Thursday, May 3, 2018

Arkham Games: The Best Place for Gamers in Allegany County


Arkham Games: The meeting grounds for tabletop gamers in Allegany County
By William Everett
Frostburg (MD)
( 1,500 words, 5 interviewees)

LA VALE – On National Highway in La Vale, several cars pass by various stops seen on most American roads. Chain restaurants like Arby’s, pharmacies like CVS, and banks like BB&T are all scattered alongside the road.

As the drivers all move along to their various destinations, most of them probably pass a certain place that isn’t a chain store, but rather, a place that can only be found there on that road in La Vale: Arkham Games.

It is somewhat hidden from view, tucked away behind other stores that share the building, so it is easy to miss. However, those who do know about the store visit often. Judging from its name, one would think that Arkham Games is a gathering place for Batman enthusiasts.
But despite its name, Arkham Games actually has nothing to do with Batman. Instead, it is a store for all kinds of games. It has a large main room with its walls and ceiling decorated with colorful posters of games and playmats labeled with price tags.

These decorations depict images of Magic the Gathering, Yu-Gi-Oh, Hearthstone, Star Wars X-Wing, Warhammer 40k, and many other popular games. 




From the entrance, the wall on the right side of the room has shelves containing boxes of board games, card games, booster packs, collector’s binders, sets of dice, and anything else a card collector or tabletop player could want.



On the other side of the room are long tables where the players gather, who bring with them backpacks and boxes of their best cards and favorite figures to play and trade. Depending on the game, they’ll either roll out their playmats, or prop up figures and miniature fortifications.



On Wednesdays in particular, the players prepare themselves for weekly Yu Gi Oh tournaments. They hold practice duels before the competition, and meanwhile, they all talk and joke with one another, like old friends at a reunion.



At the register is a glass counter filled with shiny trading cards from all kinds of games. On a certain Wednesday evening at 6:30, one of the customers spoke with the store’s owner there about the cards inside, focusing on shiny and rare golden Digimon card resting under the glass.



The owner is none other than William Howard Poland the 3rd, a young entrepreneur in the making. However, his mother nicknamed him “Trey” at a young age because she thought “Trey” was French for “third” (it isn’t.) Nonetheless, the name stuck, and all of his friends and customers call him by that name.



“I have owned Arkham since January 2016,” Trey says. He started working for Arkham Games in 2014 after being a customer there for three years. Then, just a year after that, the store’s owner of the time, John Se, offered Trey an opportunity to buy the store from him before moving to Washington state. At the time, Trey had recently dropped out of college and was looking for a way to make some extra money. Owning and managing a game store sounded like a great idea to him.



Trey says that the process of acquiring the store was a “long and weird” process, as he had to prove to the bank that the game store was profitable and he had convince his mother to co-sign the loan. After jumping through all the hoops, Trey became the owner of the game store he had been going to for years.



On a particular Wednesday evening, while everyone else was dueling with Yu-Gi-Oh cards, Trey was busy arranging rows of chairs in the store’s empty corner to have them cleaned. One of the customers said that the chairs looked like a church, and another called out “Hey Trey, are you starting a cult?”



Even though he started going to Arkham to play games, Trey now has very little time to partake in them since he has to devote most of his time managing the store. He claims that he did not think that his new job would interfere with gaming, but it keeps him much busier than he thought.



After all, as a customer, one would be able to choose when to go to Arkham’s events, and it has many. Jessie McCourt, a friendly, regular customer of Arkham for six years, says that the store has events for all kinds of games throughout the week. From board games to video games to tabletop games, “there’s something for everyone here.” Jessie is an omnivore of a gamer at Arkham, as he participates in as many games as he can. From dueling card games like Yu Gi Oh to tabletop games with figurines and dice, like Warhammer.



Another gamer, Taylor Walker, who has been a customer for four years, claims that the games are the best part about going to Arkham. The bold and hearty gamer, who wears the same hat worn by Ash Ketchum from the Pokémon anime, quietly chuckled before stating,“bitches be crazy and games be dope.”



