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Saly & Merna
We began volunteering with The Leukemia & Lymphoma Society’s (LLS) annual Light The Night (LTN) event in high school. Our hearts were touched by the courage and stories of empowerment present at the event, so we came back the following year, and then the year after that, and so on. Even through COVID, we were supporters of the event and the individuals and families there. We volunteer every year and support LLS as we learn more about friends who are wrestling with and have been impacted by leukemia and lymphoma, always praying for healing and restoration.
Mabel
My name is Mabel. I was diagnosed with acute myeloid leukemia (AML) in December 2018. I started aggressive treatment at Northside Hospital in Atlanta, GA. The Leukemia & Lymphoma Society (LLS) became my safety net emotionally and financially. Emotionally they were very present and readily available to answer any questions or concerns I had. Financially they helped me cover the costs of my private medical insurance premiums, co-pays, and co-insurance for medication, labs, and tests. I am forever thankful to the LLS because they are able to help people like me.
Oakley
Oakley was a typical 2-year-old going to gymnastics and play dates with her friends until a week after her third birthday when she began to decline health-wise very quickly. Oakley’s eyes began to swell, alternating between both eyes. We went to one urgent care visit, two ER visits, a visit with her primary pediatrician, and two blood draws before she was diagnosed with acute lymphoblastic leukemia (ALL).
Bill
My name is Bill Bannon. I am a semi-retired child support magistrate for the Minnesota State Courts. In April 2017 I experienced shortness of breath, a sore-throat and bleeding gums. I was diagnosed with acute myeloid leukemia (AML), was stabilized, and started on intensive chemotherapy. It was soon learned that I had a FLT-3 mutation of this cancer, the most serious and difficult to treat. The only possibility for any chance at survival was a bone marrow or umbilical stem cell transplant (BMT). I chose to continue my treatment at the University of Minnesota.
Julian
I was a 10-year-old kid when I was diagnosed with leukemia. I was a happy, energetic kid who loved being outside and was a straight-A student. However, my whole childhood was put on hold indefinitely once I had cancer. Rather than having sleepovers at my friend’s houses, I was sleeping over at the hospital. It was hard to lose my energy, smile, confidence, and hair as treatment took over my life. It was really hard to understand as I was just a kid getting injections, procedures, chemotherapy, and surgery without truly understanding why.
Chase
Meet Chase. Acute Lymphoblastic Leukemia Survivor. When Chase was just 16 months old, he was diagnosed with Acute Lymphoblastic Leukemia (ALL). Chase's treatment of chemotherapy lasted for three and a half years. Chase endured spinal taps, bone marrow draws, feeding tube placements, port accesses, blood transfusions, and countless medications - always with a smile. Chase triumphed; he's in remission and doing great. Chase's family is committed to finding a cure. They have participated in Light The Night Walk for the last seven years and raised more than $66,000!
Carlos
I was diagnosed with acute myeloid leukemia (AML) in June 2021 in Puerto Rico. I was introduced by a hospital social worker to The Leukemia & Lymphoma Society (LLS) for educational resources for patients and caregivers. My stem cell transplant was performed at Auxilio Mutuo Hospital in 2022. After applying for financial help from the LLS, I received help from several programs. LLS provided valuable educational materials that helped me to understand the condition and to make informed decisions. I am now 19 months post-transplant and in remission.
Madison
Hello! My name is Madison, but that's not what you need to remember. The name you need to remember is Brodie. You see, I am joining the 2023 Student Visionaries of the Year campaign in honor of my childhood friend, Brodie. In November 2018, Brodie was diagnosed with acute myeloid leukemia (AML) while only in the 6th grade. With a short fight of a long, five months, Brodie gained his wings on April 9, 2019. But today the war wages, on and we are battling this together. Our war is against leukemia, and I have no doubt we are going to win.
Tak Wah Mak, Ph.D.
A Leading Scientist Studying Precision Medicine Approaches for Leukemia and Lymphoma
Dr. Tak Wah Mak is one of the world’s most cited and accomplished scientists. After earning his PhD, Mak was recruited by the Ontario Cancer Institute (now Princess Margaret Cancer Centre) in Toronto, Canada for a postdoctoral fellowship.
Aleta
I was diagnosed on August 13, 2013 with T-cell acute lymphoblastic leukemia. It was totally out of the blue. I had been married for just a year at the time of my diagnosis and sadly my husband couldn't handle a wife with cancer and we divorced.
Andre
In July 1993 I was blessed with my son, Andre Christopher Jordan. He's my heart, pride and joy. Throughout his young life, Andre's has humbled me with his love, kindness, strength, loyalty and faith. Two years ago, he and his fiancé, Ana were blessed with their son. He was overjoyed with being a new father and had marriage plans in the works. He had just received a promotion at work that he had worked hard for and all was well. Then suddenly, Andre's life suddenly took a tragic turn.
GiGi
When I was diagnosed in 2002 I was in such a fog, all that I can really remember is the doctor saying "You have..." I had acute myeloid leukemia and given 6 weeks to live. I just felt that could not be the end for me.
