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ARCHIVES
SECTION A: JDRF and Type 1 Diabetes
8. 8-30-08: "JDRF Advocacy & American Express"
7. 6-28-08: "Divabetic—Makeover Your Diabetes" Event
6. 5-17-08: "Athletes, Bloggers, & Type 1"
5. 2-02-08: "It's the Cause"
4. 12-15-07: "My Thanks to JDRF"
3. 11-01-07: "Living with Type 1 Diabetes"
2. 10-25-07: "The Farrell Family JDRF Walk Update"
1. 10-18-07: "I'm Walkin' ... I'm Talkin' for JDRF"
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Topic of
the Day
A.8. JDRF
Advocacy and American Express
August 30, 2008
Here's an intriguing and urgent fundraising
campaign sponsored by the good folks at American Express and supported by the good folks at JDRF. As a mom who actively supports
efforts to find a cure to type 1 diabetes, I encourage you lend a helping hand. Nothing to buy—just a few clicks of
your time. Thank you on behalf of my son and children like him who live with type 1 diabetes. --Cheryl Farrell
Opportunity to Vote for a Special “Members Project” on
an American Express Website
“No More Insulin Shots Required”
The American
Express Members Project winners will share $2.5 Million in funding. Go to this direct link:
http://www.membersproject.com/project/view/OGEULA
You will
be guided to nominate this project for funding. It was submitted by a mom from Georgia whose son was diagnosed on Mother’s
Day 2007. This is her project description:
Fund continuing research for an artificial pancreas and
eventually a cure for Type 1 Diabetes.
Organizations like JDRF and NIHH
are working to make this dream a reality.
Let’s support her efforts and potentially support JDRF. The project closes on September 1st. It takes less than a couple of minutes to nominate this
project. This is an opportunity for viral marketing. Pass this message on to at least 5 members of your family and
friends. Let’s see if we can make an impact.
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Topic of the Day
A.7.
“Divabetic — Makeover Your Diabetes” Event
June 28, 2008
As
the mother of a teenage son with type 1 diabetes, I am ever on the alert for diabetes advocacy. The disease affects families,
not just those diagnosed. Clearly, the life-saving routines my son performs far exceed anything I have to do. However, my
desire over the past seven years has been to make his life as hope-filled as possible. As such, I recently decided to step
outside my insular perspective on diabetes.
My
journey yielded a referral to a diabetes “makeover” event held at the Los Angeles Paramount studios today. “Divabetic—Makeover Your Diabetes” is sponsored by the pharmaceutical
manufacturer Novo Nordisk and the Divabetic organization. The event is primarily directed toward those with type 2 diabetes
and pre-diabetes. It is day of self-esteem building and education activities. Fashion shows, cosmetic tips, nutrition help,
motivational help, and more filled the sound stage with positive attitude.
There’s
often a division of thought on appropriate support for the two main types of diabetes. In the case of type 1, the cause is
thought to be autoimmune related. The pancreas ceases to work and individuals require insulin every day to stay alive. In
the case of type 2, there’s a correlation to poor diet and lack of exercise. The pancreas supplies insulin, but does
so inefficiently. Corrective diet and exercise can in some cases reverse type 2 diabetes.
While
distinct in how the two types come about, the underlying commonality is making healthy food choices and active lifestyle.
This brings me back to the Divabetic event. I spoke to health and nutrition experts on topics that I can take back to my son.
I learned about organizations that focus on teens, sports, and diabetes. I learned of a book entitled, “Diabetes Burnout…”
by William H Polansky.(*) I learned that one of the best ways to be an advocate is to be a good listener. Indeed, lifesaving
food for thought.
I
encourage you to visit www.divabetic.org to find a tour date in your area. Through November 2008, tour cities include Washington, D.C., Cleveland, OH, New Orleans,
LA and Miami, FL. I extend congratulations to the organizers and sponsors of this excellent outreach effort.
A
famous quote applies here: “When the tide comes in all boats rise.” So, when a cure is being sought, everyone
benefits. When nutrition advice is provided, everyone benefits. When positive attitudes are encouraged, everyone wins.
