Spreading the Love, One Donation at a Time

The year was 1968. Fall was in full swing, and 14-year-old Christine Camann was sanding her family’s porch railing with bright orange Rust-Oleum. For a moment, she wondered whether they should leave it that color for the season’s festivities.

But another thought lingered in the back of her mind.

Is my dad going to be okay?

Christine’s father was scheduled to undergo surgery to replace two valves in his heart. The family had been told to expect him to remain in intensive care for about a week following the procedure. Instead, to Christine’s surprise, he returned home that same day. “They can’t do the surgery,” her father told the family. “They don’t have enough blood.”

Both Christine and her father were O negative. O-negative red blood cells can be given to patients of any blood type, making them especially valuable in emergencies. But for people with O-negative blood, the compatibility does not work in reverse—they can receive only O-negative red blood cells. For Christine, the importance of an adequate blood supply suddenly became deeply personal.

“I resolved right then that I didn’t want anybody else ever to be in a situation where the doctors couldn’t take care of them because they didn’t have enough blood,” Christine recalled. “I felt bad because I couldn’t donate. I was only 14.”

At the time, donors had to be at least 18 years old. Christine did not specify exactly when she made her first donation, but the experience with her father became part of what would inspire a decades-long commitment to giving blood.

Over the years, Christine found more reasons to continue. She read stories about patients who depended on donated blood. She knew people personally, including her father, whose medical care had been affected by its availability. And sometimes, a few weeks after giving blood, she would receive a notification letting her know where her donation had gone. Some of those messages told her that her blood had helped premature babies.

For Christine, those reminders connected the donation process to the people on the other side of it. A little time spent donating could mean something much larger for a patient or family in need.

As the years passed, the donations added up.

Christine received milestone pins recognizing how many gallons of blood she had given. Eventually, she lost count of them. She knew she had passed 10 gallons, but the recognition was never what kept her returning. Then she received notice that she had reached 20 gallons. A larger milestone pin made its mark.

“Maybe I oughtta get this one!” she said.

Christine has also watched the donation experience evolve through the years. As the Red Cross has strengthened and refined its screening process, donor questionnaires have become more detailed, while advances in technology have helped make other parts of the donation process faster and more efficient.

There is one change, however, that Christine remembers particularly well: the snacks. Years ago, organizations sponsoring blood drives were responsible for providing refreshments. Donors were encouraged to drink water or fruit juice and eat a snack after giving blood. When churches hosted drives, Christine remembers homemade treats, including pies, appearing at the refreshment table.

Today, donors are more likely to find prepackaged snacks. “I understand the reasons for prepackaged foods,” Christine said, “but boy, I thought the homemade stuff was a really good deal!” The refreshments are not the only thing that has made Christine’s donation experiences memorable. She typically donates four to six times a year and does not always encounter the same staff members. Still, some manage to remember her.

It may have something to do with the cow.

During a blood donation, donors are often given something soft to squeeze in their hand. Christine began bringing her own—a small rubber cow whose legs she could lock her fingers around while donating. The cow developed a reputation of its own. “Oh, you’re the one that has the cow!” Christine recalled hearing from staff members. Over time, she joked, the cow gained a little “infamy.”

The homemade pies, milestone pins and infamous cow bring humor to Christine’s memories, but beneath them is the same motivation that began decades ago with a 14-year-old girl worrying about her father. She knows what a blood donation can mean when someone needs it.

For anyone who has never donated but is considering it, Christine points to how much impact can come from a relatively small investment of time and effort.

“It’s amazing what a little time and effort can do for other people in need,” she said. “Go for it, that’s what I would say.”

After decades of giving, Christine’s story is marked not only by incredible commitment, but by the care, consistency and generosity behind each donation. From the pledge she made at 14 to the many donations that followed, her motivation has remained rooted in helping others when they need it most.

In Christine’s words, it comes down to something incredibly impactful but quite simple:

“Just spread the love.”

There is a critical need for blood donors as the readily available blood supply reached a four-year summer low. You can spread the love by helping to ensure that patients receive the lifesaving care they need by making an appointment to donate. 

