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| NO, NO, NO. |
Dear CrossFit: My Diabetes Homies & I Would Like You To Know....
Making fun of people with diabetes isn’t funny. It’s offensive, disturbing and it perpetuates diabetes myths instead of perpetuating and teaching diabetes realities.
And because of tweets/jokes/rubbish like yours, diabetes becomes an unending diabetes blame-game,a target and punchline, that keeps people living with diabetes and regardless of the type, in the Diabetes Closet.
Your offensive tweet also directly impacts funding for diabetes research.
Diabetes shaming is a thing and a horrific thing at that. Diabetes shaming like your unfunny tweet makes fun of a very real group of diseases (t1 diabetes, LADA type 1.5, and T2 diabetes,) that are never ending and have the potential to kill.
And just to be crystal clear, I didn’t develop my type 1 diabetes as a skinny 8 year old because I drank too much soda.
And my friend Jen didn’t develop her t2 diabetes because of soda. She doesn’t drink soda, weighs 20 pounds less than I do and has always worked out.
But Jen’s mother and grandmother have and had type 2 diabetes - so there you go.
Genetics came into play - as it usually does with type 2.
And lets just say for shits and giggles that some people living with t2 struggle with their weight - as a company that promotes fitness and a healthy lifestyle, do you really think it’s OK to make fun of others via social media (or any other platform,) struggling with their weight???
Do you think it’s OK to publicly mock people struggling with their health via social media?
NEWSFLASH: IT ISN’T.
Diabetes shaming in tweets like yours are exactly why people have difficulty managing/accepting and living with their diabetes.
Diabetes, regardless of the type, is never ending, physically and emotionally demanding - not to mention financially draining.
People with diabetes work so hard and we never get a break or a day off from living with diabetes - personally, I haven’t had a day off from diabetes in 13,687.5 days.
As a Type1, I do not have the ability to make insulin because my own body attacked the part of my pancreas (the Islet of Langerhans,) that produces insulin, way back when I was skinny eight year old. I was in the hospital for 3 weeks and put on a 3000 calorie a day diet because I looked like a concentration camp victim - my body was literally starving itself.
FTR: People need insulin to to live - and will die without. I could run marathons everyday and I would still require insulin to live.
Debbie lost her life to diabetes for a multitude of reasons - all directly related to diabetes.
Unfortunately, Debbie was diagnosed in the mid 60’s, a time when there was no such thing as fast acting insulins or diabetes technologies. The treatment for t1 diabetes back then was archaic the life expectancy of someone with t1 in the 1960s was grim.
Not to mention that no one ever considered the mental side of living with diabetes, nor was talked about, let alone treated. Her little body was ravaged from years of living with t1 and watching her die was a tragedy.
My parents never got over her death - and truthfully, neither have I.
Are you aware that people with Type 1 can die from something called “Dead-IN-Bed,” syndrome? They die from a low blood sugar in their sleep. Nothing funny about that.
Crossfit - You will never get a single dime from me.
But hopefully Coca-Cola will take the extra millions and millions of dollars they have the potential to win in a lawsuit re: your egregious use of their logo/copyright infringement, and use said money to provide funding for diabetes research for the cure, Peer to Peer Diabetes Support, Artificial Pancreas research, grass roots diabetes efforts and the likes there of.
Kelly Kunik
t1 PWD (Person with Diabetes) for almost 38 years.
Special shoutout to Moira McCarthy for showing up in my Facebook feed the minute I logged on this morning and alerting the DOC!
And because of tweets/jokes/rubbish like yours, diabetes becomes an unending diabetes blame-game,a target and punchline, that keeps people living with diabetes and regardless of the type, in the Diabetes Closet.
Your offensive tweet also directly impacts funding for diabetes research.
Diabetes shaming is a thing and a horrific thing at that. Diabetes shaming like your unfunny tweet makes fun of a very real group of diseases (t1 diabetes, LADA type 1.5, and T2 diabetes,) that are never ending and have the potential to kill.
And my friend Jen didn’t develop her t2 diabetes because of soda. She doesn’t drink soda, weighs 20 pounds less than I do and has always worked out.
But Jen’s mother and grandmother have and had type 2 diabetes - so there you go.
Genetics came into play - as it usually does with type 2.
And lets just say for shits and giggles that some people living with t2 struggle with their weight - as a company that promotes fitness and a healthy lifestyle, do you really think it’s OK to make fun of others via social media (or any other platform,) struggling with their weight???
Do you think it’s OK to publicly mock people struggling with their health via social media?
NEWSFLASH: IT ISN’T.
People with diabetes work so hard and we never get a break or a day off from living with diabetes - personally, I haven’t had a day off from diabetes in 13,687.5 days.
As a Type1, I do not have the ability to make insulin because my own body attacked the part of my pancreas (the Islet of Langerhans,) that produces insulin, way back when I was skinny eight year old. I was in the hospital for 3 weeks and put on a 3000 calorie a day diet because I looked like a concentration camp victim - my body was literally starving itself.
Do you know anyone that’s died because of diabetes?
Unfortunately I do and I can assure it’s painful, scary, and you will never get over the loss or the pain.
My older sister Debbie, who died of diabetes complications as a 32 year old type 1 in 1991, didn’t lose her life to diabetes complications because she drank to much soda. Unfortunately I do and I can assure it’s painful, scary, and you will never get over the loss or the pain.
Debbie lost her life to diabetes for a multitude of reasons - all directly related to diabetes.
Unfortunately, Debbie was diagnosed in the mid 60’s, a time when there was no such thing as fast acting insulins or diabetes technologies. The treatment for t1 diabetes back then was archaic the life expectancy of someone with t1 in the 1960s was grim.
Not to mention that no one ever considered the mental side of living with diabetes, nor was talked about, let alone treated. Her little body was ravaged from years of living with t1 and watching her die was a tragedy.
My parents never got over her death - and truthfully, neither have I.
But hopefully Coca-Cola will take the extra millions and millions of dollars they have the potential to win in a lawsuit re: your egregious use of their logo/copyright infringement, and use said money to provide funding for diabetes research for the cure, Peer to Peer Diabetes Support, Artificial Pancreas research, grass roots diabetes efforts and the likes there of.
Kelly Kunik
t1 PWD (Person with Diabetes) for almost 38 years.
Special shoutout to Moira McCarthy for showing up in my Facebook feed the minute I logged on this morning and alerting the DOC!
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