Thursday, April 3, 2008 (late post)
Today Melissa came to clinic with me (Thanks, Melissa). This was the fastest clinic visit I’ve ever had. We were in and out relatively quickly and home before noon. I think I’ll ask her to take me from now on. Sorry, Todd.
The phlebotomists weren’t all that thrilled to see me walk in. Emmit said “No way! I am not even gonna try!” So the other one did (sorry, can’t remember his name). It was only one stick today! Maybe next time Emmit will have more confidence!
Melissa and I hung out while waiting to be called back to the exam room. Like I said, we didn’t have to wait too long. Vitals all looked really good. Hopefully, I’ll be taken of the Norvasc (high blood pressure medication), although I’m pretty sure some medication I’m taking is actually causing the high blood pressure. Ugh! Medicines and their side effects!
Dr. V was thrilled with my labs today. All of my blood counts (WBC, RBC, platelets, ANC) were in range. And that’s a first since all this started! She also congratulated me again on the biopsy results and DNA tests. She asked how I was doing and I told her the same thing I tell her every visit – just plain tired most of the time and tired, achy and sore muscles the rest of the time. I also had been experiencing frequent nausea the past few weeks. Dr. V reassured me the fatigue and soreness will improve once she starts weaning me off a lot of the medications responsible for the symptoms. So she looked over my record and discovered my stomach problems and nausea started when she doubled my fluconazole dose. I have a pretty bad history with the –azole family (anti-fungal). She said that not only will I start feeling better, but, that by reducing the fluconazole, she is basically starting the reduction of the Prograf (anti-GVHD, immunosuppressant). And that’s good news! FYI: An anti-fungal medication like –azoles are used preventively (blood borne fungal infections are life threatening post-transplant), but also to regulate and maintain oral Prograf levels.
All in all, it was a short and very sweet visit. It is always nice hanging out with Melissa and having girl talk! My next one won’t be until April 17th. Let’s hope that one goes just as well!!
3 comments:
Yay! So nice to read your update. Glad things are going well and I hope you get some more energy once you're off some of those meds. Miss you. :)
Sounds like a somewhat pleasant day. Anytime with Melissa is fun though. I could only imagine. It is grea tto hear your updates of lowering meds. I am so happy for you and will continue to pray for more good news!
Hugs
Amy
Great work Courtney! It's always great to read your improvements. I'm sure it's not all rosy, but it will be soon.
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