Cool Transplant Information

Just have been reading a ton of fantastic transplant information lately and wanted to stop by and post it.  Also, wanted to let the world know Dave and I are both still doing great with excellent Kidney health.

First The University Of Maryland Medical Center successfully transplanted the first organ delivered by Drone! I feel like that is very amazing.  They are always using new technology to make transplants better and faster.  I am so happy to have been able to donate through them.

Second Maryland's Living Donor Protection Act Passed.

Thats all for now.  I'll try and remember to update again in a week on our 5 year Transplantaversery!!!!

2 Year Follow up with UMMC

So I know that our 2 year Kidneyaversery was a while ago, but about a month ago is when I finally had time to go do the lab work.  I took a day off and went down to the University of MD for my last follow up there.  After 2 years you no longer have any follow ups with them and are supposed to monitor your own kidney function with the help of you primary care doctor.  Everyone was super helpful and I was in and out quickly, which gave me plenty of time to go get copies of our marriage certificate (but that isn't important here).

After a few days the coordinator e-mailed me to say that my protein/creatinine levels were elevated and that she would like me to re-do the test because she things the results are wrong.  This immediately made me anxious because what if the test wasn't wrong and I was actually having issues with my solo kidney.  I didn't post here right away about this because I didn't want anyone else worrying about it till I knew what was up.  So I silently worried to myself while googling everything I could.  This is always a bad idea.

As soon as I could I went to labcorp and re-did the test.  Within a few days the coordinator e-mailed me again to say everything was normal!  This was great news and good to know.  So my one kidney is still doing its job!

Dave, also had an apt. recently where the Dr. said he was doing well.  He also mentioned how great it was Dave was on so few medications!   This is because transplant patients are normally on medications to control the disorders that caused their kidneys to fail in the first place, and Dave doesn't have to worry about that because he is healthy!

Well, I think that is all for now.  As always if you want to know anything else about my experience feel free to ask! 

Two years since we discovered ESRD

According to Time Hop and Facebooks new feature, on this day, I was reminded that two years ago yesterday is when we first found out Dave needed a kidney transplant.  It is crazy to look back at all that has happened since then.  I am grateful that in those 2 years we have been able to get back to a Dialysis free life and move on the best we can.  Hopefully we can keep it up and remain healthy for years to come.

I'm not sure what else to add to this post, I just thought it was something that should be mentioned.

Oh and I did get a replacement kidney tattoo the other day.  Better pictures to come once it is 100% healed and I'm showing it off at the beach celebrating our kidneyaversery in a month (celebrating a month early haha)

Also, if you have any questions, or if there is anything you want to know about, please ask!  I'm not sure what to write about now that its all pretty much over, so if you have ideas let me know and I will make them happen!