Speaking as a 10-year Myeloma survivor, this video is one of the best introductions to the Myeloma journey. The only thing missing is a referal to the International Myeloma Foundation as well.
I forgot to mention that I am a Multiple Myeloma patient; having gone through transplant and 24 month maintenance regimen. Now in remission maintaining with a cancer pill in a 28 day cycle to keep it in remission. Making healthy diet choices and keeping the exercises recommended to help stay healthy. Looking at you; I feel encouraged and hopeful that there is hope to live quality and many more healthy years. Emory Winship is the best💕thankful for inspiring stories like yours to bring hope. Thank you ❤
Very informative and encouraging. Thank you so much for giving such detailed and impressive information about living and dealing with Multiple Myeloma. You are a blessings. Let’s keep the faith ❤
Very informative, thank you for this video! I've been following y'all since my brother was diagnosed in 2001, and now I've been diagnosed with MGUS in 2022. The MMRF is a priceless organization that has been so extremely helpful to me and my family!
Speaking as a 10-year Myeloma survivor, this video is one of the best introductions to the Myeloma journey. The only thing missing is a referal to the International Myeloma Foundation as well.
I forgot to mention that I am a Multiple Myeloma patient; having gone through transplant and 24 month maintenance regimen. Now in remission maintaining with a cancer pill in a 28 day cycle to keep it in remission. Making healthy diet choices and keeping the exercises recommended to help stay healthy. Looking at you; I feel encouraged and hopeful that there is hope to live quality and many more healthy years. Emory Winship is the best💕thankful for inspiring stories like yours to bring hope. Thank you ❤
Very informative and encouraging. Thank you so much for giving such detailed and impressive information about living and dealing with Multiple Myeloma. You are a blessings. Let’s keep the faith ❤
So thankful for the info❤
Very informative, thank you for this video! I've been following y'all since my brother was diagnosed in 2001, and now I've been diagnosed with MGUS in 2022. The MMRF is a priceless organization that has been so extremely helpful to me and my family!