As fun as these games and tournaments are, as the store’s owner, Trey has to oversee all events. Consequently, he doesn’t have much time to actually play the games himself. He claims that the days fly by because running the store takes up nearly all of his time while he’s there. Trey also says that he has minor memory problems due to his health. “The days here… They tend to blend together.”



Of course, none of these games and events would be happening were it not for Trey and his management skills. And even though he can’t participate in these games very often, Trey enjoys keeping the store running very much. To him, the games are only the second best part of it all. Trey says that the most enjoyable part of the job is the people who come to his store.

“You meet so many people who play these games… The different backgrounds. You’d be surprised, they don’t fit the stereotypes.”

Many players at Arkham seem to agree with Trey: The community of fellow gamers is what makes Arkham the place to be. One of them, Christian Gillus, a skilled player and regular customer of two years, says, “Everyone is very friendly, we’re like a dysfunctional little family.”

And like any dysfunctional family, the gamers at Arkham have quite a few interesting stories to share. Christian told a story of how he once announced that his friend Craig, a fellow gamer at Arkham, “got laid two nights ago.” It became an inside joke that made everyone clap every time he mentioned Craig’s name.



Not long after sharing this story, Craig walked into the store, and Christian announced “there’s my boy, Craig!” At that statement, everyone stopped what they were doing, turned to Craig, and applauded for him.



Christian also jokingly said, “Quest tries to grope me, and that embodies the human spirit,” to which Quest Lockard, another Arkham customer of four years, nodded in agreement.



Quest is a dedicated gamer who attends the Yu Gi Oh tournaments whenever he can. He brings with him a large duffle bag and a backpack, both filled with trading cards and accessories like deck boxes and play mats. When asked what he enjoys about Arkham, Quest shuffled his cards as he answered, “should I say ‘nothing, I hate everyone’? Nah, just kidding. It’s the people.” Before going to Arkham games, he and his friend, Taylor Walker, went to a game shop in Cumberland called Geno’s Sports Cards, which has since closed down.



Quest and Taylor told a story that, one day, Trey came into the store saying he had a dream the night before where all of his customers tried to throw live fire-crackers at him. After that, Taylor spent the rest of the day trying to convince Trey that it really happened.



However, not everything that happens in Arkham is just lighthearted fun. Jessie McCourt says that, in March, he was attending one a Warhammer 40K tournament with some friends. One of them, Kyle, proposed to his fiancé, Taylor (not Taylor Walker, a girl Taylor,) in a clever fashion. The tournament had a prize drawing, and when it was Taylor’s turn to draw, Kyle secretly filled the box with cards that read, “will you marry me?” After receiving this surprise proposal, Taylor said yes.

So Arkham games is more than just a game store. It’s a gathering place for fans of all kinds a games, a place where gamers can make and meet friends, and form lasting relationships with one another. Trey says that he hopes to keep Arkham up and running for a good long while.


At the very least, until he pays off his loans. Once he passes the torch off to someone else, he hopes to start a career in real estate. Even after Trey moves on, it is hoped that Arkham will remain a popular meeting place for gamers for a good, long time.



Links to relevant websites:


