Merry Christmas from The Hubbel Family!
Happy New Year!!!
Our goal for the new year is still to bring Emily to NED. We know that we can't stop treatment and neither of her doctors here or in Michigan recommend stopping treatment. It's really just determining what we think is best next. Her doctor here thinks high dose chemo and her doctor in Michigan recommends DFMO, but she has been wanting us to do that each time. The other issue with starting a new treatment plan, is Emilys platelets... They have not been over 50 in a very long time, I honestly couldn't tell you the last time.
Emily had clinic yesterday just to check counts and platelets were at 29 again. She actually required a transfusion, but because they were closing early, have asked that she come back Friday for counts again to see if she is maintaining. She has two more days of chemo. It Is going well, but she isn't eating much. She has lost a little bit of weight again, but we are at least 10 lbs up from where we were last year at this time. Day 15 avastin is next Thursday and we are still waiting to hear from Michigan on scan dates. At this point we are figuring out next plan...
Emily had a nice Christmas and stayed up late last night to watch the ball drop.
Happy New Year!
#neuroblastomasucks #emilysjourney
www.gofundme.com/emilysjourney
Available to make donations via Emilys page
Mailing do donation to Dominion Credit Union to Emily Hubbels Account
Thank you again for your continue thoughts, prayers, love and donations, they mean more than you can imagine. Thank you for the Christmas cards, and those who sent gifts and love. Every bit helps so much, the prayers and love mean so much and for continuing to be part of her 3 year journey
Happy New Year! Hoping and praying this will be a year full of healing and health.
ReplyDeleteBlessings,
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