Monday, September 7, 2009
Big Day is Tomorrow...
I feel like all I ever do it put negative and bad stuff on the blog but after all this blog was set up to follow and update Eric's journey through his bone marrow transplant. Usually there is not alot of happy things during this kind of a process to post but I just feel it important to note that I am trying to be as positive as I can through out all of this journey. It is hard sometimes though.
Eric has been doing well so far so good today....no vomiting, no headaches, fever broke, no stomach pain. Over all a good day he slept alot of it with the constant morphine drip but that is a good thing. As long as he gets rest that is all I want. It is 11:15pm and so far still good Eric is fast asleep....I am so excited for tomorrow. It Eric's 2n d Birthday!! New bone marrow, new start.....
Bad Night....
They have placed him on higher isolation and watch now, we have to wear complete head to toe protection. Gowns, gloves and mask at all times in his room. He was having such a good day yesterday until about 9pm he started getting his cough really bad, then all of the sudden extreme vomiting, diarrhea, stomach pain that he was in tears about. He kept telling the nurses and doctors the stomach pain is so bad, he has never felt it like this. He describes as someone pouring bleach/ acid in your stomach and punching you over and over again in the gut. The doctors said it's cause his stomach lining is being sluft off, it's coming all off -the lining of his stomach and the etreme pain is from that and the rawness.
The doctors and nurses say that the chemo is taking more effects in him, that this pain will continue for weeks and get worse before it gets better so they are placing him on constant morphine drip. He finally stopped throwing up, diarrhea, pain around 3:15am this morning.Fever has been spiked and continues to hold at 103.4 They are concerned about additional infections, they are running additional tests. Eric has developed a rash all over his body and head, they are also concerned that this is a fungal infection. They have placed his last day today of chemo on hold until they can get the results from the labs on the blood tests and cultures.
I am so scared about everything going on all the sudden there is so much starting to go wrong. My prayers are pleading with the Lord to get us through this, to get to the transplant tomorrow. I have never seen anyone in so much pain, it is hard to watch and not be able to do anything. I feel as if I am watching them torture Eric and its heart wrenching. I wish I could take this away from him, I pray he will get some kind of break or comfort. I do not know how anyone gets through this! We are waiting for the doctors to come in, I will keep everyone posted. Please, please continue to pray for Eric, he needs all the prayers he can get.
Sunday, September 6, 2009
Day of prayer and fast

Saturday, September 5, 2009
Eric has Pneumonia..long,hard night and morning!

Thursday, September 3, 2009
Hair is Gone!!! Day 4 of Chemo



Well Day 4 of Chemo and Eric's Hair is gone! The surprise we had for the kids especially
Eric's day went alot like yesterday except now he completely will not eat anything at all! He is really fighting the nausea and doesn't feel like eating anything. He did walk for me today which is good, they want him to keep moving. I pray the Lord will give him strength to get through this...I thought I was ready emotionally to see his hair all gone but I started to cry, it's hard you know. Hard to see the strongest man you have ever known going through so much.
I have been looking at our family pictures, missing the kids alot. I have this picture I am posting of the kids and Eric laughing when we were trying to have them be serious and take a picture of them kissing their Dad. I don't know I just love this picture, it reminds me of how close we are as a family, how much we love the kids, how much Eric makes us laugh...How I hope to have that back again someday!
Wednesday, September 2, 2009
Day 3 of Chemo....It has hit Eric now
They are giving him pain medications through his IV for his headaches that within minutes put him into a deep sleep only to wake up within an hour to a severe headache again, so he has been pretty medicated through out the day. He is taking nausea meds Zofran but not holding back the sickness today, Eric has started to now not eat. He doesn't even like me to mention the names of food, gets sick just talking about it so we have stopped eating. The nurses say that they understand not eating but they need him to at least drink for his kidneys and liver, so I am trying to push fluids in him ( not succeeding very well at that though).
When visitors come to see Eric they have to wear a mask and gloves but I have not had to however the nurse just informed me that Eric is dropping with his counts fast and that I need to start wearing a mask and gloves at all times now in the room. They push here to have Eric get up at least 3 times a day and walk around the pod area for at least 10 minutes with his mask and gloves on, he was able to get up 2 times today due to how he felt. We will try for 3 times tomorrow! The surprise for the kids on the blog unfortunately will have to wait for tomorrow due to Eric not feeling well. The LDS missionaries came by and gave Eric a blessing today, that was nice. Hope tomorrow will be better....
Tuesday, September 1, 2009
Day 2 Chemo....


Eric is needing 2 units/2 bags of red blood cells so he is getting those transfused in him now each one takes about 3 hours to do. I am posting a picture from this morning of Eric while he was getting his chemo and blood transfusion. As you can see from the picture he doesn't feel well and he has alot of lines/ IV's hooked up to him.
Also a second picture for everyone of the MD Anderson main building/ hospital where Eric is now for visual purpose to see what it looks like. Doing good so far today other than low energy alot and the fever. We are gearing up for it though they tell us that by tonight he should be seeing alot of the sickness and effects of chemo kicking in.
We have a special little surprise for everyone that we will be posting on the blog tomorrow... this is for our kids. Especially Austin he had a special request he told his Dad he wanted....so be sure to check it out tomorrow on the blog! We love and miss Chelsea and Austin so much!!! We know they are being great kids!
We love you guys,
Love Mom and Dad