Damaged Souls

Damaged Souls
By: Kaitlynn Hamby


There’s a quote many parents use while attempting to bring awareness to childhood cancer, “The day before my child was diagnosed, I wasn’t a cancer parent either.” They’re right, you aren’t a cancer parent until you’re told your child has cancer. Your entire world changes in that one instant.
Childhood cancer is vastly different than adult cancer. For many, adult cancer isn’t a death sentence. There are plenty of treatment courses and options: surgery, chemo, radiation, bone marrow transplant, or some form of combination of these four. That’s assuming an adult decides to pursue treatment. And the patient gets to decide on a course of action. Adults also have their pick of oncologists, at least for the more common cancers, such as breast cancer. There have been so many advancements in treatment and there has been so much research that “cancer” almost isn’t scary any more. At least, if it was caught early, it isn’t. But for many children, cancer is a death sentence.
Many people have seen the stories on social media; a depressing photo of a “sick” child laying in a hospital bed, posted by the “parents” begging for prayers, or money, or cards. Anything that could help or make their “child” happy. Some have heard stories of scammers stealing photos of deceased children and passing them off as their own child for money. When people see these photos online, many people assume it’s a scam, but share it on the off chance that it’s real. No one wants to feel like a bad person for ignoring the photo, so oftentimes the photo is shared without the story being read.
Children don’t get to decide on a course of action the way adults can. They also don’t decide if they want to pursue treatment or not. Their parents and doctors make all their decisions. Treatment options aren’t as varied, either. Chemo is a necessity. This was especially true in the case of one brave and inspirational young girl aptly named Angel.
One day Angel was like the other kids her age: she was going to school, playing on the playground, spending time with her younger sister Lilly, and eating mac and cheese. Then, one day, she hit her knee on a table, resulting in a dark bruise. Her maternal grandmother began fretting that she may be sick when she saw the bruise, but Angel’s mother, Angie, told her that Angel is still a kid so she should stop worrying all the time. A little while after this, which was in early August, “We were up West Virginia and she just wasn’t really playing in the water like normal and was feeling tired. A few days later I saw three or four Petechiae on her face and something in my gut told me to take her to the pediatrician” (Angie).
When Angie took Angel to the pediatrician, she was informed that Angel’s symptoms indicated that she either had Anemia or Leukemia. “So obviously I thought it was the Anemia. They sent her for blood work. I was so proud of her she didn’t cry when she got her needle. The next day it was a Wednesday August 20th, 2014 I got a call at work. I was told to take her to Hopkins right away; that they found Leukemia in her blood. And that’s when the hell started” (Angie). According to Cancer Treatment Centers of America, “Leukemia is cancer that originates in blood-forming tissue. The disease is characterized by the uncontrolled growth of blood cells, usually white blood cells (leukocytes), in the bone marrow. White blood cells are a fundamental component of the body's immune response. The leukemia cells crowd out and replace normal blood and marrow cells.” Angie couldn’t remember the exact prognosis given for Leukemia, but said she thought it had about a 98% survival rate. When Angel was diagnosed, the doctor told Angie that if your child had to be diagnosed with cancer, leukemia is the best cancer for them to have, because it is the most curable.
That was not what Angie wanted to hear about her baby. For Angie, it was a living nightmare. “There was nothing I could do to help her feel better. All we could do was take advantage of the good days. She couldn’t go to birthday parties, or to Chuck E Cheese. We could barely take her to the grocery store” (Angie). Angel didn’t get physically sick from the chemo frequently, but she got viruses and other illnesses often because she had no immune system. Whenever that happened, Angel got stuck in the hospital for a few days. A blood infection in her port resulted in spending three days in PICU because her blood pressure dropped severely. She almost died and ended up suffering severe weight loss. Angel’s sister, Lilly, told me a story about how the nurse, “didn’t insert the tube into Angel’s port all the way, so a clamp came loose and blood from the port went everywhere.”

