AML successful treatment
Happy New Year! I want to share a happy treatment update for my wonderful response to Venetoclax and Dacogen (similar to Vidaza) for treatment of my AML. When I was diagnosed 3 years ago I was considered too old for transplant at age 78 here at the Mayo Clinic. I went into remission after my first cycle of treatment and have now stayed in remission for 3 years. My treatment has been ongoing and my team here has tweaked my routine several times to reduce side effects. Currently I am on a 5 week cycle of Venetoclax for 7 days at the same time I get Dacogen infusions for 3 days (recently reduced from 5 days). I will continue on some treatment routine as long as it is working. In the meantime I am enjoying a full life with family and friends although still taking precautions (weekly blood draws, avoiding folks with colds, etc.) .
I have learned a great deal throughout this period, including the variability of patient responses that can occur due to so many factors (genetics, other health conditions, etc.). I have also learned that there is at least one other patient here who is closing in on 5 years of remission with a similar routine! I am sharing my story to encourage you and wish all of you good outcomes as you face your treatment challenges.
Linda
Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.
@loribmt I really appreciate your housing feedback. I will definitely look into the Marriott Residence Inn!
How many chemo cycles did you do before a BMT donor was found for you? Did you & hubby stay in Rochester the whole time prior to the transplant? And then you stayed an additional 100 days? Or did you end up staying longer than the 100 days before you went home?
It's our intention to stay here until the BMT, then of course as long as needed after that.
Thank you for all this valuable information.
Xoxo Joan
@justjoan11 Hi Joan, Having to relocate long term to another city for medical treatment is basically an investment in health…but pricey for sure. There are a range of options from staying at the Gift of Life Transplant house, AirBnB, condos, hotels, etc. My husband and I are not ‘group home’ people and opted for the hotel suites at the Marriott.
For others that may read this reply, here is a link to some of the longterm housing in Rochester for cancer patients or transplant patients. https://connect.mayoclinic.org/discussion/transplant-housing-in-rochester/
If you do look into the Marriott Res Inn where we stayed, it’s the location on Center Street. They recently remodeled the suites and have limited indoor parking or the Mayo Ramp right across the street charges less…$12 per day max! Convenient!
For us it was the convenience of their location for being able walk to the clinic daily (via subway system), the full kitchen, two bed/2 bath suite, ability to do laundry in their small, but functional laundromat, grocery stores nearby, etc.. Since my insurance paid for my entire transplant, we didn’t mind footing the bill for the hotel for 4 mo.
Wherever you decide to stay, try to sign a lease. If you stay somewhere for 30 days and use a month to month lease, it saves on the county room tax. Most places are very flexible if you don’t stay the entire length of the lease. Also, many insurance companies offer a room allowance so be sure to ask your Insurance case worker about that.
You asked about my AML chemo cycles. Mine were actually done in my local cancer center. I had been admitted to the hospital as an emergency. The bone marrow biopsy was sent to Mayo for processing and when the results returned my doctors were able to start chemo. Took a while for me to be stabilized with transfusions and iv antibiotics so I ended up staying in my local hospital for 5 weeks the first time. Then every 28 days returned for another in-patient week of chemo. I had 1 induction round with Cytarabine and Idarubicin, followed by 2 consolidation rounds before my transplant. Between my chemo rounds, I convalesced at home and was fairly healthy. You live 3 hours from Rochester, can you and your husband go home between rounds?
I was in Rochester for the 100 days with the BMT, plus 15 days prior to transplant and another 10+ days after, making it about 4 months total.
If you’re planning on staying in Rochester during the entire AML/BMT adventure, that is a lengthy stent. Where are you staying now? Can you extend the lease? Is it convenient to the clinic?
PS…I sent you a private message yesterday. It should be in your notifications. Lori.
Thank you thank you Lori! Would you possibly consider giving me your private email? If that's not an appropriate ask, I apologize. I want to ask & share specific things related to my husband's situation & feel uncomfortable posting so much publicly. Thank you Joan
@justjoan11 You can contact me privately by clicking on my picture. It will take you to my page, with the little envelop link under that says, Send Private Message. Those are all private messages and can’t be read by anyone else! It comes directly to me.
I sent you a message the other day, the same way. I’m not sure you’ve seen it. If you’re accessing Connect on your phone, look at the top. There will be a little icon of a person in the upper right corner. Click that and it will open to a menu that shows notifications and messages (along with your profile, settings and the help center). My message should be waiting for you in there.