Friday, July 5, 2013

Dads Home !!!

Hello everyone!
     Yup, you read correctly, Dad is home!! On Wednesday morning, Day 20, dad was sent in for a minor surgery to take off his triple catheter and then he was home by 5pm! I want to thank everyone for their support, love, and prayers during this crazy season in our lives. The storm is over and now its time to rebuild. Dad will be going to the Sylvester center 3 to 4 times a week and then less frequent where they will keep a close eye on his progress and help him to rebuild. For the next two weeks dad is pretty limited and will be home, but we were excited that we were all able to be together yesterday for the 4th of July! Once his immune system is back to normal (Doctors estimate 2 to 3 months) he will have no limitations and be back to his normal life. Thank you all again for your continuous prayers! I ask that you pray for My dads body to be strong during this rebuilding stage!
   


Here's a little visual on the extremes the chemo took on my dads body. The picture on the left was taken today and the picture on the right was taken last summer after his first set of chemo.



Monday, July 1, 2013

Transplant Day #18

Hello everyone,
     I want to thank everyone for all your prayers and concerns! It is so amazing to have so many people behind us! Thank you to all of you at Dance Town for constantly checking in with me or joey to see how hes doing. Thank you to all that have been visiting: Omar, Diego, Frank, Hildy, Henry, Maribell, Rossy, Dan, Uncle Tony, Tia Ella, Kaki, Gaby, and my grand parents Lala and Pipo. You have no idea what a difference it has made for him to have your company!
     This past week was a hectic one. We had a couple scary nights were dads heart rate was at over 200 (the norm being 80). They gave him medicine to to normalize his heart rate until the cardiologist came. Through this, they found out he has Wolf Parkinson White Syndrome. The name is scarier then what it really is! In other words, they would need to do a minor arthroscopic surgery to a vessel in his heart. This would have to be done later on in the year because he cannot have surgery until his immune system is 100%.
     Please continue praying for physical and emotional strength. Its been a rough ride but its almost over! Hopefully dad will be home at the end of this week! feel free to visit him at the Sylvester Center. God Bless!

These are pictures from when dad was given the medication to stabilize his heart rate. He was feeling better and decided it would be a good time to do pay roll on the computers he set up in his room. You could imagine the nurses were not in agreement ! lol

Thursday, June 27, 2013

Transplant Day # 14

Hello everyone,
The pictures below were from day 9 and 10 when dad was still feeling pretty good. No, it was not my dads actual birthday. When a transplant patient finished their chemo and has their stem cell infusion, the nurses call it their new birthday! Technically they are completely wiped out and made new! (What a parallel to what God does in us!!)

If you read my last post, I told you all that the doctors were preparing us for a tougher week. That was an understatement. When I saw him yesterday, he was very weak and nauseous. Last night things went haywire and his heart rate went very high. Hes having rapid heart beat, and so he was put a heart monitor and was given an oxygen mask. He is at his worst point with his white blood count at zero a fever of 102. The doctors assume it will be about 2 or 3 more days like this and have asked that he has no visitors for the next few days.

Our hearts are heavy and we are a bit overwhelmed. We need your prayers!


  

Friday, June 21, 2013

Transplant Day #8

Hello everyone!
I hope everyone is having a wonderful day! We are finished with week one! Dad did great this first week, he's even been exercising more then when he was at home! He walked over one mile ever day ( 27 laps up and down the units hallway is a mile and he walks 30!). Yesterday was an exciting day as dad finished his last chemo ever!! Some might say its ambitious to say "ever" but I am so secure in knowing that God has healed him! Yesterdays chemo was real intense; it was only 45 min long and he had to be eating ice the whole time to protect his mouth. And Dad was so happy to have Omar Giritli come visit and spend some time with him! Since Thursday night dad started feeling crappy and its slowing progressing. The doctors have warned us that week #2 is supposed to be a nasty one, so please be praying for this week in particular, for lots of physical and emotional strength! Today is the actual "Transplant." The nurses have been going through a process all day of slowly unfreezing his stem cells and then administering them through a transfusion. So happy to say that we are slowly but surely on our way to recover! God is so good and he has held our hands through out this entire process! LOTS OF PRAYERS!!

 
 

Monday, June 17, 2013

Bone Marro Transplant Day 4

Hey Everyone!
I hope everyone had a wonderful Fathers Day, we sure did! Well all except for the Heat loosing!
We are now on day four and dad has been doing great. We have three days left of chemo and then on to our rough yet exciting recovery!! My dad is a man that never quits! He is the strongest man i know! As you can see in one of the pictures below, he has even set up his office in his room! lol Dad has been doing all his exercises with out a problem, and is ready to kick some butt!! Because this is going to be a long process I will be updating the blog every few days instead of daily. Feel free to send my dad some love directly to his cell! =)
I have always been a believer in praying specifically. So I ask that you all please be praying that this Chemo destroys every single cancerous cell in my dads body, while protecting the rest of his body. Pray for guidance for all of the doctors and nurses working with my dad. pray for healing. pray for physical and emotional strength. And pray that my dad can be a light in that hospital and to others going through a hard time! =)
God Bless!!


 

 

Friday, June 14, 2013

Dad started his bone marrow transplant

Hello everyone!
     I want to thank everyone for there continuous payers and love towards my dad and our family. Its been a while since my last post because they've had dad waiting to build up his strength and then waiting for bed availability at the transplant unit. We finally received word that there was a bed open earlier this week and dad went in this morning to begin his bone marrow transplant. The entire process will take 3-4 weeks. The first 7 days dad will be receiving intense doses of chemo, and is expected to feel a bit tyred. Then on day 8 dad will receive his stem cell infusion (Friday June 21). This process should take a few hours. The infusion marks the beginning of week #2 which is where they  expect the side effects of the chemo to kick in and dad feel his worst.This is the time we are asking most prayer for. Dad will then be on to recovery and hopefully start to feel better throughout week #3. This Chemo they will be giving my dad is extremely strong and will be on a mission to destroy, the doctors are setting him up with lots of pre meds to protects his organs and all the important stuff. They even have him doing breathing exercises daily to protect his lungs. For any visitors, they even have a washing station before you come in.
     Many Christians use the term "born again" to describe the spiritual process that takes place when we come to know God. God cleanses us of all the bad and makes us a new and pure creation. This is a perfect way to describe what God is doing for my dad physically through this bone marrow transplant. All of the bad will be wiped out of his body and he will be like a new creation, physically "born again"!
    Although we know dad is in remisson and the storm will soon be over, we are about to embark on the darkest part of this storm. Please be in prayer for my dads physical and mental strength! God Bless!
    



Thursday, May 30, 2013

PRAISE GOD!!

Hello everyone!
   Yesterday was my dad's PET scan, this is a scan that can check the whole body for cancer and determines whether or not the treatment is working. Today mom and dad went in for the results and where informed that the scans are looking awesome!! they even declared dad to be in REMISSION again! All that is left is the transfusion to make sure this does not come back again, in other words its like our insurance.  We are so overwhelmed with Joy! God is so good! While there, they checked his blood work and saw a lot wrong, nothing severe but he is extremely weak and fatigue. Because of this they are giving him a blood transfusion today and another tomorrow, and they are postponing the Bone Marrow Transplant until he is stronger again. The toughest part (physically) is yet to come, but God has just given us a glimpse of the beautiful rainbow that is waiting for us at the end of this storm! God Bless you all and thank you for all your prayers! Keep them coming!!!!