Melanie’s Story

Site created on October 14, 2023

Welcome to my CaringBridge website. I am using it to keep family and friends updated in one place. I appreciate your support and words of hope and encouragement. Thank you for visiting. Please note that I will not ask for money, so please do not respond to GoFundMe or any other financial requests.


In July of 2023, I went for a regular physical, and my blood work showed that some values were off, and that there may be something wrong with my bone marrow. I was referred to a hematologist/oncologist, where I had more blood work done, and a skeletal survey (about 30-40 x-rays of the entire body) was ordered. My only "symptom" at the time was a sore rib. It felt like I bruised my rib and had been that way for a few weeks. I thought it was just the pains of getting older. The next steps were a PET scan, multiple MRIs, and a bone marrow biopsy. At the end of August, I received the diagnosis of Stage 2 Multiple Myeloma, which is a blood cancer, and started treatment at the beginning of September. This was quite unexpected, as I do not fit any of the demographics for this cancer. The average age for being diagnosed with myeloma is 70. But, I am thankful that I was diagnosed relatively early and could begin treatment quickly.


The first part of treatment is 4 rounds (12 weeks total) of chemotherapy (both oral and shots), monoclonal antibodies (via shots), corticosteroids, and other supporting medicines. I'm also getting an osteoporosis medicine for my rib (which turns out to be affected by the cancer). After the first part of treatment, I will need an autologous stem cell transplant (meaning it will use my own stem cells). That is scheduled for the beginning of January. After the stem cell transplant, I will be on maintenance treatment for the rest of my life. This is a cancer that never goes away but can go into remission for a time.


This is certainly not what I expected this year to hold, but I'm moving forward with whatever needs to be done. I am so thankful for all of the prayers and support that I have received, and to know that I am not alone in this journey.

Newest Update

Journal entry by Melanie Winstanley

I met with the Emory doctor yesterday to get the results of my 100 day testing, and got some great news! There was no sign of myeloma in the PET scan, blood tests or bone marrow biopsy. This is called Stringent Complete Remission and is the best possible scenario. This happens in about 1/3 of people who have a stem cell transplant. Based on this response, if I did not do any additional treatment, I would have an average of 4 years in remission. However, with maintenance treatment, I would have an average of 10 years in remission.
 
At this point, I definitely want to move forward with the maintenance treatment. The normal treatment is a lower dose of Revlimid, which is the oral chemo that I was on before the transplant. However, there is also a clinical trial at Emory that I qualify for. With the trial, I would either receive the Revlimid or a different antibody treatment. I haven't decided for sure, but am considering the clinical trial.
 
The other good news is that I have been released from all restrictions. I will still be careful where I go and when I am around people. The doctor wants me to get my COVID, flu and RSV shots, but I won't get my childhood vaccines until a year post-transplant. I will also stay on the antibiotics for another 3 months and will stay on the anti-virals for the rest of my life. I am definitely ready for some semblance of normal, but it is weird to think about going out in the world again after being so careful for so long!
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