1192 results for Support
Refine Your Search
My Book About Cancer
This workbook for children, created by the Oncology Nursing Society (ONS), is available in two versions - one for the child whose mother has cancer an…
Joy
I am . I have been married for years. We have three children and four grandchildren. We are all very close. I am in remission from lymphoma. Lymphom…
Stories
Aimee
In October , our daughter Alexia was diagnosed with acute lymphoblastic leukemia (ALL) at just years old. At first, we thought she had hurt her back …
Dare 2 Dream
Stories
Matt
"The whole future lives in uncertainty. Live immediately.” – Seneca the YoungerI’m running the Boston Marathon and fundraising for Blood Cancer Unite…
Stories
Debra
In October , while at work, I fell after attempting to sit on a chair, and I went to the emergency department for . As soon as the technician began th…
Payton
My name is Payton, and I’m a young mom and Hodgkin lymphoma (HL) survivor. I was diagnosed when my baby was just two months old, a time when I was sti…
Stories
Matthew
In September, , Dr. Matthew Levine noticed that his regular exercise routine and rotations in the ER were more physically draining than usual. When Dr…
Kyle
In April , Kyle, a - football star at Glenn Hills High School in Hephzibah, Georgia, noticed a large lump on his throat while taking a shower. After a…
Maggie
My son, Benjamin, was diagnosed with acute lymphoblastic leukemia in February at the age of four. Due to the unique nature of his presentation, he wa…
Dare 2 Dream
Greg
In , our world turned upside down when my father, Greg, was diagnosed with acute myeloid leukemia (AML). The only chance to save his life was a bone m…
Natalie
In December , a week after my 15th birthday, I was diagnosed with acute undifferentiated leukemia (AUL) after having unclassifiable arthritis for two …
Myra
At age , Myra began having fevers and joint pain. Her parents took her to their pediatrician where she had bloodwork done. The results came back norma…
Krista
Where do I begin? I am a 2x acute myeloid leukemia (AML) survivor diagnosed for the first time in at the age of . My family and I received amazing su…
Suzanne
In January , I received my diagnosis after five months of multiple doctor visits, blood work, and biopsies. I had no common symptoms, such as night sw…
Alison & Keith
This is a love story about two Team In Training honorees, Alison and Keith. Keith has been a recreational runner for many years and first learned of T…
Doug
I have always been a builder. Professionally, I am an architect. You could say that I’ve spent my life building spaces where people could grow. I ne…
Gwendolyn
Gwendolyn describes herself as a wanderlust who never likes to let the grass grow under her feet. After college, she moved from her hometown in Florid…
Myeloma Rounds Philadelphia
Click here to register * Required Live Event Interactive continuing medical education activity for healthcare professionals in Philadelphia, New …
Wonders & Worries
To provide free, professional support for children and teenagers through a parent’s serious illness or injury, so that they can reach their full poten…
Luke
I had just turned one year and three months old, going into my second year of life, when my parents were told I had leukemia. Obviously, this is somet…
Stories
John
I first got in contact with Blood Cancer United when I was featured on a podcast on TheBloodLine.org. I was on there because of my cancer diagnosis, m…
Stories
Sean
I am running the New York City Marathon for everyone who is currently battling cancer, for those who have fought courageously, and for the families st…
Stories
Clinicaltrials.gov
ClinicalTrials.gov is a resource that provides patients, their family members, health professionals, researchers, and the public with easy access to …
MPN Research Foundation
To stimulate original research in pursuit of new treatments and eventually a cure for polycythemia vera, essential thrombocythemia and myelofibrosis, …
National Organization for Rare Disorders, Inc. (NORD)
NORD is leading the fight to improve the lives of rare disease patients and families. We do this by supporting the rare community – its people and org…