- Q:
Why is there a need for people to join the Be The Match Registry?
-
A: Thousands
of patients with leukemia and other life-threatening diseases
depend on the Be The Match Registry®
to find a match to save their life.
Patients need donors who are a genetic match. Even with
a registry of millions, many patients cannot find a match.
Donors with diverse racial or ethnic backgrounds are especially
needed.
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- Q:
I'm already on the NMDP Registry. Do I need to join the Be
The Match Registry, too?
-
A: Be
The Match Registry is the new name for the National Marrow
Donor Program (NMDP) Registry. If you joined the NMDP Registry,
either in person or online, you are a member of the Be The
Match Registry and do not need to join again. The name has
changed, but the goal is still the same. As a member
of the Be The Match Registry, you could be the one to save
a life.
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- Q:
What is a bone marrow transplant?
-
A: Bone
marrow transplant is a life-saving treatment for people
with leukemia, lymphoma and many other diseases. First,
patients undergo chemotherapy and sometimes radiation to
destroy their diseased marrow. Then a donor's healthy blood-forming
cells are given directly into the patient's bloodstream,
where they can begin to function and multiply.
For
a patient's body to accept these healthy cells, the
patient needs a donor who is a close match. Seventy percent
of patients do not have a donor in their family and depend
on the Be The Match Registry to find an unrelated bone marrow
donor or umbilical cord blood.
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- Q:
How do I become a bone marrow donor?
-
A: The
first step to become a bone marrow donor is to join the
Be The Match Registry. Doctors around the world search our
registry to find a match for their patients. If a doctor
selects you as a match for a patient, you may be asked to
donate bone marrow or cells from circulating blood (called
PBSC donation). Patients need donors between the ages of
18 and 60 who meet health guidelines and are willing to
donate to any patient in need.
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- Q:
Why is there sometimes a cost associated with joining the
registry?
-
A: The
total cost to add a new member to the Be The Match Registry
is about $100. This includes the cost of the testing needed
to match donors to searching patients and related costs.
-
Be The
Match relies on financial contributions to help cover the
costs of adding members to the registry. Others have contributed
toward the costs for you to join today. However, there are
not always enough funds to cover the numbers of donors needed,
so sometimes new members are asked to pay some of the registration
costs when they join.
-
Your
contribution will make it possible for more people like
you to join in the future. Every gift helps make life-saving
transplants a reality for more patients..
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- Q:
What is my commitment if I join?
-
A: When
you join the Be The Match Registry, you make a commitment
to:
- Be
listed on the registry until your 61st birthday, unless
you ask to be removed
- Consider
donating to any searching patient who matches you
- Keep
us updated if your address changes, you have significant
health changes or you change your mind about being a donor
- Respond
quickly if you are contacted as a potential match for
a patient
You have
the right to change your mind about being a donor at any time.
Donating is always voluntary.
If you
decide you do not want to donate, let us know right away.
That way we can continue the search for another donor without
dangerous delays for the patient.
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- Q:
Why does a person have to be 18 to join? Can't my parent sign
the consent for me?
-
A: We
require volunteer bone marrow donors to be between the ages
of 18 and 60, which is standard medical practice. An individual
must be 18 to donate because marrow donation is a surgical
procedure and the person undergoing the procedure must legally
be able to give informed consent. A guardian or parent cannot
sign a release or give consent because unrelated marrow
donation is a voluntary procedure and is not beneficial
or life-saving to the donor.
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- Q:
If I'm over 60, why can't I join?
-
A: The
age limit is not meant to discriminate. We must use chronological
age to determine eligibility to protect the safety of the
donor and provide the best possible treatment for the patient.
With age comes a small increase in the risk of side effects
from anesthesia.
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- Q:
If I join the Be The Match Registry, how likely
is it that I will donate to someone?
-
A: We
cannot predict the likelihood because there is so much diversity
in the population. Every person who joins the registry gives
patients hope, and new patient searches begin every day.
You may never be identified as a match for someone, or you
might be one of a number of potential matches. But you may
also be the only one on the registry who can save a particular
patient's life.
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- Q:
Does race or ethnicity affect matching?
-
A: Racial
and ethnic heritage are very important factors. Patients
are most likely to match someone of their own race or ethnicity.
Today, there simply aren't enough registry members of diverse
racial and ethnic heritage. Adding more diverse members
increases the likelihood that all patients will find a life-saving
match.
Members
of these backgrounds are especially needed:
- Black
or African American
- American
Indian or Alaska Native
- Asian,
including South Asian
- Native
Hawaiian or other Pacific Islander
- Hispanic
or Latino
- Multiple
race
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- Q:
What is the donation process like?
-
A: Adult
donors may be asked to donate in one of two ways:
- Bone
marrow donation is a surgical procedure in which liquid
marrow is withdrawn from the back of the donor's pelvic
bones using special, hollow needles. General or regional
anesthesia is always used for this procedure, so donors
feel no needle injections and no pain during marrow donation.
Most donors feel some pain in their lower back for a few
days afterwards.
- Peripheral
blood cell (PBSC) donation involves removing a donor's
blood through a sterile needle in one arm. The blood is
passed through a machine that separates out the cells
used in transplants. The remaining blood is returned through
the other arm.
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- Q:
Can I get tested for a specific patient or family member?
-
A: When
you join the Be The Match Registry, you make a commitment
to consider donating to any searching patient who matches
you. As a volunteer, you are never under any legal obligation
to donate and your decision is always respected. However,
because a late decision not to donate can be life-threatening
to a patient, please think seriously about your commitment
before deciding to join our registry.
You
can request a copy of your own testing results after you
join the Be The Match Registry. However, if you want to
be tested only for a specific patient, you will need to
have your testing done privately. You can contact the patient's
transplant center or transplant doctor for more information.
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- Q:
I've already been tested for a family member. How can I add
my results to the Be The Match Registry?
-
A: Get
a copy of your human leukocyte antigen (HLA) tissue typing
lab report and contact the donor center in your area. You
will need to fill out a health history form to verify you
meet medical guidelines. You will also need to sign a consent
form agreeing to be listed on the Be The Match Registry.
Once you are listed on our registry, we will contact
you if you are identified as a possible match for a patient.
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- Q:
I think I may have already joined. How can I verify that I
am on the registry?
-
A: Be
The Match Registry is the new name for the National Marrow
Donor Program (NMDP) Registry. Whether you joined the NMDP
Registry or Be The Match Registry, online or in person,
you are part of the same registry and do not need to join
again. If you have previously given a blood sample or cheek
cell sample to be tested for the registry, you do not need
to join again.