Kaity Tong
Jun
15
7:43PM | June 15, 2009 | comments: 3232

Do You Think You Can Help?

The story that I report on in tonight’s newscast began with a blog comment. I do read the comments on all my blogs, and this one touched me right away. It was from a guy named Paul Blum, posted on my blog of May 15th, Response to Readers Comments.

It was a plea for help for his ailing wife, Eva, who will not live much longer if she doesn’t get a bone marrow transplant. She is Asian, and it is harder to find a match for minorities who need transplants for a variety of reasons.

I went to visit them in Fairlawn, New Jersey to hear Eva’s story. For 12 years she had MDS, or pre-leukemia, which did not get worse until this past April. She was visiting her daughter Rachel, a professional dancer in California, when she was struck with overwhelming fatigue. She got the bad news from her doctor. She was heading for full-blown leukemia and her time was running out. Her only hope, a bone marrow transplant.

While she waits, she is getting chemo treatments, which has weakened her immune system to the point that she is basically homebound. She told me,” Kaity, the highlight of my days now is the trip to my doctor!”

This, from a woman whose entire life has been about fitness and being active. She’s an avid gardener, horseback rider, she loves to snorkel, hike, traveling with her husband and family to exotic and adventurous places. She can no longer do any of these things.

Her son Jason is engaged to be married next June. They say they’re discussing making their wedding date much sooner. And Eva and Paul will celebrate their own wedding anniversary next year also, their 40th. That is, if she makes it.

Paul told me he wrote to me in desperation because, as he put it, “I thought maybe your celebrity could draw attention to this.” Well, I don’t know about celebrity, but Paul, we here at PIX will do what we can to help your wife. This is not the first story we have done, publicizing the need for more transplant donors to step up to the plate, and it won’t be our last.

Tonight, it’s Eva’s story.



A bone marrow drive for Eva is scheduled to take place on Sunday, June 21 from 11 a.m. to 2 p.m. at Ch'an Meditation Center in Elmhurst Queens. The address is 90-56 Corona Avenue.

In the meantime, if you want to know more about Eva's story and how to become a donor, you can visit her website.

To access the Cammy Lee Leukemia Foundation, click here.

For more information about joining the National Donor Registry, click here.

Bookmark and Share


Comments: 3232

Posted by chuck at June 15, 2009 9:13 PM

Kaity,

Best wishes to Eva & her family,and sincere hopes that everything turns out to be alright and a suitable donor match is found.

Posted by kman at June 15, 2009 10:27 PM

Godspeed, Eva.

Posted by KC at June 15, 2009 10:34 PM

I am Chinese, may be I am able to help...

Posted by Airam da Silva at June 15, 2009 10:38 PM

Hello Kaity,

Thank you so much for the bone marrow story. I know Cammy Lee and I also have a Foundation in which recruits marrow donors. Jim Watkins MC our Fundraising Events every year. I want to make ALL of our drives available for Eva to have her friends and anyone who wants to join. Please visit www.icla.org and look at the list of scheduled drives. We have all over.

Thank you,

Airam

Posted by lanthao at June 15, 2009 10:42 PM

thank you for the story.

a friend of my in LA mentioned this to me, and i registered in may, but the kit never came. you reminded of it so i just went on to eva site and tried to register again but the code had expired.

just thought you and eva may want to know about this.


Posted by Mel at June 15, 2009 10:45 PM

Hey Kaity,

I couldn't find a way to ask Eva, but I saw that the code that is listed on her site is either not activated or expired. Hopefully she'll have that remedied so more people can sign up for the cause.

Posted by jose rodriguez at June 15, 2009 10:48 PM

i 'll like to help send me the kit at
584 E 137th st apt#13G BRONX NY 10454

Posted by Gina Sampson at June 15, 2009 10:48 PM

i watching the news and saw that you can take a take home test and mail in. Where can I get the test? Please email to the above address. Thank you!

Gina

Posted by Anonymous at June 15, 2009 10:48 PM

The promo code does not work?

Posted by Anonymous at June 15, 2009 10:49 PM

The promo code does not work?

Posted by Mel at June 15, 2009 11:01 PM

If you guys read the post thoroughly, the link is on her website. Here's the link: http://www.marrow.org/JOIN/Join_Now_Special/Marrowthon09/join_now_mt09.html
However, the code doesn't seem to register for some reason or another, hopefully that'll be resolved soon.

Also, I don't know why people post their addresses online like that. Maybe there should be some sort of a disclaimer. To be honest, it's kinda dangerous about posting it on a message board IMHO.

