Continuing the Transplant Process
Feb 10 2013 in Caring for Children by Jane
We started the transplant evaluation process in November 2012 after both Nicole’s PH specialist and her cardiologist agreed that it was time for this. She saw the heart/lung surgeon and then she saw the lung director at the transplant center.
The doctor ordered several tests which included an echocardiogram, a CCTA scan in which they inject dye into the patient and watch how it flows through the heart, a TEE which is where a tube was stuck down her throat with a camera which shows images being seen on the sonogram machine, and lastly a right heart catheterization. After the doctor had gotten the results of all these tests, the doctors at the transplant center, another heart surgeon that specializes in congenital heart defects, her cardiologist, and her PH specialist were all going to sit down to discuss a plan of action. Namely, can they repair Nicole’s heart or does she need a new one in addition to two lungs.
I know there was a meeting schedule for the second week in January but one of the doctor’s at the transplant center had a heart transplant and couldn’t attend. The PH specialist told me that only himself and the lung director showed up for that meeting. To my knowledge another meeting has not be scheduled. During the week of January 21st when Nicole was in the hospital the transplant center center had called because they had received an email about the PH support group meeting which also stated that Nicole was in the hospital. The doctor wanted his coordinator to call and find out how Nicole was doing. She also wanted to schedule an appointment to come in and continue with the transplant process and told me to call either the following week or week after.
It has been two full weeks since Nicole was released and I have been procrastinating about calling. They did call on Friday but my cell phone was in Nicole’s room as I have her medicine alarms on it. I had a call so Nicole had to take her medicine without me waking her up. I didn’t return the call on Friday like I should have either. I MUST DO this on Monday regardless of my fears.
Denise had asked me to blog about this and write out my feelings. I am hoping that this will let me come to terms with my feelings. I am procrastinating because I am afraid.
I am afraid because I don’t want to hear the results of the testing and what they will determine, I am afraid she will die during the transplant itself or after the transplant because of complications (infection, rejection). The five-year survival rate for lung transplants is not as good as I would like and, while I don’t have the exact number if front of me, I believe it is right around 50%. I am afraid I will not be strong enough to endure this as it will mean a long hospital stay and require Nicole being hooked up to many machines and breathing devices. I can’t in good conscience leave Nicole by herself in the hospital. I am afraid that they will deny her (either the transplant center or Medicaid) or we will not be able to raise the money needed. The estimated cost of a double lung transplant in 2011 was $797,300 and the cost of a heart/lung is $1,248,400.
I’m afraid that Nicole’s perception of being “normal” after a transplant is unrealistic. I don’t have the specific information in front of me but I know that, while she will be “cured” of PH and she will no longer have heart issues, she will not be able to go out into any public place like malls, Disney etc. for the first six months after transplant. She will have to wear a mask to protect from germs in public for the rest of her life.
She will have to visit the center on a weekly basis for either the first six months or year. She will also get regular testing. She will still take a lot of medication (maybe not as much as she does now). She will have to keep a daily log of symptoms and all her vitals including blood pressure, oxygen saturation levels, temperature twice a day for the rest of her life.
She will be normal in the respect that she will be able to breath normal but I don’t think she really grasp what after transplant life will be like.
The question is: Will it better than it is now or not??????

Trish said on February 10, 2013
Jane, It’s very understandable that you as well as Nicole and Rick are fearful of what is next. You have been amazing through the entire process so far not to mention throwing in an unexpected hospital stay! You are strong and you do what you have to do. Being strong doesn’t mean not being afraid – it’s just moving forward in spite of it and that’s what you’re doing. (I think someone wiser than me said that here before).
As far as normal, well, the definition of normal changes all the time. You and Nicole have both experienced that too. We have with Robert as well. In fact, our family had a similar dilemma before Robert’s brain surgeries. Will he be better off with surgery or not? Will he be “normal” afterwards? We didn’t know and knew there were all kinds of risks.
Trish said on February 10, 2013
Oops! I wasn’t done but we have this new puppy and he hit send for me.
Anyway, normal changes all the time.
I wonder if there’s a transplant support group that Nicole and you could join so you can talk to people who have been through it. People also deal with their fears differently so I wonder if Nicole is hoping/expecting “normal” after her surgery so she can get through it. So she has something to hang on to as a payoff for what she’s going through now. A support group might help her open up about that or at least listen to others experiencing similar feelings.
No matter what, I’m here to listen (we all are) about your fears. It’s a scary time but you have lots of support and positive thoughts coming your way.
ejourneys said on February 10, 2013
Jane, as I read your entry I also wondered if a transplant support group could help. You’re dealing with a whole additional layer of “what if”s and a whole new layer of scary and overwhelming. I agree with Trish — you have been tremendous through everything. That’s a lot of fear you are all pushing against and trying to push through. (((Hugs)))
I found this: http://www.transplantliving.org/community/support-groups/state-listing/florida/
@gail said on February 11, 2013
Dear sweet Jane,
First of all? I wish I had been there (and Trish where were you?) this Vride visit! I had wanted to meet you – and your brave little daughter Nicole too!
Secondly? You are as brave as Nicole. I don’t really know your husband but he must be your rock!
I agree with Trish and ejourneys. You might enjoy a group to help you or even a therapist for the three of you or only Nicole since she is an adule now. I have learned a lot through therapy!
We are all routing for you sweet Jane! Believe us! Honestly! I think you are being hard on yourself but at the same time facing your fears! {{HUGS}}
Denise said on February 11, 2013
Hi Jane–You’ve done such a great job verbalizing your fears. I understand each one because I know I would have them, too. I can see why it’s hard to move into this process because the process just seems to bring more questions and more possibility of problems.
You are a strong, wonderful woman, Jane. I’m so glad you are here and that you are part of our community. I can’t imagine what it would be like here without you. You bring a very special light with you.
Keep us posted!