Visit RedCrossBlood.org, call 1-800 RED CROSS (1-800-733-2767) or download the free Red Cross Blood Donor app to find an appointment nearest you.

Written by: Cinnamon Morris, Communications Volunteer, Red Cross of WNY

Blood Donor Spotlight: Sir Squeaks A Lot & Piggy Smalls

Every two seconds, someone is in need in lifesaving blood and volunteer blood donors are the only source.

That makes all blood donors heroes – even the furry, four-legged ones.

Photo credit: Ben Read

Meet Sir Squeaks a Lot and his partner, Piggy Smalls. The pair of guinea pigs were abandoned in an apartment hallway and recently rescued by Jess Meacham.

“A neighbor called and said I don’t know what to do,” Meacham explained. “Unfortunately, we get emergency calls all the time.”

Meacham founded the Buffalo Guinea Pig Rescue Mafia one year ago and has since helped to rescue and find homes for more than 100 local guinea pigs. When Oliver, one of the first guinea pigs she helped to place in a loving home took a turn for the worse, Meacham says she never expected what would happen next.

“Oliver’s veterinarian did a full work up and it turns out he had three bladder stones and needed surgery,” she explained. “After surgery he went down hill very quickly and his doctor recommended a blood transfusion. I’ve had experience as a human blood donor before, but never with animals.”

Given their age and size, Meacham brought Sir Squeaks a Lot and Piggy Smalls to the veterinarian to see if either might be a match for a blood transfusion in Oliver’s case. She says the veterinarian shared that given Oliver’s condition what happened next was nothing short of a miracle.

“Sir Squeaks a Lot saved the day. He’s literally a hero and saved Oliver’s life. Oliver looks fantastic now.”

Now, Sir Squeaks a Lot is looking for a hero of his own. He and his pal Piggy Smalls are up for adoption. The two come as a pair as Meacham says that Guinea Pigs don’t like to be separated from their partners.

“They’re big old sweeties the both of them and they love each other a whole bunch.”

You can be a hero like Sir Squeaks a Lot by making your own appointment to give blood or platelets and help keep the blood supply strong this summer. Type O blood products are most needed on hospital shelves right now – especially in the face of seasonal challenges like severe weather, summer fun and more.

Make the world brighter for patients in need. Schedule your appointment to donate blood or platelets today by visiting RedCrossBlood.org, calling 1-800 RED CROSS or downloading the free Red Cross Blood Donor app to your smartphone.

Trauma Awareness Month: 2x Blood Recipient & Long-Time Donor Inspiring a New Generation of Donors

May signals the beginning of a busy time for celebrations and summer holidays, including Mother’s Day. But the month of May is also Trauma Awareness Month, a time where the American Red Cross reminds donors that it’s the blood already on the shelves that helps to save lives during emergencies. 

Few people may understand that better than Paula Pimm.

The Canisteo resident first found herself in need of a lifesaving blood transfusion when she was just hours old.

“My first blood transfusion was when I was born,” she explains. “I couldn’t reproduce my own blood cells. I was jaundiced and transferred to Rochester. As the youngest of five kids, it was hard for my parents, and I needed transfusions until my body was able to work like it needed to.”

Years later, the elementary school counselor, wife and proud mother of two daughters would find herself in need of a transfusion again due to complications in childbirth.

“I was bleeding so much, and they couldn’t stop it. My doctor was a very calm man, nothing really ruffled his feathers, but he told me that I was going to deal with some difficulties because it was serious. They made my husband stay in the room with me my whole stay, and those things didn’t happen as much 22 years ago. By the time they stitched me up three hours later, I was white as a ghost.”

For Pimm, much of the experience itself was a blur and she credits her faith in helping her to pull through. But in recounting her story more than two decades later, she recalls one detail in particular that stood out to her husband.

“One of the things that my husband remembers is that my doctor actually called for two units of blood, and literally the blood bank at the hospital asked, ‘Are you sure you need two?’ It was the month of May, heading into the summer months, and I’m sure they were probably thinking that things might be low and maybe had to question whether to send two even with the circumstance that was happening.”

