#insulin4all USA
Healthcare for All: Calling for Change in the U.S.
16 Jan 2018, 2:59 p.m. in #insulin4all USA by Karyn Wofford
A single payer system removes greed from a place it certainly has no place. Healthcare should be constructed of an ambition to heal, not a hunger for money. Our greed driven system is dangerous, and is resulting in the death of our people. Read more
Pleas from the USA
4 Dec 2017, 10:57 a.m. in #insulin4all USA, Global Stories by Karyn Wofford
Why is this happening? How are millions of people slipping through the cracks? Why are we living in fear because we cannot afford to “breathe”? Insulin is oxygen; price gouging cannot go on. This is my plea—our plea— and we are in desperate need of change. Read more
Taking a Stand at Eli Lilly Headquarters
13 Sep 2017, 9:40 a.m. in #insulin4all USA, Global Stories by Angela Lautner
I joined dozens of people impacted by the rising cost of insulin in the USA in protest of those prices in front of Eli Lilly headquarters in Indianapolis, Indiana. Some had traveled many hours to join the protest, but one thing was made clear, we wanted to ensure that Eli Lilly heard our voices. We were passionate in our outcry for change and jointly understood that not saying anything is simply not an option.
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Indianapolis #insulin4all Demonstration: Stop Price Gouging People with Diabetes!
3 Aug 2017, 9:48 a.m. in #insulin4all USA, News & Statements by Elizabeth Pfiester & Fran Quigley
Patients and those who support us will be demonstrating outside of Eli Lilly HQ in Indianapolis on Saturday, September 9th 2017. See the full post for more information and join us at https://www.facebook.com/groups/insulin4allAction/ if you can be there.
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Reducing my Insulin Burden with Metformin
17 Jul 2017, 12:37 p.m. in #insulin4all USA, Global Stories by Karyn Wofford
As insulin prices crept upward, I realized I needed to figure out more ways to increase my sensitivity and reduce the large load of insulin I had to pump into myself every day. It became more than a financial struggle; I was scared that synthetic insulin could become insufficient. Then what? So with my shallow pockets and fear for the future, I talked with my doctor about the type two medication, Metformin. Read more
Recruiting for USA Insulin Access Study
8 Jul 2017, 8:55 p.m. in #insulin4all USA, News & Statements by Elizabeth Pfiester
In the wake of rising insulin prices in the United States and recent threats to public health safety nets like Medicaid, patients with type 1 diabetes are becoming increasingly more vulnerable. As a member of the T1D community and a rising second year Masters student at the Yale School of Public Health, Samantha Willner is hoping to shed light on the terrible sacrifices members of the T1D community in the U.S. have had to make in order to get the medicine they need to live. Read more
The Cost of Chronic Illness
15 May 2017, 9:58 a.m. in #insulin4all USA, Global Stories by Karyn Wofford
I’ll start out by saying I consider myself lucky. Yes, you read that right. I consider myself fortunate to be in a country that’s consider to be progressive in technology and medical care. There are people in countries where electricity, consistent food supply and medications just don’t exist. For these people, the cost of chronic illness is too often immediate death. Read more
Uninsured with diabetes in the USA
28 Apr 2017, 10:35 a.m. in #insulin4all USA, Global Stories by AnaElena Djafari
I have had times of desperation where I have used expired insulin, skipped some meals and diluted my insulin with water until I could afford to buy my next vial, but I am alive. I would like to suggest a few things to those who are possibly facing a future with no insurance... Read more
A Letter to Congress
27 Mar 2017, 11:41 a.m. in #insulin4all USA by Zach Toth
I write to you today as a young American with serious concerns for the future of health care in this country, namely with the GOP’s proposed American Health Care Act (AHCA). My health situation forces a more elevated interest in the current health care debate compared to many of my young peers because I have type 1 diabetes. My fellow diabetics and I (who number around 30 million in the US) rely on access to affordable prescriptions and health care for our very survival. When I say my concerns are serious, I am not exaggerating. Read more
Diabetes Debt: 3 Stories
14 Mar 2017, 10:57 a.m. in #insulin4all USA, Global Stories by Elizabeth Pfiester
When I was diagnosed with type 1 diabetes 38 years ago (March of 1979), my insulin cost my parents $10 a vial. Now, my co-pay for my insulin is $40 for the brand my insurance company wants me to use, or $60 for the brand that works better for me. If I choose to use my local pharmacy, and get my supplies for 3 months at a time, I have to pay the full amount of $120 for each Rx. If I use the insurance company and get everything via the mail, I only save $20. Read more