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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Tuesday, September 06, 2005



DRUGS!

Rebekah has slept most of the day.  It is likely a “drug” induced sleep caused by the Ativan that she is getting to keep her (and her systems) calm.  We are getting to the point where we are giving her drugs that can have some pretty serious risks of side effects but those risks are better than the alternative.  

The good news is that her concentration and her rate of G-Tube feeding is up and she has not thrown up since last night.  Mainly this is due to the increase of the Ativan dose and the introduction of an additional anti-nausea drug, Phenergan.    

This is great but, combined with her other drugs, Phenergan has as risk of putting her into tremors such as those in Parkinson’s disease.  If not treated rapidly they could become permanent.  Treatment is an injection of Benadryl or Epinephrine as in an anaphylactic shock.  Those drugs are in the top flip top container of her 5 drawer medicine kit (tackle box) with dosages and everything written out in big bold letters.

Because of the way the drugs all interact, we have to be on very strict 4 hour schedules.  Some drugs being given every 4, some every 8 and some on the odd schedules to the others.  Talk about trying to figure it all out – ugh!  Have you noticed that “ugh!” is a favorite expression?  Maybe its just what we are going through, I don’t know.

On another note, Maggie takes off for Disneyland tomorrow.  It is going to be a long trip for her but, if bathed in prayer, she should be able to have enough energy to see it through.  Rebekah (and mommy) got to see Maggie, her mom and dad at clinic today.  They were very grateful for all of your continued prayers – as are we.  

5 Shared:

At Tuesday, September 06, 2005 10:29:00 PM, Blogger Cristina Left a thought...

Thinking of you in Minnesota... and praying. Lately my husband and I have been on a 'media fast' and have not been posting on our blogs or surfing the net. Your family is on my heart so much, though, that everyday I turn on the computer just to see how you're doing. Hang in there. There are so many people lifting your family up to Jesus, asking for comfort and healing... I hope so much that you feel it.

 
At Wednesday, September 07, 2005 5:39:00 AM, Anonymous Anonymous Left a thought...

Prayers for you all and for Maggie's family. May God's loving presence and protection be intensely close to everyone today.

 
At Wednesday, September 07, 2005 7:37:00 AM, Blogger Alison Left a thought...

Praying that the side effects stay minimal.

 
At Wednesday, September 07, 2005 4:42:00 PM, Anonymous Anonymous Left a thought...

I just wanted to say that Rebekah's story has touched our heart's and our souls, and that I check the page daily to see how Rebekah is doing and pray for her and all of your family. I pray that you will find some peace and comfort and that Rebekah will continue to show some improvement.You are in our prayer's.
Tammy Johnson and Family

 
At Wednesday, September 07, 2005 7:30:00 PM, Blogger Jenny Left a thought...

God bless Maggie and her family as they go to Disney, and God bless all of you for sticking with this treatment and for loving your daughter so much that you will go to any length to get her well again. Amen to all the prayers here.

 

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