Thursday, November 13, 2008

Phase 2

Tomorrow (Friday) we are heading back to the clinic for Abbey to start phase 2 of her treatment. It is hard to go back after she's had this break for a couple weeks and since she has been feeling so good lately, but as much as we hate the chemo, we know we need to keep trucking on so she can beat this completely. What's so hard about going is that they need to make her sick for her to eventually get better.  We love that there is a treatment for leukemia and that they are able to kill cancer cells, but we hate the side effects that it has on her body.  It's a love/hate relationship and it is a ride with many ups and downs, but we are confident that one day this will all be a memory and we will all have grown in ways unimaginable.    

We have to be there at 9:30 a.m. for her port to be accessed, blood to be drawn and checked (please pray for her neutraphils to be above 750) and for her dose of chemo to be administered via IV.  We then have to be at the pediatric sedation unit by noon for her to have her spinal done to administer her dose of chemo in her spine.  She will not be able to eat anything after tonight so please pray for the morning to go quickly and for us to be able to distract her with enough things to help get her through the morning.  No matter how many times we go to sedation, it never gets easier.  Each time I hold her while they put this creamy white medicine into her port and she quickly falls asleep in my arms.  I then have to put her on a sterile table and we leave the room.  I know she is comfortable while she is having the procedure done, but it's so hard to leave her in the room and to not be by her side for that time.  Whenever I am not physically with Abbey and seeing her (which isn't much) I find myself feeling anxious and just wanting to see her face and know exactly what is going on.  Please pray for our thoughts each Friday while she has her procedures done, that our minds wouldn't start spiraling....  Once it's over and we get to see her again, we are always so relieved and she always makes us smile.  Her first words are 'I'm hungry' and she usually wants cheez-its.  

My sister Stacey has been coming with us every Friday and she has been so creative with keeping Abbey busy and happy while we wait for our time slot for her procedure each week.  Stacey is so good with kids (both hers and everyone else's) and she keeps Abbey (and Jim and I) entertained much of the time that she's with us.  She draws pictures of everything and anything you can imagine and makes up games that keep us all smiling.  I don't know what we would do without her and my mom as they truly have done so much for us.  I have called my mom in the middle of the night more then once because I either needed someone to talk with, cry with or pray with, or was nervous when Abbey was so sick and she jumped out of bed and rushed right over.  She stays with the boys each time we need to go to the clinic (along with my Aunt Patty on Fridays... thanks Patty :) and we can rest in the fact that our boys are very well taken care of when we aren't with them.  Between our family and friends, we have the most amazing support system and we truly are thankful and don't know what we would do without all of you.

Abbey has been talking a lot the last couple days about her sickness and different things that she remembers from what she has been through.  She has wanted to talk about our stay in the hospital (she says our hospital room with our bed), times when it was "owey" and times when it didn't hurt, times when she had fun and times when she felt stinky.  It is amazing how she is remembering things from our stay in the hospital and even talking about some of the days when she was really sick here at home.  She is starting to understand the difference between being in the hospital and just going to the clinic for a day to get her medicine.  It has been really good for us to hear her start to process some of this and see that she can smile while talking about it... even the hard stuff.  

God uses different things at different times to help us get through each minute, day and week of this journey.  He has used Abbey in so many ways these past couple days and it's so amazing to see a child's faith as we talk to her and ask her questions.  She knows God loves her, cares for her and is healing her and that is something that she never doubts.... even for a second.  We pray for faith like a child when we start to doubt or get scared and it's neat to see Abbey, a three year old little girl never hesitate when we ask her who made her, who cares for her and who's healing her.  Lord, help us to have faith like a child as we continue on in this journey.     

   

4 comments:

BethanyM said...

We will be praying more tomorrow for Abbey's testing and treatment.

That is exactly what we all need at times when our faith is challenged...the unquestioning faith of a child. Our precious three year old, Connor, has that faith as well, and God uses him to remind us of how to trust Him so completely. Their faith is so absolute and so unwavering.

You say that when this is all behind you, that you will have grown in unimaginable ways. As someone who has been prayerfully watching you endure these challenges from the sidelines, I see that you have already grown so much in these past six weeks.

It is such a blessing to us to see your faith and strength as God carries you through this. In the next two years, I'm sure you will continue to grow to meet the challenges ahead, so that you can not only endure this long battle, but thrive, triumph and shine for Him.

As we travel this journey along with you, I find my own faith growing by leaps and bounds, and even more importantly, my understanding of who God is and my appreciation for the characteristics of His love growing and deepening.

God is using you in such important ways. Thank you for your willingness to share the intimate details of this journey so completely with us.

How GREAT is our God!!!

The Gammons Family said...

We will be praying today.

The Gammons Fam

Aggie said...

The Lawlers are praying for God to wash peace and comfort over you all as Abbey continues to have treatments.

It is so wonderful to hear that Abbey is doing so well. We praise God for all that He is doing to heal your precious daughter, the way that He is working in your lives, and the way that He is using you to touch the lives of others.

Anonymous said...

Been praying for Abbey all day! God is with her!! You guys are such wonderful parents!! = )

Love,
The Mobley's