Thankfully, Mom and baby were healthy and continue to be to this day. Pimm shares that both her daughters got married in the last 18 months. It was at her daughter’s wedding that she also got to share a special dance with her father, John, her inspiration for donating lifesaving blood to fellow patients in need since she was just 17 years old.

“Whenever he could he donated. He was up to three gallons when I was a kid. When I was in fifth grade, he had a massive heart attack and in his open-heart surgery he needed a blood transfusion. So, as soon as I turned 17 and was able to donate, I started.”

As a regular donor at Red Cross blood drives at her school, it’s a story that Pimm proudly shares with fellow staff and many first-time donors, particularly high school seniors, because the blood on the shelves that could go to help a friend or loved one – might very well be their own.

“People were willing to do it for me and my Dad, so I want to help other people and give back to them in those times. I am so thankful for whoever it was that donated for me, and my Dad. He’s still alive today. As a baby, I could not have made it but then, as a new mom with a toddler and a newborn, my husband could have been raising them alone. I am a counselor and I like to help people! It’s a small way to help, but what an easy way to give back.”

While no one can predict when an emergency or accident might happen, donors can help hospitals stay prepared and stocked with blood products this spring and year-round. Donors of all types – especially those giving type O blood or platelets – are vital to patients counting on blood products for critical medical procedures. During this busy time of year especially, every single donation can help keep the blood supply stable for patients in need. You can make an appointment to help provide lifesaving care by visiting RedCrossBlood.org, downloading the Red Cross Blood Donor app or calling 1-800-RED CROSS today.

Written by: Meg Rossman, Regional Communications Manager, American Red Cross of WNY

"Take it from someone who has been there": Local blood drive host shares full circle moment

“Please give blood, you never know when you or one of yours will need it”. I’ve written those words many times over the past couple years in an effort to have people sign up for our Red Cross blood drive at St. Paul’s Lutheran Church in Cohocton, NY. My time came on November 9, 2023 when I had a heart attack that required bypass surgery. One of the last things I had to do prior to going into surgery was to be tested and to sign off on accepting blood transfusion if needed. It was at this point I was so glad that the American Red Cross does those drives.

If you’re lucky enough to have crossed paths with Carl Drum, it’s likely you received the message above late last week. Despite a lifechanging heart attack last fall, the president of the congregation at St. Paul’s Lutheran Church has been hard at work hoping to encourage others to roll up a sleeve in the midst of an ongoing blood shortage nationwide.

“I’ve always said on Facebook and anywhere that I contact people, ‘you never know when it might be you.’ And then all of a sudden, that happened. It was me. One of the last things I did in the pre-op room was sign papers saying that if I needed blood that I was willing to take your blood – actually, my blood!”

It was a full circle moment for Drum, who worked with the American Red Cross of Western New York to begin hosting regular blood drives at St. Paul’s two years ago.

“We’ve had some successful drives and we’ve had some that weren’t quite so successful,” Drum explained. “I’d previously given as frequently as I can until now. I’ll be honest, I don’t know if I needed blood or not during surgery, and I don’t care. I sincerely believe now more than ever, the life you might be saving through blood donation may be your own.”

Currently, the American Red Cross is facing an emergency blood shortage as the nation faces the lowest number of people giving blood in 20 years. As a result, the number of people donating blood to the Red Cross has fallen by more than 40 percent due to challenges like winter weather, seasonal illnesses and the COVID-19 pandemic which made it difficult to reach blood donors with community drives like those hosted by St. Paul’s.

Up until November, Drum was a steady donor and received his One Gallon Donor pin this past summer. He is recovering well from the surgery and looking forward to celebrating another year of life on January 15, while encouraging others to share theirs.   

“Take it from someone who has been there. Never in a million years did I think I would be in a circumstance where it would be my turn. Well, it was my turn. You just never know.”

