Lifeblood: plasma’s death grip on the Midwest

By Sarah Seifert @TheSarahSeifert

GREEN BAY, WI – “Easy cash.”

“I stopped going because it hurt.”

“I don’t plan on ever going back.”

“It goes on to help people who need transfusions!”

“It’s not worth it anymore.”

BioLife Plasma Services and the college students of Green Bay, Wisconsin have a complicated relationship. Some have a relative or friend with a blood disorder. Some want to feel connected to their community. Others have been permanently barred from donating, or the voluntary pain is too much.

None of these enterprising young students know exactly where the dull yellow plasma goes after it’s slowly extracted from their veins. Most are optimistic that it’s helping people. One student said he would prefer not to know. Another said he would feel uncomfortable asking.

Most who cycle through the spotless glass doors of Green Bay’s BioLife location have one thing in common: they desperately need the money.

The phlebotomist sterilizes the needle, pricks my skin, and finds a vein with little trouble. She asks for the last four digits of my social security number. Confused, I give them to her. The other donators here know how to play the game, and recite their digits with little to no reaction.

The donation process, called plasmapheresis, takes me just under an hour. The machine hooked up to my arm sluggishly fills with my blood, extracts the protein-rich plasma, then filters it back into my vein through an IV. Throughout the process, a metallic taste fills my mouth – a common side effect.

The perky trainee who checks up on me a little too constantly is called a phlebotomist, a local pre-med student trained to draw blood. She chats with the middle-aged woman in the chair next to mine, asks her about her daughter in college, and compliments her on her homemade flowered headband, before coming back to me. “You’re so well hydrated,” she smiles, giving me an overly enthusiastic thumbs-up. “Keep doing what you’re doing.”

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BioLife’s Appleton, Wisconsin location, about 45 minutes south of Green Bay. Image source: opnarchitects.com.

The colorful signs with feel-good messages are at odds with the sterile white facility. “Save a life in one hour!” a smiling woman in a lab coat promises me. In my introductory packet of donation materials, a helpful brochure informs me that my plasma will save the lives of people with blood disorders everywhere. Beyond promising that I’m a hero for donating, the information BioLife offers about the plasma treatment process is frustratingly vague.

I walk out of the doors with a newly bruised and bandaged arm, $25 loaded onto a prepaid debit card, the scent of lemon disinfectant clinging to my coat, and a headache. The BioLife location in Green Bay is in a fairly well-to-do part of town, and even though dusk is setting as I climb into my car, I don’t feel uneasy in the well-lit parking lot.

This BioLife facility, however, is the exception rather than the rule. Madison’s Interstate Blood and Plasma is located on West Gorham Street, right in the heart of the city, and is significantly less upscale. Milwaukee’s plasma donation centers are also in poor, predominantly black neighborhoods.

The plasma industry was built on the backs of prison inmates, drug-heavy neighborhoods, and poor sectors of large cities. Throughout the 1970s, 80s, and even 90s it spread tainted blood, slowly spread hepatitis and HIV, and was involved in dozens of scandals.

Is the plasma industry’s facelift enough to tempt Green Bay college students back through BioLife’s doors? The small, perfectly circular scars in the crooks of dozens of college students’ elbows are telling.

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The author’s arm, after six months of donating and two months of recovery. Image source: Sarah Seifert

As I continued to donate plasma for the next seven months, people would ask to

see the scar, some with genuine curiosity, others in horrified fascination. Other donors roll up their sleeves to compare their pockmarks with mine. The signature BioLife debit card always gave us away.

There were always tales to exchange about bad phlebotomists, needles being yanked out halfway through a donation, and shivering your way to your car – the saline solution injected as a substitute for the plasma is kept at room temperature, which is much colder than the temperature inside your veins. We exchange horror stories while sipping on coffee bought with that purple debit card.

Blood money?

Plasma, IVIG, and the American Dream

According to the Plasma Protein and Therapeutics Association, plasma contributes to treatments for patients with bleeding disorders like hemophilia A and B, Von Willebrand disease, and immunodeficiency disorders.

There’s a reason why the industry is so efficient, why one facility can filter thousands of people in and out so quickly. It has no other choice. 1200 plasma donations are needed to treat 1 patient for hemophilia, 130 to treat 1 patient for a primary immune deficiency, and a staggering 900 to treat one Alpha-1 patient (a genetic deficiency that can result in lung disease or liver disease in anyone from children to the elderly.)

