Sunday, November 19, 2006

Match?

For those of you checking in on a Lars update, I exchanged emails with him briefly last week and he mentioned that they think they found a donor match. They still needed to track down the donor to see if that person was still willing to donate, so this great news should be termpered with the fact that he's still not out of the woods yet.

Hopefully I'll have more news before Thanksgiving. This shouldn't prevent anyone who is still thinking of getting tested from continuing to do so. There's still a chance that this doens't pan out. There's also the opportunity to synch with another person in need of marrow.

More to come on Lars later.

PS, I think his Buckeyes winning is a sign of good things to come :)

Thursday, November 09, 2006

Getting Tested in Ohio

Found these testing centers in Ohio:

Ohio
Center ID: 039
National Marrow Donor Program at Ohio and Indiana Region
2 Summit Park Drive
Suite 210
Cleveland, OH 44131
(216) 447-0880
(888) 862-7769

Center ID: 039
National Marrow Donor Program at Ohio and Indiana Area
995 East Broad Street
1015 Building, Room 101
Columbus, OH 43205-1322
(614) 253-7981, ext. 2417
(800) 338-8086, ext. 2366

Center ID: 076
Community Blood Center
Community Tissue Services
349 South Main Street
Dayton, OH 45402-2715
(937) 461-3296
(800) 388-4483
http://www.cbccts.org

Wednesday, November 08, 2006

Getting tested in Michigan

As this blog starts to make the rounds, wanted to make sure info like the following gets circulated:

Reader Nicole said...

To get on the registry in Michigan call 1-800-471-3020. The cost is $25 for caucasians, free for anyone else. They will send you a consent form, I got mine in a day, you mail it back and they send you a simple swab kit. All of the people that I have spoken to from the registry are very nice and helpful. PLEASE consider doing this, no one is more deserving than the Larsen family!!


Also, here are test centers in Michigan:

Center ID: 030
National Marrow Donor Program at Great Lakes Region
100 Mack Avenue
P.O. Box 33351
Detroit, MI 48232-5351
(800) 471-3020
Upcoming Donor Drives

Center ID: 030
National Marrow Donor Program at Great Lakes Region
3100 West Road
Park Place Business Center
Building B, Suite 202
East Lansing, MI 48823
(517) 337-2980
(800) 471-3020
Upcoming Donor Drives

Center ID: 029
Michigan Community Blood Centers
1036 Fuller Avenue, Northeast
P.O. Box 1704
Grand Rapids, MI 49501-1704
(616) 233-8604
(866) 642-5663 (in-state)
http://www.miblood.org

An Open Email

This is the email I've been circulating. Pass it on to anyone that you know...

Friends -

I'm writing to ask for your help. As many of you know, our friend Lars Larsen recently overcame a battle with non-hodgkins lymphoma after 6 months of chemotherapy and radiation therapy. We were all ecstatic that Lars was able to beat this awful disease. Never one to take the easy route, Lars was recently diagnosed with leukemia.

For those of you who don't know Lars, he is one of our dearest and oldest friends. He's that person who epitomizes the term "good guy". Only this good guy has been dealt a tough hand a second time in his life, so we're trying everything in our power to make sure he doesn't fight this battle alone.

In order to help him beat this disease, we're working to help find a suitable bone marrow donor. A marrow transplant will save his life, and we're determined to help find a match. We're asking all of our friends (and their friends) to consider the gift of marrow donation.

About 30% of all patients in need of a transplant are able to find a matching donor from within their families. The remaining 70%, however, must search the National Marrow Donor Program (NMDP) Registry of donors.

Sonya and I actually joined the registry back in the 90’s, but have yet to be identified as suitable donors for anyone as of yet.

We’re asking all of you to consider this test. Entry into the NMDP could help Lars as well as many other Leukemia patients who are in need of marrow transplants.

For those of you located in the San Francisco Bay Area, the Stanford Hospital Blood Center will run this test for free for any Caucasian donor who contributes a pint of blood. Minority donors may be tested without the blood donation free of charge.

You can schedule an appointment with the Blood Center by calling Derek or Diane at (650)723-5532

For those of you outside of the Bay Area, you can find donor info at http://www.marrow.org. or by calling Irma Naverez at NMDP (510)601-6233.

For more information on donating bone marrow, the NMDP has established a great FAQ at: http://www.marrow.org/DONOR/ABCs/index.html

I’m blogging info on general marrow donation and Lars’ progress at: http://marrowdonor.blogspot.com/ The information I listed in this email and much more can be found on this blog.

This is a huge sacrifice to make, but it is one that could save a life. Help us find a donor for Lars.

Sincerely,
Mike and Sonya Lee


P.S. You can also help by spreading the word. Pass this email on to a friend or co-worker.

