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

Friday, February 14, 2020

Valentine's Update

So far, I have made it through step 1 of the process, and step 2 will be happening between Wednesday, February 19th and Monday February 24th.  If the transplant team gets all the information they need, we would quickly get to step 3 (potentially as early as February 27th!). [If you're viewing this on a mobile device, please look at the background information page first to get info on the steps]

While this is scary in some ways, it is also really comforting.  While I don't talk about it often, I have spent 13 years feeling tired, not being able to do as much as I used to (or want to), and in the last year feeling less and less well.  While transplant has risks, it also holds the hope for more energy and a longer future. So while we have a lot of unknowns, we are feeling really hopeful about and good about this journey.

Since Valentines day is also a "heart" day, we thought it would be appropriate to launch the blog today.  Once we know more about the process and what is going to happen, we will update the blog. We probably won't post everyday, but I'm hoping to post something at least once a week.  I hope you all have a happy heart day, and thank you for supporting me and Peter through this journey. 
at
Labels: ,

4 comments:

  1. UnknownFebruary 14, 2020 at 9:53 PM

    💖

    ReplyDelete
  2. GwendolynFebruary 14, 2020 at 11:40 PM

    Thanks for sharing your journey. I hope it encourages more people to become organ donors.

    ReplyDelete
  3. Dr. BranchFebruary 15, 2020 at 6:01 AM

    My thoughts and prayers are with you both!

    ReplyDelete
  4. TabathaFebruary 15, 2020 at 8:41 AM

    This reminds me that being an organ donor is a conversation I should have with patients..... I have many other conversations with them but I've never had that one.

    I will keep you in my thoughts and "on my heart" always!

    ReplyDelete

Subscribe to: Post Comments (Atom)

One month post transplant!

Wow.  It is almost unbelievable that it has been one month since the transplant.  So much has happened, with two weeks in the hospital, and ...