon. There can be a genetic component to the disease so the prevalence of having more than one family member with epilepsy is often higher. Some types of epilepsy run in families and are both inherited and genetic. Not all epilepsies that are due to genetic causes are inherited. In general, if a person’s mother, father or sibling has epilepsy, their risk of developing epilepsy by the age of 40 is less than 1 in 20 and the likelihood of inheriting epilepsy may differ significantly if a person has a relative with a known genetic epilepsy diagnosis.

Our focus now is on education and advocacy. We find it imperative to tell anyone and everyone about our story in order to normalize the disease and inform anyone who has contact with our girls or persons epilepsy on seizure first aid. The Epilepsy Foundation of Michigan has a community education team who will go into a school, workplace or any other public location to train the staff, teachers, etc. on seizures, seizure emergencies and rescue medication protocols. Additionally, it is our goal to erase the stigmas associated with the disease. A seizure can be very scary for anyone who witnesses it but if you are informed on how to help you too could possibly save someone’s life.

Now 9 years into this disease we are deeply involved with the Epilepsy Foundation of Michigan. I am the Vice Chairperson of the Board of Directors for the Foundation, we have a robust Summer Stroll team and we have raised over $200,000. I am also the co-chair for annual charity gala called the Toasting Hope Tasting Event which is a beautiful and exciting night filled with food and beverage tasting pairings, live and silent auctions, a live band and more occurring every September. For all the things this disease has taken from us, somehow it has given us an incredible community of friends and resources and we have made the most of this new chapter of our life.

 
The Toasting Hope Tasting & Summer Stroll events have raised over $200,000 in donations.

The Toasting Hope Tasting & Summer Stroll events have raised over $200,000 in donations.

Angie May & team at this years Epilepsy Foundation’s Summer Stroll

Angie May & team at this years Epilepsy Foundation’s Summer Stroll

If you have someone in your life that has had a seizure, has been diagnosed with epilepsy or has a family member in need of support, please reach out to the Epilepsy Foundation of Michigan. If you would like to get involved, volunteer or simply attend any of their exciting events throughout the year please check them out online www.epilepsymichigan.org or Facebook, Instagram and Twitter.


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5G The New Data Frontier

By Robere Lett | Publisher | Style Editor

As someone who is not particularly savvy when it comes to the advances in technology, I find that I am intrigued by the new 5G banter that has been the center of much controversy - We have been hearing about 5G and it’s potential to cause everything from Coronavirus to radiation poisoning, to various cancers (no definitive proof has been found yet).

Now, 5G or 5th Generation as you may or may not know is a grid of networks and wireless systems that carry signals to your mobile phones and other wireless devices. Upon further research it appears that 5G will have 100 times the capacity of 4G, so say you want to download a two-hour movie with 4G it would take six minutes but with 5G it will take only three and half seconds.

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If super-fast internet service is what you crave you’re in luck but what about data and privacy issues, there are mounting questions regarding this issue as it seems 5G will require more cell towers be placed closer to together due to the short-range distance needed to keep the signal strength, while 4G did not require such proximity this also allows for easier tracking. As of now, 4G can only determine your approximate location by pinging off a cell tower it is harder to determine the exact location, with 5G having closer range tracking becomes more exact. This leaves the opportunity to be tracked by your spouse or boss if you are late coming home or late to work. Of course, there are ways to abate the misuse of 5g's shadier side but let's face whenever the opportunity presents itself to do the wrong thing someone will take advantage and use it for their own good. Good or bad 5g is here! with 2020 it is already being rolled out overseas and soon to be on the mobile phone near you.

The Hautest 5G Compatible Phones