Last night around 8pm the neurologist came to our room to tell us Carter’s brain scan was clear (even though we had already received the news earlier). He also wanted to do an exam on Carter and observe his walking, which we had mentioned was a wider gate (we thought it probably just helps him balance better because he is pretty weak). The doctor had all sorts of toys with lights he had Carter follow with his eyes, and he checked the reflex on his arms and legs. He said everything looked good, but Carter has lost all reflex on his lower extremities. This would affect his walking and running. One of the chemo drugs Carter is on weekly (Vincristine) has some harsh side effects which seem to be rare, but all affect Carter. This is the same drug that causes droopiness of the eyelids and crossed-eyes. Apparently, it also strips away at this outer layer which causes reflexes. He said it will come back after Carter’s treatment, but may take months or years. Luckily, Carter is young and active and won’t let anything hold him back. Matt and I know this will all seem so ironic in years to come when Carter is a professional athlete of some sort (a parent can dream!). The good news is the doctor said neurology will no longer be following Carter.
All morning we were waiting to be discharged and finally were around 11:30am. This gave us just enough time to drive straight to Bennett’s soccer clinic to pick him up. Carter was so excited to see him, and Bennett was pretty surprised to see his little brother in the car. When we got home Bennett couldn’t stop talking to Carter asking if he’d play with this toy or that game with him. It just shows us how important it is for him to have his brother around.
We had the nurse come over after dinner and explain how to give Carter the IV treatment of the GCSF drug. We now have a pump which allows the drug to slowly go in over a 15 minute period. This one drug requires two flushes of the line before and three flushes after. So, every day we’ll do this with 6 pre-filled syringes.
Aside from coming home today and all of us being together for lunch and dinner, the best part of the day was Grammy coming over after the nurse left to tell Matt and I to go see a movie and she’d put the boys to sleep. This was SUCH a nice treat!! Thanks Mom!
Friday, July 10, 2009
Subscribe to:
Post Comments (Atom)
Have a wonderful weekend...looks glorious out! Hugs to everyone, especially Grammy giving you guys a date night! xoxo Cindy and John
ReplyDeletePraising God for the good news. Grammy Kay is a good woman! I added Carter to our church's prayer list, and we have some very faithful prayer warriors here in Temecula! Sounds as if you have many all over this country--so wonderful.
ReplyDeleteI had both my babies this week, and am so grateful for their good health. I will never take that for granted--thanks for reminding me!
Love from Hollie Woods and family
YEAH, for Grandmas!! Brothers are special too. :) My grandson, Kyle (5yrs.) is with his parents at Lake Havasu for the weekend & Mitchell (2yrs.) is with me in Mission Viejo. I'm sure Mitchell is having the better time :)
ReplyDeleteAs for the side effects of the drugs, they will be temporary & it's a small price to pay in the long run. It is good that you are following up on all of your concerns & that the hospital seems to be so timely addressing your questions.
Take care & enjoy the boys! Love, Cathy Sukiasian
So glad you are all together for this beautiful weekend! So relieved to hear of the clear brain scan. We think about you all the time! Love you!
ReplyDeleteJamie, Jayson and the girls
So glad that the brain scan was clear and that you guys are home for the weekend. We continue to think of you constantly and love you all so much. Enjoy the weekend...
ReplyDeleteXOXO,
Shan & Tony
Wonderful to hear that Matt and Kara had a night out together. Wonderful to hear all the support you are getting from your families through this journey.
ReplyDeleteMost wonderful to hear that any residual damage from the chemo will go away ...big love and hugs, julie Weaver