(*) For more information:
”Diabetes Burnout: What To Do When You Can't Take it Anymore,” by William H. Polansky
[ISBN: 1580400337]
American Diabetes Association: www.diabetes.org
Juvenile Diabetes Research Foundation: www.jdrf.org |
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Topic of the Day
A.6. "Athletes,
Bloggers, & Type 1 Diabetes"
May 17, 2008
My teenage son plays sports and lives with type 1 diabetes and so I am always interested
in updates on the two topics. ESPN reported that 25-year-old Denver Broncos quarterback, Jay Cutler was diagnosed with
the disease late last month. While it’s not unusual to be diagnosed in one’s 20’s, it’s most often
revealed in young children, in some cases in infants. My lacrosse playing son was diagnosed when he was ten years old.
Type
1 (or juvenile) diabetes is an extremely serious autoimmune disease in which the pancreas stops
producing insulin, a life-sustaining hormone that allows us to get energy from food. The condition requires patients to vigilantly
monitor their blood sugar levels and inject insulin throughout the day, every day, just to stay alive. Type 2, also
known as adult onset diabetes, is the more familiar version and is closely linked to lifestyle choices and family history.
Cutler
has been wonderfully outspoken about his condition—especially, citing the warning signs. Millions of individuals live
with the disease, and it is not easy. Cutler’s candor and hope inspire children like my son as well as their parents.
Please visit the ESPN web site for more information about this story.
Another
topic that can offer encouragement to young people with type 1 is a new blog sponsored by the Juvenile Diabetes Research Foundation
(JDRF). According to their web site:
Blogging
has skyrocketed in the past few years as a means for people to share their experiences and their opinions. In the past few
years, dozens of blogs about living with diabetes have been started by those who know the disease best: people with diabetes
and their families. JDRF is introducing a new round table series with nine bloggers in the online diabetes community. They
all have different backgrounds, were diagnosed at different stages in life and have different styles of managing their diabetes.
Please
visit the JDRF web site below for more information about the new round table series. You can also find information about type
1 warning signs, efforts to find a cure, as well as sources for family support.
http://www.jdrf.org/index.cfm?fuseaction=home.viewPage&page_id=108190 | |
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Topic of the Day
A.5.
"It's the Cause"
February 2, 2008
I again
have the pleasure of speaking for the Juvenile Diabetes Research Foundation (JDRF). Tomorrow, I will be the MC at an
awards ceremony for the Ventura County [California] walkers for a cure.
You may know by now, my life mission is to support efforts to find a cure for my son and children like him.
I am
pleasantly surprised by my willingness to go where I’ve been called, It reminds me of the familiar saying, “Keep
your eyes on the prize.” This slogan is often associated with the Civil Rights movement. Yet, focus is not only
required in social justice; it is as critical in children's healthcare.
I will
enthusiastically congratulate the efforts of the Ventura walkers
who raised over $150,000 during the fall campaign. I will continue to lobby my legislators to appropriate funding for diabetes
research. Most importantly, I will hug my son as he tirelessly performs his regimen of glucose testing and insulin injections.
Therein lies the hope. | |
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Topic of the Day
A.4. "My Thanks to JDRF"
December
15, 2007
There
is a lot going on right now. That’s likely the case for many of us this time of year. When I feel swept up in the commotion
of holiday preparations, my tendency is to clamp down and find focus again. I put aside the gigantic things-to-do list, the
gift-giving spreadsheet, and the Christmas card roster. I will think about the holiday meal later. For now, I want to think
about my blessings. For this entry, I note one very special blessing. That is the staff at Juvenile Diabetes Research Foundation
Greater Los Angeles Chapter.
I believe
the effectiveness of organization is directly related to the character of its members. JDRF is extremely effective under the
leadership of Mark Rieck and his associate, Liz Sanchez Jackson. My family has found welcoming support in living with type
1 diabetes. The outreach programs touch a broad spectrum of families and as such, we are reminded that we are not alone. My
son has met good friends through JDRF affiliated programs. With all the good times, attention never lapses from the importance
of finding a cure to type 1 diabetes.
The
numbers behind the organization tell an impressive story as well. The national organization was founded in 1970 by parents
of children with type 1. Since that time, JDRF has awarded more than $1.16 billion to diabetes research, including more
than $137 million in its 2007 fiscal year. The JDRF Los Angeles Chapter is among
the area’s leading community organizations, raising more than $38 million for diabetes research over the past 15 years.
