Patient Videos

Mike describes the symptoms and experiences he had leading up to his diagnosis of acute myeloid leukemia (AML).

Mike shares his experiences and advice for other people on their journey with acute myeloid leukemia (AML). As hard as it is, he says it is very important to be prepared, maintain a positive attitude, and to stay focused.

Gayle describes the tests and process she went through when she was diagnosed with acute myeloid leukemia (AML). She talks about her experience of being immediately admitted into the hospital, having a bone marrow biopsy, and how she felt when she learned of her diagnosis.

Marcia describes the process and tests she had when she was diagnosed with acute myeloid leukemia (AML). She also talks about what her doctor told her and how she felt when she learned of her diagnosis.

Mike describes the diagnostic process and tests he had when he was diagnosed with myelodysplastic syndrome (MDS) and then acute myeloid leukemia (AML). Mike had MDS for about 6 months before progressing to AML.

Thomas describes the tests he went through when he was diagnosed with acute myeloid leukemia (AML). He describes having a bone marrow biopsy, which he says he tolerated quite well, with no discomfort or pain.

In kind memory of the passing of Tom Greene who wanted to share his experiences with others suffering from AML.

Gayle describes the biggest challenge she has faced with her acute myeloid leukemia (AML), which is to accept that she is different since her diagnosis, and has had to adjust to lower energy levels and brain fog.

Marcia describes the biggest challenge she has faced with her acute myeloid leukemia (AML), which was to emerge from treatment and embrace her life again as the new person she has become since her diagnosis.

Mike describes the biggest challenge he has faced with his acute myeloid leukemia (AML), which is the emotional burden of the impact on his family. Mike has found great support from his wife, hospital social workers, and therapists.

Thomas describes the biggest challenges he has faced with his acute myeloid leukemia (AML), which are the impact on his day-to-day life and high susceptibility to viruses and infection. This impacts his travel and ability to be around a lot of people, but he wears a respiratory mask and takes precautions. He says he was fortunate to never experience any side effects from his medications.

In kind memory of the passing of Tom Greene who wanted to share his experiences with others suffering from AML.

Gayle talks about the positive experiences she has had so far in her journey with acute myeloid leukemia (AML). She considers the greatest success to be the bone marrow transplant she underwent. Fortunately, she had very few side effects. She also reflects on being able to accept her new life. She climbed Mount Kilimanjaro 18 months after her bone marrow transplant, which she considers a huge accomplishment although she realizes she may have pushed herself too much.

Marcia talks about the successes she has had so far in her journey with acute myeloid leukemia (AML), which is to keep going, accept her new life, and to be able to share her story with others.

Mike describes the positive experiences and successes he has had so far in his journey with acute myeloid leukemia (AML). He has a whole new appreciation for life. He has learned to know his limits and works closely with his doctors to stay on track with treatments and to stay as healthy as possible.

Thomas talks about the successes and challenges he has experienced with various treatments for his acute myeloid leukemia (AML), the most positive being when he achieved remission. Unfortunately, since then his AML has returned. Thomas says he tries to remain strong and not get too upset about it.

In kind memory of the passing of Tom Greene who wanted to share his experiences with others suffering from AML.

Ed describes the tests and experiences he had leading up to his diagnosis of myelodysplastic syndrome (MDS), and his subsequent diagnosis of acute myeloid leukemia (AML).

In kind memory of the passing of Ed Oasa who wanted to share his experiences with others suffering from AML.

Ed shares his experiences about how he copes daily with his acute myeloid leukemia (AML) diagnosis.

In kind memory of the passing of Ed Oasa who wanted to share his experiences with others suffering from AML.

Ed shares his experiences and advice for other people on their journey with acute myeloid leukemia (AML).

In kind memory of the passing of Ed Oasa who wanted to share his experiences with others suffering from AML.

Paul describes the symptoms and tests he had leading up to his diagnosis of acute myeloid leukemia (AML), as well as his experiences with AML treatment.

Paul shares his experiences and advice for other people on their journey with acute myeloid leukemia (AML).

Peggy describes the symptoms she experienced and the blood tests she had leading up to her diagnosis of acute myeloid leukemia (AML). She also talks about her treatment journey thus far, including blood transfusions and medications.

Peggy shares her experiences about how she coped in the first few months after her acute myeloid leukemia (AML) diagnosis.

Peggy shares her advice for other people on their treatment journey with acute myeloid leukemia (AML). She says it is important to trust your doctor and to lean on the support of family and friends. She also says it's important to take time to rest.

Ed describes the red blood cell transfusions he receives every two weeks for his acute myeloid leukemia (AML). He also talks about the platelet transfusions he receives for this low platelet counts.

In kind memory of the passing of Ed Oasa who wanted to share his experiences with others suffering from AML.

Paul describes the experiences and results he has had so far with maintenance treatment for his acute myeloid leukemia (AML).

Paul talks about how he manages the side-effects of the maintenance treatment he receives for his acute myeloid leukemia (AML).

Paul shares his experiences about how AML treatment has positively impacted his quality of life.

Paul describes the ongoing monitoring he receives from his healthcare team for his acute myeloid leukemia (AML).

Paul describes the expected duration of the maintenance treatment he receives for his acute myeloid leukemia (AML).

Peggy describes the medications and ongoing monitoring she receives from her healthcare team for her acute myeloid leukemia (AML). She also talks about the bone marrow tests she receives regularly.

Peggy shares her experiences about how acute myeloid leukemia (AML) has impacted her quality of life, comparing how she felt when she first started treatment to how she feels now. When she first started treatment, she was tired all the time, but now she travels and can do many of the things she enjoys. Peggy says it is critically important to lean on the support of family and friends.