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thegurns
Multiple Myeloma Discussion • June 19, 2024
Sharing a Survivor's Story of Persistence
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This book is dedicated to all my fellow cancer patients. NEVER give up! NEVER give in!! As I look back on the last three decades, I am the luckiest person on the face of the earth! Beating life-threatening brain surgery (twice), cancer (three times), and morbid obesity (only once, but it was a long hard fight) has taught me the true meaning of words persistence and relentless. For more, please visit us on the web at; https://www.amazon.com/dp/B08QRB3H3G Thanks, Keith 3X cancer survivor
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violetOstrich
Multiple Myeloma Discussion • June 19, 2024
Thriving for Years with Stable Disease
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Diagnosed January 2018. I am fortunate to be so well for so long. I have never been close to a partial or complete response but I keep going to chemo and taking revlimid and my numbers stay steady.
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blueOyster
Multiple Myeloma Discussion • June 18, 2024
Sharing My Journey to Remission
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I'm here for be a Multiple Myeloma patient since October 2019, have four months of treatments, and have a SCT -Auto in October 2020, since that date I'm in remission. My name is Jose Delacruz, Baton Rouge, Louisiana . I'm almost 71 years old
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Jewels95
Multiple Myeloma Discussion • June 18, 2024
My Induction Update: Feeling So Good Now
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I was diagnosed February 2024. I am finishing my 4th month of induction and have been told my numbers look excellent. I have 2 more months if induction therapy but my shots now will be every other week. I will then harvest me stem cells and go on maintenance therapy. My body was in so much pain in February, but I am feeling so good now. I still have fatigue but I can deal with that and rest when I need to. My doctor said live your life and that’s just what I am starting to do
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jadeFish
Multiple Myeloma Discussion • June 18, 2024
My Journey to Remission Without a Transplant
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I was diagnosed in October of 2016. A real big shock to say the least. I was started on velcade revlamid and dex. Didn't do great with the velcade so I was switched to kropilis and all my numbers started coming down. In January of 2018 I was MRD negative and have stayed the same since then. I feel good and hope ro continue on this path. I chose not to do the Transplant which I am happy about.
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Windy
Multiple Myeloma Discussion • June 18, 2024
Celebrating an Art Gallery Success
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So we're sharing our creativity? I'm smouldering, 2 years now. I'm an art therapist and paint to relax. I'm over the moon, my art has been picked for a gallery in the biggest city to me Hull in UK.
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emeraldOyster
Multiple Myeloma Discussion • June 18, 2024
Sharing My Triumph Through Pottery
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I was diagnosed in May 2023. I am in my ninth month of induction therapy. My hobby is pottery handbuilding. I created this piece to represent me triumphing over multiple myeloma. The base represents myeloma, like a vessel from a ship wreak at the bottom of the ocean, covered with barnacles and debris. The fish is me: emerging from the wreak and swimming up to the surface!
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Kathisu
Multiple Myeloma Discussion • June 18, 2024
Finding Normalcy Through Acting
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Acting is my “therapy.” When I’m performing, I forget myeloma and feel like life is normal again. I’m blessed to have these opportunities to live my best life despite my diagnosis.
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Iliana • Admin
Multiple Myeloma Discussion • June 18, 2024
Research Opportunity for Myeloma Post-ASCT
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Now enrolling people with multiple myeloma who have undergone autologous stem cell transplantation​​ (ASCT)​​. Participants in MagnetisMM-7 will advance research on a potential targeted treatment option for multiple myeloma, which could benefit future generations. For more details about the MagnetisMM-7 clinical trial, please visit: https://www.pfizerclinicaltrials.com/nct05317416-multiple-myeloma-trial?cmp=5ca0d465-6e7f-4fe9-b87d-8ed90a4bed3c&ttype=WEB