St. Paul’s Lutheran Church is scheduled to hold its next regularly scheduled blood drive on January 23. You can find a list of upcoming blood drives in your area by visiting RedCrossBlood.org, calling 1-800 RED CROSS (1-800-733-2767) or downloading the Red Cross Blood Donor app on your smartphone.

Turning compassion into action to help fellow Sickle Cell Warriors

Passion, Passion, Passion!

Jason Moore exudes passion as he talks about Sickle Cell Warriors of Buffalo.

The vice president of the non-profit explains that “Sickle Cell Disease is the most commonly inherited disease in the world.”

Red blood cells carry oxygen throughout the body; in Sickle Cell Disease, the red blood cells are mutated into a crescent or sickle-shaped form, and therefore cannot carry enough oxygen to the tissues and organs of the body – potentially leading to anemia, and tissue and organ damage. This often requires regular blood transfusions to manage extreme pain and life-threatening complications.

Jason explained that having Sickle Cell disease is a lonely life. Each patient presents with different symptoms, requiring treatment to be adjusted accordingly. Jason is happy to have wonderful providers in Buffalo to manage his care.

Jason and and his colleague, Sickle Cell Warriors of Buffalo president Juanita McClain experienced their journey side-by-side while undergoing treatments at Children’s Hospital, and at specialized camps for children living with Sickle Cell. Their care when they were younger was overseen by social workers. When they “aged out” around 21 years of age, there was no one to guide their care. They came to realize how helpful their social workers were and how much they did for them. Thus, the idea for Sickle Cell Warriors of Buffalo was born.

Sickle Cell Warriors of Buffalo programs include Education to the Community, Transitions – a program to assist teens and parents in moving into adult medical care, Care Coordination – assisting adults in finding qualified practitioners, and Support Groups for Warriors and their families.

On Jason’s good days, he states that he accomplishes so much. He’s a Community Health Worker assisting others along their journey, while guiding the Transitions participants. But on other days, he is in pain and exhausted. However, he appreciates what goodness will come about and knows there is a light at the end of the tunnel.  Optimistic and passionate!

This Sickle Cell Awareness Month and year-round, you can help support Jason’s work and Sickle Cell patients just like him in your community, by making an appointment to roll up a sleeve and donate lifesaving blood. Visit RedCrossBlood.org, call 1-800-REDCROSS or download the free RedCross Blood Donor app to make an appointment nearest you.

 Written by: Ginny Scott, American Red Cross of WNY Communications Volunteer

"Much more than living with Sickle Cell": How a Buffalo teacher's healing journey is helping to heal others

Juanita McClain is many things: a mother, educator, friend, author and a warrior – in every sense of the word.

“I was diagnosed early on. At just a few months old I had my first crisis,” she explained. “I spent a lot of time in the hospital growing up. I went through a lot of the complications. Until my late 20’s, I struggled really bad.”

Sickle Cell disease is the most common genetic blood disorder in the United States, impacting an estimated 100,000 people – most of whom are of African descent. It distorts soft and round red blood cells and turns them hard and crescent-shaped. As a result, blood has difficulty flowing smoothly and carrying oxygen to the rest of the body, which can lead to severe pain, tissue and organ damage, anemia and even strokes. Patients may require as many as 100 units of blood per year to manage extreme pain and life-threatening complications.

McClain estimates that until her early 20’s she was in the hospital receiving treatment for Sickle Cell disease at least once or twice a month, every month. In that time, she received multiple blood transfusions, had surgery to remove her gallbladder and suffered the devastating loss of her son during childbirth in the midst of a difficult Sickle Cell crisis. Despite all that, McClain is quick to point out that her diagnosis does not define her.

Instead, it’s all she’s been able to selflessly accomplish in the face of it.

“I was in college, and I was sick and missing school all the time. I started researching more about Sickle Cell and journaling about how I’d like to change my life,” she explains. “And I said I want to share my story with the world, so I wrote Living with and Surviving Sickle Cell Disease. I feel like it’s an autobiography of my life. After the book came out, I felt a relief over my life and things started to look brighter, so I kept going with it.”

