I just returned home from watching our grandson’s pony league baseball game. What a fun way to spend a Spring evening. So grateful for almost 10 years since my MM diagnosis. It’s the small things!❤️😊

Mental health doesn’t start and end in May. It’s a daily journey, and the small moments of hope, laughter, connection, and courage make all the difference. As we close this powerful month of reflection, support, and growth, we want to thank each of you for showing up, not just for yourselves, but for each other. 💚 Let’s keep that spirit alive here in Positive Shares. We invite you to post something uplifting today: 🌟 A moment that made you smile 🌟 A word of encouragement 🌟 A photo, quote, or memory that lifted your heart 🌟 Or simply a message of support to someone else in the group Your story might be exactly what someone else needs today. Let’s continue to build a space of light, healing, and strength together.

Olá a todos Meu marido foi diagnosticado em Fevereiro com Mieloma M. O tratamento que faz é Daratumumab , Lenalidomida, Dexametasona.Tem muitas fracturas em toda a coluna e muitas dores. Não pode fazer Radioterapia porque a extensão das lesões é muito extensa . Foi proposto iniciar um tratamento de ácido zoledrónico, para ajudar nos ossos. Já alguém fez este tratamento? Teve bom resultado ? Algum problema com este tratamento ?

I am abour 10 days before my SCT. 64, newly diagnosed. Where I live, the doctors do not allow me to recuperate at home. I will need to be in the hospital 2-3 weeks (ahhh - yikes!). Based on what I know, the first 7 days ish are the most intense and I have asked my family for 24/7 coverage during that time. After, I suspect I will be feeling a bit easier, and not need someone there all the time. I am asking you all if that approach makes sense? Which days are the worst, that 24/7 coverage would be wise? Or do I really need that kind of coverage? I know this will be an upheavel in the family, so I am trying to minimize the chaos. Looking for advice.

🌍 Today is World Blood Cancer Day 🩸 This day is dedicated to raising awareness about blood cancers, including myeloma, and supporting those affected. It reminds us how important it is to spread knowledge, show compassion, and provide hope to those battling leukemia, lymphoma, myeloma, and other blood cancers. Together, we can: 🔹 Raise awareness about myeloma and its impact on individuals and families. 🔹 Share experiences, tips, and support with others in the community. 🔹 Educate ourselves and others on the latest research, treatments, and ways to improve patient outcomes. Let’s take a moment to honor the fighters, the survivors, and their families. 💙 Your voice and support matter. Together, we continue to make a difference! 🩸Feel free to share your thoughts, personal stories, or any resources you’ve found helpful. Let’s keep supporting each other today and every day.

🩸 Today is Blood Cancer Awareness Day. A day to honor every warrior, loved one, and survivor affected by CLL and other blood cancers. This is also a day to come together—to listen, share, and build a community where no one faces this alone. Your experience, questions, and support can make a real difference. Let’s raise awareness. Let’s lift each other. Let’s grow stronger—together. ❤️ What’s helped you feel most supported while living with CLL?