This has changed their lives beyond imagination. Angie does her best to allow Angel to have freedom and to still be a kid, but they both suffer from anxiety, and Angie has suffered from depression since Angel’s recovery. As Angel got better, Angie understandably got worse. Not only was she depressed, but she was drinking a lot. She even contemplated committing suicide. She realized that she didn’t want to kill herself and did her best to get help, which wasn’t easy. “I love my loved ones more freely and I cut out those ones I don’t love more easily. Adult death doesn’t faze me anymore, but if I hear a cancer kid died, I’ll cry for days. I also don’t get as upset over the little things anymore” (Angie). She also suffers survivors guilt. When she is around a parent that lost their child, she feels like they resent her because her child survived. Angie stated that her contemplation of suicide as well as her surviviors guilt, is what helped her realize she is a damaged soul, “I’m a damaged soul, girl. Put that in your story.”
This was difficult for Angel, too. It was scary for Angel, but she freaked out the most if she woke up and was alone. She was so sick that she had to be homeschooled. She was a little upset about having to miss birthday parties, but not too much, because she was shy and didn’t really care too much about missing parties. While she was in the hospital she mostly watched TV and slept, because she was tired a lot. “When I was in the hospital, I would lay in bed with mom and listen to her heartbeat. That’s was how I fell asleep so quickly” (Angel). Angel hated when her hair started to fall out. After her hair started to fall out, Angel couldn’t stand looking at herself in the mirror, so they covered the hospital mirrors in coloring pages, so Angel wouldn’t have to see her reflection. Angel was so upset about it that Angie shaved her head along with Angel to show her that hair doesn’t matter. Once their heads were shaved, her confidence in her appearance, and in herself, returned. Her appetite and taste buds changed throughout her treatment, as well. When she was hungry, she usually ate a treat her dad made her: crackers covered in peanut butter and a piece of a banana with Hershey syrup. While going through chemo, she also wanted sausage and eggs, and stopped liking other foods such as mac and cheese. When asked if she wanted to add anything, Angel stated that she helps with fundraisers meant for other sick kids. There was one child that wasn’t going to make it to Christmas, so Angel sent him a card and cried when he passed. She cried when Austin passed, too, even though she didn’t know him as well as she’d known some other kids, such as her friends Bo, Richard, and Brenna. Now, Angel is in remission, but she still has anxiety. She’s afraid that every health problem is a worst-case scenario. When kids fight at school, she is terrified that they’ll hurt her. She’s had two or three anxiety attacks in school, resulting in her teacher phoning her mother about it. She’s a kid, just six when she was diagnosed. She’s ten now.

Angie and Angel aren’t the only people that do what they can for cancer kids due to a personal connection to cancer. “Tattoo” Tom Mitchell is another cancer parent that does what he can to help sick kids. Tattoo Tom goes above and beyond the ordinary and the expected for these kids. Tom’s daughter, Shayla, was diagnosed with stage 4 Hodgkin’s disease when she was 16. On his way to talk to his daughter about her diagnosis, he stopped in a store near the hospital, and purchased two feather bracelets: one for her, and one for himself. They spoke about everything and nothing, including bravery. They made a promise that they would remain brave no matter what. Shayla didn’t make it, but Tom kept his promise. His foundation, Stillbrave, and the feather logo were born from that promise. When asked why he started his foundation, Tom replied, “When my daughter died, I wondered why someone hadn’t done anything. Then, I realized that I am someone and I can do something.” Stillbrave provides nonmedical support with things such as rent, utilities, groceries, repairs, babysitting, funeral expenses, make a wish, travel to treatment, hosting events for siblings, and teen programs at Inova Children’s Hospital. Stillbrave works with a social worker at Inova Children’s Hospital to make sure the numerous families they help aren’t taking advantage of them, but they’ve still had people attempt to scam them. Another charity, Gold In Fight, has the opposite problem.
Gold In Fight is a childhood cancer foundation with a boxing theme that was started by six people, including Ms. Beth Wright Wheeler. Beth had no personal contact with childhood cancer when she started volunteering with Forever Fierce. She was empty-nesting and happened to see a child’s story online. After volunteering with Forever Fierce, Beth wanted a more personal connection to the sick kids she was helping, so she reluctantly agreed to form Gold In Fight so she could more directly help families instead of focusing on only research. Gold In Fight, especially Beth, briefly investigates the families they want to help, so they’ve been fortunate enough so far that no one has attempted to or succeeded in scamming them, but they do have families that take advantage of the help they provide. While Beth doesn’t like that some people take advantage, she finds the work very rewarding. She did state, however, that, “if I’d known about Stillbrave earlier, I probably would have started working with them instead of a different foundation.” Although different in some ways, the feathers and the boxing gloves both do their best to help families and children in need.
Stillbrave and Gold In Fight aren’t the only childhood cancer organizations out there. There are hospitals such as St. Jude’s that accept donations and organizations such as the American Cancer Society that don’t especially focus on children with cancer, but still do their best to at least make starting treatment easier for as many people as possible. When asked, the American Cancer Society worker interviewed stated that the American Cancer Society, “provides information, day to day help, emotional support for patients and their families, support services and programs, as well as funding research and providing grants.” The ACS splits their donations into different categories, “research programs, education, advocacy, service, and management and general (overhead) costs.” Nonprofits such as these are good to donate to, because you know that they aren’t keeping the donations or lying about what it is used for.
Childhood cancer is the number one cause of disease related deaths in children and about 43 children are diagnosed every day, yet childhood cancer receives only 4% of available research funding from the federal government. That’s probably why there are so few drugs that can be used to treat childhood cancer. According to a quote from Forbes, “around $170 million per year” is spent on childhood cancer, but most of it goes to research. Less and less is spent on clinical trials. The US spend more money on potato chips than it does on children. $170 million on childhood cancer compared to over $7 billion dollars on potato chips.
Next time you see that photo of the “sick” child, don’t just share it and hope someone else does something. You can do something. Take the time to find out if it’s a scam or not, reach out and see what you can do to help. Take the time to find a good foundation to donate to. Stillbrave, Gold In Fight, Alex’s lemonade Stand, the American Cancer Society, and St. Jude’s Children’s Hospital and just five of the many doing the best that they can. Speak up and speak out. Change doesn’t happen unless you make it happen.