McClain is now the proud author of three books on Sickle Cell disease, including a children’s book titled The Monster Within Me: Surviving Sickle Cell Disease; an educational story that serves as both a way for children to learn about Sickle Cell and to inspire them to achieve their dreams.

It was during this time that McClain, armed with the knowledge of the disease and her own triggers, began her advocacy work in the community. In that time, McClain has worked tirelessly to educate the community and her students at Burgard High School in Buffalo on the impact of Sickle Cell and blood donation; and helped to organize blood drives with the Red Cross ofWestern New York where she also serves on the Red Cross Biomed Committee. In 2018, McClain also launched a Sickle Cell warriors support group which has since grown into the non-profit Sickle Cell Warriors of Buffalo.

“It opens up doors for Sickle Cell warriors who have to get those frequent blood transfusions to be able to get the blood type they need, of their own blood type or race,” she explained. “My background and experience with the disease, I used those to help me grow as a person and to help me get healthier and live with the disease. And when that sparked, it made me want to do more to help others do a turn around in life and look at the disease in a different manner and want to be more than just living with Sickle Cell disease. And here we are today, and we’re doing so much!”

This fall, McClain’s students will help her to organize two blood drives with the Red Cross of Western New York as she also plans a number of community events with Sickle Cell Warriors of Buffalo, including a walk for Sickle Cell awareness, now in its fifth year, and a holiday event to help support local families impacted by Sickle Cell.

As for the mother of three and her own battle, she has this to say of her journey: “I feel the best that I’ve ever felt in my life these days. Things have improved drastically.”

Sickle Cell Warrior Uses Voice To Advocate For Fellow Patients

Sickle Cell Warrior Uses Voice To Advocate For Fellow Patients

“I use the word warrior a lot when I talk about people who battle with sickle cell disease and their families because a lot of times it is a battle.”

It’s a battle 33-year-old Stephanie Ramos knows all too well. It’s one she’s been fighting since birth.

“I was born with Sickle Cell disease. I have a twin brother who has the Sickle Cell trait.”

From roughly six months of age that meant episodes or “crises” as Ramos describes it, each time requiring lifesaving blood transfusions to alleviate what she recalls as tortuous pain.

“If you asked any Sickle Cell warrior, they would tell you it feels like being stabbed. It feels like being hit with a bat. Every second, every minute, every hour that it’s not being treated or taken care of.”

Sickle Cell disease is the most common genetic blood disorder in the United States, impacting an estimated 100,000 people, most of whom are of African descent. The disease distorts soft and round red blood cells and turns them crescent shaped. As a result, blood has difficulty flowing smoothly and carrying oxygen to the rest of the body, which can lead to severe pain, tissue and organ damage, anemia and even stroke.

“It causes a decaying effect in that particular part of the body,” Ramos explains. “It’s not getting the proper oxygen it needs so it starts to die and that’s what we call an episode. It’s pain and a lot of times it causes hospitalization and then most importantly, that leads to a blood transfusion.”

Ramos estimates that she received at least two blood transfusions per year from birth to age 25. In some cases, patients may require as many as 100 units of blood per patient per year to combat the painful effects.

“I always had to take a pack or two of blood. It’s a scary thing. Receiving life from someone I don’t even know. When you donate, you’re donating to someone like me who is in need and it’s needed more than ever.”

Like so many battling Sickle Cell disease, Ramos knows that frequent blood transfusions can make

finding compatible blood types much more difficult and that most often, donations from Black and Brown donors are the most compatible blood types for treatment.

Because of that, Ramos says she was forced to find her advocacy voice – for herself and now others, at a very young age.

“They pump new blood into us. Literally,” she explains. “So, when I tell people about donating blood, I tell them you are literally giving life again to someone whose life is fading away. When I speak to individuals from my background, from my Black and Brown communities, I say we scream that all lives matter – well, this is the start. If my life matters and yours does as well this is the start to show how much we matter to each other, by donating.”

In remission since a bone marrow transplant eight years ago, Ramos is now using her voice to help her fellow warriors through Sickle Cell Advocates of Rochester, or S.C.A.R. The group works to support patients and families affected by Sickle Cell in the Rochester area, hosting educational and social events, fundraising and much more.

