Today marks one year since this journey with my new liver began. I have been thinking a lot about how things were before. I do this to keep perspective on how far I have come in the past year. There are mixed feelings about almost everything as I look back. There are things that I have done since surgery that I wish I hadn't. There are many more things that I wish I would have had the courage to do.
The past year has both flown and creeped by all at once. Looking back, I can't believe that a year has past, but as I was going through some of the trials it seemed so slow. I have had relatively few setbacks, the main one being the sinister CMV.
Today was a great day, though I was tired. Craig and I spent the weekend in Bristol at the race and got home around 3:30 AM. Three hours later, I was out of bed and getting ready for work. The day was non-stop with surprise after surprise. The people that I work with went completely out of their way to make today all about me and the transplant. Through some sneaky planning, my class made pancakes for me(blueberry with peanut butter, my favorite), my co-workers made a huge spread for lunch, and the faculty showed up for a party at the end of the day. They also had a lady from Lifelink (the organ procurement agency for Georgia, Florida, and Puerto Rico) come discuss organ donation with the faculty and give out some Donate Life goodies. The school wore green today for organ donation awareness and I knew nothing of the entire thing. I, of course, was wearing my green "Recycle" t-shirt (photo to come). There were some sneaking suspicions, but I never imagined the extent they would go to make me feel special. I am not the type who enjoys being the center of attention. I actually tend to shy away from the spotlight, but today was nice. It is a great feeling to know that you have people who are there for you. That people are willing to take time out of their busy schedules as moms and teachers to plan something that is special to me. Organ donation has become one of my passions and I am trying my hardest to get more and more into furthering the cause in any way that I can. The people that I work with realize this and are helping me to meet this goal. These types of things do not go unnoticed. I will honestly remember this day for the rest of my life. I cannot remember a day where so many people came together to show me that they love me. It still amazes me and more than once today it choked me up, and is again as I type this.
It is so easy to lose sight of all that you have to be thankful for. There is the obvious, the transplant, that is the reason that I am here and able to type this today. But there are many other things that I have to be thankful for. I am thankful for the donor family, who in extremely hard times, were unselfish enough to donate their loved ones organs to me and possibly others. I intend on writing a letter to them when I find words that can BEGIN to wrap around the love that I have for those people. There are my friends and coworkers who show their love everyday, in ways they do not even know. They show their love even in times where I am extremely close to unlovable. My family, who has stood beside me through this entire process. There have been many ups and downs that they only know about, and even more that Craig only knows about. He has been the one that I lean on, he has been the one that I can tell when I hit rock bottom. He is the one who constantly pulls me back up when I am ready to give up. That has been more than once. Sarah, though she came after the surgery, has been another person that I can tell anything to in confidence and know that I will not be judged. She has been my motivator and does not let me use the transplant as an excuse to give up on anything. For that I am thankful because there are times that I get lazy and would use it as a crutch. She pushes me to better myself constantly. There are so many people that I could name that have been an inspiration to me. There are the doctors and the nurses on 9E and in the transplant clinic who never told me that my goals were unreachable. They told me they were lofty, but that I should shoot for them. If any of them happen to read this, I want them to know that each one was met. I returned to work in August, I went hiking, I am back on my mountain bike, I am working out, and I am enjoying life like I never thought that I would again.
There are many things that I haven't done and at times I feel like I am still not living. I want to step out of my comfort zone and make a difference in the world. I don't need to make a big difference, just a little ripple will be fine with me. I want to make my donor and their family proud. I want them to know that their decision was not made in vain. Their loved one is living on inside me and I tell our story everywhere I go. I am thankful for so much and this post barely scrapes the surface of all that I am feeling at the moment. I thank God for giving me the faith to trust in him, the strength to carry on through hard times, and the time to make a difference in the world for him. I want Him to be proud of me when it is my time to go more than anything else. Happy 1st transplantiversary to me! Happy 1st transplantiversary to my donor! Happy 1st transplantiversary to all those who have stood by me and loved me through it all.
3.26.2007
3.20.2007
2 for 1 deal
As I was checking my email this morning, I noticed the top story on Yahoo! was about liver transplantation. It was an awesome story which will no doubt raise ethical concerns in the near future. As a transplant recipient and knowing about the organ shortage it was nice to see that organ donation and transplantation had front row seats on one of the most popular websites on the internet!
The story told of a 21 year old college student who got the call that she was to receive a new liver. When she got to the hospital, she learned there was a baby girl who was in serious need of a liver as well. She asked the doctor if he could split the liver and give part to the baby. The liver is able to regenerate itself in about a month with enough blood flow. Most pediatric livers use only one lobe of the liver and often times the other is given to someone else or thrown away. The doctor agreed to split the liver and now two lives were saved with one organ.
This is a fascinating story about a brave girl who was willing to risk her chances to save someone else. She is my newest hero! That is one heck of an example of unselfish love for your fellow man. I applaud the doctor for taking the chance as well as the young lady who was able to be so unselfish at a time when she had every right to be selfish!
The story told of a 21 year old college student who got the call that she was to receive a new liver. When she got to the hospital, she learned there was a baby girl who was in serious need of a liver as well. She asked the doctor if he could split the liver and give part to the baby. The liver is able to regenerate itself in about a month with enough blood flow. Most pediatric livers use only one lobe of the liver and often times the other is given to someone else or thrown away. The doctor agreed to split the liver and now two lives were saved with one organ.
This is a fascinating story about a brave girl who was willing to risk her chances to save someone else. She is my newest hero! That is one heck of an example of unselfish love for your fellow man. I applaud the doctor for taking the chance as well as the young lady who was able to be so unselfish at a time when she had every right to be selfish!
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3.08.2007
Q&A update
Yesterday was the Q&A at Children's Healthcare of Atlanta. It went surprisingly well even though I could barely talk! It never fails that I lose my voice on the days that I am required to talk in front of people. Oh well, it was a very informal support group type meeting so no big deal. I think that Jenn and I did a pretty good job and hopefully calmed some of the parent's fears. I feel for the parents of these children who are never going to know a life without medication and doctor's appointments. I hope that seeing Jenn and me as productive citizens post-transplant will give them hope for their children to live fulfilling lives.
We got some good feedback from some of the people running the show and have invited us back for something similar in the future. I can't wait to go again. I honestly think I could do that everyday. It has been exciting meeting so many people here lately who are passionate about organ donation and transplantation. I admire each one of them, but some have never even been directly affected, those I really admire. They have a love and a passion for others that hopefully one day I will realize. They amaze me.
18 days until my 1st transplantiversary!!
We got some good feedback from some of the people running the show and have invited us back for something similar in the future. I can't wait to go again. I honestly think I could do that everyday. It has been exciting meeting so many people here lately who are passionate about organ donation and transplantation. I admire each one of them, but some have never even been directly affected, those I really admire. They have a love and a passion for others that hopefully one day I will realize. They amaze me.
18 days until my 1st transplantiversary!!
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3.01.2007
Walking and Riding for Organ Donation
Next Wednesday is the big day! I am going to talk to the group of parents at Children's Healthcare of Atlanta and I am getting excited about going. I am going into this blind, not knowing what to expect but I am looking forward to talking to people about my experience with transplantation. I have no idea what I am going to say. I hope that I will be able to say something worthwhile to the parents. Brent left a comment on my earlier post telling me to be honest about my feelings. He said that the parents are wanting to know what is going on inside of their children emotionally so they can help. I think that was great advice and I will be taking that with me to the session.
I have also been in contact with others who are active in the organ donation world. It seems I have been meeting lots of wonderful people lately. First there was Kim, from Pensacola, which I mentioned in an earlier post.
In the past week, I have been fortunate enough to speak with two other people through email. The first was a lady named Amanda Prather from Jasper, Ga. Her father received a kidney from her sister through the living donor process two years ago. She is organizing a walk for organ donation in Jasper on April 14, 2007. The name of the walk is Donate Life Walk: Raising Awareness One Friend At A Time. Here are pictures from last years 1st annual walk. If any of you are willing to walk, I am going to try and get a group from Dahlonega to head over to Jasper that morning to show our support for organ donation as well. If you are interested let me know and I will get you a registration form. There is a registration fee that includes a T-shirt. All of the proceeds will go to support the Georgia Transplant Foundation.