Posted by lanthao at June 15, 2009 11:09 PM

just found a new code so that the test can be free, otherwise it's $52. i just registered. hopefully this time the kit wil be mailed to me....

code: ICLABTM09

Posted by dolores healy at June 15, 2009 11:12 PM

I was just diagnosed with CML, and my heart and prayers goes out to Eva. I pray someone comes to Eva's needs and donates the bone marrow.

May God Bless you.

Posted by dolores healy at June 15, 2009 11:12 PM

I was just diagnosed with CML, and my heart and prayers goes out to Eva. I pray someone comes to Eva's needs and donates the bone marrow.

May God Bless you.

Posted by dolores healy at June 15, 2009 11:13 PM

I was just diagnosed with CML, and my heart and prayers goes out to Eva. I pray someone comes to Eva's needs and donates the bone marrow.

May God Bless you.

Posted by Catherine at June 15, 2009 11:13 PM

http://www.matchforevalove.blogspot.com/ (this will link you to get a kit @ Marrow.org)

FACEBOOK/Groups-Bone Marrow Drive for Eva


Please check out these websights for Eva as well!

Posted by Mel at June 15, 2009 11:21 PM

Thanks for the code lanthao, it works.

Posted by catherine at June 15, 2009 11:39 PM

Lanthao-Thank you very much for pointing out that our current code had expired!!! We have updated our webpage at Matchforevalove.blogspot.com with this new code!

Thanks again!!!

Posted by KC at June 15, 2009 11:49 PM

I think I already have record in the NMDP system, any way I can verify that? If I am, I won't need this.

Posted by Catherine at June 16, 2009 12:02 AM

KC-try and order a kit for yourself, I would think that if you are already on the list, it will reject you from ordering a new one.

Thanks!

Posted by Cammy Lee at June 16, 2009 12:19 AM

Hi Kaity,

I hope a lot of people saw Eva's story. As Kaity mentioned, I recieved my life saving marrow transplant 16 years ago and am doing great! Those who would like to help Eva and others find her match, can request the kit and registration form from the Cammy Lee Leukemia Foundation Inc. at www.cllf.org

Posted by Linda at June 16, 2009 5:52 AM

I just saw your show about an Asian woman's plea for bone marrow. It puzzles me how particular people are chosen to appear on national TV when others requests go by the wayside.
I have a personal friend who is in great need of Howard's help and has been trying to reach him for months. I wonder what she might have to do or be to receive such attention.
I do wish the woman good health as well as any others who need help as well.

Posted by Bruce Solomon at June 16, 2009 5:58 AM

Kaity,

Being an anonymous donor myself through The Gift of Life I know the importance of this. Jay Feinberg from Gift of Life is a friend of mine.

Maybe they can help as well.

Let me know.

Thanks.

Bruce Solomon

Posted by Bruce Solomon at June 16, 2009 5:59 AM

Kaity,

Being an anonymous donor myself through The Gift of Life I know the importance of this. Jay Feinberg from Gift of Life is a friend of mine.

Maybe they can help as well.

Let me know.

Thanks.

Bruce Solomon

Posted by M Wong at June 16, 2009 10:09 AM

Where do I order the kit? I looked at several websites and can't locate it. Is there a charge to donate?

Posted by M Wong at June 16, 2009 10:09 AM

Where do I order the kit? I looked at several websites and can't locate it. Is there a charge to donate?

Posted by Amanda at June 16, 2009 10:47 AM

I hope you find your perfect match, Eva!

Please register as a life-saving donor today!

You can register anytime by going to http://www.dkmsamericas.org/marrow-donor-form

The testing fee is NEVER mandatory. DKMS only asks for donations to cover the tissue typing costs

Posted by paul at June 16, 2009 12:53 PM

if you register and donate thru Eva's website (above) there are no fees to pay at all!!!!

Posted by paul at June 16, 2009 12:53 PM

if you register and donate thru Eva's website (above) there are no fees to pay at all!!!!

Posted by Debra McCabe at June 16, 2009 1:32 PM

I am 42 years old and was recently diagnosed with MDS myself. I was told by my doctors that I have about 5-10 years before what is happening to Eva happens to me. My community on Long Island is having a bone marrow drive for me June 20th. I had never heard of MDS before this and When I saw Eva's story I could not stop crying for her and for myself. I want Eva to know that I am truly praying for her and hope that my drive may also possibly bring her a donor. I am so happy that you did this story, I do realize that different ethnic groups have a harder time finding donors and I thought that the story really was effective in explaining to people how easy it is to test and possibly be a donor and save a life. I wish people could really understand that this could be them or their loved one and would wish for the same from other people. We all need to do for one another.

