Announcement About Angel Donor

This pandemic hit everyone pretty hard over these past few months. People are getting sick, losing jobs, and businesses are closing. The writing industry is no different, especially for smaller publishers. 

My book, Angel Donor, was created to help other children going through the transplant process. It is more than just a book to entertain. It is a book to provide help, connection, and comfort to those children going through the same thing. So it is with this in mind that I am sad to report that the pandemic made it too hard for my publisher to sustain their business, and they had to shut down. 

However, since I feel that this book is important and needed, I've decided to republish it now that I have the right reverted back. Illustrator Samantha Bell has granted permission for continued use of the illustrations. While I am sad to part ways with Guardian Angel Publishing, I'm happy and relieved to be able to create a second edition of this book. 

One of my plans is to create a hardcover edition, which I believe has always been missing. I'd also plan to do another Kickstarter or Indiegogo campaign to help make this happen. More updates will come as plans develop. 

For now, know that this is not the end of Angel Donor, but a new beginning. 

Feeling Thankful

I've always been grateful for Jackie and Anthony's medical teams. They truly stopped at nothing to make sure they were in the best of health despite the horrible diagnoses they had. So many times they exceeded my expectations. Whether it was tending to their care, stabilizing them or coordinating emergency care, they have always come through. So, it is no surprise to me to see the dedication and bravery the medical profession is showing in combatting the novel Coronavirus.

As a mom of 2 transplanted children, this disease scares me to death. I constantly worry and make sure they are not exposed. Yet, when the rest of the world is distancing from it, the medical profession is gunning for it head-on.  Knowing doctors and nurses as long as I have, I know they would settle for nothing less.















For all the help they have given my family I wish there was a way to help them now. And so I do what I often do when I want to help but have no means to do so - I write. So, medical professionals everywhere, this is for you.

What Happens After a Transplant

It's been over a month since my son recieved his #giftoflife . Life is very different after a transplant. Sometimes it is tough to get used to it. For example, there were so many medicines he had to take while managing his kidney disease. Now he has a whole other regimen that is completely different. The doctors told us as he gets farther out from transplant that some of the meds will wean down and will be stopped.  As much as we were aware that he would have different medications, it felt strange to just switch it up. But it is a change we are glad and grateful to make!

Another  thing he is getting used to is taking precaustions so that he doesn't catch any colds, viruses, etc. They can easily turn into a more serious infection since he is now taking medications to suppress his immune system. Handwashing and sanitizing are constant.

Doctor visits are frequent the first few months so that they can monitor the healing process and help stabilize the amount of medications needed.

The toughes in my son's experience is the amount of fluids he is required to consume. His kidney needs to be well hydrated so they want him drinking 2 liters a day.

As time goes on, these things ease up more and more. Pretty soon there will be a stable routine. All of these things have greatly improved his quality of life and he is forever grateful to his donor and donor family.

A day's worth of meds

Anthony and Kidney Transplant

Who knew just two months ago with my last post that Anthony would already have his new kidney. I'm this was due to a mix of divine intervention and timing.

The process of being listed for a kidney transplant lasted from the end of December through the beginning of April. We were always visiting the hospital getting tests and evaluations to ensure Anthony was a good candidate to receive a kidney.

It seemed the odds were stacked against us from the beginning. Just as the evaluation process started, we discovered a temporary lapse in insurance. Thankfully the hospital was able to work with the insurance and minimized the time  we had without coverage. 

Another thing that came up during the evaluation was concern about papilledema (swelling of the optic nerve.) However, everything finally worked out and he was officially listed as active on the kidney transplant waiting list on April 9th. Meanwhile, his aunt was going through evaluations to see if she could be a living donor (Thanks Aunt Amy.)

We were relieved that the process was complete and knew that waiting for a kidney could take a long time.  However Sunday evening on April 14, the transplant team called and said they might have a kidney for Anthony. We left for the hospital that night. After testing both Anthony and the donor's kidney again, the doctors felt that the kidney was a good match for Anthony and he went into the OR early Tuesday morning.  We found it a blessing that he received his kidney not only during National Donate Live Month, but also during Holy Week.   Many people have been keeping Anthony in their prayers, and I have no doubt that they have been heard and answered. It truly has been a miraculous journey.

In my local community we are raising funds to help with the initial costs of recovering from the transplant. One of the ways we chose to do this was to remind people of the book Angel Donor. Whenever Angel Donor is purchased (especially through Guardian Angel Publishing), I earn royalties which can be put towards the costs.

You can read about his updates on his Go Fund Me Page as he continues the recovery process. 

Twice in One Family

I felt it was important to talk about what has been going on lately. Yes, Angel Donor was inspired by my middle child who was born with a liver disease and needed a liver transplant. Angel Donor was a way for us to tell her story.

Now, it is her brother who is going through the transplant process. He is in need of a kidney. It is rare for something like this to strike a family twice in a row.  He was born with only one kidney and that kidney is in the advanced stages of kidney disease. 

In January he began his evaluation for a kidney transplant. The process is still going on, but should be finishing up within a month or so. 

They say every experience is different, and this is no exception. I catch myself thinking, "I don't remember it being this stressful before." Maybe it was just as stressful, but everything moved so fast.

Howevers tressful it is, we know we are aiming for a healthy and better quality of life. 