Monday, November 06, 2006

ABCs of Marrow or Blood Cell Donation

Reprinted from: www.marrow.org - ABCs of Marrow or Blood Cell Donation

What is a marrow or blood cell transplant?
A marrow or blood cell transplant is a potentially life-saving treatment for patients with leukemia, lymphoma, and other blood diseases. A transplant replaces a patient's unhealthy blood cells with healthy blood-forming cells from a volunteer donor. Patients who do not have a suitably matching donor in their family may search the NMDP donor Registry for a donor. The three sources of blood-forming cells are marrow, blood-forming cells collected from the blood (called a PBSC donation) and umbilical cord blood.

How are patients matched with donors?
Blood or cell samples from adult donors or cord blood units are tested, and the tissue or cell type is added to the NMDP Registry. Doctors can search this Registry when they need to find a donor whose tissue type matches their patient's.

How does a person's race or ethnicity affect matching?
Because tissue type is inherited, patients are most likely to match someone of their same race and ethnicity. There is a special need to recruit more donors who identify themselves as: Black or African American, American Indian or Alaska Native, Asian, Hawaiian or Other Pacific Islander, Hispanic or Latino.

How are blood-forming cells collected?
Marrow donation is a surgical procedure performed in a hospital. While the donor receives anesthesia, doctors use special, hollow needles to withdraw liquid marrow from the donor's pelvic bones. Many donors receive a transfusion of their own previously donated blood. A donor's marrow is completely replaced within four to six weeks.

PBSC donation takes place at an apheresis center. To increase the number of blood-forming cells in the bloodstream, donors receive daily injections of a drug called filgrastim for five days before the collection. The donor's blood is then removed through a sterile needle in one arm, passed through a machine that separates out the cells used in transplantation, and the remaining blood is returned through the other arm.

Cord blood is collected from the umbilical cord after a baby's birth. The cord blood is taken to a cord blood bank where it is tested. Cord blood units that meet eligibility standards are frozen and stored for future use. The collection does not pose any health risk to the mother or baby, and does not affect the birth process in any way.

Does donating hurt? What are the side effects?
Marrow donors can expect to feel some soreness in their lower back for a few days or longer. Donors also have reported feeling tired and having some difficulty walking. Most donors are back to their usual routine in a few days. Some may take two to three weeks before they feel completely recovered.

PBSC donors report varying symptoms including headache, bone or muscle pain, nausea, insomnia and fatigue while receiving injections of filgrastim. These effects disappear shortly after collection. During the collection, donors may experience a tingling feeling or chills. These effects go away shortly after donating. When asked about their discomfort, most donors are quick to point out that it was worth it to help save a life, and they would be willing to do it again.

How does a patient receive a transplant?
After a patient undergoes chemotherapy and/or radiation treatment to destroy their diseased marrow, the healthy donor cells are given directly into the patient's bloodstream. The cells travel to the marrow, where they begin to function and multiply.

How does a person become a volunteer donor?
Potential donors must be between the ages of 18 and 60 years old and meet health guidelines. A small blood sample or swab of cheek cells is taken and tested to determine the donor's tissue type. Potential donors also complete a brief health questionnaire and sign a consent form to have their tissue type listed on the Registry.

Creating More Marrow Matches

Reprinted from The Marrow Foundation - Creating More Marrow Matches Through
Recruitment of Potential Donors with Diverse Tissue Types


Because tissue types are inherited, patients are most likely to find a match within their own racial or ethnic group. People of color represent only about one quarter of the total volunteer donors on the National Marrow Donor Program® (NMDP) Registry. Because the Registry holds fewer potential donors with the same racial or ethnic background, those communities of people are less likely than Caucasians to find potentially matched donors.

There is a special need for volunteer marrow donors from the Asian/Pacific Islander, Hispanic, and American Indian/Alaska Native communities. And the need to recruit more Black and African-American donors is particularly acute, because their heritage tends to be the most diverse. Every new potential donor could represent a unique tissue type. However, it has been shown that minority volunteer donors add unique tissue types to the Registry at a higher rate than do Caucasian volunteers.

While volunteer donors from all racial and ethnic backgrounds will continue to be the core of the Registry, The Marrow Foundation is devoting its resources to support the NMDP's efforts to recruit more ethnically diverse donors. In this way, the NMDP can assure that the Registry more nearly reflects our nation's population.

About 30% of all patients in need of a transplant are able to find a matching donor from within their families. The remaining 70%, however, must search the NMDP Registry of donors.

The Process to Join:

When volunteers join the NMDP Registry, they are tested to determine their HLA type. A small blood sample or swab of cheek cells is collected from the volunteer donor and tested to identify which HLA markers are present. Information on each potential donor is added to the NMDP Registry, which can then be searched by physicians who are considering a transplant for their patients.