Student Support Services: Ensuring Your Academic Success

Are you starting your first year in college and need guidance? Are you a first-generation college student? Then Student Support Services will be the right program for you. Student Support Services is a program at Frostburg State University that helps many students throughout their college experience. The advisors of the program are the director, Tam Lowry, Shawn Jones, Don Maxwell, Holly Clark and Bridgette Karalewitz. The program’s main mission is to help students stay in college until they graduate and give them the support they need to stay motivated. The program is funded by the U.S. Department of Education and has set guidelines for students who are eligible to be a part of the program.
            Student Support Services is also a part of the Academic Success Network. Frostburg has the Center for Academic Advising and Retention (CAAR) office. The CAAR office’s main job is to direct and help students search for programs that promote academic success and helps them stay on track. The services and programs included are an intro to Higher Education course, assistance with transitioning for first-year college students, an Academic Enrichment workshop, advising for students who are on academic probation or have warnings and other academic help.  
CAAR also has PASS which are Programs Advancing Student Success. PASS offers free tutoring services for 100 and 200 level courses such as Math, Computer Science and Economics. PASS also offers writing assistance. There’s also a Developmental Math Program that offers pre and intermediate algebra courses to help students who struggle in math increase their skills and prepare for future math courses needed for their studies. Disability Support Services (DSS) are also provided. The purpose of this program is to give an equal academic opportunity and enhance learning for students with any disability. Depending on the student’s disability, special accommodations and services are provided for them such as; Extended time for testing, Assistive technology, readers and scribes, private testing and interpreting services.
            Student Support Services was created in the late 60's when President Lyndon B. Johnson had concerns about poverty in America and wanted to help first-generation college students graduate. The program has been in Frostburg for about 44 years. When asked about the origins of the program Tam Lowry added that it started along with the Trio program which started in high schools. In order to participate in the program, you have to either be a first-generation college student, your family’s income is within the set limit given by the Department of Education or if you have a documented disability. When asked about the qualifications for SSS Tam Lowry added, “Students must show an academic need, meaning they have a GPA below a 3.5 or a low high school GPA.”
Photo of Advisor and Director of SSS, Tam Lowry.
Tam Lowry takes the role as both an advisor and director of the program. She’s filled with a lot of energy and is very welcoming. When asked about her role in the program she stated, “So, I advise about 80+ Student Support Services students and then we do a lot of cross referencing meaning I might work with a student for accounting help or tutoring or they might meet with Holly or Shawn or Don for advising, if they’re one of their regulars, but we each have about eighty something students.” Lowry called the SSS program a “one-stop shop for anything college” because of the resources that are available to students who are part of the program.
Photo of Academic Counselor and Student Developmental Specialist, Shawn Jones.
Shawn Jones is an academic counselor in the program, but he helps students outside of the program as well. He stated that the main goals of Student Support Services are to work with first-generation college students, help students meet Financial Aid guidelines and provide all of their services and resources from one year to the next. He has a lot of responsibilities that includes being the advisor for multiple organizations, Jones stated “Right now, I am the advisor of… a couple of organizations on campus. So that’s a way to actually spread awareness about Student Support services as well.” Shawn Jones does a lot of counseling for students and makes sure that they have the right mindset in and outside of their studies. “Being an advisor, everyday is different, and we focus on academic achievement,” Jones said.
Like Shawn Jones, Holly Clark is also an academic counselor. When asked about her role as an advisor she said, “I work with students individually on things like financial aid and career counseling.” She also stated that she leads SSS workshops for things like academic counseling or student loan help. Clark connects well with her students. When I asked how she personally connects with her students she said that she likes asking them questions about their lives, tries to attend events that the students are performing in or leading and shows that she cares about them more than just being a student at Frostburg.
