Day 17 - Hey, it's Saturday.

Ok, it's official.  I have been in here too long now, as I no longer know what day of the week it is.

I seems the graft is starting to settle in.  The white count is up to 0.7, and the others are falling very slow.  The platelets might be gaining, but I had a transfusion yesterday so it's hard to tell.  (I don't have the 'post transfusion' counts).

I am NOT feeling much better though.  I am still sleeping/zoned out/etc. through the day, and having crazy dreams, etc. and uncomfortable sleeps through the night. 

It hurts to swallow.  So, when your crazy thirsty at night, because you have been sleeping with your mouth open, because your nose is blocked up from not being able to blow it due of nose bleeds, you are in for a world of hurt.

I have managed to build up enough get up and go to get the computer on to post on the blog, check facebook, and put some audio-books onto my mp3 player.

My blood sugar level was a bit high in my morning blood tests, so for the short term I have been put on closer watch, and insulin injections.  I have been told that this is very common, but I am not pleased.   I am going to have to try doing more walk in place exercises, etc.

Comments

AJ and Dexter's Mom said…
So glad to see you feeling well enough to get the computer out.

Thinking about you, Babe.
11/13/2010 2:29 PM
Al & Bren said…
welcome back !!! it is nice to hear from you again!
11/13/2010 3:53 PM
Tony said…
Hey Richard,
Glad to see you back online too!! Yaaaa Neutrophils, Go Leukocytes Go!! Come on Hemoglobin!!! Platelets, Platelets, Platelets, (or as my italian mom used to call them 'piglets') LOL
Sorry I haven't been by lately but I've been feeling a little under the weather so I didn't want to bring you any unwelcomed presents!! Lolita (you met her with me at Light The Night) says hello and asks how you are everyday at work. I've given her your blog address as well (your developing a following!!)
Keep getting better, we're all with you!!!!!
Ciao for now!!
Tony
11/13/2010 4:02 PM
Anonymous said…
Hey Richard,

Glad to hear from you! Thinking about you and the fam.

Cheers,

Ryan
11/13/2010 4:18 PM
Anonymous said…
Richard must be getting better beacause he is now a smart ass!!!forgot to tell me about high blood sugars so I just called him to see if I should still go to the Island tomorrow for a few days. His reply was yes, UNLESS i had the magic touch instead of insulin, invented a pressure bandaid for nosebleeds, and found the cure for hiccups caused form chemo, that I should take a break. So, I will head home tomorrow.TONY- Loved the book. What a hoot!!! Thx from Richard's Mommy
11/13/2010 8:37 PM
Anonymous said…
It's good to 'hear your voice" so to speak on the blog...Not that we haven't been enjoying Sonja's updates, but your dry humour makes us laugh! and Hey, one condition is enough...You are NOT allowed to be diabetic too!

Kim and Nathan
11/13/2010 11:15 PM
Post a Comment

Popular posts from this blog

Someone's like me.

I was back in at the LBMT Thursday afternoon for blood work, hickman line flushing, and news. The good news is that there seems to be a very good chance that they have found a bone marrow match for me.  Dr. Bernard, who gave me the news, said a "95% chance" - mostly to give an out, as there are a lot of things that can go wrong still. I don't know how far along they are in the process with the donor but they are looking at starting the transplant in the next 2-3 weeks, early-mid October.  I will know more shortly after a yet to be scheduled meeting with Dr. Nevill. So, if you are one of the recent people who signed up for the registry, and have been magically called as a match, you might very well be my blood brother/sister so to speak - lol. The coming transplant scares the willies out of me as it will be the most intensive event I have been through in this whole thing, since the start over a year and a half ago.  Any grief, discomfort, etc.  I have been thoug
Read more

Thurdsay - My New Nemisis ?

Wow. Today was nasty. Tossed and turned most of the night, and then barfing in the morning. Nothing to come out, just there to taunt me, and let me know who's boss. Then there was the tightness of the chest, and some pain in my arm. Well, that started a flury of activity. ECG, blood work, etc. ECG looks good, there were some blood signed that the heart might have been in distress. They will be putting me on some drugs to help my heart mellow out just in case. It's all fine now, but they are being on the safe side. Tired. So very tired today. I slept most of the day, and I am only now getting into doing some stuff on the computer. Catching up with work, blog, etc. I don't have my totals for today, but the platelets and red blood cells mean I will probably be getting a transfusion tomorrow. I got to have a shower today - Yippie ! My last bag of the nasty "Red Koolaid" of death was today, so only the one Chemo drug left on tap. Still a potent brew at that, bu
Read more

2012

2012 I made it to another year ! Yay me! Another stellar delay before posting an update, but it has been a very busy time - work, Halloween, work, trip to the Island, work, Christmas, work, New Years, work. In my last update, I was off Prednisone, and now, I am off Cyclosporin. I am still on the Anti-Pneumonia, Anti-Viral, and blood pressure pills until the end of the month, and then I can stop all but the blood pressure pills. So far everything has been clear for GVHD, but my energy levels have been taking a pretty big hit. Next doctor visit is in March.
Read more