I am so tired. My head hurts and I just feel exhausted. I think it's just my nerves. We don't really do that much, basically just go to the hospital about 2-1/2 hours each day. Tanner told me last night that I looked nearly as bad as he does. Hah! He knows how to make his mom feel better.
I went to the store this morning and got the risers to put under the couch so Tanner won't have so far to rise when he gets off the couch but the darn thing is so heavy there's just no way I can put them all under the legs by myself. I got two of them under the legs, but couldn't lift up the other end by myself to get them inserted.
Tanner's dad and step-mom are going to try and come up here Wednesday so maybe Tim can get them under the couch for us. If somethings happens with his job to where he can't come, I'm sure I can get Aunt Tencey's son-in-law to help us out. At least I know they will fit.
If Tim and Janet get to come, I think I'm going to run back to Fort Worth for a few days. I need to go into the office and if I can, I need to get the air conditioner fixed on my car. Nancy (who I work with at PIE) has a friend who works on cars and he's checking prices for me.
I think it's going to be hard for me to leave Tanner this first time. You know how us mom's are when it comes to our babies. He told me last night I should go home for a few days while he's still feeling pretty good and, oh by the way, while you are there you can get my computer games and bring them back with you? I'm sure I will worry more being away from him than he will miss me while I am gone.
I was helping him back to the couch last night and he stopped and asked me for a hug. It's times like that when he truly touches my heart.
In July 2009, the world, that seemed to be going like every 17 year old expected, was completely knocked off its axis with the diagnosis of Multiple Myeloma. We are now on a journey that we never expected to be taking. We appreciate the support we have received from so many of our friends and family. This blog will allow you to join us as we charge head long into the unknown as we journey towards a cure.
Showing posts with label Last chemo day - at least for now. Show all posts
Showing posts with label Last chemo day - at least for now. Show all posts
Monday, August 10, 2009
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