The other person that I have been talking to is from California. (This is where technology amazes me. I never would have known about Team Donate Life, let alone talk to someone involved if it weren't for the internet.) Kent Mulkey and I have been exchanging emails lately about biking and organ donation. Mr. Mulkey is riding in the Race Across America (RAAM) for Team Donate Life. He will be riding over 1500 miles in 8 days on a bicycle. He became involved in organ donation after his best friend and best friend's dad went through the living donor process. He is now the main man in charge of Team Donate Life as well as his own life. Check out Kent's blog, An Unfinished Life. It is an inspiring one!
I think that it is cool how many doors have been opening up lately for me to get to know so many people in the organ donation community. I enjoy meeting everyone and hope to meet many more in the future!
I have also been in contact with others who are active in the organ donation world. It seems I have been meeting lots of wonderful people lately. First there was Kim, from Pensacola, which I mentioned in an earlier post.
In the past week, I have been fortunate enough to speak with two other people through email. The first was a lady named Amanda Prather from Jasper, Ga. Her father received a kidney from her sister through the living donor process two years ago. She is organizing a walk for organ donation in Jasper on April 14, 2007. The name of the walk is Donate Life Walk: Raising Awareness One Friend At A Time. Here are pictures from last years 1st annual walk. If any of you are willing to walk, I am going to try and get a group from Dahlonega to head over to Jasper that morning to show our support for organ donation as well. If you are interested let me know and I will get you a registration form. There is a registration fee that includes a T-shirt. All of the proceeds will go to support the Georgia Transplant Foundation.

