Wednesday, May 28, 2014

Cyberknife Treatments Complete! ✔️

Last week I completed the cyberknife radiation treatments to the third and final lung tumor scheduled for treatment.  I went to Stanford on four consecutive days to receive the treatments.  Each treatment took about 20 minutes to do the scans that verified the precise positioning needed to deliver the radiation and about one minute to deliver the treatment.

Here is a photo of me on the table just prior to my last treatment. That device above my chest circled around my body - a complete 360 while delivering the radiation to the tumor.

The tumor will be progressively destroyed over the next several months.  I will have scans to check the progress in late August.  I had vertually no side effects, except for being tired from getting up early to fight the traffic on the way to Palo Alto.  If I am to have any side effects, they will likely show up in about 4-6 months.  The most common side effects of cyberknife radiation to the lungs are a cough, indication pneumonitis (inflammation in the lungs), that may require steroids and pain & weakness in a rib if it is near the tumor site. Let's hope neither of these occur to me.

Cheers!
As my husband so eloquently stated, "Check one more treatment off the treatment to-do list!"  We celebrated several times this weekend the fact that I am now three tumors closer to beating this cancer than I was about a month ago.  I am almost recovered from my lung surgery & the neuropathy pain from the surgical incisions is getting better each week.  So, WOO HOO!!!

We also enjoyed a visit from Elyse this weekend, had a great hike at Freemont Alder Open Reserve, had a wonderful dinner with friends, and enjoyed a couple of fun events at Brookside (our local family tennis and swim club).  It's shaping up to be a nice summer!


   
Hike with Hubby and Elyse
My girls enjoying cheese fondue together
Now I move on the next procedure - never a dull moment around here! ;-). On Friday I will have my colonoscopy, as it has been one year since my colon cancer diagnosis. We do not anticipate finding anything suspicious, as my recent CT scans have shown no findings in my liver, abdomen, or pelvic (yay!!!), but my surgeon wants to take a look at his surgical handy-work, specifically at the anastemosis (the technical name for the area where he attached my small intestine to my large intestine after removing the section of bowel that contained my tumor).  He will make sure there is not excess scar tissue present and verify that indeed I otherwise have a health happy gut ;-).

June 2nd marks the day I start back on chemo. I do not look forward to returning to this every two week regime.  I think it will end my post here and not think about this until I have to.

On a happier note, I think I will begin to ease back into playing some tennis in the coming weeks. Nothing too competitive.  Just social tennis to start, but it makes me very happy just to think about it! ❤️

I hope you all had a wonderful Memorial Weekend too!

Cheers, Jacki


Wednesday, May 7, 2014

Recouping Well from Surgery... Thanks to my Team!

I can always tell when I'm overdue for a blog post.... My People start calling, texting, and generally reaching out requesting more details.  I have such a wonderful supportive team of people in my life, & I appreciate all of you so much!  So, here goes....

Surgical Post-Op Report:
Today is 2 weeks and 3 days post-op from removal of the TWO, left upper & left lower lobe, lung tumors & the day of my surgical post-operative appointment.  For the most part it was all good news :-)!  Dr. Burt told me that the final pathology report showed clear margins (clean of cancer cells) for both removed tumors!  WOO HOO!!!  He reviewed my chest x-ray and looked at my surgical wounds, and reported that all was healing as expected.

I have some annoying residual post-op pain & numbness in my left rib area that refers forward from where the chest tube was inserted.  This kind of nerve pain is called "neuropathy".  It may be temporary while I am healing, but for some it can persist. I hope not for me, as it is really uncomfortable at times & I hate taking pain meds.  He started me on a pain medication specifically for nerve pain called Gabapentin or Neurontin. I hope it doesn't make me too sleepy, as I understand it can have this affect :-(.  I need to be functional!

Otherwise, I am regaining strength & energy each day. I have been out walking and beginning to increase my distance and elevation. I do get short of breath a bit, but it sure feels good to expand my lungs and  exert my self!  Cooper is enjoying it too!


So, what's next....
The other appointment I had today was a 4 hour radiology cyberknife preparatory appointment. They made a mold of the back side of the upper half of my body & marked my skin to ensure that I will be in the exact same position for each radiation treatment. Then they prepared to do a PET Scan.  For this scan they had me not eat for 8 hours, then deliver sugar tracking medium, had me wait in a quiet dark room & rest (zzzzzz......), then put me in my upper body mold (made earlier) for positioning & run the scan to detect the areas of faster sugar uptake (tumors metabolize sugar more quickly than normal healthy cells).  Without letting me move, they then deliver IV contrast & do a CT Scan of my chest on exhale & one final chest scan without contrast on inhale.  All three of these scans will be overlayed on each other to create the radiation delivery parameters to obliterate the remaining right upper lobe tumor.  That all took about 4 hours this morning. Then…, I finally was allowed to eat!  I am now prepared to have the cyberknife (a.k.a. SBRT) treatment on 4 consecutive days; May 20th, 21st, 22nd, & 23rd.  The tumor destruction & scar remodeling takes several months to complete following the radiation treatment, so they will monitor my scans every 3 months for the next year+ to ensure there is no further tumor growth in the area.  With any luck, this will be it for that tumor!

Plan for restarting chemo:
Craig & I met with my oncologist just prior to surgery to discuss my long-term chemo plans.  I will restart every 2 week chemo on June 2nd for about 3 months.  The plan is to give me what I was previously on, Folfuri (Arinatecan & 5FU), as it was working to stall tumor growth, plus add the drug Avastin.  Avastin is a targeted therapy that targets the blood supply that sustains & allows tumor growth.  Avastin has been proven very effective and has very few side effects.

After three months of the above plan, if all scans & labs look ok, I will stop getting Arinatecan, start an oral daily version of 5FU (pills taken at home), and go in to the infusion center every 3 weeks for Avastin only.   This will continue with monitoring & guidance though regular scan results &/or until I am declared in remission.

More Scans & Procedures Pending:
With all the attention on my lung scans, we are behind in checking my abdomen & pelvis.  So, next week I will squeeze in a CT scan with contrast of my abdomen and pelvis to ensure no tumors have cropped up in those regions.

May 1st marked the one year anniversary of my colonoscopy that unveiled my cancer diagnosis.  So, I am due for a repeat colonoscopy. With all the other treatments going on, I will fit this in around
mid-June.

Keeping up with my treatments, procedures, & scans has been a full time job of late. It has been challenging to keep up with my daily green smoothie commitment, exercise routine, meditation/yoga/relaxation, not to mention, the rest of life with three kids and a dog plus preparing Kayla for prom and graduation!  I am still on track, but it's quite a challenge with all that has been going on.  I am hoping things will slow down into a quieter routine for the summer, because right now I'm pooped!

I'm off to bed; today was a very long day!!!

I will close with a video that expresses my feelings about cancer at the moment.
Thanks, Rasheeda, for sharing this with me.