Short Executive Status (Summary) -- Blog is below

Active Tumors:
»
5+ liver tumors -- largest is 7 cm by 5.2 cm (70 x 52 mm), Gold tracers inserted Nov 21 for CyberKnife x-ray 3D movement tracking. Thu Dec 1st,2011, CyberKnife planning. Dec 16th, treatment 1/3 done to whole liver. Dec 19th, treatment 2/3 done to whole liver. Dec 21st, treatment 3 failed, couldn't get tracer alignment. Dec 22nd, treatment 2.5/3 done using 2 of 4 tracers. Final 0.5 treatment was to be done Tue Dec 27th. Cancelled due to complications and hospitalization.

»
12 lung tumors -- largest is 8 mm in size (0.8 cm)

»
1 lymph node tumor -- near left renal vein & artery of left kidney (1.4 cm). Nov 14th: Ultrasound done of both kidneys and bladder area, all 3 areas are cancer free.

» 3rd-8th brain tumors -- 6 new brain tumors. Sizes all less than 5mm(0.5cm). Some as small as 2mm(0.2cm). Full brain radiation or CyberKnife TBD in Jan after 2nd MRI to see speed of growth.

Inactive Tumors:
» 2nd brain tumor -- Killed via CyberKnife Sep 29/2011, 5 mm in size (0.5 cm).
» 1st brain tumor -- Killed via CyberKnife May/2011, was 20 mm in size (2 cm). Nov 21st, still showing brain tissue swelling, but not active.
» Original Esophogeal Cancer tumor (source of everything) -- Surgically removed June/2010 by 3-field Esophogectomy. Was roughly large egg sized.

[ Note: 2.54 cm = 25.4mm = 1 inch ]

5 pictures included in album


2011_11_16, Shane in BIG CHAIR



Link to 34 surgery June 2010 pictures and some post surgery shots.

Latest Picture

Latest Picture
Shane - 2011_11_27, Photo Shoot lighting prep

Wednesday, September 22, 2010

What I can do?

To answer some questions:
  1. Yes, I physically can eat more often than I do.
  2. It isn't what foods I'm putting in, it is how often and how much.
Here's why:
  1. I have a huge sore in my throat that hurts like the dickens if ANYTHING goes past it. Water included.
  2. I need to have my throat enlarged again, so it is back to baby food, so if food isn't pre-prepared (whipped) then I'm very hesitant to eat it as it gets stuck (and hurts, with or without the sore that is in the same place!)
  3. It seems that practically every food I consume ends up hurting my small intestines. This combined with the chemotherapy results in my throwing up after every meal. This has lead to an aversion to many, many foods I would normally consume in mass quantities and can't even look at them now.
  4. I have no appetite. The desire to eat plays a large part in how much and how often you eat. The steroid provided to me should help with that this week. Also, removal of the nauseating chemo pump should also remove many aversions.
So hopefully with the proper diet suggestions I have from all my friends and family (no need to provide any more, I'm overloaded). Then I just need to eat MORE. That is all.

Note: one of the reasons I have to eat more is that I'm not eating fast food any longer. No tacos, no chicken wings, no hambergers and fries. Therefore I have to eat more because the calories of what I am eating are less. Health food isn't all it is cracked up to be for someone like me that can't eat much.

Shane

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