Husband, father, coach, athlete

Kevin is no stranger to rising to a challenge. As a professional swimmer and coach, he spent years pushing himself to perform at his best while training his athletes to do the same. But nothing could have prepared him for the toughest fight of his life—first battling cancer, then facing graft-versus-host disease (GVHD).

In 2019, Kevin was diagnosed with T-cell acute lymphoblastic lymphoma and leukemia. He and Jaqi, his wife and caregiver, fought through months of intense treatments and a bone marrow transplant. Always a competitor at heart, Kevin set his sights on beating his expected recovery times. He was out of the hospital in just 25 days—and declared cancer-free in 2020.

But the fight wasn’t over. A few months later, Kevin started noticing sores and ulcers on his tongue, around his gums and inside his cheeks—making eating, drinking and brushing his teeth incredibly painful. He was diagnosed with GVHD in his mouth. Just as he was feeling better again, it felt like his health was slipping away.

That’s when his care team stepped back in—especially Jaqi. She worked closely with Kevin to track his symptoms, relieve his pain, research GVHD treatments and speak up for Kevin’s needs with his doctors. Together, they all worked to stay ahead and keep Kevin moving forward.

^“Anyone going through GVHD knows it’s an everyday battle. You’ve got to stay positive, and you’ve got to trust your care team. Just know that you’re not alone, and you’ve got people around you to support you getting through this journey.^”

Wife, mother, CEO, caregiver

With a family, three companies and a full life that never slowed down, Jaqi was no stranger to thinking fast on her feet and making things happen. But when her husband, Kevin, was diagnosed with T-cell acute lymphoblastic lymphoma and leukemia in 2019, her tenacity was put to the test. For six months, they fought his cancer all the way to remission. Just when it seemed they had won the battle, graft-versus-host disease (GVHD) came out of nowhere.

When Kevin first started getting sores and ulcers in his mouth, Jaqi didn’t know they were GVHD symptoms or how to care for him. She’d heard of GVHD before, but in that moment, there were so many other things she feared it might be—like side effects from treatment, or worse, the cancer coming back. Even after they found out what it was, she still didn’t know where to start. So, she did what she always does. She jumped in, figured it out and took action.

Jaqi dove into learning everything she could about GVHD. She tracked Kevin’s symptoms, changed his diet and found ways to ease his discomfort. She worked with Kevin’s doctors, researched new GVHD treatments and never stopped pushing for better answers and options. Jaqi did everything in her power to get Kevin back to his healthy self—while being his strength and support through it all.

^“GVHD is exhausting. It’s unpredictable, and you really never know what’s going to happen. But it’s all about constantly monitoring new symptoms and at the same time trying to remain positive and seeking out the best care possible.^”

Medical student, former teacher, daughter, sister

As a young college graduate one month into her career as a high school teacher, Ananya’s cancer and subsequent graft-versus-host disease (GVHD) diagnoses came out of left field. Her head was spinning – what would this mean for her future? In that moment and with the support of her “fans” – including her devoted students and brother who was her BMT donor – Ananya made a choice to challenge GVHD head-on. By tracking her symptoms and reporting changes to her care team, Ananya is managing her health while still planning for her future.

Shortly after receiving a BMT in 2023 as treatment for her leukemia, Ananya began experiencing nausea, abdominal pain and digestive issues, which are potential signs of GVHD. But like many people post-transplant, she wasn’t sure which symptoms were a result of her cancer treatments and which were potentially dangerous GVHD complications.

At first, Ananya found her symptoms embarrassing to talk about, but she soon realized that being transparent about her experiences enabled her to receive the care she needed. Thanks to her openness, Ananya’s healthcare team was able to diagnose her with GVHD and quickly put together a plan to manage her symptoms. Ananya continues to closely track her symptoms and share anything out of the ordinary with her healthcare team to stay on top of her GVHD.

Ananya feels lucky to have her wonderful family and “fans” in her corner. But she’s also found support online by connecting with other GVHD patients who understand what it’s like to live with complex symptoms.

