Do I have anything to say?: The Life-a-Thon

Thursday, May 31, 2007

The Life-a-Thon

Organ and tissue donation is an issue very close to my heart because of the work I do. Because of this, I decided earlier this year that I wanted to run the 10K at the "Life-a-Thon" this year, an event to promote organ and tissue donor awareness and also to celebrate donor families. Five or six years ago, I did a couple 10Ks and a few 5Ks, but hadn't really run much since then. When it was about 5 weeks before the race, I decided it was time to "train". My training consisted of running 5 or 6 times, the farthest being 4 miles 5 days before the race. Somehow I managed to run the entire race (it took me a little over 70 minutes to run the 6.2 miles, but I did it!). I think it was because of the cause (and probably a few special angels cheering me on!). The photo above is me after the race with a transplant recipient and her sister, who probably will also need a transplant someday.

***More than 94,000 Americans are currently waiting for an organ transplant. Over 2,000 of them are children. Approximately 17 patients die each day, before receiving their lifesaving organ transplant due to the organ donor shortage.***

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Privacy Statement

This blog purposefully is left full name and location free out of respect to my family and to my patients/families. Due to the nature of my work, and having foster children in my home, it is important to maintain privacy and confidentiality. All photographs of patients were either given to me by the families or taken with family permission. Thank you for your understanding and support in helping me protect myself and "my people" =) If you have any questions, or want to know more about me, feel free to email me at iloveblogs44 {at} gmail {dot} com.

Who's Who

Updated September 2013

I have one sister who is married and has two boys. "A" was born June 2009 and "I" was born March 2012. We are both really close to my parents and have lots of "family dinners".

I wrote a lot about my patients when I first started this blog. Some patients are still growing and thriving, and others have lost their battles.

My first foster placements lived with me from June 2010-September 2011. They were sisters who were 15 and almost 3 when they were placed with me and are now 18 and 5. I called M "the teen" and L "the little one". They live with their mom who still has many issues, but are doing well (ok) and I still have (not enough) contact with them.

My second foster placement came to me September 6, 2012. I call her Zoe and she turned 5 in April. She has cystic fibrosis and has been a patient on my floor at the hospital. The plan is still reunification.

Ivy is a 17-year-old whose mom died just before Thanksgiving. She has a Guardian, but is unable to live with him due to some family issues. She has no other family who is willing/able to take her. She moved in with me the beginning of February. She moved to a group home at the beginning of August as her needs were too great for me with my schedule and having another child with special needs.