A little about us...

My name is Ryan and my wife's name is Amanda. We are just two people with a lot in common that fell in love. Just so happens that one of those commonalities is Cystic Fibrosis (CF). We are breaking all the rules with being together, but love knows no boundaries.

Amanda and I met a few years ago at a CF walk kick-off event. Who knew our path's would cross again.

I was going through a rough time in January 2012, and a friend of ours mentioned to Amanda that I might need someone to talk to. Being the caring person she was, she contacted me to talk. We had an instant connection. She had previously gone through what I was going through, and was there to lend an ear. We started talking more frequently and feelings started developing. When we saw each other, there was a feeling that we had never felt before, almost like in the movies, love at "first" sight. Our friendship was stronger than ever and with feelings developing stronger and stronger every day, we decided that we had to make a hard decision. Being that we both had CF we had to decide where this relationship was going, did we want to take it to the next level, or was it going to end at just being friends. After a little time we both decided we were ready to take it to the next level. There was no turning back. We were in love, and took our last first kiss.

Sunday, October 21, 2012

1 week down! Approximately 51 to go…


Tonight was my last IV for the first week. Every week I will need to have a new port needle put in. What this means is the current port needle will have to be de-accessed, and then my port re-accessed with a new needle. Luckily I de-access myself, but don’t know how to re-access myself yet. Eventually Amanda will learn to access it so that will eliminate the need for a home health nurse weekly. I will still need one bi-weekly to draw blood labs to check kidney functions etc.

After my IV tonight I de-accessed my port. That will give me almost 24 hours needle free before the home health nurse comes to re-access me. When I am de-accessed I can take a shower without worrying about covering my port and making sure moisture doesn’t get in. I can clean my skin where the tegaderm was and sit in the hot water longer. This is nice because when I have to cover my port to shower it limits what I can do and makes it harder to shower. I feel clean.

After a week of antibiotics I am starting to feel better. I am a little more tired, but at least I feel better. I have not had a lot of bad side effects from the antibiotics, and I keep praying that I wont. After doing my IV every night, I am a little bit nauseated, but not bad at all. I have not had to use my anti-nausea meds, which is good.

Yesterday was the Williamson County Great Strides Walk. My team Bad to the Boone raised around $5000 if not more, and the walk exceeded our goal. I wish my team was bigger, but it gives me a goal to reach next year. With everything going on this year I did not have the time I have in the past to put together a team and manage it. I did exceed my goal for fundraising, so next year I will raise the bar.

Today Amanda and I met Sierra, Tory and Logan at the house and picked up our washer and dryer, so we can finally wash clothes at the apartment. After unloading the washer and dryer we went and picked up our new couch. It was good seeing Sierra, Tory and Logan, and nice of them to help us out.

Our apartment is coming together quite nicely. It’s not the house, but we are making it home. I miss my neighbors and the quiet of Hutto, but I love being in Austin with plenty of places to go and more things to do.  We don’t have to worry about what we are going to eat dinner if we forget to take something out, and on the weekends if we forget to get breakfast stuff, there are plenty of places to eat breakfast food.

Now off to finish treatments and get some sleep. Another week starting tomorrow, hopefully I can get some rest and not wear myself out.

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