Thursday, December 27, 2018

Christmas 2018

Christmas 2018 update 


Grandson Alejandro and I goofing around. 
Here to fill you in since my last post, I now have a granddaughter, Gabriella!  Counting up to my fifth heart “birthday” and life is good! My daughter, Kasey and her husband Nelson are fantastic parents and Vickie and I are blessed to be grandpa and g’ma!


God is Good, All the time, and,

All the time, God is Good. 



Friday, April 22, 2016

21 Months Post-Transplant

Yes it's been quite a while since my last post.  I'll try and fill you in on the little that's going on in that time.   Let me again thank all those who have participated in my treatment and care including the family of my donor. Life is good and filled with wonder! "God is good, all the time; and all the time, God is good!"

Just 20 days after the transplant my wife and I were with the family and greeted our first grandchild, Alejandro, into this world! My "little girl" Kasey was now a mommy and we all were there to celebrate, she and her husband Nelson's joy! The first grandchild of both the Corl and Palacios families, "it's a boy!" He's now 20 months and I'm 21 months. Vickie says I'll always be five years old though. 


To start at the beginning, go to Start Page
http://heart56.blogspot.com/2014/06/the-new-normal.html


I spent two months of "house" arrest during the "sterile" phase of recovery. Folks could visit though and did. Vickie had to watch me like a hawk because of the powerful meds and their affect on my thinking.
Yep, I was on drugs! I had my "release date" countdown on my calendar and when it arrived:
I celebrated with a drive in my little, yellow roadster! Woo Hoo! I found out later that I have "misunderstood" that I could go out at two months, I wasn't to drive until three months. Oops

The meds were reduced in quantity and variety as my health, strength and quality of life rapidly improved. Down two just two handfuls; pillbox refill went from one-two hours to just fifteen minutes!


 “The Shakes” It is common to have hand tremors after transplant – these start out bad and lessen over the first year. Due to the drugs being reduced and you become adept in what to, and not to do. Making decisive and direct movement with the hand and not “hovering” helps. Do not drink from crystal stemware for quite a while (oh yeah – no booze either.)

The "New Normal" just becomes the normal. Life is good, very good. I got back at church, getting with friends, managing my business and singing praise to God for the Corl Family’s "Year of Blessing!" I was normal again and was free of heart disease and failure that, over ten years, had shrunk my world and my life. Now, life blossomed like a garden in spring!

I can say that I am changed, profoundly changed.
I did not have any “out of body”, “visit to heaven” or other experience but if you read on – I’ll tell you about the change and the wonders I’ve been a part of. That telling is in the audio link below.
In October the church heard testimony of my journey and how the Lord gave me exactly what I needed, at exactly the time when it seemed as if all hope was gone. Time and again, over and over, I was shown that in all things, "God is in Control". Hear the recording is at the St. Andrews Presbyterian Church Dunedin website sapcd.org under  "Teachings". Quick link to the recording http://goo.gl/Tp7iB4 The text and graphics link will be added, soon. 

There are times when the church needs to laugh, sing and shout for joy - for celebrating the very Greatness of Our God, this was one of these times! We celebrate Victory! There are worlds beyond our limited vision that we are shown in Christ Jesus.

We have a purpose here - and - this is the point, God is in Control.  If your are happy with the evil and hurt of this world and want to continue under your control, God will honor your desire: but, when you give God Control through Christ, love becomes the purpose of life. God's love in you will become love for each other. The New Life!

When you get a new heart and a new life, every effort is made to assure that it beats on and that you continue to health and long life.  

During the first year this means tests, blood and biopsies of the new heart. Many, many, many heart biopsies. I was thinking of getting a "welcome mat" sticker for my left groin - their 'entry point of choice'.  First its weekly, then bi-monthly (the 'off' week' means a day-long visit to the transplant clinic) then monthly until "The Annual" Yes, you make friends that are pre and post transplant, and with heart and lung transplant folks. Heck - its a regular family gathering.  

You also get to talk with terrified pre-transplant folks and answering their questions and calming and ministering to them in their own, time of great need.  I learned from newbies and veterans alike. You also learn where the sandwiches, frozen yoghurt and good coffee are!

I made Facebook posts to let folks know when I was “in” for biopsy and the results a few days later.

The “feet” are before and “Zero Man” is the after the results. The reason is that the best “score” from heart biopsy is Zero rejection in all samples. Zero is Good!



