Thursday, February 18, 2010

Late to the usual

Hey there, I'm lying here sick as a dog and catching up on email messages when I saw that I had missed a very important message.

My dear, dear blogging sister Kelli has been waiting almost 4 years for a new kidney. Obviously, this is an issue close to my heart. It is time for Kelli to get her kidney. Things are finally in place to test donors and the search has begun to save my friend's life. Since, as I mentioned, I'm really sick and coherent thoughts are not possible, I'm just going to copy and paste the information I received.

If you don't know Kelli, I highly recommend that you spend some time in the archives of her blog Living in Grace. After you get to know her, please consider how you might be able to help. Not only does Kelli need a living kidney donor, but she also needs financial gifts to pay for expenses associated with the whole process that insurance doesn't cover. Thanks for taking the time to pray for and help my friend.

I will now return to my not-quite-but-really-close-to-death bed.

Thank you for offering to be a part of the call for living kidney donors, and to help with our fundraising efforts. It is a true blessing for this family, and we love you all.

Here is the basic info on being a living kidney donor and the process. Feel free to put in out in whatever way you see fit, letting me know if you need further info or anything.

1) I will be listed with OHSU in Portland, OR. If someone is interested, they should contact us at and we will get them the contact info they need.

2) Because of some complications, I will most likely not be able to use a cadaver donor, although I have been listed with another hospital on the UNOS list for 3 years.

3) I will need donor with the A or O blood type. If you don't know your blood type, they will have you get tested.

4) All medical costs are billed directly back to OHSU where my insurance covers 100% of all incurred costs. This allows the donor candidate to have all testing up to the end done at their local hospital or Dr. office at on charge to them.

5) Pre-screening involves an over the phone health questionnaire, then a simple blood test where my blood and theirs are combined and cross-matched. If that is ok, then they will have a series of tests done locally to them and billed directly to my insurance.

6) All this will lead up to a scheduled date for everyone to meet in Portland for transplant. The process, from the time a suitable candidate is found, is about 3 months to the actual surgery.

7) Fundraising is currently under way for all costs not covered by insurance (all non-medical). This includes things like travel and lodging for the donor, my housing and support for the month or more I am required to stay in Portland after surgery, etc.

We are going to be using for the fundraising efforts.

The fundraiser is located at:

Thank you again everyone, and please let me know if I can give you more information.


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