Sam and I spent the better part of Monday and Tuesday in the hospital. On Monday, they checked out his floppy foot and said it was NOT "foot drop", which was good news indeed. The muscles, tendons and ligaments can often become very tight and sore with chemo drugs. With Sam still trying to play basketball outside and practice with the boys grade 6/7 volleyball team, he exerted those muscles, tendons and ligaments which left him very sore. He slows down when he is sore, but barely! It's hard to keep this young man from doing the things he loves. Dr. Bond said he knows what his body can do, and when he gets too sick he'll ease off of everything.
Sam is feeling more nauseous again and has been vomiting throughout the past 4 days. It is not surprising when we realize that he his starting dose of methotrexate was 100 mg per meter squared on Sept. 17 and this week he is up to 300 mg per meter squared. If his counts are still high enough they increase by 50 mg each week. We are thankful that no mouth sores have appeared and that he can usually keep some food down each day! He has been resting more and enjoying some movies his friend lent him to watch.
Yesterday Sam received PEG injections in his thighs by 3 wonderful nurses. Ugghh...I forgot my camera to update the blog with PG hospital pictures. One of the many benefits of being home for treatments is that we know some of the people working at the hospital. Two of the hospital pharmacists we know, one from our church, and the other one used to be one of Ger's students and basketball players. One of the nurses that came to give the PEG was a friend of mine from church. Then I ran into another friend of mine, who has a son in K8's class, so we had an impromptu meeting to discuss some upcoming fundraising events for our kids for their big grade 12 trip next fall. These connections are truly wonderful and the conversations and care we receive because of these relationships, is precious...special blessings!
The kids have 6 days off because of their teacher's convention in Abbotsford and the Thanksgiving weekend. Sam will catch up on his homework and the girls are planning to work a couple days at Ness Lake Bible Camp and hang out with some of their friends. Ger will be back on Friday night so we can be together for our Thanksgiving.
Often people stop Ger and I to ask about Sam and the rest of us and how we are doing. We are grateful for your concern and feel so very encouraged as you remind us that you are praying for us...we love that we do not have face this on our own, and that we have this amazing network of people who are supporting us and praying so specifically for Sam. You have made a huge difference in our lives these past months.
I've have to take Lucy out for her morning walk and blueberry feed! Enjoy your day!
Blessings,
Debbie
5 comments:
Sometimes in my magical way of thinking, I wish I could take on Sam's illness and treatments so he could return to good health. But then I read about the needles and the nausea, and am glad it's not me getting the treatment. Better someone brave like Sam. I'm such a wuss. I've almost got a runny nose, and I'm impossible to live with.
Thoughts and prayers,
Dennis
Hi Deb!
I'm thankful for you all, and your steadfast trust in God. We are praying that God will bear Sam up during his treatments and the dreadful aftereffects. And you, too, while you watch him. You are such an encouragement to me!
I sent the link to your blog to three families we know who are facing cancer right now, and I'm hoping they can draw hope from the same well. Even in your suffering, your story is blessing others.
It's cold but sunny here, and we are working away today on some home improvement projects. We'll do our big family dinner on Monday with my brother Dale and his family, and my niece and nephew and another young married couple. So it should be fun!
Lucy looks like a real treasure, it's amazing how much pets add to your life. Kohl is such a good buddy - gets me out walking everyday. And it's good to watch him do what God created him to do - he leaps and plays at the offleash park and you can see joy in every fibre of his canine being. He reminds me to do the same!
Love to you all,
Heather
hey sam,its catie! i'm sorry to hear that you are feeling nauseous again. i was looking forward to getting together with you when you phined me up! well, at least your preety well caught up on school work.i hope god will provide you with enough strengh to continue playing 6\7 volleyball . You are an amazing at vb! can't wait to seeya back at school !
FROM:Catie G.
P.S Lucy is soo cute!
Hi Debbie and Sam,
Happy Thanksgiving to you and your family! I can smell your turkey from here :) We are not having turkey tonight but I do have a frozen one in the freezer for this coming Saturday. This Friday is Jayden's birthday. So we will have dinner with his grandparents and godmothers on Saturday. I don't think I can make 2 "big" dinners within a week...hehe...
Blessings,
Evelyn
P.S. Jayden also says "Happy Thanksgiving"!
Hi Sam..thinking of you today!How thankful we are that you can be at home with your family,especially at a special time like Thanksgiving.
We continue to lift you up to our heavenly Father every night as a family. We pray for strength for each new day, to be encouraged and to have joy that can only come from the Father in difficult times.For God to touch your body, and finally we thank him for you! For creating an incredible, wonderful child that keeps pressing on and has grown in his faith and has helped in strengthening ours!
Happy Thanksgiving to you and your family,
Love the Belbecks
Post a Comment