Christmas, Easter, New Years, birthdays and get togethers are sweeter. The air smells scented, well, when 'outside the glass' of the hospital - even diesel fumes smell sweet.  
I settled in to my transformed, New life. That means all of the good and all of the bad that everyone has but, the second time around is different because I am different. Some call me “short bus” different.

This brings me to my first “birthday” July 23, 2015

The medical 1st Annual is two days of glorious fun, with all the tests and scans and yes, another heart biopsy! That was in early August of 2015. Skipping ahead, it’s now January 2016 and I got an unwelcome visitor.

CMV for short, became active. We knew it was in the donor heart and I was on a drug to suppress it until after the Annual plus a few months. Like Mono, CMV makes you very tired, has some flu-like symptoms and just, su..., er, is unpleasant. It’s over it for now – but unlike true love, CMV is forever! Dermatology is a constant thing for me, immune suppression lets skin pre-cancers go wild. If you look at my face at the top of this post you will see the results of ten sessions and multiple PDT peels. I'm in at least quarterly and now I'm doing PDT on my arms. OUCH!

I'm good, it's great to be alive and thriving! My second birthday and Annual are coming in July. 

Oh! One more thing – many ask if I know who my donor is or have had any contact with his family. There is a contact process and there is a grief process, after long thought I decided that the latter should be most respected, so, no, but they didn't contact me either. I have the greatest respect for my donor's family and encourage all to be or become donors. 


The good time to "sign up" and to "sign up" family is at Easter or Thanksgiving. What better way is there to give thanks but by giving up to 8 people life and taking your family "off the hook" should something happen. Hispanics and Blacks are real important as few are donors. As the population increases these groups have to rely on white donors and that math is failing now! Sign up - it's right, not white. Be an organ donor, prove that we are all "God's children."







Monday, August 25, 2014

Having the Words (revised)


Words (revised)
Anger vs. Peace
Words.
Not having them. Here is the story I want to share from my second week in TGH Heart Transplant Recovery - or “Eight West”. Eight West is a place of miracles, healing, cures, and great joy. Eight West / Tampa General Hospital / all hospitals are places of great grief and anguish, too.

There are statistics on survival and recovery but for any individual, there are only two, possible outcomes. Life and Death (ok, continued disease, too, but I'm counting that in the Life outcome).Couple of other things collided outside my door on Eight West. - words and inconsolable grief / anguish.

I startled awake from a mid-afternoon nap by the angry yelling and curses of a young, black father in anguish and pain over learning that his only child, his eight year-old daughter, was near death. She needed transplant or she would die. He was not married to the mother of his child, was estranged from her and had no rights in his daughter's care. His mind could not accept it and he couldn't express it except in anger, profanity and threats of violence. I had no idea what he would do, I couldn’t get up to close the (un-lockable) door - I was stuck, finally, I remembered I had some cheap, hospital headphones and plugged into the tv and turned up the volume! Before that, I heard enough and I could hear him above the TV volume.

It became clear to me that the chance of violence was slim as the nurses, assistants, docs and a psych nurse continued to gently speak to the young man. Security was nearby but not in view. The caregivers “talked him down” and walked him out without physical contact. I prayed for him. I wondered what to make of this and it came to me - words. He did not have the words. He had “street”.

Street was all he had needed to “do” life and interact with his world and culture but he is suddenly outside his world, and was lost.  Lost, lost, lost. It broke my new heart and was ground glass to my soul. His pain and anguish that could only be expressed by street. He only had street for words, for thoughts, for coherence of his own mind and for expression to others.  It was Primal. Raw. Angry. Vile. Profane. Threatening. Violent. It was street.

Eight West is a place of healing, grace, mercy and love. Compassion, patience, training, inner-peace and faith of the caregivers was all that was needed. My nurse, Rodrigo, was one of these. He stands all of five-foot, four and probably weighs in at 140 soaking wet - not the Hulk by any means. Others took the lead but Rodrigo stood with them.

He could not, discuss the matter with me later as they all keep their silence in patient matters, but we shared the peace and joy of the resolution.  The young, un-married father had the space to settle down but he didn't have the words to understand, conceptualize, or understand that his baby girl was going to get her heart, soon, and have a great chance at a full life. 

He cried, “She’s my life!, She’s ALL I GOT” in a mix of tears, curses and taunts.
He didn't have the words, or “The Word”.

He cursed in the hallway outside my door, he yelled curses from around the corner, he screamed angry threats from the elevator lobby and down the elevator. He returned an hour later and screamed and yelled violent taunts and curses from the elevator lobby again.  Still, no security - just faith, patience, care and compassion in response.