Posted by Debra McCabe at June 16, 2009 1:32 PM

I am 42 years old and was recently diagnosed with MDS myself. I was told by my doctors that I have about 5-10 years before what is happening to Eva happens to me. My community on Long Island is having a bone marrow drive for me June 20th. I had never heard of MDS before this and When I saw Eva's story I could not stop crying for her and for myself. I want Eva to know that I am truly praying for her and hope that my drive may also possibly bring her a donor. I am so happy that you did this story, I do realize that different ethnic groups have a harder time finding donors and I thought that the story really was effective in explaining to people how easy it is to test and possibly be a donor and save a life. I wish people could really understand that this could be them or their loved one and would wish for the same from other people. We all need to do for one another.

Posted by Sal Butta (Cel Art Film Service) at June 16, 2009 1:50 PM

Hi Eva, I saw your story on the WPIX news with Kaity Tong. I'm sorry to hear that you're ill and hope a donor will be found quickly to help you get better. I have many fond memories working with you at Cel Art. Regards to Aileen and Juliana. Cant believe all these years have gone by. Good luck. You'll be in our prayers.

Posted by Sal Butta (Cel Art Film Service) at June 16, 2009 1:50 PM

Hi Eva, I saw your story on the WPIX news with Kaity Tong. I'm sorry to hear that you're ill and hope a donor will be found quickly to help you get better. I have many fond memories working with you at Cel Art. Regards to Aileen and Juliana. Cant believe all these years have gone by. Good luck. You'll be in our prayers.

Posted by ASIANS FOR MIRACLE MARROW MATCHES at June 16, 2009 2:53 PM

HELLO EVERYONE! SORRY FOR THE CONFUSION. HERE IS HOW YOU CAN HELP:

1. Log on to join.marrow.org. The promo code to use is "marrow99". USE THIS PROMO CODE AND NOTHING ELSE!!

2. Email me at gsanagustin@ltsc.org if you would like to request a home kit. I will send it to you by mail. Email me your: name, mailing address, phone number, and ethnicity.

3. Attend a bone marrow drive. A complete listing organized by zipcode is available at marrow.org. You may also email me where you are from and I will let you know where to go.


For all other inquiries (volunteer opportunity, hosting a drive of your own, etc.), email me at gsanagustin@ltsc.org or call me at (213) 625-2802 ext 107.

THANK YOU

Posted by J.Hein at June 16, 2009 3:57 PM

Dear Kaity,

Wanted to commend you for trying to help Eva and
spread the word re Leukemia & bone marrow transplants.

Note to Eva: I will say prayers for you that you receive an acceptable donor real quick. Lots of Good Luck & more years of happiness. I have been diagnosed recently w/CLL & hope to live a longer life, too.

Thanks for sharing.

Posted by Maureen Duggan at June 16, 2009 6:05 PM

I have worked with Eva at Grand Union. I have been registered as a bone marrow donor for at least 15 years. Hopefully, mine can help if suitable.

Posted by Maureen Duggan at June 16, 2009 6:05 PM

I have worked with Eva at Grand Union. I have been registered as a bone marrow donor for at least 15 years. Hopefully, mine can help if suitable.

Posted by mc in PA at June 16, 2009 8:50 PM

A great story that hopefully will help have great results. I wish Eva best wishes in finding a match and I commend you,Kaity, for bringing this issue to the public's attention.

Posted by suiling feng at June 16, 2009 9:30 PM

Hi Kaity,

I am Eva's sister, Thank you so much for helping her. We are doing a drive this Sunday at ChanCenter.Today, World Journal also wrote an article about Eva. I'll be glad to help anyone who has difficulty to get a kit. My tel:516-484-6737
many thanks! Suiling

Posted by KC at June 16, 2009 11:09 PM

Instead of being rejected from ordered the kit, is there a better to to verify whether I am already in the system?
I did the test some years ago, but I want to verify.

Posted by SuiLien Feng at June 17, 2009 1:56 AM

Hi Kaity:
Thanks so much for the great story for my sister Eva. Eva was helping my older sister to fight for a breast cancer 12 years ago, when she first diagnosed with MDS. She could put her illness behind and visited my sister at hospital every day. I admired her braveness and being such careful person. Today she has to fight for her own illness. She still stands as brave and strong as 12 years ago. I hope she will be the lucky one can find a match and thanks for all of you who have be involved to encourage her

Posted by Glenn San Agustin at June 18, 2009 2:27 PM

Hi KC,

Glad you asked. There is no need to re-register if you have already done the test in the past. You are automatically removed from the registry when you turn 61.

To check if you are already registered, please call the Be The Match marrow registry at 1-800-MARROW-2 (1-800-627-7692). They can check if you are already registered and you can also update your information over the phone.

Email me if you have other questions. My name is Glenn and my email is gsanagustin@ltsc.org.

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