My name is Elisha.  I am twenty-seven years old and have cystic fibrosis.  In July of 2011 I went to New York City to meet with a lung transplant team for a double lung transplant.  That is when I decided to start a blog to document everything I was about to go through.  I am not going to do this on a daily basis (I never was any good at keeping a daily dairy when I was younger lol), but I will write about what is going on every once in awhile to keep everyone up to date with where I am and how I am doing.

A lot of people don't really understand the struggles that come along with Cystic Fibrosis.  This even includes the people that are around me and know me very well.  For the most part, if you just see me, you wouldn't really know how sick I was.  I don't look sick and most of the time I don't act it either.  I put up a good front and barely ever complain about what is going on.  Some of it has to do with the fact that I am use to it.  This is my life...I have always had CF and I don't know anything different.  Another reason is because I want to live my life as much as I can.  I want to stay positive and not dwell on what is hard.  Things are getting more difficult for me as I get sicker... but I want to continue doing the things I love and I refuse to just completely stop . I know things are going to get harder, but that is not going to bring me down because there is light at the end of the tunnel. I have a second chance at life when I get these new lungs.

I am starting this blog for a couple of reasons.  One is to keep my friends and family up to date on everything that is going on through this lengthy process.  Also I want to do this for other people who are going to be getting lung transplants in the future.  Now I know every situation is different, but I hope this will be something that they can sit down read and learn something from.  Maybe get an idea of what to expect. or maybe reading this could give some insight to ease a little of the anxiety or just read because it is something they can relate to and know they are not alone.  I am going into this completely blind and learning as I am going, so if this helps one person out just a little I would be thrilled.

There are going to be some ups and downs throughout all of this, but one thing I promise to do is stay honest.  This includes what I am actually going through and how I feel.  So feel free to ask questions if something doesn't make sense, you don't understand something or if you are just interested. I am not too shy. :)  Either leave a comment using facebook or send me a message using the contact icon.

Double Shot

Written by Elisha. Posted in Elisha's Blog

The hospital stay went smoothly and I was able to come home last Friday.  I am so grateful I am able to do that because after a little while in there I am ready to get out.  If it wasn't for some of the respiratory therapists, the procedures that go along with them and the food, I wouldn't mind being there as much.  Even if everything was perfect in there though it is nice to be home, sleep in my own bed and be able to do things with people.  I would do the whole thing at home except that first week I really am too sick to do it all by myself.  It is better to let my nurses set everything up with the port and allow them to nurse me back to health those first few days.  The coughing that I did the first few days were rough.  I blacked out once for a few seconds while on the phone with Jason, so obviously safer for me to be there.  I can't go anywhere in that condition anyways.  It's the second week when I feel better, but still need the meds...

Candles on the Cake

Written by Elisha. Posted in Elisha's Blog

Today is my 27th birthday.  I am still in the hospital, but to everyone's surprise not too upset about it.  It is not where you are, but the people you are with and today many people have made this day special for me....

Thank You for Being a Friend

Written by Elisha. Posted in Elisha's Blog

I am back in the hospital for an exacerbation.  I made it a little longer than last time and this month was a good month.  My coughing has gotten more rough, a lot of unexpected coughing fits that bring me to the verge of passing out, but I am learning to get through those.  I can't complaining about this because I had some energy to go out and do things with people the last few weeks.  I did not have this luxury the previous month and it was horrible.  My friends and family have been coming over and taking me out a lot, even if it's for a little while.  It isn't always easy or go smoothly, but I am grateful they all put up with it for me.  And when I am too tired and can't go out they just come over and we have a good time here.

Stronger

Written by Elisha. Posted in Elisha's Blog

I am home, off the IV's and feeling ok for the time being.  There are a few things to catch everyone up on, but not much.  I am also going to start something new.  I am going to use my twitter account, which is attached to the home page and to my facebook page https://www.facebook.com/Journey2NewLungs, to update how I am feeling on a more day to day basis.