Monday, December 1, 2008

Homecoming

Marianna will return home today. We hope the ambulance can transport her early this afternoon. Unfortunately this homecoming is not the celebration we had hoped for.

I am sorry to say this on a blog, and I hope we have been able to speak by phone to those we could....but Marianna is coming home under Hospice care. The cancer has spread to her lungs, and the battle is over. We will make her as comfortable as possible for the time she has, which she wants to spend surrounded by you, her family, friends, and neighbors. With luck and God's grace we may have her with us for Christmas. I am sorry. Very sorry. But in the weeks she has, she wants to make every day count! She has clung to a phrase we just recently heard,

"Life is not about surviving the storm, but about learning to dance in the rain."

Marianna wants to spend these last weeks dancing, and we are going to help her do that. For today, calls and visits will be limited, she is having an exhausting adventure with an ambulance ride, and the nurse will be checking on her and prepping us. But beginning tomorrow we invite you to check in and see if she is up for a visit. Cynthia and Tommy will be at the house full time, and of course we will be there as much as possible. You can always call us for information as well.

Love to you all,
CW

Saturday, November 29, 2008

Saturday morning, November 29

I am sorry I was unable to update the blog yesterday. It was a bad day.
Marianna's fight is not going as we had hoped. It is essential to contact us before contacting the hospital please. Let us bring you up to speed so Marianna does not have to.

You can reach us at:

Richard 714-292-0045
or
Cynthia 714-292-0042

Thank you for your ongoing support, we are all going to need each other.
CW

Wednesday, November 26, 2008

Wednesday, November 26 morning update

Frustrating. Dr. Schlessinger called this morning, while Marianna's abdomen is healing nicely, her lungs continue to be a challenge, and her breathing is getting worse. Even more frustrating, I have caught the flu bug the boys had over the weekend, and cannot see Marianna. She has banished all of us (Ward family) from the room, in case any of us are "carriers", and while we cannot blame her, it does not make it easy when ee know she is struggling again. We are keeping up with the nurses and doctors by telephone, and may send Cynthia to stay with her if warranted. All we can say is please keep praying, her lungs have to stay strong for the chemo. Sorry for such a bummer report when we are trying to gear up for the holiday. I comfort myself with the knowledge that the Lord had every opportunity to call Marianna home last week, and especially over the weekend, indeed on Friday night/Saturday morning we believed He was doing just that. But He chose to heal her then, and I have to cling to the belief that He has a plan for her future and will work this out.

Tuesday, November 25, 2008

Tuesday morning, November 24th

Today is our daughter Elizabeth's 20th birthday, with extra celebratory appeal that we have Marianna to share it with! We will visit tonight with the whole family and Gelato so she can participate.

While visiting last night the cardiopulmonology kid (they keep getting younger) mentioned Marianna had mucus in her lungs when he listened. I'm sure they will get it taken care of, but if you are going to call please listen for her to get tired or winded. I suspect she feels so much better that she is overdoing it. By all means call, but as usual, keep it short and really listen for her breathing, OK?

Thanks to all.
CW

Sunday, November 23, 2008

What a Difference a Day Makes!

Wow! Amazing! I would call our girl's recovery unbelievable, but then it IS Marianna. We have heard back from all of her doctors, they are all THRILLED at her progress. The collapsed lungs are back and working on their own, the bowel is working, and she is sitting up running the hospital from her bed. So if ya wanna chat, have at it. If she is tired, she will shut off her phone. Just try to keep it short still, and listen for her struggling for breath.

She will need to stay for at least another week, but then if she is doing this well they can start a low dose round of chemo and begin beating back the cancer! She will need to stay there for that as well, it sounds like. So we have some time before she comes home, but that's OK, she will come home to us when she can.

I have to share what she would call a "Grammie story". On Friday night, Marianna was out and out delirious, the Adavan really made her not herself, and she spent the night talking to people who were not there. She needed someone to be with her all night, to keep from pulling out tubes and wires. To say it was the low point was an understatement. But in her confusion, talking to someone clearly not in the room, we heard her mutter, "But we don't let little things like that bother us, do we?" Even in her worst time, she was still Marianna. And God Bless her for it.

Saturday, November 22, 2008

Big Victory! WooHoo!!!

Get our your best Southern Baptist accent for a great big THANK YA JeeZus!!!!

Dr. Tran (pulmonologist) was able to remove a LOT of mucus from her lungs, which will let her breathe. I will be honest, if they could not do that, we would have no choice but to honor her wishes and let her come home on Hospice to say goodbye. It was that bad. Her lungs and the tube in her nose were so miserable that she had to be sedated with medication that made her essentially incoherent. We have never had a more heartbreaking 24 hours in our lives.

So we are up and over a MAJOR hurdle! Next step is to get her bowel to work. Until both her lungs and bowel are functioning on their own and she is healed from surgery, Dr. Park cannot start chemo, so we are in a race to get her body better before the cancer gets worse. So keep praying because it is working! We have a long way to go, but right now it at least looks like we are moving in the right direction!

She will still have a very sore throat for a few days, so i will let you know when she is ready to talk on the phone. She may even call out if she feels up to it, and again, if she calls out try to do a lot of the talking and keep it short, save her from herself please!

One of the big things we need to fix is the despondency she was in, so IF she continues to do well we MIGHT be able to get a few of you in for very short visits. Again, what she is like in the morning is not always the story in the afternoon (it has been a real roller-coaster ride) so I am reluctant to make promises, but if you want to visist, please call me and I can let you know how that might work, or not.

Thanks again, y'all must be really good at prayer, because something is working!
CW
714-292-0042

Small Victories, We Will Take Them Where We Find Them

Dr. Schlessinger (surgeon) called. He is concerned at the lack of "sparkle" in our girl, which has us concerned as well. We've never seen her like this. The good news is, he is removing the gastric tube that was snaked down her nose into her stomach, and was her greatest discomfort. So that should give her MUCH more comfort today. He will also let her have a drink of water, which does not seem like a big deal, until you go without it. So the quality of her day should improve, and we are grateful for that. Will report in after they check her lungs, but wanted to be able to say something positive for once.

CW