Marrow Donation FAQ

I found a great Frequently Asked Questions post on bone marrow donations and the National Marrow Donor Program (NMDP) Registry on the AMA website at:

http://www.ama-assn.org/ama/pub/category/12080.html

Check it out if you have more questions on donating bone marrow.

How to become a marrow donor (SF Bay Area)

Reprinted from Stanford School of Medicine Blood Center - How To Become A Marrow Donor

Health & Safety Requirements
- Be between 18 & 60 years of age
- Weight normal for height and age (not more than 25% over)
- No auto-immune disease
- No personal history of cancer or diabetes
- No hip, neck or back problems
- No asthma

1. Contact Stanford Blood Center's Marrow Donor Coordinator and make an appointment to donate blood and request that it be screened for the National Marrow Donor Program (NMDP). Phone 650-723-5532 or e-mail NMDP_SMSBC@hotmail.com. A limited number of screening appointments are available to blood donors each week and at no charge.

2. Your blood will be HLA-Screened for the NMDP when you donate a pint for the community. HLA typing (Human Leukocyte Antigen) and virology (infectious disease) testing is done at Stanford laboratories. After eligibility is determined, your blood donation will be used to meet local patient needs. Your HLA type is entered at the Stanford Blood Center and forwarded to the National Marrow Donor Program electronically. The NMDP searches for matches for patients worldwide. Only the Blood Center knows donor names and addresses.

Note: The Stanford blood center offers marrow testing without blood donations for minorities.

3. When a preliminary match is determined by the NMDP, you will receive a call or letter from the Blood Center asking you to give another blood sample for further testing. If the tissue typing determines you are compatible, a special informational meeting with a Blood Center physician and the Donor Coordinator is scheduled. The Transplant Center caring for the recipient will inform us whether they want you to undergo Marrow Harvest or Peripheral Blood Stem Cell (PBSC) collection. After being fully informed, you then can make the final decision on giving your stem cells.

4. You will be given a complete physical exam at the Stanford Hospital and Clinics and meet the Transplant Team. There is no charge to the donor.

5. Prior to a bone marrow harvest, a donor gives at least one unit (pint) of blood for their own use prior to the marrow collection procedure in the event a transfusion is needed. PBSC donors receive granulocyte colony stimulating factor (GCSF) injections prior to their procedure.

6. Marrow/Stem Cell donations are scheduled at least two weeks in advance, giving the donor time to arrange business and personal commitments. Your "Living Gift of Life" will be delivered to your patient by the Blood Center staff and you will be released from the hospital the day after your donation.

7.The Blood Center staff will keep you informed of your patient's progress. The names of the donor and the recipient are kept confidential. Donors and recipients may sign a special release to allow direct contact one year after transplant.

Make an appointment via this online form now to donate blood and be tested. Testing facilities include:

Stanford Blood Center
780 Welch Road, Suite 100
Palo Alto

Stanford Blood Center
515 South Drive, Suite 20
Mountain View

Lars Bio

Lars Larsen's Bio:

Currently I am a 39 year old man with a wife named Monica and two children, Savannah, age 5 and Sorina, age 2. I grew up in San Jose California and attended Silver Creek High School and then attended San Jose University in which I graduated with a degree in advertising. After a few years I decided to go back to school studying sciences with hope of working in the medical profession. In 1993 I moved to Ohio and attended the Ohio State University. In 1995 I was accepted to the Ohio State University Dental School in which I graduated in 2000.

I worked five years as a dentist and then was diagnosed with non-hodgkins lymphoma. After a rigorous 6 months of chemotherapy and radiation therapy I was determined to be in remission. In September I had fallen out of remission and the disease had transformed into leukemia. I love my job but more important to me is the time I spend with my family. Although the disease has taken a devastating toll on my body it has brought me extremely close to my core family and my extended family.

Currently I am being treated for leukemia with hopes that my body will go into remission again and I will find a suitable bone marrow transplant match. My will to live is strong as I realize I have so much to live for. I am relying on complete strangers for a suitable bone marrow donation and I am thankful for anyone who is willing to give some of themselves so that I may live.

I thank you in advance for giving part of yourself in hopes that me or some other individual in my situation may benefit. You are truly providing somebody with the possible gift of life.

Regards,
Lars

Welcome to Marrow Donor




Welcome to marrowdonor.blogspot.com! This is a blog that has been setup in support of our friend Lars Larsen, who was recently diagnosed with Leukemia. Lars is a 39 year-old, married father of two beautiful little girls, currently living in Columbus, Ohio.

Lars originally hails from San Jose, California, which is where we met him. We're trying to rally support for him on his quest for a suitable bone marrow transplant. This is where you can help Lars, and the myriad of others who suffer from this disease.

We'll use this as a forum to track Lars' battle and to post information on donating bone marrow. Please spread the word, by passing this on to anyone you know.

Help us, help Lars.

Thanks,
Mike & Sonya Lee

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