He finally left and I did not hear from him again. 


We think in words in a language. Core beliefs are held in our mind in words. When we think of self, place, others, anything other than base groans, primal expression of need or pain we require words. Words are important - have them, and you have rich, complete and nuanced  thought and can express your thought to others in words that have clarity, and from clarity comes understanding and from understanding, maybe agreement.  We respond to words from within and from without.

I choose a photo that tells a story, too. I like that we are the one above after looking at men of the street culture. I thought, who mostly determine our outcomes? I like that the photo above promotes a positive, wholesome vision, rather than "street" photos, I prayed for that young man that day and during my stay at the hospital and I pray for him to have peace and his daughter to be healed. I wonder what could have been this distraught dad's life if he had been taught the words, or most importantly, “The Word”?

--
image ©Corbis Images: licensed use by permission.
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Sunday, August 17, 2014

Repost: "Post" post - my new birthday 7-25-14 post




I didn't know whether to share this - but decided to and revised this post.  

Revised August 17, 2014:

My new birth date is July 23, 2014. That's what they say around here when you get a new heart.

I'm in ICU and have been since surgery, it's taken a while before I could write. Wow, had some crazy dreams, visions and hallucinations over the last two days. The great care staff, Vickie, Tom and Nancy kept guard over me and talked me through the worst of them - at 3:00 AM!. Reaction to the drugs I was told. I have experienced events that have changed me and how I will view the world. I have an understanding of mental illness - it was so real, but my mind was in paranoid overdrive. Nothing the staff hasn't dealt with before and was not ready for. I am thrilled and really drugged. Should be getting most of my tubes out today. I'll be in the hospital for 2 to 3 weeks. Thanks for all your prayers everything is going great right now.

Special thanks to Meghan (with apologies), and to Lori and Lorna, all of TGH ICU. Tom and Nancy picked up Vickie and they came to my aid at 3:00 in the morning! How can I say what good friends they are. God bless these, God bless us all. 

This was my original post:
My new birth date is July 23, 2014. That's what they say around here when you get a new heart.

I'm in ICU and have been since surgery, it's taken a while before I could write. I am thrilled and really drugged. Should be getting most of my tubes out today. I'll be in the hospital for 2 to 3 weeks. Thanks for all your prayers everything is going great right now.

Saturday, August 16, 2014

Grace and Peace


There's A Story Here
St. Andrews Presbyterian Church


Update: these people have been with me - heart transplant 7-23-14. They helped me qualify for the transplant by pledging and signing up to provide transportation, care and assistance and certifying to the transplant center.  They have been mighty in their love and prayers, visited me, cared for Vickie and support her as my primary by being her backup. Good friends that came in the middle of the night in support! Unqualified love - this is the true church in action!

Grace and peace - God's love is poured out here. Joy, laughter, fulfillment, truth, compassion, friendship and help for the tough times. Baptism of our daughter, her growth in faith, confirmation and marriage. Now, herself a mom! Thanks to her wonderful husband, Nelson. Pastor John married them and I hope they choose him to baptize my beautiful, new grandson, Alejandro.

What of a church life? Looking back - I can see how they helped me grow in maturity, it doesn't happen all-at-once, but by "catching the wave" and being propelled by a mighty power to strength and peace not attainable without God's provident hand.

Sharing life with good friends in all the wonders of raising families, working shoulder to shoulder on building lives filled with grace, peace, hope, promise and love. Sharing and celebrating all the great times and being there for the others. Seeing God's active hand in this world and working tirelessly for its reconciliation and peace. Being the body and face of Christ to the greatest and the forgotten.

Being equipped and taught by mighty men and women of God who have discipled me and helped me see beyond this meanness of this world at the glories all around us. Living looking up and ahead and moving away from the regrets of a past that can be left behind - by  grace being granted joy.

Vickie, Kasey and I have had their support and strength through the pain of the deaths of my dad, mom, sister, Vickie's brother, step-brother, gran, dad and mom. Through times of great joy and pain - through life, good and bad! 25 years and many dear friends. There's a story here - come and be a part of it!

