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MANY AGAINST 1.
MANY AGAINST 1.
At JDRF, we're leading the fight against type 1 diabetes (T1D) by funding
research, advocating for policies that accelerate access to new therapies, and
providing a support network for millions of people around the world impacted by
T1D.
At JDRF, we’re leading the fight against type 1 diabetes (T1D) by funding
research, advocating for government backing and expanded access to treatment,
and providing a support network for millions of people around the world impacted
by T1D.
THE LATEST
2X YOUR GIFT FOR 2X THE RESEARCH
Every day, JDRF works to further innovations for the type 1 diabetes (T1D)
community–but we’re coming up short on our 2021 fundraising goals. Pitch in with
a DOUBLED gift before it's too late.
I’ll close the gap yes
THOUGHTS AT YEAR’S END FROM JDRF’S CEO
Read More yes
FIRST-IN-HUMAN GENE-EDITED STEM CELL TRIAL? CHECK.
Read More yes
MAXIMIZE YOUR HEALTH BENEFITS BEFORE 2022
Read More yes
ADVANCING ON MANY FRONTS
JDRF is the world’s largest nonprofit funder of type 1 diabetes research. Our
in-house scientists oversee a diverse portfolio of research tracks, leaving no
stone unturned in our search for a cure.
Learn More about Advancing on many fronts
IMPROVING LIVES, TODAY AND TOMORROW
While our focus is on curing type 1 diabetes (T1D), we also pursue new
treatments to keep people with T1D healthy until that day comes. Outside of the
lab, we push for increased government funding for research, and work with
academia, clinicians, insurers and regulators to get new therapies and devices
to market quickly and safely.
Learn More about Improving lives, today and tomorrow
TYPE 1 DIABETES RESOURCES
Connect with others or find useful guides for navigating some of the trickier
moments of life with type 1 diabetes (T1D).
JDRF BAG OF HOPE®
DIABETES HELP, ON CALL
T1D CONNECTIONS PROGRAM
T1D MANAGEMENT 101
See All T1D Resources
JDRF ONE WALK®
Our biggest event of the year is a fun way to connect with people in your area
who understand what it’s like to live with T1D, while raising money and
awareness. Walk on your own, or register with your family, friends, classmates
or colleagues.
Find a Walk
Want more ways to connect with your community? JDRF hosts a variety of events
year-round, including golf tournaments, galas, summits, support groups, research
opportunities and rides.
See All Events Near You
Be the first to know about T1D news, local events and more.
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MEET SOME OF THE PEOPLE BEHIND THE MOVEMENT TO END T1D
“WE ARE ALL IN THIS TOGETHER.”
“JDRF HAS ALWAYS BEEN MY BEST RESOURCE FOR THE LATEST INFORMATION.”
“JDRF REALLY IS SO TREMENDOUSLY POSITIVE AND EFFECTIVE.”
“I CAN’T IMAGINE HOW DIFFERENT THIS JOURNEY WOULD HAVE BEEN WITHOUT JDRF.”
“JDRF IS ... A STRONG FORCE FOR CHANGE.”
“I OWN THE FACT THAT I HAVE T1D.”
Stories From Our Community
KEYOSHI CARR
“We are all in this together. To be able to go to the Walk and see that we are a
community makes all the difference to my family,” Carmen Carr, Keyoshi Carr’s
mother.
Keyoshi’s family changed forever when her older sibling was diagnosed with T1D.
They quickly became active members of the JDRF community, doing school
fundraisers, T1D education workshops and starting a JDRF One Walk team.
Six years later, the unimaginable happened again. Keyoshi was diagnosed with
T1D. She had been a participant in TrialNet, a JDRF-funded program that offers
risk screening for relatives of people with T1D. She had tested positive for
antibodies, so her parents we’re watching for the symptoms. They credit TrialNet
with potentially saving her life.
DAN HAMILTON
When Dan Hamilton was diagnosed with T1D in 1972, the doctor told him he
wouldn’t live past 50. Fast forward 45 years, and Dan is strong and healthy at
59. He credits his health to the advancements in treatment and care over the
years. He has been an early adopter of every technology that has come along, and
exercises regularly as part of a healthy lifestyle.
Dan has found he has had to be a strong advocate for himself with healthcare
providers. He had made sure to work with clinics and professionals that
specialize in T1D and keep up with the latest technology and treatment options.
He enjoys mentoring others with T1D and helping them discover a path to staying
strong and minimizing complications.
MADDY ARNSTEIN
Maddy Arnstein has lived with T1D for over 50 years. She became involved with
JDRF when she saw the dramatic difference technologies like the insulin pump
could have on her life. Maddy was quickly drawn to advocacy—initially to help
secure continued renewal of funding for the Special Diabetes Program (SDP). But
once she started using a continuous glucose monitor, she dedicated herself to
fighting for Medicare coverage.
In 2017, Maddy took part in JDRF Government Day, meeting with her members of
Congress. She offered a unique perspective, as she’s seen first-hand how far
research has come over the years.
“Because I’m very action-oriented, I can’t tolerate just sitting around and
discussing something with no results,” Maddy says. “Through JDRF I can actually
help make things better for the next generation.”
WILL STEVENS
When Will Stevens complained of aches and pains, the doctor advised his mother,
Cassie, to give him a baked potato before basketball practice and to make sure
he had plenty of Gatorade to drink. Will’s health went from bad to worse. He
lost weight and was tired all the time.
When they went to the hospital, Will was diagnosed with T1D. The family spent
four days at the hospital learning a “new normal” and trying not to feel
overwhelmed.
Soon after, the Stevens started participating in JDRF events and became part of
the JDRF community, something they describe as a “game changer.”
ARIANA SHAKIBINIA
Ariana Shakibinia decided to study public health in large part because she lives
with T1D. She had always been interested in public policy, but she says living
with this disease has made her more vested in the healthcare conversation. “ I
am living with what is essentially a pre-existing condition. I’m fortunate
enough to have good health insurance, but it makes the potential financial
burden of T1D management much more visible and relatable.”
The JDRF community has enabled Ariana to connect with people across the country
she wouldn’t normally meet. She finds it incredible how JDRF advocacy has
mobilized a small group of people to do big things—like securing bipartisan
support for the Special Diabetes Program, which provides $150 million annually
to T1D research.
TYLER NEWBOLD
“I own the fact that I have T1D, and am grateful about some of the things I’ve
learned and the people I’ve met throughout my experience,” says Tyler Newbold.
Tyler played college basketball at Utah State from 2007-2011, and had the
opportunity to play in three NCAA tournaments. His coaches and trainers always
had Gatorade or candy on hand in case his blood glucose dropped during a game.
Tyler tested his blood glucose right before training, and during halftime
breaks. He says working out and playing basketball has helped him to better
control his T1D.
Tyler got involved with JDRF One Walk when he was in college; as a basketball
player, he was asked to be the celebrity speaker. “It was an awesome and
humbling experience to help younger children understand that they can still
achieve their dreams.”
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YOUR VOICE COUNTS
Whether you advocate at a grassroots level or support the work of our policy and
regulatory experts, every action you take advances our mission to cure, prevent
and treat T1D.
HEALTH INSURANCE: EXPLAINED
In addition to assistance with cost of insulin, JDRF’s T1D Health Insurance
Guide helps families navigate topics including prior authorizations, denials and
appeals, and applying for an exception.
Learn more
See All Campaigns
Join the movement to end T1D
Your gift today gets us a step closer to a world without T1D.
Donate Now
Also of Interest:
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* Type 1 Diabetes High Blood Sugar Symptoms:...
* Low Blood Sugar: Symptoms, Causes, and...
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