Plasma’s precious ingredient, one that scientists have not yet found a way to manufacture, is intravenous immunoglobulin (IVIG). Plasma fBiolife_1rom thousands of donators is pooled, treated with chemicals to eliminate blood-borne pathogens and extract the immune globulins.

IVIG treatments are nearly impossible to conduct without insurance coverage – $100,000 to $350,000 per year, per patient. The relatively tiny cash compensation for donors, $50-$70 per two donations in the form of a prepaid debit card, might seem strange, given the precious value of IVIG.

The U.S. is one of only two countries that has not outlawed paying plasma donors (China is the other). “It is banned…for ethical reasons and in order to assure the safest supply possible,” said London School of Hygiene research fellow Lucy Reynolds in 2013.

“Hospitals, Red Cross units, and nonprofit agencies reject the plasma center model because cash incentives may give donors an incentive to lie,” said The Atlantic’s Darryl Wellington in 2014. People with transmittable infections will donate anyway, especially since the current low-paying system is focused on those who desperately need quick cash, Reynolds argues. She warns that another deadly outbreak of blood-borne disease is not only likely, it’s inevitable.

Bad Blood

The plasma industry is desperately trying to recover from the image it cultivated in past decades. Scandals upon scandals erupted due to erratic testing.

In a polarizing 1998 article, a Salon journalist reported that Arkansas was the last state to outlaw selling prison inmate’s plasma in 1994. However, throughout the 1980’s at one of the most notorious prisons in the state, prisoners were donating a pint of blood for a mere $7. The prison reaped the rest of the financial benefits.

Multiple prisoners who were known hepatitis B carriers were allowed to donate blood. It was pooled with dozens of other prisoners’ blood and shipped to Switzerland, Japan, Italy, and Canada. Connaught Laboratories of Toronto bought into the tainted units and sold them throughout Canada. The simple oversight erupted into a national health crisis.

More that 42,000 Canadian citizens had been involuntarily infected with hepatitis C and HIV. That negligence will most likely soon result in at least 7,000 Canadian deaths.

China, the only other country that uses a paid plasma donation model, has had its own blood contamination woes. A 2007 Reuters journalist said “Blood transfusion is still a major channel for HIV-AIDS transmission in China, and patient infections from blood-based drugs made with tainted plasma are reported sporadically by local media.”

Gregory Maddy of Spokane, Washington brought a medical malpractice suit against CSL Plasma for contracting a staph infection shortly after donating. The court ruled against Maddy, saying there the only possibility that donating plasma had caused his infection would be a contaminated needle. But is contamination really a stretch?

Plasma is precious – and pharmaceutical companies are realizing its true value. It’s now being used to treat a much wider variety of health problems – authors of a 2008 review of unlabeled uses of IVIG (IVIG being used to treat health problems other than primary immunodeficiency diseases) found that it was also being researched to develop treatments for childhood asthma, obsessive-compulsive disorder, and neuropathic pain.

Better treatments for more people sounds positive. If we continue to feed the plasma machine, how fast will it take before people begin dying from contaminated blood?

A Poor Man’s Game

The U.S. is the plasma industry’s top producer. “The OPEC of plasma,” a top executive of America’s Blood Centers calls it in a New York Times article. It’s a part-time job for many; the sole income source for some.

America has 495 plasma centers, compared to Europe’s 100, spread over Germany, Hungary, Austria, Belgium, and the Czech Republic. The real question about America’s plasma fascination is this: why are the majority of centers concentrated in the Midwest?

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The “red zone” of plasma centers is the American Midwest. Image source: DonatingPlasma.org.

Furthermore, why are nearly all facilities in large cities found in high-poverty, primarily black, or drug-ridden neighborhoods? Detroit alone boasts eight centers; Chicago has seven. Wisconsin, with its affinity for small towns, hosts nineteen.

A 2003 American Journal of Public Health study found that commercial plasma donation clinics were overwhelmingly located in high-risk city areas – meaning areas with “active local drug economies.” Income and education, however, also play their part.

The average household salary in Madison, Wisconsin is sixty-one thousand dollars a year. The average household salary on Gorham Street, the location of Madison’s main plasma center? Seven thousand a year. Milwaukee isn’t much better, with an average household salary of forty-three thousand compared to the plasma center neighborhood’s average of eighteen thousand. Almost every Wisconsin city with a plasma center – Eau Claire, Green Bay, Beloit, Janesville, La Crosse – has a higher average household salary than its plasma center’s neighborhood.