The First Surgery #JackiesStory

The days before Jackie's surgery went by in a rush. While we were still at the surgeon's office the day of her diagnosis, the doctors were already scrambling to set up a date for surgery. They insisted the earlier, the better. With Biliary Atresia, the longer the bile flow is blocked, the more damage is done to the liver. I didn't know it then, but as I learned more about the disease, I found out that this surgery(called the Kasai procedure) worked best if it was done within the first four weeks of life. The longer we waited, the less likely it would be successful. The Kasai essentially is a surgery to create another way to restore bile flow by attaching the intestines directly to the liver in place of the damaged bile ducts.

                                                         Jackie and Mom a few days before surgery

The morning of Jackie's surgery I felt like I was caught in a dream. We were moving around, gathering her things and making sure we were ready to go.At the same time, I was full of anxiety. What was going to happen? What if something goes wrong? Will her liver be okay?  I remember my husband at the time took a picture of me holding her. I wasn't sure how I felt about it at the moment (though now as I look back, I'm glad he did.) since my mind was racing with such anxiety. 

The whole process of checking into the hospital and arriving to Surgery seemed so detailed, however as the years moved on, it became a second nature to us. We checked in and waited in the waiting room. A few moments later we were called by a nurse to the intake area. We had to change Jackie into a gown as the nurses gathered all her information. We met with so many people: nurses, her surgeon, the anesthesiologist. Finally the time came for them to take her back to the surgical area. 

This was a moment I still remember clearly. There are few times in life when a memory is so clear and so vivid that it seems like it just happened. This was one of those memories, I gave her a kiss and then the nurse gently took Jackie from my arms and began to walk away with her.  As they moved, they became smaller and smaller until I could barely see Jackie's yellow gown. My only thought, even though I knew she would be well taken care of, was , "They took my baby." I tried not to think of all the "what ifs" that ran through my mind earlier. 

The next several hours seemed endless. The doctors sent updates out to us as time went on, but I was still a bundle of nerves. Finally, around 6:00, Doctor M, (the surgeon) came up to us. He told us she was out of surgery and should be waking from the anesthesia shortly. He then talked about her liver. He was so relieved we had the surgery so quickly. The condition of the liver was pretty bad. He said the color was brown. I had a maroon sweater on that day and he said a healthy liver is more the color of my sweater. He reassured us that they will do everything they can to get her better.

After the surgery I began to seek out online support groups. My favorite has always been Class Kids.This is an amazing website dedicated to helping families of children born with liver disease.  I'll talk more about them as the posts go on, as they have been with us for much of Jackie's journey.  

Once we came home a few short days later, I knew we had a long way to go, but hoped this surgery would provide her some healing. Stories I heard about other babies who had the Kasai procedure gave me hope. There were some "babies"  who have gone all the way into adulthood without many complications. As for us, we were grateful she made it through the surgery fine and we took it one day at a time.  

The Diagnosis #JackiesStory

Before we knew it, we were on our way to Jackie's appointments.  The first stop was in Radiology for a Hida Scan, a test that can diagnose diseases of the liver and bile ducts. She had to get an IV with fluid that would make the liver and bile ducts visible in the image.  

After that, we went to see the GI doctor. At this point we were getting tired and were continuing to hope that this was all about the doctors being cautious. However, those hopes diminished when we visited the GI. As we waited in the exam room, I changed her diaper. Right in the middle of that, the GI walked in and asked to see it. The contents were a pale white. He expressed concern at the coloring and told us he was going to send us to the surgery office immediately. When he returned from contacting Surgery, he briefly explained that the white color in her diaper was a sign that there was no bile leaving her liver. 

I was too confused and shocked to really react to what I was told. At the moment, I was still experiencing the situation, and everything was moving too fast to react right away. I do remember that as we pushed her stroller across the parking lot to the main hospital, I had an epiphany. (I had lost my job at the end of my pregnancy and was questioning my direction in life). It was at that moment when I knew. This was what I was here for. This is what I was put on this earth to do. 

Jackie Pre-Surgery

Once we arrived at the surgeon's office, things seemed to move even faster. Doctor M already had all her information in front of him. He explained that what our baby had was called Biliary Atresia. In my head I wasn't even sure I heard that right. "Billy who," I asked myself.  The doctor explained it in concrete terms for us. He described it as imagining you are trying to get out of your front door and instead of an open door, there is a brick wall. There is no way for you to get out. He explained the bile ducts (the doors in the liver) are blocked (the brick wall) and can't exit the liver.  He explained this leads to scaring and infections. I think he knew we weren't ready to process the fact that it can also lead to liver failure.

He then told us that he wanted to do the Kasai procedure, a surgical procedure to help restore some bile flow in the liver. He told us that it may not be a permanent fix. He had us wait in the waiting room as he scheduled the surgery. He said it worked best when done within the first month of life. Yes, this was all before she was 4 weeks old.

I don't remember much from the blur of that day, but I do remember getting a call from the pediatrician's office while we were still at the surgeon's office. The doctors and the surgeons were telling me that this disease was not my fault or the result of anything I did when pregnant. 

We finally left the surgeon's office. I'm not sure how I was able to sleep that night. I was still processing the last 3 days and nothing seemed "real" at the time. I knew I had to get some rest, though because we had to be ready for the surgery that would be happening in just a few short days ahead. 

Up Next: The Surgery