Day 283 - More chemo...

Ryan was a bit tired today after his chemo dose.  While both his ANC and platelets are still down, the doctors went ahead with this dose.  I think they are happy that he is in-patient and willing to be a bit more aggressive.  He got two different chemo drugs today (PEG and vincristine), but I don't think he gets anything else for the rest of the week.  He should get another dose in about a week, and then we are done with this phase.

Once we are done with this phase, we will wait until he 'recovers' and then start the final phase.  Each phase should be about 2 months, but with Ryan, it seems as though phases are taking about 3 months.  So, hopefully, this last phase will go by in about 3 months and we can talk about moving on to the maintenance, which means the boys might someday get to come home!

Thank you all for the continued prayers and good thoughts!

Comments

  1. Lois HillJanuary 28, 2018 at 10:51 PM

    that is great that he got to finish this phase of his treatment. I hope this last one is on schedule of 2 months not Ryan's schedule of 3 months!!! and we get to see their smiling faces in Raynesford, Montana :)
    McDonalds French Fries are good
    LUV U all

    ReplyDelete

Post a Comment

Popular posts from this blog

Day 500 - wow...

Image
Today - Sept, 2018 So, this is day 500.  500 days since we found out Ryan had Leukemia.  It's been a very strange year and a half, and you all have no idea how much I appreciate your support and your prayers.  For the last 500 days, I have posted an update every evening. I have tried to keep my posts positive (sometimes more for me than for anyone reading them).  There are things that I have not talked about, perhaps because putting those things into writing will make them possible.  Mostly, I have avoided any writing that implies that there is any alternative to things working out.   When we were first diagnosed with Leukemia, our doctors came in to give us 'the talk'.  For anyone who has gone through this, you know about 'the talk'.   Since Ryan had a small bowel and liver transplant, odds were that Ryan would not survive.  We knew this.  However, Ryan is an amazing kid, always defying the odds. May, 2017  (first month...
Read more

Day 490 - A bit smoky

Image
We've mostly recovered from our emotional day yesterday, only to wake up to a very smoky day.  We decided that Ryan could plant his flowers another day, as he probably shouldn't be outside too much on days like today.  So, it was a video game inside kind of day (after our school work was finished, of course!) We got a call from our Great Falls oncologist, who spoke to the Seattle team about Ryan's low magnesium numbers.  They want us to get labs tomorrow, and probably a bolus of magnesium to get him through the weekend.  Depending on his numbers, we might come in next week as well until the TPN can get this right composition of mag (there is a shortage right now). Hopefully, these fires can get under control and the air quality can get back to our beautiful Montana weather, so we can enjoy the outside again... Thank you so much for your continued prayers and good thoughts!
Read more

Day 498 - Visit to Ft. Benton

Image
I spent the day in Fort Benton with my mom and her friend... It was nice to spend the day walking around the fort and the museums, and just enjoy the beautiful day. Ryan stayed home with Patrick, so it was kind of a break day for him as well!  He woke up late and didn't have to worry about his school work all day... But, he will make up for the missing work tomorrow... One of the side benefits of homeschooling! His belly has completely closed up, now that he's been without the IV chemo for 2 weeks or so.  It looks great and hopefully will stay that way for a while.  We don't have another spinal tap until October, and I don't think we have the week long IV chemo for another few weeks.  Just enjoying feeling good! Thank you all for the prayers and good thoughts!
Read more