Oscraps

Tomorrow may be discharge day! eek

CookingMyLife

Well-Known Member
This is an update written by my xh's wife Amy. One blessing that has come out of all this is finally after 25 years post our divorce, having some kind of relationship with them. It's also one where we are all looking at the same picture and working amongst ourselves to find workable options. Amy is a clear thinker and a say what you mean person as much as I am. We are on the same page with this daughter.

Update via Amy McC (ty Amy for taking notes! I uh...used another method...nuff said)

So we all met with Dr. Cullen this morning.(Jan 21) He's the A team for this type of cancer. (eta..Dr Cullen strongly advised us not to transfer Liz from UMD MC and we concurred.)

Elizabeth will finish this course of chemo on Monday. They will evaluate her then to make sure that she is eating, is mobile and is able to manage the pain. She will still have the headaches but the Dr. felt that the chemo will have lessened the pain to a level which would be managed by prescription drugs. Right now Elizabeth is very nauseated and has not been able to keep food down because of the chemo. Also she dozes most of the time and has been reluctant to get out of bed.

Upon her release she will be going to stay with her mom and Dick in Annapolis. She will have an appointment with Dr. Cullen in about a week and at that time they will set up the next round of chemo. That next round would occur in about 3 weeks. Elizabeth would come into UMMC infusion center, get hooked up with the chemo and then would be released (after many hours at the hospital!) that same day with the chemo to return to whereever she is staying. The chemo is 24 hours a day for 4 days. Then someone comes and disconnects her. Then there are more checks with the Dr. and then 3 weeks later, the next round starts. This will be done through the UMMC.

Dr. Cullen anticipates 2/3 rounds of chemo - each cycle 21 days so he figured 9 weeks for that. Concerning radiation treatment, she will start that in about 6 weeks There is an initial evaluation in a month, then two weeks after that Elizabeth will start daily radiation treatment,Monday through Friday, for 7 weeks. That will be done in Annapolis. (eta by Maureen - This is still dependent on Dr. Cullen's advice on release to another facility. But at least much of our winter weather could be over.)

Of course, these numbers of weeks and days are not set in stone -- they are hardly set in paper!! Timing and medication and treatment will all depend on her condition and response to the treatment.

So that being said, Maureen and Dick and Vince and I will work out who does what when and where. We will not be taking her to NC until we see the results of the treatment and the Dr evaluates her. So we will be coming to MD to stay when it's our turn at bat. Those details follow when we have them.
 

faerywings

The Loopy-O
CHEERY O
I just posted on FB, but will add my prayers here as well.

*fingers and toes all crossed for all of the best of everything*
 

Kiliki

Well-Known Member
*hugs* i wish there was something i could say that would make you feel better....but know that i am thinking of you and your family during this time.
 

LSlycord

Well-Known Member
Oh Maureen...such a difficult situation. But it sounds like you are all focused on what is important. Continuing to pray!
 

donnagoar

Well-Known Member
Maureen, best thoughts for all of you. Continued prayers. Find some time to take care of YOU too.
 

Ellen

Well-Known Member
tough times ahead for all concerned but at least it has brought all of you together to put your shoulders under it and support each other.

wishing you lots of strenght
 

Bush Girl

Well-Known Member
How wonderful that Elizabeth has you all pulling together to take care of her and see her through this dark period of her life. My thoughts are with you all for the coming weeks.
 

taxed4ever

Administrator Crazy about the "O"
CHEERY O
Maureen sending you prayers and healing thoughts to give you all the strength to continue to provide care for your dear daughter :hug: Don't forget to take of yourself along the way!!
 

mrstoa

mrstoa
Big warm hugs for you Maureen and prayers for all the family and of course, you!

It must be a huge relief to have the families pulling together for your dear daughter.
 

sberkan

Well-Known Member
Hugs to you and your family Maureen! So glad to hear that everyone is working together in this to support your daughter! Take care of each other!
 

snowdropz

Well-Known Member
Glad to know that you have worked things out for your daughter. Hope she responds well to the treatment given.
 

scrap-genie

Well-Known Member
Thoughts, hopes and hugs to you all, Maureen. She is fortunate to have all four of you planning and supporting her.
 

hondachicc

Well-Known Member
Most definately the time to pull together....

I am glad she will is well enough to come home...I will be praying for your family and for her that she will come through this with shining colors!!! Lots of love and hugs for you all too!!!
 

digigal

Well-Known Member
So nice to have a whole "team" supporting her and what a wonderful mom you are. I agree with Donna, you will need some time also to yourself. Thinking of you!
 

wombat146

ONA - Administrator
CHEERY O
All the best for the coming weeks Maureen, it is going to be so hard on you all, especially Elizabeth. Sending you lots of positive and healing thoughts!!! xx
 

clarabear

always chatty at the O!!
I am so happy for you that you are in a place to be doing something for your daughter. Those few days when things are being figured out have to be soooo long. I know Chemo and radiation are scary things and the outcome is always unknown, so I'll pray that results will be seen quickly and have the desired results. It is so great that you are in a position to be able to bring her into your home and be the support she needs. She is soooooo lucky to have family that is so willing to jump in and do what's needed. Hugs and lots of prayers!!
 

KerryHalasz

Well-Known Member
Maureen, I'm so sorry about this. Sounds like she's in good hands. I'll keep all of you in my thoughts for a full recovery without too much pain. Hugs to you.
 

CookingMyLife

Well-Known Member
Well, no discharge, but that didn't surprise me. WE didn't think she was eating or was mobile in most any way, but the real reason was that she doesn't finish this cycle of chemo until 03:00 tomorrow. Oh well. We did have a chance to speak to the one dr and strongly state that she was not eating - being asked if she wanted it and with little response she just sleeps, no nurse was getting her up and moving etc. I know the onus will be on us when she gets home but until then when we aren't there, I'd have hoped they'd push her a bit more. At least get her to the bathroom instead of just the potty chair. Oh well...

We call tomorrow after 10 to see if the drs and staff feel she's ready to leave. Personally, I can't imagine such a change from 3am till 9am when they meet but God knows, not me. Dick and I are really appreciating this time home alone with no other responsibility knowing that it's fleeting. The NC parents said their goodbyes today and that relationship is a profound blessing. Doesn't god have a sense of humor!!

Anyhow, we did some more shopping this afternoon and feel a bit more settled tonight. That's a nice nice feeling.
 

suezeeq12

Cupcake Ninja
Maureen my gosh you are such a trooper staying so strong! God does operate in weird ways sometimes, that's for sure.

Everyone continues to be in my prayers. I think you are an extraordinary woman and I admire how strong you are.
 
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