Coming on this trip was a calculated risk for us. But a risk that we and our doctors decided was necessary and worthwhile. We have enjoyed our time away immensely. It has been a blessing to see so many of our friends and family- some we haven't seen in a long time. It was good for all of us. It was great to see so many of the people out there following our story and praying for us on a daily basis. Some we have met before, others we saw for the first time. It is humbling to know that so many people are interceding on our behalf. I pray God blesses each and every one of you and your families. Thank you for holding us up!
But now we are suffering the consequences of breaking out of our bubble. I took Carter to the ER when we got home Sunday night. They took him right back and took full precautions. After a full work up they told us he had a virus, possibly flu. They sent us home with Tamiflu and instructions on quarantine for our household. "No contact between the kids. Everyone wearing masks and gloves. Complete cleaning and disinfecting when moving from one child to the next. etc." After they read me the list, they smiled and said it would be really difficult, near impossible, to do with preschoolers. No kidding!
Carter rarely if ever tells us if he doesn't feel well. But it is very easy to tell because the child that never stops moving is stopped in his tracks. He actually fell asleep Sunday afternoon. His only symptoms so far are lethargy and fever. We pray he doesn't get worse.
So that's where we were going into chemo today.
It feels like such a long time since we came to the hospital. Julia was happy to see everyone again and them her. She was painting in no time and driving the firetruck all over the clinic.
Today she received vincristine, dactinomycin, and zofran. This week is her first of four high doses of vincristine. Because of her age jump and the higher dose she is actually receiving double the dose strength she started with. Dr. McLean spent a lot of time talking to me about this. They expect her pain to increase steadily. He said not to be surprised if it prevents her from eating and limits her ability to walk in the next weeks. The dactinomycin will also likely make her nauseous.
She cried today for the first time during treatment. When Ms. Karen started her port access, she lost it. I hate having to force her to do this. She said having the access pushed in really hurts. This is the first time she has ever talked about how all this feels. My heart aches for her having to go through this process. Julia, you are my hero.
Please pray for strength for Julia and minimal side effects. Please pray for Carter's quick healing and protection for all of us from illness. Also for strength, encouragement, and faith for all of us during the next weeks recovering at home. Thank you for your continued love and prayers during this long journey...
3 comments:
Amber, we are praying. Is there anything I can bring you? Any shopping you need done? I'd be happy to bring it, drop it off on your porch, anything you need. Just let me know.
I am praying for all of you! I hope carter gets better soon and it stays contained. Let Julia know there are so many people praying for her who do not even know her and I think she is so strong! I will pray extra strong and loud today for your strength and hopefully all virus will go away! Thinking about you all.
Julie J.
I know about the quarantining, girl! We're in that boat together this week. Continuing to lift you ALL up in prayer...
Love you!
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