Search Results
Liam
One of the Boston Bruin’s biggest fans, Liam Fitzgerald garnered national recognition as the “fist bump kid” and went on to raise almost $153,000 for The Leukemia & Lymphoma Society (LLS) to help fight blood cancers.
Henry Jr
I was the longest leukemia patient on G111 at the Cleveland Clinic. I spent 135 days on the floor fighting every day. I was there so long that when they could not find a way to get my numbers back up, we would call it Ground Hog Day. Every day for about a month, nothing would change. Finally they said that they can keep me alive like this for only nine months, and I have used five of them already. It was time for a bone marrow transplant.
A. Timothy Lunsford-Stevens JD
In 1970, I was playing baseball in high school as a freshman, playing second base. A bully made a hit and ran from first to second base, tackling me. I got into a fight with him because of the pain I was feeling in my left hand. After the fight, I needed to go to the hospital. In setting my broken hand, they also did a blood test. The results showed why my hand was so fragile; I had acute myeloid leukemia (AML). I had chemotherapy but no radiation or other treatment. I lived in Georgia and went to MD Anderson in Houston for chemotherapy.
Minerva
On October 6, 2015, at 26 years old, I was diagnosed with acute myeloid leukemia (AML). A month later, I was in remission. I completed six months of chemotherapy and am so grateful to be back at my normal life.
One thing I learned early on is that when one person is diagnosed with cancer, so are their friends and family. My journey has not been one I have gone through alone, I have gone through it with the love and support of the people I love.
Robert
I was diagnosed on August 28, 1999 with acute myeloid leukemia (AML). I was told at that time that I would not survive the next week.
Well, at 28 years old, I did not accept that sentence. With a lot of good medical technology and the love of my family and friends, I was able to overcome the odds. I am going on my 16th year cancer free. I do have a lot of health issues due to the intense chemotherapy but I am blessed to still be here.
Suzanne
My mother was diagnosed with multiple myeloma (MM) in February 1987. She passed away in December 1997. I was diagnosed with MM in February 2017. My diagnosis was not only a surprise but daunting because I was my mother’s caregiver and experienced what she faced battling this disease. I’m currently undergoing treatment with the bispecific drug Teclistamab with success. The Leukemia & Lymphoma Society (LLS) has provided me with educational and financial assistance, so I greatly appreciate this organization.
Rhonda
This is my second time participating in the Light The Night as a cancer survivor. I have had blood cancer twice.
In 2012 I was diagnosed with Non-Hodgkin Lymphoma. After being in remission for almost 7 years on December 17, 2018 I was diagnosed with Acute Myeloid Leukemia. I had a bone marrow transplant in March and I am in remission.
I must say I’m grateful that team NCA (National Christian Academy’s school cheerleaders) would do Light The Night in my honor.
Taylor
Meet Taylor Carol. survivor to singer. Taylor started singing in the 4th grade, until he was diagnosed with acute lymphoblastic leukemia at just 11 years old. For about 2 years Taylor's health kept him from singing, but after he went in remission he came back with an even greater passion. Since then Taylor have been given the chance to sing at incredible venues and share his inspirational story of hope and passion.
William
Hi, my name is William Yank and I am a 23-year-old, three-time leukemia survivor from Indiana. My story begins at the end of my junior year of college. I had just secured an internship in Washington D.C and was excited to finally spend a summer on my own. The summer started off pretty rough. I struggled to find affordable housing in D.C, I had no idea how the transportation system worked, and food was twice as expensive as compared to Indiana. Not to mention, I was only 20-years-old having fun was next to impossible.
Melanie
I beat stage 4 lymphoma last year after six months of aggressive chemotherapy. Honestly, I wasn't given much information from my centers, but The Leukemia & Lymphoma Society (LLS) reached out to me to inform me about all the aid and grants they offer to help those going through cancer. Their representative stayed on the phone with me for over 40 minutes and was one of the most helpful people. When you're going through cancer with very little education, EVERYONE helps.
Dr. Adams
Jerry M. Adams, Ph.D., leads an LLS Specialized Center of Research grant.
His team is investigating apoptosis, the nature process of cell death. When apoptosis goes wrong it can lead to proliferation of cancer cells. It cells fail to die when they are supposed to they can develop into leukemia, lymphoma or multiple myeloma, and become more resistant to treatment. To improve treatment, the team is studying new drugs, used either alone or in combination with other therapies, to flip on the cell death switch.
Erica
As you can see, she's the beauty in the grey sweatshirt, mi amor. My daughter Erica survived leukemia, she was diagnosed when she was only two years old.
I'm the blessed momma that gets to celebrate this amazing woman of courage, who is now 28 years old!
Thanks to her awesome team at children's Hospital of Denver and the numerous supporters along the way. You’ve made the celebration of an important life possible.
Blessings, Erica’s mom, Rhonda Lee Salazar.
Kevin
In 2011, I was given two months to live after I was diagnosed with acute myeloid leukemia (AML).
I had to stay at the Bone Marrow Transplant Center at the Salt Lake City Hospital for a very long time and undergo a very hard fight.
My aortic valve failed this year from the chemo, but I had open heart surgery in May 2017 and I am grateful to be alive!
I live in honor to all that passed in our family and those who are still fighting blood cancer.
Steven
I have a rare blood cancer. It is Waldenstrom macroglobulinemia (WM), a type of non-Hodgkin lymphoma (NHL), but some doctors say it has the same characteristics as POEMS syndrome.
I have very painful neuropathy, and it affects my legs and feet to the point that some days I cannot walk.
I have a spinal cord stimulator with the battery implanted in my back.
I am thankful to The Leukemia & Lymphoma Society (LLS) for my grants and all the other assistance, especially through this COVID pandemic.
Disease Complications
As myelofibrosis (MF) progresses, complications may arise:
Follow-Up Care
Click here for information about follow-up care, including what to expect, long-term and late effects of treatment, survivorship clinics, and other resources such as The National Comprehensive Cancer Network (NCCN) treatment guidelines.
Use the Survivorship Workbook to collect all the important information you need throughout diagnosis, treatment, follow-up care and long-term management of a blood cancer.
Michael
In 1995, Michael’s daughter Carley was diagnosed with acute myeloid leukemia (AML), M-7 – a rare form of blood cancer – at just two and a half years old. For the following year, Michael and his wife, Liz, practically lived at Rady Children’s Hospital in San Diego while Carley underwent heavy chemotherapy treatment.
Myra
At age 2, Myra began having fevers and joint pain. Her parents took her to their pediatrician where she had bloodwork done. The results came back normal except it showed she was a little anemic.
“Myra never had any bruising or any issues other than the recurring fever,” according to her father.
Zainab
I'll never forget the call I received on April 17, 2017, when my then-three-year-old niece, Zainab, was diagnosed with leukemia. At the time, she was a bubble-blowing, pose-striking, diva princess. But for the next 2½ years, she became a tiny superhero whose mission was slaying the evil villain cancer. I've always felt a special connection to Zainab starting from the day she was born ― on my birthday, which I also happen to share with my younger sister Noura.
Mollie
Although I was a cancer patient many years ago, survivorship is a journey I take every day. Ever since my diagnosis, I’ve spent my free time engaging with the childhood cancer community and learning more about myself.