On behalf
of the Farrell clan, I send heartfelt thanks to Mark, Liz, Frances, Anna, Cindy, Adrianna, Denise, and Erika for all your good work, support,
and best wishes. Our hope remains alive and well because of you.
–Cheryl
General Diabetes Facts
Diabetes
is a chronic, debilitating disease affecting every organ system. There are two major types of diabetes: type 1 diabetes (an
autoimmune disease also known as juvenile diabetes) and type 2 diabetes (a metabolic disorder also known as adult onset diabetes).
Type 1 (Juvenile) Diabetes Facts
Type
1 (juvenile) diabetes strikes children suddenly, makes them dependent on injected or pumped insulin for life, and carries
the constant threat of devastating complications. While diagnosis most often occurs in childhood and adolescence, it can and
does strike adults as well.
For
more information about type 1 diabetes and how you can help find a cure, please visit www.jdrf.org.
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Topic of the Day
A.3. "Living with Type
1 Diabetes"
November 1,
2007
I asked JDRF to
send the following letter to California legislators on my
son's behalf. It is part of the effort to retain research funding to cure type 1 diabetes.
My sixteen-year-old son Alec was diagnosed with type 1 diabetes almost six years ago. His father and I
have a long history of checking with pediatricians for the mildest of symptoms. Our hyper-attentive parenting paid off because
his diagnosis came before he developed serious complications. Nevertheless, Alec’s diagnosis caught us by surprise.
We did not know about the disease and it does not “run in the family,” as we are often asked. We did not know
the symptoms—we just knew something was not right.*
I noticed my son’s rapid weight loss and constant thirst. I travel for work and I
naively thought he was reacting to my being away. These days living with the disease, my son enjoys lacrosse and wrestling.
However, he manages a complex set of calculations many times a day. He factors in carbohydrates in his meals, exercise, how
long he sleeps, how he feels, and other considerations to stay alive. While
treatment varies, my son’s daily routine is to test his blood sugar (glucose levels) six
to seven times a day in addition to taking insulin throughout the day. For parents of young children, this regimen often includes
multiple visits through the night—every night—to test and to supply
insulin.
A big
concern for us now is how as a teenager, Alec must negotiate his disease with his social life. He doesn’t want to stand
out or be defined by diabetes. How do you date and explain you must test your blood before a meal? How do you explain the
difference between type 1 and type 2 diabetes? It’s not about being overweight or eating too much sugar. How do you
excuse yourself repeatedly from class to urinate which is an indication of high glucose levels? It’s a job staying alive
that never takes a vacation.
I am
a member of the Clue Crew on the TV show Jeopardy! I am also a volunteer for the Juvenile Diabetes Research Foundation (JDRF).
As part of my advocacy work, I have interviewed parents of children diagnosed with type 1 diabetes in order to share their
stories and help raise awareness. Those stories can be found at www.bayheartmusic.com under the writing link.
Thank
you in advance for any and all support to finding a cure to type 1. My son’s life depends on it.
*For warning signs of type 1 diabetes, please visit www.jdrf.org. Education about type 1 diabetes symptoms is critical because they can be mistaken for more common illnesses. | |
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Topic of the Day
A.2. "The Farrell Family
JDRF Walk Update"
October
25, 2007
(Includes post script—November 4, 2007)
The following is an email I sent to friends
and extended family about the JDRF Family Walk Update. I hope you are inspired.
10-25-07
7AM
Hi all. This is my Juvenile
Diabetes Research Foundation (JDRF) Family update. Our focus this year is to keep the cure for diabetes top of mind. I know
that you are often approached by friends and colleagues requesting financial support for very worthy causes. As citizens of
the world, asking and giving is the business we’re in. However, the Farrells don’t want to wear out their welcome
with you. By the way, I’ve been working on ways to raise funds via mass market. Stay tuned…it’s in
the works.
In the meantime, I’m
compelled to keep the message of hope alive—finding a cure for type 1 diabetes. I see hope in Alec’s activities.
It’s been six years since he was diagnosed at ten years old. He’s a strapping lacrosse player with his sights
on sports medicine as a college major. It’s subject to change, but he’s heavy into high school chemistry and physiology.
