You Can Make a Life or Death Difference

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A name is added to the national organ transplant waiting list every 10 minutes. And each day, 18 people on that list die because compatible organs can’t be found in time. As I write this, a San Diego woman—Katrina Bischoff-Howell—is on that waiting list and hospitalized on a ventilator. (To the left is a photo of her taken during a somewhat “healthier” time, when she was on oxygen, but not yet on a ventilator.) Cystic Fibrosis has wasted her lungs and she now has a very small window in which she can receive a transplant…or never be transplanted. Her husband tells me that after two weeks on a ventilator, the body deteriorates and is weakened. He would know: He has CF, too, and received a lung transplant six years ago. Now it’s his wife who is in desperate need of one. You can read and watch her story here:
http://www.10news.com/news/28115787/detail.html

But rather than only read or watch her story, will you act to possibly save a life? Here’s a letter written by Katrina’s mother, which I share with her family’s permission:

Hello Friends and Family:

Yesterday, my daughter, Katie was moved to ICU at Thornton and was put on a ventilator. This means bluntly that we have only two weeks to discover two donated and fully vetted and qualified transplantable lung lobes or to have a cadaveric transplant and to successfully transplant those lungs. After two weeks on the ventilator there is no more opportunity for transplant. Moreover it is extremely tough for a CF patient to be able to live after being on life support for that length of time.

Here is exactly what you can do to help.

·· If you are under 55, have type A or O blood and are at least 5’ 9” and are willing to give up one of your five lung lobes to Katie, call my husband at (760) 579-8275 and we will get you tested to be a cross-match. Katrina is a very difficult match because of being transfused years ago and therefore her blood chemistry changed. The test to see if you are a suitable cross match is simple and painless. If you are a match, USC will take it from there.

·· Post the need for transplant donors to every friend and Facebook contact right now! Please ask them to consider giving one lobe to her IF they qualify. Please make certain that they understand how critical it is to act now.

·· Please ask your friends, family and congregations to pray for Katie now.

·· Because of the length of time it takes to find a donor…and now we have only two weeks to accomplish this…we can only identify potential donors for testing through this first week. Please understand that there is absolutely no time to waste.

Please I implore you to act now, right now. Please do not hesitate.

Thank you for your consideration in lovingly and prayerfully considering this massively bold request immediately. Please help me save my daughter’s life.

Do you want to know the amazing story of how I learned about Katrina’s situation? From my friend Sharlie Ross Kaltenbach—also living with Cystic Fibrosis. Here is a woman who is in need of a transplant herself, asking others to support her friend. I am not the least bit surprised that Sharlie is reaching out on behalf of her friend—that’s the kind of giving, loving and compassionate person I know her to be. Make no mistake, Sharlie is also in need—her lung function is at a mere 18%. That’s why those of us who love her have mounted a fundraising campaign to help cover the expenses associated with her needed lung transplant.

Here’s how you can help Sharlie: Buy a product from this website and personally ask three friends to do the same:

http://breathlessmom.com/products?r=4551

We believe in the power of three! Do you remember the movie Pay It Forward? The main character helped three people and asked them to “pay it forward” to three more people, so nine people would be helped. Then those people would multiply into 27. Then it would spread to 81. Then 243. Then 729. Then 2,187. And on and on. That’s the model on which we’ve based this fundraiser. We ask you to buy one product for $27 and ask three people to do the same and “give forward.” In a very short period of time, hundreds of thousands of dollars could be raised to fund Sharlie’s transplant and associated costs, with any excess going to others living with CF and to the Cystic Fibrosis Foundation for ongoing research for a cure.

All of the products offered will enhance your life, too! Please check them out here:  http://breathlessmom.com/products?r=4551, buy a product and ask three friends to do the same, to continue “giving forward.” Simple way to make a difference.

Another way to get involved is to sign up for the donor registry. You can do that here: https://www.donatelifecalifornia.org/ Will you join me? I’ve been on the registry since I first met Sharlie and her family about 20 years ago.

If you live in another state, go to the US donor registry site and search for your state: http://www.organdonor.gov

YOU can make a life-or-death difference. Will you?

Please share your thoughts, insights and questions below. Your participation provides wisdom that all can benefit from. Thank you!

Denise Yamada © 6/2011

 

1 comment to You Can Make a Life or Death Difference

  • Sad news to report: Katrina Bischoff-Howell went into kidney failure and passed away today, just as two lung lobe donors were found. Holding her family and friends in prayer tonight. Gratitude to all of you who forwarded her story with pleas from her mother for donors to be tested as possible matches.

    But our work is not done: We’re still raising funds for a transplant for my friend Sharlie, who also has Cystic Fibrosis. Please buy a product, ask 3 friends to do the same, share the link, save a life: http://breathlessmom.com/products?r=4551

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