The other person that I have been talking to is from California. (This is where technology amazes me. I never would have known about Team Donate Life, let alone talk to someone involved if it weren't for the internet.) Kent Mulkey and I have been exchanging emails lately about biking and organ donation. Mr. Mulkey is riding in the Race Across America (RAAM) for Team Donate Life. He will be riding over 1500 miles in 8 days on a bicycle. He became involved in organ donation after his best friend and best friend's dad went through the living donor process. He is now the main man in charge of Team Donate Life as well as his own life. Check out Kent's blog, An Unfinished Life. It is an inspiring one!
I think that it is cool how many doors have been opening up lately for me to get to know so many people in the organ donation community. I enjoy meeting everyone and hope to meet many more in the future!
Labels:
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organ donation,
PSC,
transplant,
waiting list
2.23.2007
March 7 - Parent Q&A
Well, I have been kind of dry lately. Not so much across the board, but about organ donation and anything to write on here. As always, I have plenty to say but I am trying to keep this blog semi-focused. I am still wondering about the direction it will take. I am sure that it will still focus on organ donation, struggles with transplantation, others going through the process, and me as well. I am just wondering if I need to expand it a little to include some of my bigger thoughts about other things that I feel should be shared. I don't know. Guess I will ponder it more. Any feedback would be appreciated as well.
As for me, I am doing well. I got a couple of weeks off of going to the doctor which is great. My truck is thanking me that is for sure. I changed my oil 3 weeks ago and have driven 1900 miles since then. I didn't realize I was on the road that much until I started logging it.
I am looking forward to March 7 with much anticipation and nervousness. I have never been really good at talking in front of people, though in the past 4 or 5 years I have forced myself to do it a great deal. For those that know me can attest to the fact that I am painfully shy when the group gets above 3 or 4. I basically shut down in the conversation that is taking place.
On March 7, I am going to Children's Healthcare of Atlanta to speak to a group of parents. I will be on a panel of 7 young adult organ transplant recipients answering questions for parents of children who are waiting for a transplant. We will be telling them how transplantation has affected our lives. I feel for these parents who are no doubt worried about whether their child will be able to live a normal life. I am not a parent and don't really understand that side of the card, but I do remember how nervous I was about my own life changing. I am happy to say that it has been the catalyst for the improvement in my quality of life. I have taken up some things that I had given up when I was sick and also made some changes in my life that are much healthier. I hope that through this experience, the parents will be more at ease with how their children will live post-transplant. I am exciting about the opportunity to speak, but I am nervous about opening up in a public setting. I say a lot on this blog that I would never say in person; it is easy to hide behind the computer screen!
Guess I wasn't as dry as I thought.
As for me, I am doing well. I got a couple of weeks off of going to the doctor which is great. My truck is thanking me that is for sure. I changed my oil 3 weeks ago and have driven 1900 miles since then. I didn't realize I was on the road that much until I started logging it.
I am looking forward to March 7 with much anticipation and nervousness. I have never been really good at talking in front of people, though in the past 4 or 5 years I have forced myself to do it a great deal. For those that know me can attest to the fact that I am painfully shy when the group gets above 3 or 4. I basically shut down in the conversation that is taking place.
On March 7, I am going to Children's Healthcare of Atlanta to speak to a group of parents. I will be on a panel of 7 young adult organ transplant recipients answering questions for parents of children who are waiting for a transplant. We will be telling them how transplantation has affected our lives. I feel for these parents who are no doubt worried about whether their child will be able to live a normal life. I am not a parent and don't really understand that side of the card, but I do remember how nervous I was about my own life changing. I am happy to say that it has been the catalyst for the improvement in my quality of life. I have taken up some things that I had given up when I was sick and also made some changes in my life that are much healthier. I hope that through this experience, the parents will be more at ease with how their children will live post-transplant. I am exciting about the opportunity to speak, but I am nervous about opening up in a public setting. I say a lot on this blog that I would never say in person; it is easy to hide behind the computer screen!
Guess I wasn't as dry as I thought.
Labels:
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liver,
organ donation,
PSC,
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waiting list
2.14.2007
National Donor Day