Not only are Wisconsin plasma centers found in poor neighborhoods, but in uneducated ones. 47% of Madison dwellers over 25 have a bachelor’s degree; only 37% of Gorham Street inhabitants do. Comparing education level data in neighborhoods with plasma centers can be risky business, however, because college towns are an instant draw for the plasma industry. The built-in market in any town hosting a university would make any company jealous.

The plasma industry has never tried to deny it: college students, the poor and homeless, and the uneducated are their primary targets.

Community Service or Russian Roulette?

            Plasma centers, without fail, offer an incentive for twice-per-week donation. Some give bonuses, coupons, gift cards to local businesses. However, the Red Cross’ recommendation is far, far less – once every 28 days, or about 13 times per year.

Asking the plasma industry to cut their revenue by seven-eighths to ensure the safety of donors is laughable. But why the discrepancy? Why do plasma centers downplay the risks of donating twice per week, ad infinitum?

            Donors seem to accept that twice-per-week means migraines, fatigue, and a hugely increased risk of getting sick. “All I can say, I just got sick a lot. I easily caught the flu. Then, you know, I would go back and do some more, so I would get even more sick and wouldn’t even think about it,” laughs a UW-Green Bay senior, 27-year-old Benjamin Koenigs who donated twice a week for two months.

Like many other donors, Koenigs seems to realize the consequence of donating twice a week – migraines, weak immune system response – but plasma centers offer incentives. “I was trying to get Packer tickets. They were handing out tickets to anyone who donated eight times a month,” Koenigs says, rolling his eyes.

He lost his shot at the football tickets after developing a hematoma in both arms, blood pooling underneath his skin after a phlebotomist inserted the needle too far into his arm. The pain and frustration with BioLife kept him from returning.

If he knew the Red Cross recommended a donation rate of only once a month? “Unfortunately, if I needed the money, I’d probably still do it,” Koenigs says, looking more than a little guilty.

The Wisconsin Plasma Giant

BioLife, CSL Plasma, OctaPharma, and Interstate Blood and Plasma all pop up in poor towns around the state – but BioLife dominates the Wisconsin landscape, with 10 out of the state’s 19 total plasma centers. It was founded in 2000, a relatively new plasma company, and perhaps is untainted by the hepatitis and HIV scandals of older entities.

But in the town of Green Bay’s population is overrepresented by both college students and the elderly; furthermore, the city is known for its heroin problem. These factors combine to make Green Bay the perfect target for plasma donation. While the facilities sparkle and most of the phlebotomists are a certain Midwestern breed of friendly, many UW-Green Bay students regard BioLife with unease, distrust – or hostility.

Ashley Wisneski is a 23-year-old alumna of UW-Green Bay who donated a mere five times. The extreme fatigue after a donation is somewhat common, but after her arm began swelling and fell asleep mid-donation, she stopped making the ten-minute drive from UW-Green Bay’s campus to the BioLife facility. “It’s so uncomfortably painful and I was always worried about which nurse I would get,” Wisneski says.

A UW-Green Bay female student, who wishes to remain anonymous, says donating affected her health for several months. “I was getting sick all the time. I swear after I would donate, a few days later I would get a cold.” Towards the end of the six-month period of donating twice a week, she would experience constantly illness for nearly a month. “It was…pretty much destroying my immune system,” she says.

Yet another donor’s vein ruptured when a phlebotomist inserted a needle upside down and attempted to turn it while still inserted. Crystal Gruselle, also UW-Green Bay alumna, says attempting to donate plasma gave her a fear of blood and needles. After re-inserting the needle several times, Gruselle’s blood pressure dropped so quickly that facility staff had trouble finding a vein. Gruselle says she couldn’t bend either extremely bruised arm for over a week.

In 2013, a Washington woman sued BioLife for misdiagnosing her with hepatitis and HIV. The story is eerily similar to that of a UW-Green Bay student, David Burish, who was misdiagnosed with AIDS at Green Bay’s BioLife location in 2015. “Only working part-time gives you so much money, and you know, easy cash for an hour twice a week,” Burish said. He donated twice a week for four to six months, only experiencing the occasional migraine, before a confusing exchange led to a shocking email.

“I went to schedule my third appointment, and they wouldn’t let me. About two weeks later I called…they had the wrong ID under my name. Finally when I got a response back, I got this letter in the mail. It said their tests showed I had a diagnosis of AIDS.”

