I started this blog as a way to support a fellow Mom and friend with her son's brave journey through cancer. Megan and Carter have inspired many moms and friends through the internet, so this is our way of giving back and helping them through this hard time. Most of the posts are copies of ones that she wrote to our internet group or on facebook. Thanks for reading Carter's story!
Saturday, February 18, 2012
Friday, February 10, 2012
Megan's final update for a while :(
For the last 8 months I was dreading this most.
Carter has gone into relapse and has a brain tumor. They were able to remove over 50% of it. But there are also other tuners wrapping around his spine that cannot be removed. They will try chemo. But the issue with that is they are afraid he will not survive long enough to get chemo. They have to wait for him to heal from brain surgery in order to do chemo. We have been told that he could pass at any time, or in weeks.
There are alot of details that are very hard for me to type only iPhone.
The short version is
We thought he was constipated, went to the ER a few times, then nothing was adding up and one of his symptoms were making them think of neuromuscular problems, so they did a CT scan. They found a tumor covering a quarter of his brain and more cluttering around his spine. Them we were given a decision to operate, hopefully remove the large tumor, and relieve pressure, hope that they can figure out what type of tumor is is and a small possibly of chemo if he survives long enough to heal from the surgery, and prolong the inevitable. Or, not have surgery and just make him comfortable until he passes.
We made the decision to operate and have a tiny chance.
We have now found out that he has relapsed. Which is less in his favor as most infants with AML do not survive. They only thing we can hope for and donor is keep him comfortable.
I really don't know how to end this post.
I am sorry that you had to read this horrible news. But I am eternally greatful for all of the love and support you have all given to us.
I will be taking a break for a while, as I need as much time with him as I can get.
I love you all
Thank you
-Meg
(Posted to BBC on 02/10/12)
Carter has gone into relapse and has a brain tumor. They were able to remove over 50% of it. But there are also other tuners wrapping around his spine that cannot be removed. They will try chemo. But the issue with that is they are afraid he will not survive long enough to get chemo. They have to wait for him to heal from brain surgery in order to do chemo. We have been told that he could pass at any time, or in weeks.
There are alot of details that are very hard for me to type only iPhone.
The short version is
We thought he was constipated, went to the ER a few times, then nothing was adding up and one of his symptoms were making them think of neuromuscular problems, so they did a CT scan. They found a tumor covering a quarter of his brain and more cluttering around his spine. Them we were given a decision to operate, hopefully remove the large tumor, and relieve pressure, hope that they can figure out what type of tumor is is and a small possibly of chemo if he survives long enough to heal from the surgery, and prolong the inevitable. Or, not have surgery and just make him comfortable until he passes.
We made the decision to operate and have a tiny chance.
We have now found out that he has relapsed. Which is less in his favor as most infants with AML do not survive. They only thing we can hope for and donor is keep him comfortable.
I really don't know how to end this post.
I am sorry that you had to read this horrible news. But I am eternally greatful for all of the love and support you have all given to us.
I will be taking a break for a while, as I need as much time with him as I can get.
I love you all
Thank you
-Meg
(Posted to BBC on 02/10/12)
Wednesday, February 8, 2012
Update
Update: Carter had a good day today, he's still very tired and sore, but was able to eat a total of 10 oz today!! Way to go buddy!! Keep making us proud!
*each minute is an extreme blessing that we will cherish forever. We love you prof *
(Posted by Megan to facebook on 02/07/2012)
Tuesday, February 7, 2012
Out of surgery!
Carters surgery went well, they were able to remove most of the large tumor. He was kept sedated last night because he is incubated, and should be waking up over the next few days.
Carter still has a long fight to go, and we can just hope and pray that he comes out the champion
Thank you all for your support, it helps us keep going
(Posted by Megan to facebook on 2/07/2011)
Monday, February 6, 2012
Sad news for Carter and family
After feeling that something was off based on Carter's behavior, Mom Megan brought him in to the doctor and was met with devastating news:
Carter has a tumor covering a quarter of his brain.
Thank you everyone for your thoughts an prayers. We are in total shock and devastation. It's very grim.
He is in MRI right now getting more of a look at the tumor. We won't know the next step until they know more about it. My heart hurts like I could never have imagined. We can only hope that he pulls through this. He is staying in the ICU to make sure they can keep him stable. His heart rate fluctuates from very low to the low side of normal and his oxygen is low. While he is under sedation they will incubate (breathing tube down his throat) to help stabilize him
I will post updates when we know
Thank you again
(Posted by Megan Whipple to Facebook on 2/06/2011)
Thursday, January 5, 2012
Carter's Article
An article on Carter is in our local news paper!
www.hamiltonnews.com/community/resi...
www.hamiltonnews.com/community/resi...
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