Search Results

Chemotherapy and Drug Therapy

Treatment of CLL is started when symptoms develop that are associated with active disease. Before starting treatment, it is important to have another FISH test to see if there are any changes to the genes and/or chromosomes of the CLL cells. 

Pilar

My name is Pilar, and I am 34 years old. I used to work for the workforce board of Philadelphia, working with youth, until I was diagnosed with acute myeloid leukemia (AML) back in October 2020. It has been a hard battle, but I am positive and blessed to have the support of my family and friends. Additionally, I was very fortunate my sister, Marcela, was a match to be my donor.

Stephanie

I was diagnosed with stage 2 Hodgkin lymphoma (HL) in 2000 and had seven months of chemotherapy (ABVD) and 20 rounds of radiation. I have not had a reoccurrence of HL, but in 2014, I was diagnosed with chronic lymphocytic leukemia (CLL). I see my oncologist every four months to check my white blood count, and so far, I am still in a watch-and-wait situation. I work full-time in a high-level, stressful job, have two children, and thankfully, have the energy to do it all and have not had to resort to any treatment yet.

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.

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).

Julia

My daughter Julia is 13 years old and was diagnosed with Hodgkin lymphoma on October 19, 2020. She had intense itching episodes on her arms and legs along with swollen lymph nodes that her dermatologist misdiagnosed her for along time with different things. We wanted answers.

After many tests we had answers, she has stage 2 cancer. And her itch is a Hodgkin itch, a rare symptom. Julia just completed her second cycle of chemotherapy and her itch has subsided. We are just beginning her journey.

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.

Monica

As a First Connection® volunteer with The Leukemia & Lymphoma Society (LLS) for almost two years, I have had the opportunity to connect with patients and survivors to share their stories and experiences while battling this deadly illness. Every day I come across so many touching and courageous stories that inspire me to do more and more to support this cause.

Elizabeth

I was diagnosed with lymphoma in October 2017 after three months of dithering doctors even though I live in New York City and had good health insurance. After three months of dithering and a diagnosis, I was told the next appointment at the treatment department was in two months. I had the good fortune to have heard about Dr. Morton Colemen because he had treated a friend's mother 15 years before. He became my doctor that day, and I revere him.

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.

Geoff

I was diagnosed with acute myeloid leukemia (AML) on April 13, 1995, at Arlington Hospital (now VHC Health) and was hospitalized there for 32 days for chemotherapy. I received a second round of chemotherapy (high-dose) at Memorial Sloan-Kettering Hospital a few weeks later. Afterward, I received an autologous stem cell transplant at Sloan Kettering. I was discharged on August 13, 1995, and readmitted in late August for two days for an infection. I have been cancer-free since then.

Reduced-Intensity Allogeneic Stem Cell Transplantation

Reduced-intensity allogeneic stem cell transplantation (sometimes called mini-transplant or nonmyeloablative transplant), like a standard allogeneic stem cell transplantation, uses stem cells from a donor, but the conditioning treatment contains lower, less toxic doses of chemotherapy and radiation. This type of SCT may be an option for certain patients who are older or who are otherwise not healthy enough or strong enough to undergo standard allogeneic SCT.

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.

• Download or order The Leukemia & Lymphoma Society's free booklet, Chronic Myelomonocytic Leukemia (CMML) and Juvenile Myelomonocytic Leukemia (JMML) 

Lashelle

In 2019, knots started to appear on my neck and jawline. My face was also massively swollen. I was unrecognizable. I had difficulty breathing, and major parts of my body were swollen as well. After several tests and two surgeries, I was unexpectedly diagnosed with non-Hodgkin T-cell lymphoma (NHL). I was told that if the cancer had stages, I was considered stage 4.

Lia

Hi Everyone! My name is Lia Sartorio and I am 21 years old. I am Stage 4 Hodgkin's lymphoma SURVIVOR! My world was turned upside down on May 6th, 2019, when I was diagnosed with lymphoma. I had been experiencing severe back pain for a few months, and after many unsuccessful chiropractic visits, I was prescribed an MRI. Expecting to see nothing but a pinched nerve, the MRI uncovered that I had abnormal bone marrow in my lower back and pelvis. Within two weeks of my MRI, I underwent a CT Scan, a PET scan, a bone marrow biopsy, and a surgical Lymph Node Biopsy.

Amy

I am a stage IV non-Hodgkin lymphoma survivor (NHL). The diagnosis came as a complete shock since I was a relatively healthy, active young adult working and enjoying life with family and friends. With a family history of breast cancer, I was advised to start having screening mammograms in my 20s. After a few clear screenings, I approached my 2018 screening and annual health visit to my primary care doctor's office with optimism. Within 48 hours, I received the dreaded call many women fear ― abnormal results.

James

I am a cancer survivor and my story starts in the summer of 1999. On June 9, an MRI revealed a tumor the size of a golf ball in my brain. A biopsy showed it to be a primary central nervous system non-Hodgkin lymphoma. I remember this date vividly because it was my wife’s birthday and she had to break the news to me. This marked the beginning of our journey.

Jacqueline

It’s been five years since my daughter was diagnosed with stage ¾ Hodgkin lymphoma (HL). She had just graduated college, and she had a lump on her right clavicle area. We went to the doctor, and then it all started, from CT scans to biopsy to telling us that it would be six months of chemo, and that’s it.

Lenny

I am nominating an extraordinary person, that I have never met in person before.  This person truly changed my life in many ways.   He has performed many positive actions that changed my perspective and outlook of people for the better. He truly has the power to change millions of people's and or their family's lives, and my family and I were fortunate to be the recipients of access to his extensive knowledge base and his immediate comforting support.  

Gianna

My story began nearly seven years ago on February 28 when I received the call from my doctor and heard those dreaded words, “You have cancer.” A week prior, I had gotten a lymph node biopsy for a lump that randomly grew on my neck. As a healthy 19-year-old, cancer was the furthest thing from my mind, and receiving a diagnosis of Hodgkin lymphoma (HL) was simply unbelievable to me and my family. Hearing this news began a three-week blur of diagnostic testing and meetings with oncologists, fertility specialists, and surgeons before my first chemotherapy treatment on March 23, 2015.

Jill

My world changed forever in April 2021. Life was going so well . . . I was 35 years old, my kids Henry (9), Olivia (7), and Ruby (5) were getting excited about summer break (and all the trips we had planned), my insurance business was in full swing, and all my plants and flowers were in bloom. I was doing what I loved most, working in the yard, when I noticed my right pinky finger was going numb, and I began having trouble walking. We immediately went to the ER. The doctors initially thought it was a stroke, but luckily a fantastic neurosurgeon was on call and saw the MRI.

Yaneiry

Certain things come into your life to show you how strong you are. Life is so fragile, and we don’t know if we will be here on this earth in the future. This process shows me that the most important thing in life is having health and making beautiful memories with loved ones. 

Barry

I was diagnosed with non-Hodgkin lymphoma in May of 2003.  The diagnosis came after three or four months of tests attempting to diagnose a lump from my neck (which was ultimately removed).  My wife and I were told that I had a disease that was considered treatable but not curable.  My particular sub-type, follicular, has a tendency to reoccur.  I was referred to MD Anderson Cancer Center in Houston.  The staging test results showed I had a very small amount of the disease on the whole, but it was present in my bone marrow, which is considered Stage IV, or

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.

Russell

In the tapestry of life, there are moments that test the strength of the human spirit, moments that challenge our resolve and redefine our sense of purpose. For Russell, a Filipino-American music artist and entrepreneur, such a moment arrived six months after marrying the love of his life ― a moment that would alter the course of his life forever.