I went through the chemo, hospital stays all while trying to raise 4 small children and I made it through it all. Thank goodness, right? Fast forward to 2017 the day after my 48th birthday. I began to feel weak and extremely fatigued, without trying to "self- diagnose" myself, this feeling was all too familiar.
Zeke
On April 16, 2022, I brought my son Ezekiel "Zeke" to a sick appointment because of leg pain, stomach pain, and a fever over the last few days. We were sent for some additional testing (bloodwork and an X-ray of his stomach area). Later that day, we received a call from the doctor saying we needed to get Zeke back to the hospital fast because his bloodwork wasn't normal, and he had an enlarged liver and spleen. We woke up Easter morning in the hospital for the first of what would become over 100 nights at the hospital throughout his treatment.
Sue
It’s 2015 and I am doing my happy dance! It’s been 20 years since my bone marrow transplant for my chronic myeloid leukemia (CML) and I am still here enjoying what life brings my way.
Patty
On January 19, 2012, I lost the love of my life to acute myeloid leukemia (AML). We were together for 21 years and this was not how our love story was supposed to end. Too young, too soon… still so much to do, to see, to experience – How do you go on? How do you continue life without the other half of you? How do you stop crying in the shower, before the water runs cold? How do you get dressed, put on a smile and face the world – alone? How do you believe again, when everything you believed in is gone?
Jordana
Jordana was busy being a mom, wife, and radio host when she began experiencing fatigue, hot flashes, and bruising in the fall of 2020.
“I've been feeling crappy for a few months, very fatigued. About two weeks ago I noticed some large bruising on my legs but didn't remember bumping myself,” Jordana wrote in her first journal entry on CaringBridge. “I went for some bloodwork. Tuesday night my doctor called and said I need to go to the ER as my platelets were low. They admitted me, did a bone marrow biopsy, and 12 hours later told me I had leukemia.”
Maurice
On July 15, 2018, I went to the ER after feeling sluggish and weak the day before. I was kept in the hospital and on July 17, I was diagnosed with acute lymphoblastic leukemia (ALL).
Leukemia changed my life. From that day, I received chemotherapy for 43 days. It took me at least eight months to achieve remission and it was and still is a very hard fight. But I refused to give up. I am now a candidate for a bone marrow transplant.
Allison
My story is not all that different from many others. It began with two-year-old me not feeling well and my mom taking me to the pediatrician on a Monday. They diagnosed me with an ear infection and gave me antibiotics. On Friday, still not better, my mom asked my dad if they should let the doctor take another look at me. In my mom’s words, “Something’s not right with my little girl.” Fortunately, the doctor ran a platelet test. My results were so off the charts that she also ran the test on herself to make sure the machine was not broken.
Joey
Joey Renick is a three-time acute lymphoblastic leukemia (ALL) survivor. He was first diagnosed at the age of 3, then 18, and again at 22. Joey has received years of chemotherapy, radiation, and a bone marrow transplant. Since receiving his bone marrow transplant in June 2016, Joey has married his wife Caylee, completed nursing school, began and continues to work as a bone marrow transplant nurse, and will be a dad soon.
Wendell
Wendell Ison was diagnosed with chronic lymphocytic leukemia (CLL) on June 6, 2006. It was through his own battle that he decided to create the team known as "Wendell's Warriors" as a way to give back and make a difference in people's lives by raising money for the Leukemia Lymphoma Society (LLS).
Anna
As many of you know, in 2015 our daughter Anna was diagnosed with acute lymphoblastic leukemia (ALL). She had a very successful treatment, and God answered my wife and my prayers. As of March 2023, Anna has been cancer-free for five years making her a cancer survivor. On October 21, Aimie, Anna, and I will participate in the Light The Night (LTN) walk for The Leukemia & Lymphoma Society (LLS). Funds raised through LTN allow LLS to fund treatments for patients who have blood cancer. As you can imagine, this cause is very special to Aimie and me.
Sydney
My grandfather, Michael, passed away from leukemia in 1991. While I never had the pleasure of meeting him, I have always considered him to be my guardian angel. My grandmother and best friend, Patrice, has been a loyal advocate, supporter, and donor to The Leukemia & Lymphoma Society (LLS) ever since his passing. Additionally, she served as vice president for two years and president of LLS for four years. We love how committed LLS is to the research and care of those with blood cancer.
Jeffrey
My name is Jeff Kurowski and I am 35 years old. I have lived with chronic myeloid leukemia (CML) for two years and Crohn's disease (CD) for 20 years. I have had three feet of my intestines removed. I now depend on daily bowel suppression medication, monthly B12 shots, biologic therapy for a quality of life, and a daily targeted chemotherapy pill to stay alive.
Jude
From 2013 to 2014, after he was diagnosed with acute lymphoblastic leukemia (ALL), Jude endured four cycles of intense chemotherapy, lengthy hospitalizations, difficult side effects, and months of home isolation. Jude's younger brother, Finn, was born in May 2014 in the middle of Jude's chemotherapy cycle. In August 2014, his family finally celebrated as Jude finished the more difficult part of treatment.