St. Andrews Presbyterian Church
705 Michigan Blvd.
Dunedin FL 34698

727-734-5493

On the web
sapcd.org

Contact by email
Connect with St. Andrews


Map and directions (click map or here)

 St. Andrews Presbyterian Chuch - map and directions


Friday, August 15, 2014

Joy


I have never smiled so wide or been more joyous.
I returned home from Tampa General Hospital on Sunday, August 10, 2014 after a Heart Transplant on July 23 and that was joyous.  To my delight, that joy was surpassed on Tuesday, August 12, when my daughter and her husband had their son, my first grandchild, Alejandro (Alex) and the smile above is the following day when I got to hold him for the first time!

Joy upon joy, blessing upon blessing! I am now a member of two, joyous "clubs" - Transplant and Grandparent! The joy of the first may fade with "normalcy" but I look forward to the other joy growing and growing. Wow! Grandkids Rock!


Sunday, August 10, 2014

Discharge to Home

My last mobile blog from Tampa General Hospital. I will keep you updated through the first year.

--

Transplant plus 18 days. It seems like a wonder to me now. The last tube is out.

I am free of all stents, pumps, infusers, defibrillator and drain. Other than dental and the wires in my breastbone - I am free of metal and stuff for the first time since September, 2007!

I am "natural" again.

The new life launches! My thanks and my prayers for the loved ones of my donor - his heart is filled with his love for you! May this be a comfort to you in your grief - my prayer is that joy will one day return to you.

Thank you for your love, prayers and support. Thank everyone involved over the years. Thank my pastors and church. Thank my family Thank my wife, Vickie. Thank my God.

Vickie and I will have many things to deal with in this critical first year. I have to encounter the virus that the donor had that's being suppressed.

There may be other, serious battles ahead, but today, today -
today is a day of great joy!

My first grandchild, Alejandro, will be born this week.

Truly, how much can one man be blessed?

Saturday, August 9, 2014

TGH Burger and Home!

For long-term patients of TGH Saturday noon's hamburger is the most anticipated meal of the week.

This is my third TGH burger. I am definitely ready to come home.

Dr. Hoffman says if my meds stay in control overnight that I will be home tomorrow afternoon.

I have to return on Monday for retesting. She asked if I'd like to stay over Sunday night since I have to be retested on Monday - I declined. I had to really control myself to keep from laughing!

She understood and said well, "there's no place like home!"

Friday, August 8, 2014

Blanketed in Love

A package arrived at home today - blankets of love from the blanket ministry of Alpharetta Georgia First United Methodist Church. They are both beautiful and heartwarming.

What a wonderful surprise - good friend Dale S had shared my blog with them.

Vickie and I are deeply moved and humbled by the outpouring of love coming our way.

I had shared with my pastor, Rev. Dr. John Fullerton, how I could actually feel his prayers, and the prayers of the saints, "cover me like a blanket".

This ministry perfectly competes that metaphor. Thank you for this joyous and unexpected gift.

Bless you for your ongoing thoughts and prayers, we are truly united in the love of Christ. God bless us all.

Update: Success!

I actually received edible food from TGH kitchen. Yes, it took two weeks! LOL

I'm still doing great and everything is doing great. I hope to hear soon about the results of yesterday's biopsy. The first biopsy of the new heart last week showed zero signs of rejection six samples. That's what we're looking for again.

Wednesday's operation to take the fluid off of the heart was a success and I'm hoping to get the drain lines out today.

I was correct in thinking that the new heart goes in the old sack or pericardium. That sack was too large for the new heart and that contributed to the fluid. The body should adjust for the difference in time.

I asked Dr. Mackie (transplant cardiologist) about the condition of the heart and he said the fit is near perfect, it was a three on a scale of four in the "cardiac index." That index relates the size of the body to the cardiac output - it's an exponential scale so three and four are almost identical. Truly a fantastic match.

The donor did have one virus, CMV, that I did not have an so they're keeping that reaction suppressed for six months. The infectious diseases doctor say that I will eventually have to encounter this disease but they want to choose the time that it expresses itself so that they know what the symptoms are in contract quickly. Range of symptoms could be from nothing more than a head cold to something more dire. The heart was so perfect that they rarely ever reject a heart for that type of condition.

I've still got tubes and sutures and things that will have to come out before they're going to let me go home but I'm feeling feisty enough now to start asking, when?

It's all good, now, even the food (sometimes).

Wednesday, August 6, 2014

Resistance is Futile

Yes more tubes. I do feel like a character from a Star Trek show.

Everybody's doing what they need to do to get me fixed up.

Of course great people here and great saints.

I'm feeling fine keep the prayers coming.

Tuesday, August 5, 2014

Too much water in the pool

Going to be enjoying the hospitality here at Tampa General Hospital for a few more days.

