BACKGROUND

As many of you know, Jodie was born with congenital heart defects and had surgery at 10 days and 18 months old. She did ok throughout childhood, but had to be on some medications through high school, then another was added in college. Jodie went on to grad school, and unexpectedly required a valve replacement in 2007. It turned out she was in the early stages of heart failure, but only found out after the procedure. She needed to get a pacemaker since her heart stopped beating on its own, and then a few months later upgraded to a pacemaker/ defibrillator due to low heart function. In 2008, Jodie was told that she would eventually need a heart transplant, and that the doctor predicted it to be necessary within the next 5 years.

In the 12+ years since then, Jodie was upgraded to a bi-ventricular pacemaker/defibrillator which helped her feel better but didn't improve her numbers, had it replaced two more times due to the battery almost running out (normal process), was put on a new medication that helped her feel much better but still didn't improve the numbers. Then in April of 2019 things started to get interesting. Jodie went into an atrial flutter and after 3 weeks, had to be cardioverted (think being shocked with paddles, but more controlled and while under anesthesia) to get her rhythm back to normal. Then over the summer she started feeling more and more tired, and having slightly worse symptoms. Jodie had some tests in August that showed things were worse, and the doctor told us in October that we would need to check back in early 2020 to see how things are. After having those tests, its clear that Jodie needs to have a heart transplant.


WHY DID WE START THIS BLOG?

Jodie and Peter decided to keep this blog for a few reasons. First, as a way to keep our friends and family up to date. Second, as a way to share how we are doing and what we are going through (and potentially what we need). Third, as a way to document this journey.

We have learned that we want the people around us, and those who care about us, to know what is going on, but don't always have the energy to talk about it over and over. We will be sharing was is "on our hearts" as we go through this journey. We welcome you to check in as often as you like. Thoughts and prayers are much appreciated. You are always welcome to reach out individually, but please feel free to leave comments on our posts and we will try to respond to everyone when we can. We are also planning to use this platform to share news when we don't have time or energy to send to everyone.

Some of our posts may be more emotional, and some may be about more mundane things. Once we get to step 4, it could take anywhere between 1 day and a year or more to reach step 5. We have no way to know. As we are in that waiting period, we do know that one of the things that will be helpful to us will be to keep busy - board game nights, movies, etc. If you are nearby, please do reach out. While Jodie can't be doing anything too strenuous right now, we still want to connect with people. If things come up that we need or could use help on, we may post it here, or reach out specifically to those who have let us know they want to help.

Thank you for walking with us through this journey as we share what is on our hearts. Please check back for updates. We will add information as it becomes available and as we go through the process ahead.

God bless,
Jodie & Peter Elliott

Sunday, March 15, 2020

So it's been a week

Sunday last week we were getting ready and going to the hospital to get Jodie a new heart. A ton has happened in seven days: a dry run, a short ICU stay, fever, mandatory isolation due to Covid precautions for 3+ days, and finally back to the cardiac floor. It feels like it's been way more time than just a week.

I was holding off on a lot of the news lately waiting until Jodie got more stable. And she
is now feeling more like herself, talkative, and animated; better all around. However, we have been noticing her energy depletes much more quickly, so waiting here for a heart really is the best option. She was finally approved to get a regular room on the cardiac floor today, and got special permission to treat herself to a shower. Feeling like there is some normalcy in her life again will do wonders to make her more comfortable.

Feeling clean for the first time in a week!

So now Jodie is back on the transplant list, and the plan is to stay at the hospital until a better heart becomes available.

Short update tonight, but good news. Jodie is planning a much more detailed post for later.

God Bless,
Jodie and Peter
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3 comments:

  1. Sarah WelchMarch 15, 2020 at 7:12 PM

    Such good news! It’s great to see your smiling face, Jodie! Love to you both 💕

    ReplyDelete
  2. UnknownMarch 15, 2020 at 7:24 PM

    Thanks for the updates! We are thinking about you all the time and sending you lots of love from OH-IO! XO Patty and Jay

    ReplyDelete
  3. UnknownMarch 16, 2020 at 3:52 PM

    Thanks for the update Peter. Nice to see your beautiful smile Jodie! Glad that you are back on the list and that you are doing well. Thinking of you both with love, Aunt Elaine

    ReplyDelete

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