hammond newsletter julypdf
TRANSCRIPT
8/9/2019 Hammond Newsletter JulyPDF
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Building Community at HometownOur first event led by local familiesBy Kim Hammond
We moved into Hometown on
May 16th. In two months we have
taken over the Community Events
for the neighborhood, some 1200
homes, 3500 people. Over 50%
are Hispanic and the rest are made
up of Black Americans, Asian and
others. Our estate is in East
Aurora which is one of the
poorest areas in Illinois. I love that
we are serving with local families,
and with our friends who all live in
Hometown and have kids our age.
Every Monday night we (thanks to
our friends the Moberly’s) are
running T-ball and Baseball for over
60 kids in the neighborhood.
In a few weeks we will begin an
open meeting once a month for
anyone in Hometown wanting to
join us in transforming the
neighborhood. Whether they want
to help us form a community
Neighborhood Watch committee
or help with art classes in the local
school, they can be part of our
team. We are hoping to transition
from Baseball to Soccer to
Basketball through the next few
seasons. We have also been given the
keys to an empty cafe in the
middle of Hometown that we
plan to renovate and turn into
a community centre. We plan to
run youth events and community
events and would love to see a
functioning cafe open again. We
also are working with
Community 4:12 in collecting
goods for a local food pantry.
Over 600 goods were collected
from around Montgomery
including Hometown. It is all run by
Angela, who also lives in Hometown
Our first community event, our July
4th celebration and parade, saw
250 people come out for face
painting, family games, craft, snow
cones and a picnic.
Lachlan Hammondwith his friend Jeremyleads 250 people inthe July 4th parade atHometown, Aurora .
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;k;.
Our kids are involved in every part of missionLachlan, Carter & Jordan are on mission too
H A
M M O N D M O N T H L Y
Lachlan is growing up right
before my eyes.
(He is nearly 5 ft 3!). He is as
committed to mission here as
anyone of us. As we walk
back from baseball he gets off
his bike and walks next to
kids who don’t have one and
chats to them. He has made
lots of friends with the kids
around our neighborhood.
Hometown Events
The next event we are running is Halloween. We hopeto have fixed up the cafe, form a neighborhood housecommunity, start after school mentoring, a drop incentre and build a strong team among the communityand see increased community involvement.
“Baseball is an American past-time. Every
kid dreams of playing baseball one day.
Find an open park and you will find kids
playing catch. We are providing a safe
place for kids to play sports and make
friends. Our plan for the year is to offer
baseball, soccer then basketball.
More kids turn up every week from the
surrounding houses (including nine last week!)I think it’s hilarious that an
Australian is teaching American young
people how to play baseball. But I
love being around my kids and their friends,
and I love watching my kids make new
friends.”
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We moved to Chicago Dec 16 to begin two new roles: I
am the Director of Missional Imagination for
Community Christian Church in Chicago (a multi-site
church with 11 locations reaching nearly 7000 people weekly),
and I am launching Forge America as the National
Director.
After being here 1 month, my son Carter (7 years old)
complained of chest pains & broke out in spots, so we rushed
him to the doctors to hear the words no parent wants to hear,
especially a million miles away from home & family: “Your son
has Leukemia.” Carter was rushed to the University of
Chicago where he was immediately sedated & underwent
several blood transfusions. ( A.L.L Leukemia is cancer of the
BLOOD that happens when the bone marrow which should
produce white blood cells that fight infection produces
"immature" cancer cells instead that fill the blood.) Carter had
100% leukemia in his blood, his platelet count was
dangerously low (what CLOTS the blood) & his immunesystem was shot.
I cried every day that week as he went through several
life-saving blood transfusions, spinal taps (needles into the
spine), bone marrow scraps in his back, and a line put into his
arm that went all the way to above his heart for
Chemotherapy. My little brave boy never complained and
never cried when they stuck him with needles & I all I could
do is weep saying to God “please don't let my son die.” I
have no brave prayers, I am carried by all of yours, like the
crippled man on a mat carried to Jesus. I am paralyzed by
grief. So your prayers mean a lot to me. 50 years ago all kids
who were diagnosed with Cancer died within two weeks.
Today, depending on the type, they have a 80% -90% chance
of beating it. However, I don't want any chance of my child
dying—would you? I hate it when people say “they are good
odds”--how would you feel if you had kids & I said there is
a10%-20% chance of your kids dying?
The health system here is costly & complicated
We had not been paid yet, had not received any of our
support, & had only just filled out the health insurance form
which will cost us $8000 for the insurance, when we had to $4000 for the deductible. (You pay the first $4000 before
anything is covered-- the first Hospital bill was $64000 for fo
days.) 6 months in, Carter is responding to treatment. He is
low risk, and is responding to the Chemotherapy & the
cocktail of drugs, including a heavy dose of Steroids. His ha
is falling out & he will soon lose all of the hair on his body.
The pick has been removed from his arm & a port has been
inserted into his chest for the next three years of treatment.
Every day is a challenge, from headaches from the spin
taps, rage & mood swings from the steroids, & tears with the
weekly day in hospital where he is still prodded & poked. It
tiring every week having blood taken and spending a whole
day in hospital, even more tiring for Carter who can’t eat for
12 hours before. Maria does the 1.5 hour trip to the City ev
week. We have a website for Leukemia research & for the
medical costs associated with the costs of having a sick child
The web site is called www.clippersforcarter.com
In a foreign country with no family or long te
friends we have had to lean on God and build
support base from scratch-it has been hard.
especially feel for Carter who got sick a monafter we arrived so hasn’t made many close
friends and all his life long school & church
friends are back in Australia.
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Carter still fights
Cancer
Photo 1: Each beadrepresents a needle,bone marrow scraps,spinal taps, bloodtransfusions, chemotreatmentsetc....Photo 2: Part of the side effects of the
treatment is loss of hair, sunken eyes,puffy checks, weightgain, headaches, back pain, vomiting andnausea.
Carter Hammond’s fight with Leukemia
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Every Dollar you give allows usto do mission here in America
Thank you for your
ongoing support and friendship.
Your support means more to us
than you could ever imagine.
Your support allows us to
minister in the following roles:
Director of Missional
Imagination: At Community
Christian Church in Chicago. I
train, coach and teach across all
11 campuses, soon to be 18,around 7000 people. I continue
to work 20 hours a week in this
role and volunteer at
Montgomery campus by
preaching teaching, greeting
and pastoring people.
National Director of
Forge America. We have
hubs in Alabama, Kentucky,
California and Chicago all in
the first year. We are also
establishing a partnership with
Shapevine through the
rebranding of MQuest to be
under Forge America.
Lastly, we are committed to
leading the Mission in
Hometown. We will seemultiple missional communities
planted here in our
neighborhood.
We can’t do this without
you. Please keep in contact with
us: us: [email protected]
www.kimhammond.com
Skype: kimhammo
Twitter: /kimhammond
Facebook: kimdhammond
www.forgeamerica.com
twitter.com/forgeamerica
We loved July 4th in America. It was ourfirst one and we alldressed in Red Whiteand Blue.
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