Within a week, the local STD testing center had delivered Burish his actual test results: negative. BioLife had sent Burish a false positive, and as a result, he is barred from donating for life.

The Midwest is slowly becoming a more popular venue for plasma donation centers, and is relatively safe. But the plasma donation center model of payment is clearly taking advantage of poor populations, and in Green Bay, Wisconsin, college students are slowly becoming disillusioned with the shiny silver-gray BioLife building next to East Mason Street, and the fast cash it promises.

 

Cover Image: WordPress.com

Cast in the shadows: The forgotten Phoenix

By: David Burish

Most students attend a university to pursue a career that they will have for most of their lives. Others use the opportunity of a college education to network and create a group of people they can rely on in future endeavors. And some use it to fulfill the opportunity of a lifelong dream. So is the case for UW-Green Bay junior Warren Jones.

Jones is pursuing his degree in communication after transferring from Bradley University last summer and is on track to graduate next year. His main goal in college is to play the game he loves: basketball.

“I first started playing basketball probably when I was five,” Jones said. “I started playing on a little tikes hoop when I was young. My mom told me that I would never shoot on it until she would raise it all the way up and that’s the only way I would shoot on it.”

Jones looked to college to pursue the game he loves but it wasn’t until high school in his hometown of Centralia, Illinois that he saw it as a legitimate option.

“I started getting letters from some colleges and I realized that I can do this. I can play college basketball.”

Jones’ journey was not a typical path through college but he succeeded early. He started attending Southeastern Community College in Burlington, Iowa where he helped the Blackhawks to a 25-7 record in 2013-2014 averaging 16.8 points and 3.5 rebounds a game.

The college experience

After two years at SECC, he transferred to Division 1 Bradley University and again became an instant success for the Braves. But it came with a price for Jones.

“It was up and down all year. I was the leading scorer all year but I actually had a stress fracture in my foot,” Jones said. “I played nine games and after six games it was hurting and I would take pills and stuff before the games and I couldn’t feel my foot. I had 33 points and then the next game I played and got  seven and could barely walk the next day.”

Jones was in a walking boot for the next eight weeks and had to watch his team from the sideline. After his injury had healed, Jones was ready to get back on the floor and in 2014-2015 he led his team in scoring with 11.9 points per game.

He was looking forward and began to workout for the summer. That offseason Bradley had hired a new head coach, Brian Wardle from UWGB to lead the team. Jones said he got along really well with Wardle and wanted him to be a major part of his team. But things got more difficult for Jones.

“At the end of the summer, there was this math class that I wasn’t doing so good in and I got some help for it but it wasn’t the kind of help I was supposed to be getting,” Jones said. “He told me then that was like my last strike and I ended up leaving because I would’ve had to sit out some games and I didn’t want to do that.”

The transfer process

Jones went back home and began looking into other colleges. He joined many students who look to transfer to a new school. According to statistics compiled by the NCAA, 528 male basketball athletes transferred to a new school in 2015-2016. Of those transfers, 44 percent of them transfer from one Division 1 school to another and 90 percent of the total athletes said they looked to transfer “for athletic reasons.”

Jones looked into many options and even looked at transferring to a smaller school.

“I took a visit to UW-Parkside,” Jones said. “Actually I committed there and told the coach I was coming. So me and my mom we drove to Parkside. That’s eight hours from my house.”

While Parkside became the main option for Jones, he took a visit on a whim to UWGB, even though he never considered it as a serious contender.

“Two days later we flew to Green Bay and then flew back the next day. But coach worked me out and showed me some tape of what they wanted to do here, how they wanted to play and that’s the kind of player I want to be.”

Jones committed to UWGB after that visit and he was told early on that the process to a new school would not be easy.

“They knew it would be hard for me and when I transferred here I had to do so much paperwork and it was a lot of work, more than I thought it would be.”

The paperwork for student-athletes to transfer is extensive. The NCAA guide book on transferring is a 20-page document in itself. The book opens with a question for potential transferring students that asks, What should I think about before transferring?

The NCAA suggests, “NCAA transfer rules are designed to help student-athletes such as you make sensible decisions about the best place to earn a degree and develop athletic skills. The decision to transfer to another school involves important and sometimes difficult choices.”

NCAA rules state that if a student athlete decides to transfer from one Division 1 school to another, the athlete must sit out one full year of eligibility. Student-athletes have a five year window to compete in four years of eligibility.

