HAIRY CELL LEUKEMIA🫶💪 warrior!Hey 👋 👋 My name is Jimmie Lou and I was diagnosed last year of May 2022! It felt really hard knocks because my dad just passed away a month... By JIMMIE Lou1 min readBookmark for laterReactions 0 reactions Comments1 comments
Jak 2 Mutation in MeMy bone marrow-blood cancer called Primary Myelofibrosis 'MF' started on a festive Cinco de Mayo 2015. It was a normal typical work day for me and all of the sudden... By MASoto4 min readBookmark for laterReactions 0 reactions Comments2 comments
Cancer no way!Hi,my name is Donna, on June 19 2022. I was diagnosed with stage 4 cll and sll! I was in the hospital for 45 days 21 blood transfusions 18 platelet... By CommunityMember2062161 min readBookmark for laterReactions 0 reactions Comments4 comments
My Blood Cancer Story (PV) Polycythemia VeraAloha, my name is Maka. I am a 64 year old female who was diagnosed with PV in April 2020, just when the Panademic started affecting people's lives. I was... By CommunityMember1116b31 min readBookmark for laterReactions 0 reactions Comments1 comments
Living Well with CancerDisclaimer: What follows is just what has worked so well for me that it has taken me from essentially being bed-ridden for the better part of nine weeks (including four... By CommunityMembercfef252 min readBookmark for laterReactions 0 reactions Comments2 comments
A Hermits LifeI'm in my 3rd year of stage 3 CLL. My husband died of lung cancer the year before I was diagnosed. Having seen what he went thru I decided to... By Bhambrick1 min readBookmark for laterReactions 0 reactions Comments10 comments
Living With Lucy Part 4Now I need to tell you that Lucy is still mean. Yes, the targeted therapy helps, and I feel good. But my arms and hands get black and blue bruises... By Editorial Team3 min readBookmark for laterReactions 0 reactions Comments3 comments
Living with Lucy Part 3Let’s talk about blood donations for a minute. First, thank you if you have ever donated blood and to those of you who are multiple-time donors, a huge THANK YOU... By Editorial Team2 min readBookmark for laterReactions 0 reactions Comments0 comments
Living with Lucy Part 2That visit was soon followed by a hematologist/oncologist consultation because he specialized in dealing with folks who live with Lucy or one of her cousins. He explained that I was... By Editorial Team3 min readBookmark for laterReactions 0 reactions Comments0 comments
Living with Lucy Part 1By Linda Gainey Smock Lucy is a mean girl. Oh, I know, not all girls named Lucy are mean. In fact, I have a friend named Lucy who is one... By Linda Smock3 min readBookmark for laterReactions 0 reactions Comments0 comments
MPN DiagnosisI was diagnosed with Polycythemia Vera by my general practitioner, essential thrombocythemia by my hematologist and Myeloproliferative disorder by my oncologist take your pick. I was handling the diagnosis ok... By ritamorse21 min readBookmark for laterReactions 0 reactions Comments0 comments
Surviving Multiple Myeloma Since 1992When diagnosed with stage 3 myeloma in 1992, an oncologist gave him 3 years to live. Jim asked more questions that led to a new oncologist & hospital where he had... By Patient0072 min readBookmark for laterReactions 0 reactions Comments0 comments
ET? PCV?My husband was diagnosed with blood cancer over ten years ago. They did all the blood tests, and bone marrow tests. It was narrowed down to either ET or PCV... By CommunityMember10061 min readBookmark for laterReactions 0 reactions Comments3 comments
Multiple MyelomaI'm 58 yrs old and 2 yrs ago I was diagnosed with multiple myeloma and stage 4 CKD. Since then I had stem cell transplant and I am in remission... By Alycev641 min readBookmark for laterReactions 0 reactions Comments0 comments
So?For the past year and a half I felt so weak and fatigued. I had just moved down to a more so part of Arizona. I knew no one. My... By CommunityMember9aba1b1 min readBookmark for laterReactions 0 reactions Comments2 comments
Fatigue and More Fatigue!I am in remission for CLL and was doing ok, except for the fatigue. After retiring in 2017, I thought I had the world in my hand. CLL is behind... By aldrich471 min readBookmark for laterReactions 0 reactions Comments2 comments
PolycythemiaI kept going to the doctor's office and complaining of a headache, fatigue, itching, and just general malaise. The PA would have me go to the lab and say there... By CommunityMember682e161 min readBookmark for laterReactions 0 reactions Comments0 comments
Some Things I Can No Longer DoI didn’t think of it as an excuse, it’s my new reality. I’m grateful for 10yrs in remission of Stage 4 Hodgkin Lymphoma. There are just some things I can... By CommunityMember58a29e1 min readBookmark for laterReactions 0 reactions Comments1 comments
Cinderalla EffectHaving both CLL and NHL my wife has named the "Chemo fog" effect to Cinderella effect. Sometimes in the afternoon, I get really foggy. Yesterday we were shopping for groceries... By Craig1 min readBookmark for laterReactions 0 reactions Comments8 comments
My Diagnosis and Living with Polycythemia VeraI’m Nathan, I'm 47 years of age, and I was diagnosed with polycythemia vera in 2020, 2 years ago. I live in Sydney, Australia. I was in my prime in... By CommunityMembera1b02c3 min readBookmark for laterReactions 0 reactions Comments4 comments