Welcome back to the next Thriving
not Just Surviving blog post. Its been a quiet, but productive past few
weeks. Progress has been slow, but I feel that I am getting closer to "normal".
I have continued to attend physical therapy twice a week and
rehab of my right shoulder has begun. I do brisk walking for 30-40 minutes
several times a week in addition to my stretches and exercises from physical
therapy. Pain in the right shoulder is minimal and only bothersome at night. I
rarely use the sling and the rehab exercises have greatly expanded the range of
motion. When I saw my oncologist on Thursday the first thing he said was “This
is the first time I’ve seen you over the past two months when it doesn’t look
like you’ve had 5 beers to drink.” I’ll take that as a compliment because I
know I’ve been "out of it" due to the seizures and various medications.
Earlier in the week I underwent another brain MRI. Once
again, it came back clean. We weren’t expecting to see anything, but my
oncologist ordered it as a precaution. The blood work that was testing for an
autoimmune response from cancer treatment also came back negative. This means
that we can officially rule out an autoimmune response as the cause of the
seizures. My oncologist said that its nearly impossible to rule out cancer as
the cause of the seizures because there is always the possibility that a tumor
small enough to be undetected could be present. However, this is very unlikely
given that the first seizure occurred over 6 weeks ago and a tumor would most
likely have grown large enough to be detected by the most recent MRI. The major
takeaway from the recent batch of tests is that my cancer continues to be under
control and its extremely unlikely that the cancer or cancer treatment
contributed to the seizures.
I still don’t have an exact date for my return to Kansas
City, but my lung cancer is no longer a barrier. The focus now shifts to my
neurologist and his comfort level with the effectiveness of my anti-seizure
medication. I’ve now been seizure free for over 5 weeks. The neurologist said
that 1-2 months of no seizures means that the medication will most likely be
effective for the long term. My follow up appointment is scheduled for April
16. I’m hoping that I will have a return date to Kansas City following that
appointment.
It feels great to get all of these issues under control. I
feel much better physically, emotionally, and mentally. Back in February it felt like the medical
issues were really starting to “pile up” and I was left thinking to myself,
“What else is going to go wrong?”. Excellent medical care, a healthy lifestyle,
prayers, and support have been the perfect medicine over the past few months.
May God bless you. I pray for your continued improvement.
ReplyDeleteGreg, Sorry I haven’t checked your posts for a while, but you have remained in our prayers. Hope you and Maureen have a wonderful summer! Mrs. Lanari
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