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Old 09-23-2011, 08:06 AM   #286
deb_U_taunt
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You are amazing..HUGS and LOVE to you and your mom

Quote:
Originally Posted by JustJo View Post
Hi everyone,

Just doing the "mom update."

I find myself sighing heavily a lot lately. It's just crazy-making.
I talk to her every day, and she's is better some days, worse others....to be expected.
Unfortunately, what I posted before may not be the case now....



After undoing some of the damage done by my sister (which is good...the doctors are now actually communicating with my mother like a competent person again and respecting her wishes)....we appear to be back at "we can send you home to wait out the month."

Naturally, Mom is all for this...and they are training her to do the TPN/IV fluids changeover, with the understanding that once she can do it with no prompting or assistance....she can go home.

A friend has offered to spend the better part of each day with her...do any cleaning, cooking, take her to appointments, etc. And the nurse will come twice a day (once paid for by the insurance, once by us)....so that part is good...she'll have help.

I still have mixed feelings.

I know she'll be far more comfortable and relaxed there...which is important. I also worry because every time she's gone home, she's gotten worse. She's never had a nurse visiting her daily at home either though (as I remind myself), so any "worse" wouldn't get too bad before they put her back in the hospital.

My bigger worry is that Mom is now saying she didn't realize that the TPN was a "forever" thing, that the IV was a "forever" thing...and that she's unwilling to live that way. And, of course, the cancer isn't gone....there's more still there to be treated...and it's complicated by the long term Crohn's, which isn't gone either and never will be. She simply no longer has enough intestine left to support her life, period....so those artificial supports are not optional, and won't be "healed" out of....ever.

I respect her wishes. The choice, ultimately, is hers. No doubt she isn't the first person with stage 4 cancer to be ponderig the decision of ending medical treatment. It's just a tough thing all around.

I've told her that I am her ally. I will defend her choices, stick up for her, insist on everyone respecting her wishes...whatever they are.

When I said that, she started crying and thanked me...saying that all her friends, and my sister, would no doubt sell everything she owned, stick her in the closest nursing home and think they had done the right thing. She's right...they would...they started to until I intervened.

Thank you Tommi for the link to 5 Wishes. I read everything on the site, and printed it out....and it's coming with me, along with the composition book and a good supply of pens, when I get on the plane Wednesday.

I'm also reading "The Memory Palace" by Mira Bartok that someone (ack....maybe Novelafemme?) suggested to me. It's hard reading, but helping right now....and I'm grateful for the suggestion. Dealing with the mixed feelings coming up right now is hard going, and it's truly moment to moment and one step at a time.

Hugs,
Jo
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