While his banter with his younger sister is annoying at times, we know it comes from love and will create a long lasting bond
between them.
Alec has an excellent endocrinologist.
Thankfully he has presented Alec with the latest technology to inject insulin and measure glucose levels. The work of JDRF,
the researchers it funds, and medical equipment suppliers continually make progress. It’s evidenced in Alec’s
life and the lives of children like him.
But you know the drill:
technology is not a cure. Finding a cure is the primary objective of JDRF. We believe it’s a reachable goal. That’s
why our family participates each year in the Walk to Cure Diabetes. I was recently the MC at several local events and will
be walking November 4th at Dodger Stadium. Okay, for those clamoring to support the cause financially, it’s
not too late to register to join us at the walk. Please see below.
In any case, we feel your
support in thought and deed and we are grateful.
Ways to Support Finding
a Cure for Diabetes:
1. The “Promise to
Remember Me” CDs that I recorded a few years ago on behalf of JDRF are still available for purchase. (Thank you for
your past purchases.) You’ll find more information on my website:
www.bayheartmusic.com
A CD order form can be
printed on the link entitled, "How to Order." ("Promise”)
2. To pledge for the Walk
to Cure Diabetes, please go to our donation site:
http://walk.jdrf.org/walker.cfm?id=86747373
3. Keep those prayers and
good thoughts flowing. We cannot make it without them. You have ours for the work you do.
Thanks for indulging this
long message. All the best to you.
Gratefully,
Cheryl Farrell and Family
P.S. Nov.
4, 2007 @ 3:55PM
The walk was completed
a few hours ago and the numbers are in. The Shining Stars, the Farrell Walk Team made its goal! Thank you to all our incredibly
generous supporters. As before, I saw thousands of walkers in their colorful team shirts all moving in the same direction
toward a cure. It's an amazing sight to witness the power of hope. It makes it easier to get up every day to face the challenges.
Thank you all for your love, prayers, and support.
—Cheryl |
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Topic of the Day
A.1. "I'm Walkin'
... I'm Talkin' for JDRF"
October
18, 2007
This week’s topic is
not a tribute to Fats Domino. My walking has to do with a role I’ll play in a few days. I will serve as MC for the 2007 JDRF Walk to Cure Diabetes in Ventura, CA. (Side question: Does “MC” generically stand
for Master of Ceremonies as opposed to the female version, “Mistress of Ceremonies"?) Whatever the phrase, it’s
the third time in the past few months that I’ve supported the JDRF LA chapter in this way. I’m thrilled to do
it. I help in other ways, but cheering a crowd on, particularly for the very important cause of finding a cure to diabetes
gives me a special buzz.
As you may know, my teenage
son Alec has type 1 diabetes, along with millions of other people in America.
Also known as juvenile diabetes, the rate of new cases increases every year for this autoimmune disease that mainly strikes
children. For families with a type 1 child, the only statistic that matters is the one that affects your family. However,
when a cure is found, the wealth of opportunity is shared by all. So, despite the natural reflex to nest and go inward, I
reach outward to find a cure.
I spend a lot of time explaining
the difference between type 1 and the often misapplied version of type 2 (adult onset diabetes.) No, my son did not eat too
much sugar; no he is not obese; no, it’s not about lack of exercise—in fact, he’s an avid lacrosse player.
Both type 1 and type 2 versions share a common name because they both affect the pancreas—the insulin producing organ
that helps sustain life.
Children are the least equipped
to defend themselves against the false stigma of juvenile diabetes. The good news is that they can rely on their advocates
in parents, siblings, aunts and uncles, neighbors, friends, colleagues, legislators, generous businesses owners, and many
others. We all talk and we all walk for a cure.
I invite you to walk with
me and hundreds of thousands of other walkers across the county over the next few weeks. For information about a walk in your
area, please visit www.walk.jdrf.org
Register Today for the 2007 Walk to Cure
Diabetes!
Sunday, October 21, 2007-
Oxnard State Beach Park
Saturday, November 3, 2007-
Yokuts Park- Bakersfield
Sunday, November 4, 2007-
Dodger Stadium, Los Angeles
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