Grier Martin Christenbury(age 2 1/2) was diagnosed with stage IV neuroblastoma on Tuesday, March 27, 2007- This blog is to help family and friends know how he is doing with treatments. Go Grier Go! www.caringbridge.org/visit/grierchristenbury
Monday, March 31, 2008
We made it---!
Sunday, March 30, 2008
Here we go again!
We have had several corporate angel flights cancelled this time so we just booked a USAIR flight--- !! I was going to go crazy with all those phone calls this week regarding changing flights-- so we decided to book a flight instead of waiting to see what happens at the beginning of the week--
The good news is that we will finish accutane tonight--- YEAH--!! His mood swings have been trying and we basically walked on egg shells last week!! His skin was much better this time--- we used SWEEN creme ( a tip from Marett's friend) and it seemed to help--- LIPS are the hardest to keep from cracking especially when the wind and cold came a few days ago!! He will have 14 days off -- and then back on again for the 3rd cycle-- There are 6 in total-
He will have an MIBG injection on Tuesday -- then a MIBG scan on Wednesday-- And Thursday he will have a CT and Bone Marrow tests-- I hope to be home by Friday-- but if the HAMA tests says he can get another round of 3F8 then we will stay next week!!!
I guess the next update will be from the Ronald--- maybe the weather will be warmer than here???
Thursday, March 27, 2008
1 Year~~~ we made it with the help from so many!
The blog has helped me stay in contact with friends and family without spending hours answering phone calls and emails—But I must admit it makes me very tired to read the early entries – I can not believe Grier went through so much as well as the rest of our family, especially the supersibs—It also gave us strength from the entries from Grier’s team… there were some that would write everyday and still do!!
I can happily say we made it with the help of family and friends and our faith—WE MADE IT! Grier did far better than expected and in some ways carried us through this-- We are now living WITH cancer and still live day by day—I know some will find that odd but it is the way we have survived for so long—
I am reminded everyday (yes, I read caringbridge sites too, and I am a lurker!!) that we are not the only family living this way-- we have met some wonderful people from all over with their own pediatric cancer story and they are just as strong and courageous as Grier and our family—I remember going to the clinic for the first time and meeting Julia… she was dressed up in a princess outfit with a grin on her face—the nurses and staff were welcoming to all that entered and I was numb—but gaining strength watching the veterans of the clinic—and now I can say we are a veteran of not only our Charlotte Clinic but MSKCC as well-- WE MADE IT! We made it through a 10-hour surgery (with a huge sense of peace around noon that day). We made it through so many ups and downs. We made it through the first “buzz” cut and later the first sight of him bald. We made it through 7 rounds of chemo- We made it through so many scans. We made it through countless pokes and injections. We made it through 14 radiation treatments. We made it through 2 cycles of 3F8. We made it through the unknown. We took all of this and made it our new normal— We do not take any of this for granted… We know of far too many kids that did not make it this past year—They “lost/won?” their battle with cancer and became ^Angels^. Pediatric Cancer research is still lacking appropriate funding—we need to do more so these brave kids that fight everyday can just be normal kids – and a cure can be found so no family has to have an anniversary of a diagnoses!
I wish I could say we are done… but we are far from it- We still need a cure! Or the very least a treatment that is not so toxic to the kids.
Each set of 3-month scans brings back a lot of uneasiness and fear that the scans will find more NB in his little body. And if they do… we will make it again and start all over knowing we have wonderful friends, family and strangers that are supporting us everyday as we battle the beast called Neuroblastoma—(I know what it is now!!!)
Thank you again for all that has been done for our family this past year… meals, rides, donations, organizing help, wearing a Go Grier Go Bracelet, Putting a magnet on your car, prayers and good wishes, phone calls, visits, gift cards, flowers, TOYS, hats, cards, and the list could go on—
This day will be marked in our lives forever… but so will all the acts of kindness given to The Christenburys— THANK YOU! THANK YOU! THANK YOU!
GO GRIER GO--!!
