Sunday, May 9, 2010

Bravo's Design by 9 Supports the Bone Marrow Donor Program

Do you watch the Bravo tv show "9 By Design?"

Their next episode airs on Tuesday May 11 at 10:00 PM on Bravo. It's a show that follows the husband and wife property design and developers as they work on multiple projects throughout the season.

I'm sharing this with you because part of the next episode will feature a fundraiser that was held for little Jasmina Amena. The hosts of the show, Robert and Cortney Novogratz, were personal friends of Jasmina before she passed away and are still friends with Jasmina's mom Thea. Because of what happened to Jasmina, Robert and Courtney were able to create a feature on their program to help spread Jasmina and Thea's message: To raise awareness about Leukemia and the need for more people to join the registry as willing donors.

You may remember reading about Jasmina here on Tami's blog in the past. She was an adorable and courageous little girl who got to meet President Barack Obama just weeks before she passed away. CLICK HERE for to read the memorial blogpost I wrote about Jasmina.

Friday, May 7, 2010

I Am an official SMART volunteer for Be The Match

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.

The journey I have taken into being a volunteer advocate over the past year has been more heartbreaking then 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.

Wednesday, May 5, 2010

Shaquille O’Neal Supports Be The Match

Read about Taylor on the Mid Dekalb news website by CLICKING HERE

Press Release from Be the Match:

Shaquille O’Neal has teamed up with Be The Match to challenge Americans to “Be the one to save a life.” Starting today, three public service announcements will hit the airwaves and the Internet to help the thousands of patients like Taylor John who need a marrow transplant.

Unlike most 15-year-old girls, Taylor isn’t eagerly anticipating her 16th birthday. She has severe sickle cell anemia and a marrow transplant is her best hope for a cure. But there is no matching donor in her family or currently on the Be The Match Registry. And because of the progression of the disease, doctors say Taylor may run out of time if a match isn’t found before her 16th birthday, which is this August.

Taylor and thousands of other patients are counting on the Be The Match Registry, whose 8 million volunteer members stand ready to become marrow donors. While many patients do find the life-saving match they need each year, more donors are needed, especially those from racially and ethnically diverse communities.

You can be the one who helps save a life. Take the first step by joining online at BeTheMatch.org.

Sunday, January 17, 2010

New Tutorials

Yesterday and today I added the following tutorials to the Marrow Drives website:






They're designed to help patients in need of a bone marrow or stem cell transplant to learn how to effectively launch their own marrow donor drives.


Thursday, December 10, 2009

African Descent Marrow Donor Urgently Needed to Save Zyreal

I'm begging here. If you are of African descent (No matter what continent you live on) and if you are not in a National Marrow Donor Program PLEASE consider joining to help save Zyreal. Also please forward this message to anyone you know who might be able to help him.

Zyreal is an adopted 7 year old boy who suffers from Sickle Cell Anemia. He recently underwent a cord blood (stem cell) transplant to save his life but today his family found out the transplant failed. This means he is now left with no working bone marrow. His body cannot produce new blood cells or platelets so for the time being he will have to rely on transfusions to buy him more time. A better match must be found ASAP if Zyreal is going to survive.

Ethnicity is crucial. Any patient in need of a marrow transplant will most likely find a match within their own ethnic group so Zyreal needs more people of African descent to join the marrow donor program in case they are the one who is going to be able to save his life.

___________________________________________

IN THE UNITED STATES

If you live in the United States please go to Be the Match and enter your zip code to locate a live drive in your area:

http://www.marrow.org/JOIN/Join_in_Person/index.html

It takes 4 cotton swabs that you wipe on the inside of your cheeks to find out if you are the match that can help Zyreal. It can then take up to 10 weeks for the test to be processed. Zyreal cannot wait so please do not delay in locating a drive.

___________________________________________

ALL OTHER COUNTRIES

There is also a list of international marrow programs at this link:

http://helpingtami.org/asian_stem_cell_transplant_int_marrow_programs.html

Please contact a program near you to locate a live drive. In most countries testing is simply swiping the inside of your cheeks with 4 cotton swabs. It can then take up to 10 weeks for the test to be processed. Zyreal cannot wait so please do not delay in locating a drive.