Today is National Donor Day! Yes, I know it is Valentine's Day as well and hopefully everyone is having a great one. You girls are getting all the gifts you want from your men and guys.....hopefully you will get whatever you are waiting for from your girl. For just a few minutes though, I want to shift your focus to something that is important to me, organ donation.
On this day that is characterized, thanks to Hallmark, as the day that we show our love to those around us, remember there are some out there who will lose a loved one because of a shortage of donated organs. I am not writing this to change anyone's mind about organ donation, I just want everyone to have some facts about the process.
- Almost 100,000 men, women and children currently need life-saving organ transplants.
- Every 12 minutes another name is added to the national organ transplant waiting list.
- In 2005, there were 7,593 deceased organ donors and 6,895 living organ donors resulting in 28,108 organ transplants.
- An average of 18 people die each day from the lack of available organs for transplant.
- 90% of Americans say they support donation, but only 30% know the essential steps to take to be a donor.
I encourage you to evaluate your stance on organ donation today. If you choose to become an organ donor, know the steps to make sure your organs are donated. You can find out your state's requirements by going here. If you live in Georgia, you can become a donor by marking the option on your license and by signing a donor card. In Georgia, your family is ultimately the people who decide if you will become an organ donor. Be sure to let them know your wishes concerning organ donation upon your death.
This being National Donor Day, I want to encourage everyone to donate blood and bone marrow, as well as their organs and tissue. 60% of people are eligible to donate blood, but only 5% of the population actually donates!
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2.11.2007
Therapy

Today, I did what I have been wanting to do for a long time. I went back to one of my favorite places, Preacher's Rock. This was one of those places that I went to a lot when I first found out that I had a liver disease and it seemed my life was changing for the worse. If nothing else, it seemed at that time like my life was in a blender and I had no idea what this drink was going to taste like when the blades stopped. I used to go up there to just sit and clear my head. It is one of those places for me that I can "breathe." From this rock, the world, it's problems, my problems, and even I seem insignificant. This is the ultimate meaning for the metaphor of being "on a mountain" versus "in the valley." Life seems okay and good when I am up on the mountain and the problems "down there" seem to melt away. I haven't been up there in a little over two years and it was so much better than I remember. I am sure that nothing really has changed in those two years, but my memory had failed me at just how beautiful it is "in my little heaven." I have had some tough times alone on that rock, some arguments with God and myself, as well as some good times with God I will never forget. There are a lot of my feelings up on that rock and today more were left. This time I am glad to say that they were positive feelings.
I went up there today with a purpose of getting a picture of me, an organ transplant survivor, for Kim, a lady who lost her son to cancer shortly after receiving a liver transplant. She is now a strong proponent for organ donation and shares the story of her son, Willam McMahon, with countless others. Kim had sent me a shirt and asked that I take a picture wearing it. I decided I would go back to my favorite place, a place I would never have been able to return to without a new liver. I am glad that I did. I was able to find my center again and realize that what I am going through, though tough and sometimes aggravating, is not so bad. I was able to have some quiet time up there and reflect on how good God has been to me. I was able to say a prayer for Kim and to think about William. This is a public thank-you to Kim, for the shirt and for giving me the reason to return to "my little piece of heaven." I encourage you to read William's story.
If you are not an organ donor, I encourage you to become one. By donating your organs, you could save up to fifty lives.
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2.03.2007
Organ Donor Waiting List hits 95,000
I just wanted to post this to get you thinking about the need for organ donors. I know it isn't a comfortable topic and not what you want to be thinking about on a beautiful day. There are people out there today who are waiting, wondering if they will get their organ before it is too late. I have been there, I understand. Please consider becoming an organ donor, and if you decide to do become a donor, INFORM YOUR FAMILY OF YOUR WISHES! THEY ARE THE ONE'S WHO MAKE THAT DECISION IN GEORGIA! Waiting list candidates as of today 11:22am | |
---|---|
All ![]() | 95,066 |
Kidney | 69,983 |
Pancreas | 1,745 |
Kidney/Pancreas | 2,389 |
Liver | 16,988 |
Intestine | 239 |
Heart | 2,857 |
Lung | 2,864 |
Heart/Lung | 135 |
![]() |
Transplants performed January - October 2006 | |
---|---|
Total | 24,445 |
Deceased Donor | 18,793 |
Living Donor | 5,652 |
Based on OPTN data as of 01/26/2007 |
Donors recovered January - October 2006 | |
---|---|
Total | 12,401 |
Deceased Donor | 6,750 |
Living Donor | 5,651 |
Based on OPTN data as of 01/26/2007 |

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2.01.2007
The Dog in the Snow....FUN!!
I took Mia out in the snow for a little bit today. She loves getting hit in the face with snowballs!! I think she has some "special" problems. I got some good pics out of the deal though. Thought I might share!



Here is a pic of Cas, too!



Here is a pic of Cas, too!

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Snow Days in Georgia

Gotta love snow days in Georgia!! This is a ton of snow for us! That is a 20 oz Dasani water bottle in the snow! I have no real desire to go out in it....but it sure is pretty to look at and it got me out of work for a day!


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