Sunday, March 23, 2008
Wednesday, March 19, 2008
Friday, March 14, 2008
We are still living our new "Normal"
I can not believe it has been TEN days since the last time I updated this blog!!! We have had a very normal past ten days at home with a few breaks for me--- the beach and a wonderful visit with a friend and her family- I was lucky enough to be there when she had her second baby-- Some days I look at Grier and forget that he has NB-- it is easy to do these days since treatment has stopped for awhile-- I am thankful for these days-- but hope that his HAMA goes away so we can get 2 more rounds of 3F8 -- A total of 4 has better odds so that would be great-
Grier is doing well-- the 14 days off of accutane have been great... he will start that again on Monday--- so we will once again deal with mood swings and DRY skin!!!!!-- We did find out that we will be in NYC April 1-3 for scans-- As you all can imagine, scan times make us nervous but it something we have to do-
The most exciting news today was that Grier made a visit to preschool--- he went and played on the playground with Mrs. Leary's class at First Pres! He was VERY timid at first but warmed up quickly to all 3 teachers!!! He later warmed up to some of the kids on the playground-- By the end of the visit he had let go of my finger and was sliding down the slide... and driving a truck-- It made my day to see this happen-- He told the teachers he wanted to come back and play so I plan to do that as time allows- It is my hope that we ease back into school before the end of the year-- obviously waiting for results of the April scan before we make the full transition-
Tuesday, March 4, 2008
Change of plans--- not going to NY this weekend-
Please see below for an explanation of HAMA--
What is HAMA?
HAMA stands for "human anti-mouse antibodies." HAMA measures how strongly the body's immune system is reacting to 3F8. 3F8, like most monoclonal antibodies, comes from a mouse white blood cell. This means that 3F8 looks different from a human antibody, and a human will form antibodies (HAMA) against 3F8. If a patient has HAMA, there is no point in doing 3F8 treatments because the HAMA will block the 3F8 from getting to neuroblastoma cells. However, HAMA can disappear, and 3F8 treatments can then resume. Patients are checked for HAMA by means of a blood test. Patients with HAMA do not have pain or other side effects of 3F8 treatment, but patients without side effects sometimes do not have HAMA (and can continue to be treated with 3F8).
Sunday, March 2, 2008
We are doing OK!
This week we will begin shots on Wednesday to prepare for 3F8-- cycle 3--- We need to be in NYC by Sunday the 9th-- And we expect to be there for a week for 3F8 only! It is hard to believe how fast this time at home has gone--
I also have a few Thank Yous--- Thanks to Nancy and Ralph for sharing their house-- I was able to rest and relax with friends for the first time in a year! It is amazing what the beach can do to your attitude--! Thanks to my friends for allowing me to relax in my favorite spot and letting me set the pace this weekend! Also-- thanks for the dinners that are still coming to my house-- And THANKS to everyone who has jumped on board with the Go Grier Go magnets ( especially the stores that have allowed us to use them as a pick-up location!)-- I have seen them as I am driving and I look forward to seeing more and more-- Hopefully people will become aware of neuroblastoma when they see the magnet !
I will update by Tuesday to let everyone know the results of the HAMA test--
If you would like a magnet--- please see earlier posts-- lots of stores are helping us sell them!
GO STEEL FAB!
Go Grier Go Magnets are Here!
Grier's address in NYC
Ronald McDonald House of New York
405 East 73rd Street
New York, NY 10021
Before 3F8
After 3F8
Grier leaving NY-pres and going back to MSKCC
Grier going for a ride in the ambulance across the street
Grier patiently waiting surgery to remove tumor
Go Grier Go Picnic in the Park
On the way to NYC!
Grier at the "new" clinic at CMC
Some of our team at the Hopebuilders 5k
HOPE IS GOOD!!
Supersib- GRACE
If you have time-- these are great WEBSITES to look at!
- Grier's CaringBridge Site
- GO Grier Go! -- website
- Dilworth Little League--Steel Fab (Majors)
- Childhood Cancer Awareness Video
- The Loneliest Road Campaign
- Children's Neuroblastoma Cancer Foundation
- Community Blood Center of the Carolinas
- Coaches Curing Kids Cancer
- SuperSibs
- Levine Children's Hospital
- curesearch