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I’m going for a bone marrow biopsy Monday. I have all these symptoms for over 20 yrs only to get a blanket diagnosis of fibromyalgia. 😑 doctors are human too, but I still feel mishandled. God bless everyone going through this. ❤
Hey there! Just stumbled upon your video and I want to thank you for sharing such a poignant and important conversation. As someone who runs the Christian channel focused on themes of hope and compassion, I deeply appreciate your willingness to delve into such difficult topics and provide support to those in need. Your message of resilience and support truly resonates with me, and I've subscribed to your channel to stay connected and learn more. Keep up the incredible work, spreading awareness and offering comfort to those facing challenging times.
Alyssa goes to my school she is a strong brave and a kind person I so glad she's back in school. And ok❤ I was speaking to her at the start of the school year and really comforted me
Not brave enough to watch but so happy for Alyssa, Kiona and family. Love always 😘 (was this filmed in a lift lol, those buttons on the wall look familiar 😉).
Dear Stephen Fry. I am your deepest admirer. I belive you can be healed. The story should have plenty of healing. I love you. Yours Most sincerly. Jeremy
The forum is very helpful if you are looking for a source of information or just a chat with people who are going through the same journey. Whether it’s a loved one or yourself the forum is always open for discussion or information.
@@BloodCancerUK My wife died from AML 26yrs ago, I wish there was something like this forum back then. I was diagnosed with CLL 3yrs ago and if I’m feeling a bit down I fire off a post and always get some positive feedback, especially from Erica and Willow. Coping with CLL on my own can be a strain at times, knowing that there is someone to share with is an important aspect to my journey.
Very apt campaign. I was in hospital and told that I had an MPN called Essential Thrombocythaemia. My other half is a nurse and said it was blood cancer. I was dumbfounded and asked the doctor to confirm this, which she did. Why don't they just tell you that it is blood cancer instead of confusing you with medical jargon?
❤❤❤❤❤ I was diagnosed 5 years ago with multiple myeloma, had a stem cell transplant (with chemo blast to kill off my immune system) in Feb ‘19, and have been in remission since April’19. There have been SO MANY advancements in blood cancer treatment in the last handful of years! You. Have. GOT. THIS!!! ❤❤❤❤❤
You need the GPs to know the symptoms as well. I was attending a GP for two years with these symptoms, and several others, such as dizzy spells, fainting, headaches, tingling in my fingers, ulcerated feet and toes without getting diagnosed. I only got diagnosed when I was hospitalised and lost a toe. I told them that I thought it was cancer and they laughed at me