“I use my voice because it’s all I’ve ever had. This is part of our toolbox. I’m lucky to be a person who walks in faith and since I can’t donate, let me be a person who can use my words to help bring others to donate and serve as an advocate.”

Part of Ramos’ own toolbox is hosting blood drives through S.C.A.R. and regularly encouraging others in the community to donate. While she recognizes a fear associated with donating, she has this to say on behalf of her fellow warriors.

“We have to watch out for our communities, because if we’re not looking out for ourselves, who is? If fear is the reason you don’t want to donate, then volunteer. Help us out and maybe you’ll learn it’s not a scary thing. And know that for two seconds of being scared, you just gave someone another two seconds of life back.”

One in three African American blood donors are a match for people with Sickle Cell disease. To help ensure patients have the lifesaving blood products they need, the American Red Cross of Western New York works with partners like S.C.A.R. to grow the number of compatible donors. You can help Sickle Cell warriors in the community by making an appointment to donate by visiting RedCrossBlood.org, calling 1-800-REDCROSS or downloading the FREE Blood Donor App on your smartphone.

As nephew battles pediatric cancer, blood donations take on special meaning for Gates woman

It was a normal day at the office when I virtually “connected” with Lisa Bubel in March. 

The Spencerport native and mother of four tagged the Red Cross in a photo on our Twitter account. It was a picture of Bubel donating blood, part of a series of regular appointments the One Gallon donor proudly keeps.

What struck me, though, was that she also posted a photo of a young boy receiving blood – her two-year-old nephew Landon, currently battling cancer.

“I’m donating and I find out that my nephew is receiving blood at the exact same time,” Bubel explained. “It hit the heartstrings even more.”

Bubel is acutely aware of the lifesaving impact donating blood can have. Donating for the first time nearly 15 years ago, the lieutenant with the Rochester Fire Department and part-time Emergency Medical Technician, says she sees the critical need on an almost daily basis.

“So many people need it, people you don’t even realize. We need the blood supplies in stock and ready to go. God forbid there is a major disaster or injuries, you need it for that. But also cancer patients and people with various illnesses. It’s so important to have it in stock.”

Diagnosed at four months old after his parents discovered a lump on his nose, Bubel says Landon is in his second round of treatment and has received blood and platelets several times throughout his fight. Since then, donating blood has become something of a family tradition with future plans to hold a drive in Landon’s honor.

“It makes it much more meaningful when you know someone who has needed a transfusion. I know he’s not getting my blood, but I know that when I’m donating that it’s going to be used. He’s had times where they’ve needed to send him in now to get it. So I have that personal understanding of what it means to have everything stocked up and ready to go when its needed.”

That need, as Bubel well knows will become even more critical as we head into the summer months. As people resume normal summer activities, the likelihood that blood donor turnout and the blood supply is impacted becomes even greater. Every two seconds someone in the United States is in need of lifesaving blood and donating blood or platelets is not only an easy way to give back, but also to make a difference for those in need – people like Landon.

That’s why Bubel is encouraging family and friends to donate as often as they can. For her part, she’s even turned it into a friendly competition racking up badges on the Red Cross Blood Donor app and comparing milestones with loved ones.

“I can’t talk enough about the app! You can pre-register, fill in questions and schedule your appointment with the click of a button. I schedule my appointment before I walk from donating, it’s so easy,” Bubel laughed. “It’s just that first step of going into the unknown. Take that first step and donate. It’s helping so many people and it’s just so worth it.”

Worth it, indeed.

You can make an appointment to donate blood and provide help and hope to patients like Landon by visiting RedCrossBlood.org

 

Red Cross Western NY region staff member shares the special meaning behind his dedication on the job

 

Jason Fogg's infant son, Jackson, required a blood transfusion related to an emergency heart surgery in 2018. Today, he is a happy, healthy 2-year old.