They've found that there is excess fluid around my new heart so tomorrow it's off to the OR.

Dr Hooker, transplant surgeon, will remove the excess and I'll have a drain for a few days.

Alas, this means more culinary delicacies from the hospital kitchen! Vickie has been great bringing my fav, chick salad on pump in so I have a backup. I do have a small fridge in this private room to hoard my "stash".

The second biopsy (checking for rejection) is also tomorrow. The first showed none.

The extra fluid is causing A-fib pattern so it needs to go and before they finish they will shock me back into rhythm if needed. I'll be out, thankfully.

The new, healthy heart is more compact so there's extra room in my chest than needed. The body is adjusting and this will help.

Morale is still high, Vickie and I appreciate all your love, prayers, cards, offers of help. It truly does increase our joy in this time of change. Bless you all, I'll post after.

http://en.m.wikipedia.org/wiki/Atrial_fibrillation

http://en.m.wikipedia.org/wiki/Pericardial_effusion

Saturday, August 2, 2014

Great hearts begin with his.

Dr Cintron, the founder.

Bio: http://www.tgmg.org/providers/cardiology/guillermo-cintron/

Much of what has become one of the leading transplant centers in the country is at his doing.

I was happy that he was able to stop by and examine me. This man possesses a depth of knowledge and skill that a few of achieved.

But truly his greatest gifts are his countenance and as an inspirational leader.

He sat with me and we discuss the history of heart medicine and transplants rising from the mere 50% survival rate to near 95% today.

He told me of the 80 people that sprang into action when my organ became available. And there is a backup for every process and person. Five helicopters and two jets aid collection and transport.

But is staggering as the logistics are - the most impressive thing here is the attitude, commitment and dedication of the people who do this work.

That begins with Dr. Cintron.

Thursday, July 31, 2014

The beat goes on!

Having so much fun here I've decided to stay a few more days. The good news continues- the first biopsy shows no rejection at all!

Dr Kumar did the cath and said,"the heart looks fantastic!" That's what I want to hear!!

Staying on to improve red count, balance anti-reject meds and fluids. There's a lot of complex chemistry.

I'll be here over the weekend and maybe as long as Thursday - the 2nd biopsy is Wednesday so they may just keep me till then.

Visitors are welcome. I'm feeling great and getting excellent care. The chaplain visits me and is a hoot, too! What a great servant of The Lord!

Kasey & Nelson came yesterday- they are so great together and Kasey is just precious, she's due to deliver their son, Alejandro, by the 14th! The first grand for both families.

Vickie and I get rounds of education on our "New Normal". It is a lot but they are great teachers so we'll be fine.

The profound take-away is that the old, diseased life is over and a new, healthy life has begun. I feel this heart beating so strong at night that I hear it move the pillow case beneath my neck.

The donor heart is chilled and implanted and then the bypass ends - when warm blood fills the heart it beats on its own! It beats because it must beat, it beats because it was created to beat and even has a brain of its own to make it beat!

I praise you because I am fearfully and wonderfully made;
your works are wonderful,
I know that full well. Ps 139:14 Praise You, O Great God of Glory!

Thanks for your cards, thoughts, love and prayers!

Tuesday, July 29, 2014

Home Friday is the plan!

Proved to be overly optimistic. I can be patient, it's been an eight-year run of heart failure and I'm in good hands. Need more time - balancing the really complex chemistry and heart rhythm. My spirit is high and I'm feeling good. 

Monday, July 28, 2014

Sunrise Davis Island Tampa

I got moved from the intensive care unit after midnight last night into the larger recovery room. All transplant patients on this floor, heart kidney and lung. The sun is beautiful rising in the clouds over downtown Tampa and Davis Island. I was able to lie back and feel the beating of my heart. Wow, is the only word!

Sunday, July 27, 2014

Moving Day

Surgeon Dr. Farber the cardiac surgeon that I had not yet met (Calderia, Hooker) was by to tell me that they really like the way it's looking and are going to move me from ICU onto the treatment floor (Dr. Mackie has been caring for me here in ICU).

The new heart is beating strong normal and well. I can feel its beat! It is an amazing feeling!

Doing physical therapy - made a lap of the ward this morning. Getting stronger of course there's aways to go yet. Much more freedom up on the upper floor where the standard Transplant rooms are.

The rooms are single private rooms and they have a couch so it's easier to visit.

All functions have to be returned to normal before the let me out of here. But that's all going along great so the move is on.

