To Read Tami's Story from the Beginning

Just CLICK HERE. Her blog begins on March 12, 2009 with a post titled "Tami's Myelodysplasia Diagnosis." Then at the bottom of each post, click on the words "Newer Post" located just below the comments section on each page.

Friday, May 7, 2010

I am an official SMART volunteer for Be The Match

Stacie here: At the end of last year I was contacted by a representative from Be The Match (The National Marrow Donor Program) who informed me that they had noticed the volunteer advocacy work I had been doing online to help my cousin Tami and other patients who needed to find marrow matches to save their lives.

They had noticed there were many people like myself, out there doing their own thing to raise public awareness about Be The Match. So they wanted to create a program that would offer us up to date information as well as an actual liaison at Be The Match who could assist us in our online advocacy efforts. Great! I need all of the help I can get.

I was asked to a part of a focus group that would help to develop information for the program over the course of several weeks. I joined the group, answered lots of questions, then they took that information and developed the "Social Media Action Response Team" program and I'm very excited to say that I am now an official "SMART" Volunteer for Be The Match. You can read about the volunteer program in their BLOG by CLICKING HERE.

The journey I have taken into being a volunteer advocate over the past year has been more heartbreaking than joyful but ultimately even through the sadness it is rewarding because even though many of the patients I wish had found matches in time didn't, it doesn't mean that the effort to help them was wasted. In fact the patients themselves are usually the first to point out that even if a match isn't found for them, they know that people who joined the donor program to try to help them, might someday help another patient in need, and that means the world to them.

Yesterday was a bittersweet day.

Rob Harder is a young man who was entering the prime of his life in 2009 having just graduated from college. Early last year he was diagnosed with an Aggressive T-Cell Lymphoma. He set up a blog, a Facebook Group (which is how I met him) and shared his story with the world. Yesterday his family posted on his Facebook Group that he is nearing the end of his battle and on his behalf, bid his friends and fans farewell. (ETA: Rob did pass away that same evening. May he RIP)

At almost the same moment that Rob's family posted that he was not in pain and surrounded by his loved ones, who want to be there to comfort and love on him as he passes, little 8 year old Natalie Nakatani's family posted on Facebook that she had finally received her bone marrow transplant yesterday and now has a chance at surviving the Acute Myeloid Leukemia she suffers from. You might recall from a previous post that her doctors had given her less than 6 weeks to find a match before they felt it would be too late, when, with I think less than 2 weeks left, an international donor match was found for her in China.

What has become normal for me is simply fielding some questions to the proper places that can help those in need. For instances a few weeks ago I received a desperate plea for help from a man in Europe who was told there was no hope for a transplant for his condition because the cost was too prohibitive and another inquiry from someone here in the U.S. who wanted to set up a donor drive for their sick cousin. I was able to direct both of them to the proper agencies who could help them. The man in Europe I found a group that might be able to get him into a clinial trial offering some hope and more time with his family. The woman in the U.S. I was able to direct to both Be The Match and DKMS to help her set up a donor drive.

So emotionally it is often hard on a good day and absolutely heartbreaking on a bad day. But I believe if more people get involved and if more people are willing to donate their stem cells or marrow to a stranger in need, we can turn this whole thing around and begin saving more patients instead of watching them wait and wait for a marrow match that never comes or is found too late. The donation process has become very straightforward using a newer method 75% of the time called Peripheral Blood Stem Cell donation (PBSC) where the stem cells can be harvested through your blood instead of marrow being extracted from the hip bone. CLICK HERE to learn more about the 2 donation methods.

Each of us can make a difference. We can be willing to donate our marrow or stem cells to a patient in need and/or help encourage others to join the marrow registry. Please contact me if you have any questions at all. I'm happy to help find you some answers.

1 comment:

  1. You will do a stellar job! Thank you for being such an amazing resource. Let me know if they're looking for other help as I'd be happy to volunteer as well.