Visit Rebekah's Page to get updates, read messages and send messages to Rebekah and her family through comments. This is a public "diary" of a family whose little girl started a battle with inoperable cancer in April 2005. In December 2007 our house burned down. And in September 2009 Mommy was diagnosed with a terminal disease (a genetic form of ALS) that took her to Heaven in July, 2011, leaving Daddy and two young girls to make it on their own. Over several years of ups and downs, you will get into our hearts, minds and souls as we share joys and sorrows. It can sometimes be very difficult to read. We hope it is also uplifting. Please find joy in what you read here.
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Monday, January 16, 2006



Monday Evening

Our clinic appointment went well. Her counts are still doing well and all is generally good. We do not need to go back to clinic until next Monday when we should be admitted for our last Chemo treatment. Rebekah's Chemo Pal met us at clinic and played with Rebekah and helped to entertain her while we waited. It was good to see her again.

Don't get me wrong, Rebekah has issues. She continues to sneeze and need an antihistimine. Her occasional cough seems pretty painful and she needs at least one dose of morphine most days. She eating only an occasional bite here and there (she did eat 3 or 4 bites of cooked carrots tonight - the most I've seen in weeks), so basically all of her nutritional needs are having to be met by g-tube feeds. She has bouts of throwing up. It just seems that nothing has gotten dramatically worse in the last few days. With as many kids as are having serious problems, I count my blessings that we are hanging in there. Yet it makes me wonder what sort of issue might be around the corner for us and when will it hit.

Rebekah's left eye is a little puffy (but not red) and I was a little concerned about whether it might be infected. I didn't really think so, but knowing that her tear duct is blocked it had me concerned. That was one of the things that the eye doctor wanted us to look out for, and if it became infected he would want to unplug it before we were done with chemo. I asked the Nurse Practitioner if I needed to be concerned about it and she told me it did not appear to be infected. That was good to hear.

We saw Kennedy's mom (and Kennedy) at clinic. She is still having a rough time. She is at home, but having lots of struggles. Please continue to pray for her and her family. Kennedy seems really sad and could use some encouragement.

After Clinic, we headed up to the floor to check in with Gage and his Mom. We chatted for a while. They are hoping to go home tomorrow. His counts are coming up a little. He can still use a lot of prayer. Gage isn't wanting to do much other than lay in bed and watch TV.

Grandma M stayed until both girls were in bed. Daddy wasn't home when Rebekah went to Bed (he was at Fire Department Drill) and she was not at all happy that she couldn't give him Night Nights. She tried to get out of bed a couple of times to go find him. I explained to her that he wasn't home, but it took quie a bit of convincing.

There are some changes to the right hand side of the blog. Check them out! There is a second "Prayers for Rebekah" button. Also, toward the bottom is a list of "Referring Web Pages" for the last 24 hours. You might find these interesting.

7 Shared:

At Tuesday, January 17, 2006 3:28:00 AM, Anonymous Anonymous Left a thought...

Glad to hear that Rebekah's counts are still doing good, (thank the LORD)
my heart goes out too, the kids and their family, my prayers are with you all :)
huggs
janice

 
At Tuesday, January 17, 2006 6:55:00 AM, Blogger Katie Left a thought...

Still praying for you family and those other famlies that you so lovingly share with us. What a testament to your hearts that you covet not only prayers for Rebekah but for all children who share in the hurts and struggles of these diseases.

 
At Tuesday, January 17, 2006 7:31:00 AM, Anonymous Anonymous Left a thought...

Dear loving people who follow this blog,

Please understand that this family will continue to need prayers and financial support LONG after chemo has concluded.

Chemo is a major phase to get through, but there will be other things for a LONG time, if not for life. Not trying to be a downer, just trying to be realistic. I am a cancer survivor myself and I hurt for little Rebekah and the other kiddos. It was bad enough having it happen to me, I can't imagine how it would be if my CHILD had to suffer.

Praise God for bringing everyone THIS far. That is NOT a given either.

PLEASE plan to fervently continue your prayers and other support for as long as God gives you strength to do so.

Thanks.
God Bless you all.

 
At Tuesday, January 17, 2006 8:19:00 AM, Blogger Rebekah Christine Left a thought...

Thank you anonymous. Yes you are right on all accounts. And yes we knew what we were up against when we choose treatment and not just to let little Rebekah die.

Now when it is finally starting to hit us, however, it is a big comfort to at least see that others recognize it too. So many people think we are "Done".

 
At Tuesday, January 17, 2006 1:27:00 PM, Anonymous Anonymous Left a thought...

Hi Rebekah and family
I'm glad to hear that Rebekah is doing ok.I pray for that beautiful little girl everyday.I lost my daughter last year on jan 20th.It is the worst possible thing to happen.She was 22 and commited suicide.Good luck and God bless you all.

 
At Tuesday, January 17, 2006 3:29:00 PM, Blogger Darlene Schacht Left a thought...

This is off topic, but I thought that you may want to know. Mito girl's link on your sidebar is a site that hasn't been updated since November. However, I tried www.thismomslife.com (their other site) and found out that Mitogirl had severe heart failure late in December. She has been in hospital since and needs a heart transplant. They need prayer.

 
At Tuesday, January 17, 2006 7:16:00 PM, Anonymous Anonymous Left a thought...

I am so glad you are "hanging in there" so well. Hope you and Scott are feeling better and that the Lord continues to hold you all dear to His heart.

 

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