I should be here for another two weeks so getting out of the noise and confusion and chaos of ICU is always great.

Getting all your messages about your prayers, thank you for all of your attention, all my love, John.

Saturday, July 26, 2014

Selfies

Kasey and Nelson stopped by as did Banks and Lois. Vickie was here earlier to.

Friday, July 25, 2014

A selfie with all my tubes

Actually that's just the top half of the tubes

"Post" post - my new birthday



I didn't know whether to share this - but decided to and revised this post.  
Revised August 17, 2014:

My new birth date is July 23, 2014. That's what they say around here when you get a new heart.

I'm in ICU and have been since surgery, it's taken a while before I could write. Wow, had some crazy dreams, visions and hallucinations over the last two days. The great care staff, Vickie, Tom and Nancy kept guard over me and talked me through the worst of them - at 3:00 AM!. Reaction to the drugs I was told. I have experienced events that have changed me and how I will view the world. I have an understanding of mental illness - it was so real, but my mind was in paranoid overdrive. Nothing the staff hasn't dealt with before and was not ready for. I am thrilled and really drugged. Should be getting most of my tubes out today. I'll be in the hospital for 2 to 3 weeks. Thanks for all your prayers everything is going great right now.

Special thanks to Meghan (with apologies), and to Lori and Lorna, all of TGH ICU. Tom and Nancy picked up Vickie and they came to my aid at 3:00 in the morning! How can I say what good friends they are. God bless these, God bless us all. 

This was my original post:
My new birth date is July 23, 2014. That's what they say around here when you get a new heart.

I'm in ICU and have been since surgery, it's taken a while before I could write. I am thrilled and really drugged. Should be getting most of my tubes out today. I'll be in the hospital for 2 to 3 weeks. Thanks for all your prayers everything is going great right now.

Dr. Caldeira, transplant surgeon


Dr. Caldeira, transplant surgeon

My brother got this photo of Dr Caldeira when he came to give my family the good news that the heart looked perfect, the transplant went well and that I should recover shortly. 

It is kind of unusual but sometimes the last person you meet in the transplant process is the actual transplant surgeon. I was finally able to meet Dr. Caldeira at this afternoon. The surgeons take different weeks in rounds. Dr. Hooker is rounding this week so it was nice for Dr. Caldeira to stop by.

Wednesday, July 23, 2014

Still on track


Dr Caldeira
Transplant Surgeon

The donor organ continues to check out. Now transplant operation isa scheduled for late morning or early afternoon. I've been in a comfortable room on the post-transplant floor since 4:00 AM. This is a private room with a couch, recliner and chairs. Vickie can "stay over" with me, she is currently bedded down on the couch and I had a "chill pill". Nurses, docs and techs scurry in and out as we wait for news. In another room, somewhere else in the southeast US, another family is gathered. That family is dealing with a tragic event. The donor is brain-dead and they are in grief. 

My prayers are for comfort and healing in their loss of their, now brain-dead, loved one. I thank them for the gifts of life they are giving to me and others. Their doctors and councilors are with them and will be through this all. They will say their goodbyes and let him die, leave the hospital and began their lives as his survivors.  
Remember them also in your prayers 

This type of "beating-heart" cadaver allows the heart to be transplanted without it being ischemic (without blood flow) for a long period of time. That is the best for the quality of the organ. The recovered heart will be chilled to about 45*F to preserve it and ready it for transplant. The "harvesters", a team of organ recovery specialists have come by jet or helicopter and will recover the solid organs - heart, lungs, kidneys and liver. That equates to up to right transplants from this donation. Eight lives will continue or be lived more fully from this one gift. The donor will have passed life on to us in these gifts.

The truth is that all of this is scary but I am comforted by your prayers and support.

--
Later

Surgery is still scheduled for today. The surgeons will have a visual on the donor organ around noon. If everything still checks out I should be in surgery between two and three. The transplant will take between three and four hours so I should be out of surgery between five and seven.

Once it begins I won't start remembering anything for a day or so due to the drugs. I will look and feel pretty bad at first. I'm being pre-medicated with powerful anti rejection, anti viral and anti bacterial drugs now. Some of them are messing with my thinking and are giving my a tremor. Typing this is getting harder so I'll put this down, now

Vickie will be able to see me  -  I'll be in ICU several days. Once the tubes come out I'll get to a regular room (two - three weeks).

Tom and Nancy will be with Vickie here at TGH for the surgery (thanks!)





JohnCorl@gmail.com