^“Getting diagnosed with GVHD feels isolating. Being on social media and connecting with people who also live with GVHD has been incredibly meaningful and helped me deal with my diagnosis. Now I know I’m not alone.^”

Mother, dancer, social media influencer

Tia is an avid dancer. Despite the joint pain and stiffness that often comes with graft-versus-host disease (GVHD), she doesn’t let her health journey define her or dampen her spirits. In fact, she manages to still live life to the fullest and be a shining light for others facing their own health challenges. Her adoring “fans,” including her five beautiful kids and husband, remind her daily that she has the grit to challenge GVHD.

In Tia’s case, her journey began in April 2020, when she was diagnosed with acute myeloid leukemia (AML) and had to undergo intense rounds of chemotherapy, which her body ended up rejecting.

Luckily, Tia’s brother was a perfect match for a BMT. A few months following her transplant, she noticed that the skin on her face and body was thick, difficult to grab hold of and felt as if it may split when she moved. Her healthcare team immediately knew what the cause was and began treatment right away.

^“I fight through the difficult days for family. My hope is to show – not just to my social media followers that are watching, but to my children – that you can do hard things and that no matter what life throws at you, you can endure and find a way to enjoy life.^”

Writer, advocate, father

Brad’s cancer and graft-versus-host disease (GVHD) journey was so challenging that there were days he considered giving up. As a writer, during the toughest times, Brad wrote poetry about his experiences to help cope with his feelings of frustration. His writing, along with the incredible support from his family, kept him going. Today, by tracking his symptoms and working closely with his healthcare team, Brad is managing life with GVHD and encouraging other patients living with chronic illness to do the same.

Brad received a BMT to treat his lymphoma in 2016. Before his transplant, he learned about the potential for GVHD complications. When he started experiencing symptoms, like rashes and digestive issues, he immediately talked to his healthcare providers.

That eventually led to an acute GVHD diagnosis, which progressed to chronic GVHD over time. Like many others living with GVHD, for a while, Brad felt like his life had come to a halt. Extreme exhaustion kept him from doing the things he loved, like playing sports. Brad also went temporarily blind, forcing him to relearn how to navigate the world while working to combat his GVHD symptoms.

When Brad began to lose hope, it was his desire to be there for his daughters that motivated him to push through and find a medical team that could help him manage his GVHD.

^“My main motivation is that I want my daughters to have a dad. During the toughest moments of my GVHD journey, my youngest daughter made me pinky promise that I’d live to see her future children born. My kids are my biggest fans, and I’m their biggest fan, too.^”

Author, health advocate, touring speaker, mother

Loriana has been through more than most. When her son was only two years old, she was diagnosed with leukemia and her world turned upside down. She subsequently developed graft-versus-host disease (GVHD) and eventually breast cancer.

She survived two cancers and her GVHD battle has been long and complex, but she hasn’t done it alone. Though she has faced many unforeseen obstacles, her loved ones — or her “fans” — have been by her side the whole time. Her son is her “North Star,” her husband is her “rock” and they both motivate her to challenge GVHD.

In 2014, Loriana received a BMT as a treatment for her leukemia. At the time, she knew there was a chance she could develop GVHD post-transplant. Not long after surgery, she noticed rashes and started experiencing stomach issues—both potential signs of GVHD.

Loriana was proactive in flagging these symptoms to her healthcare team and was diagnosed with acute GVHD, which ultimately progressed to chronic GVHD. At the time of diagnosis, her everyday life changed dramatically. It became consumed by a maze of doctor visits and specialist appointments. Her work and hobbies fell by the wayside. Yet, through it all, she struggled the most when seeing the impact her GVHD had on her husband and son.

^“When you go through two cancers, you start to see life through a different lens. I am really passionate about making an impact on the world through my health activism and improving the path for other patients because I feel no one should suffer the way I’ve suffered…If you’re going through GVHD, whether it’s acute or chronic, the best thing you can do is advocate for yourself. Don’t stop, and never let up.^”