Postby kpjpmom » Fri Apr 03, 2015 4:02 am
Kenny,
CT scan and bone biopsy were what they used to confirm. Targeted the one area that was giving me fits. I kept pointing to lower spine, tailbone area...that is where the met was on the spine. Spine eroding and small cracks around the bone. The tumor is up in the spinal column and eating away. Causes much nerve pain and down the left leg. Feels like sciatica if you have ever had that. To hold the spine together they injected cement right after the bone biopsy to shore up the spine that had already been eaten. Radiation is to help shrink tumor off of root nerves that run in that area. Roots like legs and bowel and bladder funciton. I am paralyzed somewhat down there. I cannot feel when my bladder is full and well you know.......a river runs through it! LOL Gotta have some humor in these stinking situations. Also, having to stay on a bowel regimine now since I have to get that %^&* out of there. They are hopeful I will get these nerves back since they are peripheral nerves. Hope this helps and yes now cea is a marker for me after 4 years of not really being sure we were dealing with cancer.
DX March 2011 stg 3 cc
Kidney cancer May 2011
Folfox 6months (12 rnds)
It's Back! October 2012 colon resection, kidney removed.FOLFIRI/Erbitux starts Jan.2013
Completed FOLFIRI June 2013, Erbitux continues
March 2015 Met to spine. Radiation 15 treatments
Folfri, 5fu dropped after 3x, Erbitux and Iri continued CEA rising. Moved to
Folfox, Xeloda,Avastin until Feb. 2016 oxilap. Neuropathy returns.
Xeloda,Avastin continues.