Wednesday, November 25, 2009

2 Easy Ways You can Help Janet Find Her Cure for Cancer!

1. Business Cards
These are Janet's new business cards. You can order some from me (for free) to hand out to friends, leave a pile on your desk at work for colleagues or customers or keep a few in your wallet or purse to hand out to people you meet. CLICK HERE to place an order online.

This is the front of Janet's business cards

And this is the back



2. Flyers
If you have a computer and a printer and somewhere to hang or hand out a flyer (i.e. your office at work, a community bulletin board, your church, a club or group, etc.) you can help me to help Janet. There are two parts to this flyer, the information sheet that you can print and hand out and the tear away tabs that can be added to the flyer for bulletin boards so that readers can take one with them to remember the website url when they go back to their computer.

(These links will open in new browser windows and may take up to 1 minute to load as they are high resolution, printable flyers.)

CLICK HERE to download the PDF of this flyer.

CLICK HERE to download the tear away tabs that can be attached to the bottom of the flyer.



And this is Janet. You can visit her WEBSITE by CLICKING HERE. There you can learn more about her, how to join the National Marrow Donor Program and leukemia. For current updates visit her BLOG by CLICKING HERE.

Will you help her by joining the registry or by spreading the word that she needs more help and more people to register?

On August 24, 2009, 22 year old Janet Liang was diagnosed with acute lymphoblastic leukemia, a form of blood cancer. Janet is currently living in the Bay Area and is undergoing chemotherapy in the hopes that she can attain a successful remission. If the chemo fails she will need a stem cell transplant. She will then be faced with the daunting task of locating a marrow match from the national or international registries after tests revealed that her only sibling is not a match. Processing new donor samples can take up to 2 months or more so it is crucial for people to be tested asap before her need becomes critical.

Already in the registry? No matter how long ago you signed up you will remain in the National Registry until you turn 61 years old. If you move or change your phone number you can update your contact information by CLICKING HERE.

Last year more then 4,400 people missed their opportunity to save a life when Be The Match was unable to locate them after they were a preliminary match for a patient in need.

Thursday, October 22, 2009

Chinese and Asian Americans Please Help Me to Help Janet Liang

People this is the real deal. Twenty two year old Janet Liang is a patient in critical need. She was diagnosed just months ago with acute lymphoblastic leukemia (bi-phenotypic).

This is Janet's desperate truth, her plea to help her save her own life that I read last night in her most recent blog post. Many of the people who she thought would reach out to help her have not:
"I became distraught because an urgent email was sent from a coordinator at Asian Miracle Matches to 70 of my closest friends in Southern California that I was willing to burden. Only 2 of them replied. No, I’m not popular at all."
I am hoping that all of you will reach out to help her. There is something you can do. You can join the registry or if you already have I implore you to reach out to anyone you know who is of any Asian ethnicity (particularly if they are Chinese) and ask them if they have joined the registry.

Janet's match could be anyone you know and of any Aisan ethnicity whether they are a friend, family or extended family member, a colleague, neighbor, or anyone you might happen to meet in your day to day life. The base requirements are that they are 18-60 years of age and in good health.

If they say they are not in the registry please direct them to any of the following websites to learn more about the pain free registration process and the donation process that is not, contrary to popular beliefs, excruciatingly painful. Most people who donate their marrow or stem cells suffer from relatively little discomfort if any at all. Nausea and a bruised sensation is usually the worst of it. They can learn more about the donation process on theHelpingTami.org website by CLICKING HERE.

They can also learn where live drives are held nationwide or how to order a home test kit at:

Live Drives Nationwide Using their Zip Code Locater
The National Marrow Donor Program website: www.BeTheMatch.org

Southern California Live Drives
Asians for Miracle Matches website: www.AsianMarrow.org

Northern California Drives
Asian American Donor Program website: www.AADP.org


More words from Janet:

"There’s an overwhelming amount of guilt I feel and frustration, because all I can do is keep asking and begging. That’s all I’m good for these days with no guaranteed promise of the ability to return your favors. I also understand that many of you have fruitful, promising lives/futures and are extremely busy. All I can really tell you is that I have about 3-4 months time to come up with some kind of bone marrow donor match. That is nearly impossible. The pressure is on, as my doctors and bone marrow transplant coordinator continuously remind me of the time-sensitive nature of treating this disease. If not, they’ll continue to drag it on and on, keeping me alive with one chemo round after another until I become resistant to it and there’s no other alternative except an umbilical cord transplant, which will buy more time and is currently in the research/experimental stages."