But, today is a better day. Actually, yesterday, 09-09-09 was the day - my NG tube came out - for the 4th time, but I think this time it is for good. They still aren't letting me eat yet, but I know that is the next step. Once I can eat, (and, of course, poop), I think I might actually be released. I feel like I have been here forever. You may all be asking, "What have you done for the past 3 weeks"? OK, this is a good exercise for my brain. Hmmmm, what have I done during my stay at Stanford University Hospital? Well, let's see:
- I've spent many hours feeling very sorry for myself
- I've counted my blessings
- I've watched a ton of really stupid TV and a million infomercials
- I've appreciated (so much), visits, cards, emails, phone calls and gifts
- I've met about one hundred nurses
- I've gotten about 8 accupuncture treatments
- I've had a massage just about every day
- I've had two sessions with ancient Tibetan "singing bowls" (amazing!)
- I've had a Jin Shin Jitsui treatment
- I've had a ton of foot reflexology
- Richard, and my wonderful friend Susan Meadows have spent hours sitting with me here in my lovely room
- I've heard from so many old, old friends on Facebook (many of whom have been incredibly generous by donating to my swim: www.swimacrossamerica.org/teamsusansurvivies
- I've watched hours of programming on the FoodNetwork because the doctors told me that if my brain got stimulated by food it might inspire my gut to start working.....watch out, I just might become a gourmet cook after this!
OK - that's all the psychic energy I can muster up for this blog. More will follow - with photos, I promise. I'm doing better, hour by hour, day by day. There is a light at the end of this long, dark tunnel. Thank you for reading my blog and for your interest in my cancer journey.
Dear Susan,
ReplyDeleteI think you are an amazing woman and I have been thinking about you and praying for you everyday! Stay strong!
Love, kisses, and hugs,
Martha Salomon and family