Yesterday was Mebsie's 6 Month Anniversary of her Double Lung Transplant! I'm so very proud of her! She has spent roughly 5 of the past 6 months in the hospital dealing with complication after complication, yet she still came out on top! I am so honored to call her my friend! It's been a long journey, and it's really just beginning, but I know she can beat anything!
I just wanted to do a short update. Please forgive any typos that may appear in this blog, I don't usually blog from my phone.
Anyway, I'm currently in California! It's my last night. :(
I flew out for my friend's wedding, which I was actually in! I have known this friend for over 9 years, via the Internet. But this was the first time I met her in person! She's absolutely fabulous and I had a great time with her. I wish that I could stay longer, but unfortunately she needs to be admitted to the hospital, and I'm not feeling so well either.
Her wedding was on Halloween! It was lovely and she looked beautiful. Later that night I took her and Randy (her husband) out to eat. We went in costume, of course.
That's really the whole blog, but I felt it was important enough that it had to be posted. Now have some pictures.
I'm Kate, but my friends call me Ducky. I'm 26yrs old.
I'm have a huge heart.
I cry when I'm happy. And when I'm sad. I'm very sarcastic. I live online.
I hate the idea of smoking!
I'm a twin. (My sister died at 13months from Muscular Dystrophy)
I was employed as a PCT at a hospital. but had to leave for medical reasons.
I'm a huge supporter of organ donation.
I have been working with the Cystic Fibrosis Foundation since I was 16,(2005)(A friend with CF died on my 16th birthday). I'm addicted to charity work.
---For more info, check out my about me.
you all know my life's dream is to see the day when Cystic Fibrosis is cured!!
so make with the donations pleaseeeeeeeee ♥
and together we can make "CF" stand for "Cure Found"