Don Maxwell is known as the Math Specialist in the SSS office while also working as an advisor. Maxwell said his main role as an advisor is to help students stay on track and be successful in their courses. When asked about how the program helps a student’s college experience Maxwell stated, “I try to get students to take advantage of all the things college has to offer, we (the staff) advise them to get involved with campus organizations and we help them negotiate some of the difficult parts of college like Financial aid.” Maxwell also offers tutoring for students in math and science courses.
Bridgette Karalewitz is the administrative assistant of the program. Karalewitz has a bright attitude and is very happy to help students with anything they need. She showed that she really cared about her students, like when I asked how she personally connects with them she said, “Oh that’s a hard one… I feel like I’m the mother of our students, does that make sense? Because I send them emails… I get a personal connection with some of them and some I don’t get to know as well, but of the 275 sometimes I say I’m the mother of the 275 students in the program.” Karalewitz made it clear that the SSS advisors are there to help the students with many things ranging from academic to personal problems. She also said that they are there from the beginning until their students graduate. She added that the staff can be considered as “all around advisors” because they help with more than just school life.
Students have responsibilities of their own once they’re in the program. These include making satisfactory academic progress and developing and reaching their goals in an educational plan and goal statement. This is effective for students who have trouble planning ahead and being prepared for graduation. Students are also required to meet with their set advisor at least three times a semester, inform the staff of any changes and to complete their FAFSA application by February 1 of each academic year. These requirements actually help students stay on track with their studies and keep the right mindset throughout their college career.
Once students are approved to be a part of Student Support Services, many resources are readily available. The program has many types of workshops made to ensure each student’s academic success. The workshops are held both in person and online through Blackboard. The program also offers financial guidance, professional tutoring, help with study skills and has a voucher program. The voucher program is made for students who wants to attend cultural events, trips or other events like plays and concerts but can’t afford them or need help with getting tickets. The program allows students who are in SSS to get a voucher from the office and go to the event for free. Financial help is also offered for students like scholarships and grants. There’s a $342,918 budget for the participants of the program so most of that is used for grants. Tam Lowry stated that financial help is mainly offered to “first and second-year students because it’s such a pivotal time.”
Director Tam Lowry provided some information on the statistics of the program. From 2015-16 the six-year grad rate was 63%. There was a 90% persistence rate and 93% for those with a good academic standing. The statistical reports are always a year behind meaning you can expect the reports for the 2017-18 school year in 2019. All of these stats are needed by the Federal government and she stated that this is the their way of keeping track of the success of the program.  Lowry added that all of their numbers are really good. The max number of students allowed into the program are 275.
I asked each advisor about ways to make students more aware of the program. The tactics mentioned were student marketing, tables being set up in the Lane Center, word of mouth, through FSU’s preview day, weekend events and working with other organizations. These are all good ways to spread the word quickly about Student Support Services and all it offers. It’s also a great way to connect with students before they’re enrolled into the program.
Overall, Student Support Services is a helpful program that aids student in their progression through college. Many resources are available to ensure that each student enrolled into the program reaches their academic goals. Success is the main priority of the SSS staff. So, if you qualify the best thing for you to do is drop by the office located in Pullen Hall room 133 and talk to the one of the advisors about getting enrolled in the program. It will help you build your future.

