Hey Everyone! I'm looking for advice on meeting new people without shaking too many hands and still being warm and welcoming. I'm a 41 year old with High risk CLL and just started Calquence (acalabrutinib) and I receive monthly IVIg treatments because my immune system was really struggling. This week my family (husband and almost 10 year old) head out on a family retreat we do annually with several other families from around the state. Many events will be outside. My concern is that I'll be meeting or re-meeting several people, which of course involves hand shaking. Has anyone figured out a way to politely meet people without shaking hands? I'm trying to keep things as normal as possible. Thanks! Mollie

🎗️ 💜June is Cancer Survivor Month, and we want to honor and celebrate the strength, resilience, and courage of survivors like YOU! 💜 We invite you to share your inspiring story with our community and remind others that survivorship is about living. How to participate: Send us a photo of yourself or a symbolic visual of hope and share your journey in a short caption. For example: Meet [First Name], a [cancer type] survivor. Diagnosed in [year], faced [brief challenge] but never stopped [something inspiring you continue to do]. If you would like to participate, please email support@healthtree.org. Remember, by sharing, you can change a life. 💜

🎗️ 💜June is Cancer Survivor Month, and we want to honor and celebrate the strength, resilience, and courage of survivors like YOU! 💜 We invite you to share your inspiring story with our community and remind others that survivorship is about living. How to participate: Send us a photo of yourself or a symbolic visual of hope and share your journey in a short caption. For example: Meet [First Name], a [cancer type] survivor. Diagnosed in [year], faced [brief challenge] but never stopped [something inspiring you continue to do]. If you would like to participate, please email support@healthtree.org. Remember, by sharing, you can change a life. 💜

Copays .org gas financial copay/co-insurance/deductible (medications and office visits) assistance available for AML patients. Max award $4,000.00/yr. renewable yearly. 500% or less of Federal poverty levels. This is adjusted for Cost of Living Index. You must be on Medicare, Medicaid, or Military Benefits.

copays.org has financial support for patients for Cancer genetic and genomic testing. $250/yr.

Hi everyone! I'm Diana, Product Designer at HealthTree. We're working to make your experience with our products and resources even better — and your feedback plays a key role in that. If you have 5 minutes, we’d greatly appreciate your input through this anonymous survey: 👉 https://forms.gle/aLChy5jwzUVQhox36 Thank you so much for your time and support!

Hi everyone! I'm Diana, Product Designer at HealthTree. We're working to make your experience with our products and resources even better — and your feedback plays a key role in that. If you have 5 minutes, we’d greatly appreciate your input through this anonymous survey: 👉 https://forms.gle/aLChy5jwzUVQhox36 Thank you so much for your time and support!

Anyone have t17 tp53?

#healthtree #myeloma #aml There is a saying I found that helped my husband and I get through many treatments for AML, maybe someone here will find it worthwhile. It goes like this: "You never know how Strong you are until being strong is the only choice you have" I find this to be so true in my life and I see it in so many coaches that I have had the pleasure to interact with.