Since my last post, I have continued to have horrible bone pain. This pain, coupled with not sleeping, has made for quite an emotional woman. Russ e-mailed Dr. Shiftan on Thursday to let him know how bad I was and asking him about different pain medications. He responded quickly and offered 2 more drugs that might help. The problem I have is the pain medicine make me throw up and doesn’t touch the pain. I try to have a full stomach before I take the meds, but I regret the full stomach once I start throwing up. So I have tried, Tylenol with codeine, vicodine, percoset and darvocet. All of these make me very sick and don’t relieve the pain. So we got the prescription for a new drug, Marinol, called in after a series of events. Apparently Marinol was a triple duplicate medication so we were going to have to wait until Friday morning to drive to San Diego to pick up the prescription, and then take it to a pharmacy and have it ordered. On Thursday afternoon it looked like I would have to deal with the pain for at least another night. My pharmacist Vijay, who is a very sweet man, looked up the drug and found out the category had been changed to a 3 and that meant the doctor could call it in. He also found a pharmacy that carried it (Costco). So with this great new news we try calling one of my doctors, Karin, to let her know we didnt’ need to wait another day. But it was already 6PM and hard to leave a message. So we called the on-call oncologist and explained everything. Dr. Sally was the Doctor and he also believed you had to have the triple pad but was willing to give it a shot. He called back in minutes and said it’s there you better hurry it closes in 15 minute. So we RACED out of the house to get some new drugs. I didn’t even grab a hat or scarf. I went in with dark circles under my eyes, pale face and a bald head. I looked terrible! We got the prescription just in the nick of time. I was so happy and hopeful that maybe this would finally help the pain. There was a little kid screaming to his Mom, “Mommy, Mommy look at that lady!” The Mom was trying to ignore her child and think he would let it go. She turned and pretended to be distracted. Again the child starts yelling louder. The poor mother is mortified. I had to giggle! Kids are always the ones who are most shocked by my bald head. I think it is cute! The poor Moms I know are terribly embarrassed by their children pointing and yelling at me. I forget I’m bald until someone reacts and then I remember. I used to care a lot about what other people thought about me. It is amazing that now I really don’t care. I have a new sense of drive and focus that I don’t give a second thought about what strangers think of my round head. This is a quality I have always wanted. I have tried all my life to not care what other people thought. But I always cared. I cared a lot. Even worse, I would worry about what I thought other people thought. I’m sure I put quite a spin on what they were thinking. I could make myself believe people were thinking all kinds of negative things about me. All the things I was most insecure about I was sure they noticed and spent lots of time thinking about my bad qualities. It was SICK and I do know it was a problem. The truth I have found is, it doesn’t matter. Who cares if a stranger might think something about you. Only I know who I am and only I can judge myself. We all have a pile full of trials, and we are all dealing with them in our own ways. So maybe what has changed is the way I look at others. I no longer judge. When I don’t look at others with criticizing eyes I no longer feel or care about what other might be thinking. It is an amazing freedom! This is one of those things I never thought cancer would teach me. I’m becoming mentally stronger and healthier in spite of a body repeatedly going through a process of actively dieing and then recovering.
I took a pill right then. Nothing……….. (more to come)
Hope that the new meds are helping by now. We got the plane tickets!! So we will be seeing you soon. How was the boys trip to Montana?
Love you lots.
I can’t wait to hear if the new meds are helping…I pray you will find something soon. I can’t wait to see you. I think the kid was pointing because he was amazed by your beautiful glow and radiance. =) Love you.
Beautiful! What lessons you are learning and teaching. I hope the new stuff works…I hate the nauseated stuff that goes along with most pain meds. I have never been able to tolerate any pain medication. Good wishes for some pain relief and some much needed sleep…
Chris lets me read your blog every now and then and she told me about this bone pain thing. We both agree that this hopefully (prayers in here…) means that the chemo is working and it is doing what is is supposed to do. Keep your chin up and ge SURE to let us know if there is anything we can do to assist.
We think you look absolootely maaahvalous with no hair and I’ve just happened to have mine cut short as well (in support, of course…it has nothing to do with being military…uhm, of course not). It’s short enough that Ethan thought I was bald too with a hat on!
We’ve got our fingers and toes crossed that the new regimen of treatment works out for you.
Susan,
Eric and I want to thank you for spending one of your very limited good days with us. Brining the Lord into our marriage and knowing you were there to witness it made it even more special. I hope keeping you so late made you sleep well. You looked wonderful and it was so nice to talk. From the outside it seemed the new meds might be working, or you just faked it for us. I hope it was the meds, I wouldn’t want you to hurt yourself for us.
I will try to be less judgemental and maybe caring what everybody thinks can be cured from me too.
Thanks for the inspiration.
I will see you Tuesday.
Love ya,
Michelle
Susan,
I was just noticing that this is about the time you should be feeling better, so I hope you are! I’m still thinking about you
Mary
Hi Susan,
I’ve been so effected by your “blog” and how it has opened my eyes to what trials other people have. I’ve stopped whinning about some of my difficulties and realized that others have harder, more difficult challenges. Thank you for helping me see this. If I could, I would take a day of pain for you and have it so you could have a break. You are blessed with a great supportive family!
Colleen