For more information related to SSS, click the links below:

WMHS Cardiac Health Unit: A Gem Within Our Community




Hidden within the walls of the Western Maryland Health System Regional Medical Center is a special team of highly trained professionals who love their jobs. This is our own Cardiac Health Unit. They have saved the lives of thousands of folks in our area and have been recognized as developing one of the best Cardiac Health programs in the country. In 2013, my family went through a scary time, but this group of tremendous people made it so much better. We very well could have lost my father. At the time he was working at North Branch Correctional Institution, which is known for causing its employees a vast array of medical problems due to the high stress work environment. Fortunately, my mother has been a nurse for over 30 years and pushed my father to get a stress test after he came home with chest pains one evening. It was that stress test that saved his life, well many people were involved in saving his life, the point to be explained here, is that it took a whole team of amazing people, not any one thing saved my father.
My father, brother, and myself were all hunting together shortly before the Christmas of 2012 when my father experienced some chest pains. At the time we didn’t think anything of it and neither did he. It wasn’t until it happened again that my mother picked up on the issue. My father came home from working second shift at the jail one evening after having had a rough night with a former coworker. He complained of chest pains and numbness in one arm, so my mother gave him baby aspirin and took his blood pressure. Not being satisfied with her findings, she called and scheduled a stress test for my father for 30th of January 2013. During this stress test, my father actually passed for his age and weight bracket, but it was his stubbornness that helped save his life. He asked them to go a few steps further than his bracket, to someone 20 years younger and in runner’s shape. After some convincing, they cranked him up and then they could see what had happened to him twice before, once in the woods and once at work. They then determined that they needed to do a catheterization, so that they could physically see the problem.
On February 8th, 2013 the same date many years prior that my father’s father had his heart attack at the very same age of 59 years, my father had his heart catheterization. They determined that stents would not be possible, and that triple bypass surgery would be needed. They gave him a few options; a drug regimen over the course of 6-8 months to see if any changes would occur or schedule him for the next available date for open heart surgery. Now, my father has never had any kind of major surgery, everything that he has experienced up to this point has been outpatient care, all done in the same day, with minimal recovery. So naturally he had lots of questions and concerns. He knew he had plenty of time saved up at work that he could go ahead and take the next surgery date, but the decision was still his.
        
         Fortunately for my father, my Uncle David had just had this surgery the year prior and was given a full briefing of the surgery before deciding when to go under the knife. David experienced chest pains for roughly six months but didn’t take it seriously. On Saturday the 27th of July 2012 around 5:30 PM he had the first of three mild heart attacks. By 8:45 PM he had a heart attack so severe that he agreed to go to the hospital via ambulance. During the ambulance ride he was given three doses of nitroglycerine spray and upon arrival at WMHS, he had a heart catheterization with an attempt to install stents. However, his left internal, main was blocked beyond 90% (“actually 96-97%”) so open-heart surgery was indefinite. The following morning at 7:00 AM “they wheeled me into the operating room and started” he said. “I don’t remember much until Sunday evening when they took the breathing tube out of my throat. Uncle David became patient number 3269 of the Cardiac Health Unit on that very day. He then spent the following six days in Cardiac Intensive Care Until he was released to go home on the 2nd of August 2012.
        
         After speaking with my uncle several times, and much deliberation from the whole family the date was set for my father to have open heart surgery on March 7th, 2013. Dad became patient number 3394 when he had three bypasses completed. The bypasses were to fix three different blockages, one at 50-60%, another at 50-60% with a narrow portion downstream at 70%, and an 80-90% blockage at the circumflex. He spent 5 days recovering in the Cardiac Intensive Care Unit, during which he walked as much as they would allow him. He said the whole process was “scary, but the care was excellent. I was treated very well.” My mother was with him as much as she could be, she’d stay every day until visiting hours were over and we would make her go home. She had seen her father go through open heart surgery twice, then helped her brother through it. “When it is your significant other it shakes the core of your world,” she exclaimed. “I felt a lot of disbelief, this can’t be happening. I worried about having a son about to graduate from high school. I came to realize [that day] that any plans we had for the future could just end abruptly, I made a decision to push my husband as hard as I could to make it through.” My mother, having worked in surgery now for around eight years and having been a nurse for 33 years at the time of dad’s surgery, she knows many things about the process that ordinary people would not know. I believe that they would not have been able to get my father or my uncle off the breathing machine without her. She is and always will be a nurse, with incredible patient care abilities. She has helped prep operating rooms for these surgeries and helped patients into and out of the operating room and into recovery. “I’ve been fortunate to watch Dr. Nelson and his team provide excellent care to many patients over the years.”
        