A lesson learned by former University of Northern Illinois punter Peter Deppe.

The lawsuit

According to a story in the USA Today, Deppe was looking to transfer from UNI to the University of Iowa.  Deppe had a year of eligibility remaining and the University of Iowa athletic department declined to file a waiver to exempt Deppe from sitting out a year.

Deppe is now being represented by Hagens Berman Sobol Shapiro LLP out of Seattle in a lawsuit filed in March that claims, “The NCAA’s limitation on the mobility of college athletes is patently unlawful. For a striking contrast, one can simply examine the unfettered mobility of the players’ coaches. Football coaches, including assistant coaches, are free to leave a school at any time they choose to take another job in the college or professional football ranks. This ability to better their own situation has allowed coaches to reap enormous financial benefits…”

The NCAA responded later citing back to previous, unsuccessful lawsuits.

The Deppe complaint repeats many of the same arguments made by the same law firm in other cases against the NCAA,” Donald Remy, chief legal officer said. “Repeating allegations and legal theories does not make them true. As a result, the lawsuit should be dismissed.”

While Peter Deppe is in a far different circumstance than Warren Jones, the consequences of selecting a new school to transfer to does not come without some difficulty.

It’s a tough rule,” Jones said. “I don’t really see the point of it but a lot of stuff the NCAA does, I don’t see the point of it.”

Jones found the rule most difficult after showing what he was capable the last three years.

“I already had been playing and been the leading scorer on my team. I already had my name out there so it’s kind of like you’re put in the shadow and put away for a while.”

The struggle continues

Jones said the process has been especially hard this year. After moving nine hours away from home and only knowing a couple of players from years at Southeastern Community College, Jones was alone on a campus and could not participate fully in the game he loves.

“When everyone’s gone, especially for the first half of the year, I was alone. Me and David (Jesperson, another transfer student-athlete from Pepperdine University) didn’t really hang out outside of workouts and practice. It was like I didn’t really know anybody so I was always by myself. I didn’t talk to anybody so no, it didn’t help me.”

Jones continued to find a way to workout with the team and practice as hard as he could. Jones said that the year got easier as it went on. He began making friendships with his teammates and hoped they continued their success.

This year the men’s and women’s basketball teams succeeded more than in two decades. They both won the Horizon League championship and earned automatic births to the NCAA National Tournament. In their game against Texas A&M, Jones was watching like the rest of us.

“I was at a bar watching the game, just a little sports bar watching the game. I just went by myself.”

Jones worked all year to help his team be as successful as they could and all he could do now is wish he was there.

“Every game I watch on TV I wish I was playing but this one, I really wish I could be playing just because it meant so much more being in the national tournament. In the last 20 years, it hasn’t happened so it meant a little more and I wish I could be there but I couldn’t.”

What the future holds

Jones said despite his wishes of being there with his team, the team has been a great support system. He said after the game he was on the phone with teammates and discussed what had happened.

“I have a relationship with all the guys,” Jones said. “I work hard just to get them better cause you know you’re not going to play but the coaches encourage me to keep working hard for them and myself.”

UWGB coaches and other players were unavailable for comment on their transfer athletes. The Director of Strategic Communication, Joseph Daniels, responded to an interview request with this comment.

With the success of both of our basketball teams this season, we received a lot of national media attention as well as a handful of local media requests. While I understand your request is for a class project, this is something we have simply declined in the past. Our men’s basketball student-athletes receive a ton of attention in the media nationally and regionally and this request is among the many that we decline.”

Since Jones and Jesperson had transferred to the university in the summer, there were no stories written about them by the national or local media outlets.

Jones however has remained optimistic and looks forward. Building into another year and looking to get his chance and contribute on another successful season.

I got to practice with a great team for a year which made me better. It’s like up and down thing. It has it’s positives and negatives.”

According to UWGB statistics on the 2015 student body statistics, the total enrollment at UWGB is 6,779 students and 661 were new transfer students, including Warren Jones and myself.

Jones has been looking the last couple of years for a place to achieve his dream of being a basketball player and a university graduate. His struggle is familiar to many and he said that this time has given him a great gift.

“It helped me mature. It helped me think about things I was doing, things that weren’t right and just try to better myself. A lot of time to think. A lot of time.”

The NCAA rules prohibit him this year from being a part of a game that reminds him of home, his mother and a life that could be. But Jones will play next year, and he looks forward to getting the opportunity that has been taken from him.