January is National Blood Donor Month. Without volunteer donors, blood products for hospital patients like Jackson – young son of Rochester collections specialist Jason Fogg – would not be readily available.  
 
Fogg has served the Red Cross Western New York region for two and a half years, but he was only a few months on the job before he experienced an even deeper appreciation for the organization’s lifesaving mission. 
 
In early 2018, 2-month-old Jackson was diagnosed with an extremely rare, life-threatening congenital heart defect, which caused the passage of blood to be slowed due to an extra chamber in his heart’s left atrium. With very mild symptoms, the Foggs were lucky to have caught it as early as they did. Within 24 hours, Jackson was undergoing emergency surgery, and required a blood transfusion. 
 
At that time, Fogg had only recently started working for the Red Cross. “It was an eye-opener to me for a lot of different reasons, but it made me appreciate the work that I do even more,” said Fogg. “I reached out to our team and said, ‘make sure you tell everybody in collections and everyone around you right now, thank you for everything that you do.’” 
 
Thankfully Jackson, now 2, has made a full recovery.  
 
“I have this motto on a bracelet I wear and it says ‘do it for Jackson’ with a little blood drop on it,” said Fogg. Whenever days are getting tough or things are not going well, I look at it as a reminder that this is important work and I take a lot of pride in what I do.”
 

Esteemed recognition

Fogg’s responsibilities include setting up blood drives, training and coaching staff, and managing the drives entirely. In his terms, this means “taking the moving pieces and making them all work to collect blood products as efficiently as possible.”  
 
With his dedication in mind, Fogg was recently nominated for and awarded the Red Cross Presidential Award for Excellence. Fogg received a pin and certificate (pictured above) in recognition of this national-level achievement.
 
The Presidential Award for Excellence is presented to employees or volunteers who demonstrate exceptional performance or service in support of the organization, delivering on its multi-faceted mission. Nominees actions must go beyond meeting organizational goals and expectations and be exemplary of the highest level of commitment to Red Cross values and the execution of superior service and performance.
 
“Jason cares deeply for the mission of the Red Cross and works hard to fulfill it and serve as an example for other employees. He is an innovative problem solver. He finds new ways to enhance the donation experience, realizing that even the smallest, everyday efforts make a difference,” said Hanna Malak, Western New York Regional Donor Services Executive.
 
Humbled, Fogg is quick to share the credit.
 
“I am only as strong as the team around me and the management that puts me in the position to succeed,” said Fogg. “Those are the people that I feel are just as responsible for this award and nomination as I am.”
 

Overcoming a challenging year
 
2020 posed many challenges, however the response from the Rochester community and supporters across the region has been nothing short of inspiring. 
 
“It has been a difficult past year,” said Fogg. “It is a testament to what we have in our area, Western NY in general. We have amazing people that really understand the importance of humanity.”
 
Even with strong turnouts, the need is constant. Especially for blood donations from those who test positive for COVID-19 antibodies. 
 
For COVID-19 survivors, there are two ways to help – through a convalescent plasma donation or by simply giving whole blood. Plasma from whole blood donations that test positive for COVID-19 antibodies may be used to help COVID-19 patients. Those who have recovered from COVID-19 can sign up to donate convalescent plasma now by visiting RedCrossBlood.org/Plasma4COVID.
 
“It is nice to get the chance to speak with them [donors] and watch them go through the experience of a first-time donation,” said Fogg. “We get to make their experience extra special, answer any questions, and remind them that they are doing great things with their blood, literally helping save lives.”
 
Health emergencies don’t pause for holidays, game days or a pandemic – blood is needed every two seconds in the U.S. to help patients battling injury and illness. The Red Cross has teamed up with the NFL to offer those who come to give blood, platelets or  plasma, Jan. 1-31, 2021, a chance to win a getaway to the 2022 Super Bowl LVI in Los Angeles. Terms apply; visit RedCrossBlood.org/SuperBowl for more information.  
 
Appointments can be scheduled through the Red Cross Blood Donor App, visiting www.RedCrossBlood.org or calling 1-800-RED CROSS.

Story by Nicole Mauro, American Red Cross