         Another person we are all fortunate to have in our lives is my brother’s fiancé Leslie. Though she was not a physical part of my father or uncle’s heart surgeries, she has been a part of Dr. Nelson’s heart team for four years. In fact, he specifically asked her to join his team after hearing about her work ethic. She has been a Surgical Scrub Tech for 12 years now and she said she “had always wanted to be a part of the heart team, but the opportunity just wasn’t available.” Then, “when a fellow employee of the heart team decided to go back to nursing school full time they decided that they could no longer be a part of the team anymore. When they asked me if I would be interested, I jumped at the opportunity!” When asked how she liked the position Leslie exclaimed, “I absolutely love my job, the fact that I get to help people every day is a very rewarding and satisfying career. I love my job so much that I recently decided to go back to school and become nationally certified, because I was trained on the job when I first started.” When asked about the stresses involved with such an invasive job she said, “I do consider my job a very high stress job, I believe that [working in] the operating room in general is a high stress job. [In] the heart room we work on the sick, unhealthy, and probably [the] most scared people [to] have surgery. I mean imagine you are coming in to the hospital for a routine heart catheterization and they take you back to the room and start the procedure. All of a sudden, they say that you have had a heart attack, and need emergency CABG (coronary artery bypass grafting). This is why I love my job, we get people in the most vulnerable time in their life and make them well again.”
         I was able to get a hold of Dr. Nelson through Leslie for comment for this article. He is an extremely intelligent man who is passionate about what he does and the people that he has chosen to work with him. To date, he has done over 4000 heart cases at WMHS and 7000 heart surgery cases in his career “including my fellowship training.” That is a lot of people for one man and a small team of highly trained individuals to have people’s hearts literally in their hands. When asked if he enjoys what he does, Nelson stated, “in general I enjoy what I do, but not always. [We’re] working in an imperfect environment with expectations of perfection. [It’s] unrealistic and can lead to lack of enjoyment and frustration.” He also noted that, “the pre-operation and post operation periods can be complicated and prolonged, which can also lead to less than enjoyable working conditions.” So, the job isn’t all it’s cracked up to be, saving lives for a living. Which led me to ask him if he felt any level of heroism in his work, to which he said, “I wouldn’t say I feel heroism, that would suggest arrogance or lack of humility. Gratification that a patient has benefited from surgery is perhaps the proper perception [for me].” Clearly this man is very humble about his work, which is something that I personally like to see in people so talented at what they do for a living. My final question for Dr. Nelson was how he chooses who he has on his team. He then explained that “the organization of the heart team is a multistep proves [that] involves extensive training and of course a strong interest and work ethic.” Sounds to me like our dear Leslie is definitely in the right place and surrounded by good company.
         I feel that though the Western Maryland Health System does put a lot of pride and marketing into their Cardiac Health Unit, the individuals themselves do not get enough recognition. Something that genuinely bothers me is that people in this area still believe that we don’t have excellent healthcare here in our area. I hear folks say all the time, that they think they should just go to Morgantown, or Baltimore, or Pittsburgh for their care. Sure, those facilities provide excellent care and have wonderful trauma centers, but our own hospital has some truly amazing healthcare professionals operating within its walls every single day. These individuals have been a part of my life since my mother has been a Registered Nurse for 38 years as of last month. They have saved many members of my family including my Uncle and Father. I will stand behind our hospital and its care because of the amazing work that departments like the Cardiac Health Unit do over and over again. It is some truly amazing work done by some incredible people.

Relevant URLs:


Images:


My Father's Heart Pillow with the hand drawn diagram by Dr. Nelson








Dr. Nelson's Signature on every patient's Heart Pillow