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My Spin On The Diabetes Civil War - I Say Unite & Fight Against The Real Enemies

My Spin On The Diabetes Civil War - I Say Unite & Fight Against The Real Enemies

So, I’ve gotten a lot emails asking me my thoughts on the Diabetes Civil War and name change - So, to paraphrase an old Toyota commercial from the early 90’s: You asked for it, you got it, Toyota.

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In my eyes, the whole diabetes civil war thing creates conflict and separatism among those of us living the diabetes life, instead of the unity in our diabetes community.

Unity in community = power. Cracks in a foundation (be it in a community or structure) lead to that community or structure crumbling.

I've been a type 1 for 33 years and have, and have lost, many loved ones in my family to type1. And I want us to find a cure, BIG TIME. I'm tired of losing family members to this disease, and my heart always breaks when I hear of another type 1 diagnoses.

And I've also felt the hurt and shame every time someone has blamed me for my disease, or my sister for causing her own death. That hurt, shame, and pain never goes away. That hurt and blame did nothing but continually put me on the defense, and prevented me from developing a good diabetes offensive for quite sometime. That time I can't get back, and I'm sure it's caused damage to me physically, not to mention mentally.

I don’t want to fight others with diabetes just because they have a different type.

I don’t want to take away from their diabetes issues and pain, and I sure as hell don’t want to blame them for their disease.

And I’ll be honest, before I become friends with people who were type 2, there’s a very good chance I might have joined the separatist movement. But thanks to the Diabetes On-line Community, I’ve wised up. I’ve learned that their diabetes struggles mimic my own and that we are on the same side, and when I think back of my type 2 prejudices, I’m ashamed.

Many people with type 2 diabetes have a genetic link to the disease, just like a have a huge genetic link to type 1 diabetes. 
And regardless of the type, once a person is diagnosed with diabetes, they will always be diabetic. They will always have to stand watch and continually be on guard for diabetes complications.

Many of my type 2 friends work very hard on managing their disease - the very same disease that their parents and grandparents.

And many people don't have a genetic link to diabetes, regardless of the type.

The same thoughts apply for my brothers and sisters with 1.5 Diabetes. Before I became part of the DOC, I had no idea that they even existed. Now, I learn from they every day.

No, I don't want to change the name of my diabetes. I'm Ok with being called a person who has type 1 diabetes.

And I'm OK with people with type 2 diabetes being called a type 2 diabetics, or people with type 2 diabetes. Same goes for those who are type 1.5 diabetics, a.k.a., type1.5-LADA diabetes.

No, what I want to change is the public perception of diabetes - and I will fight to do just that.

My weapons of choice will be education and a loud and constant voice of many, not just my own.

And I say let's start the rumble in the diabetes jungle with the media!

LIsten up Media, I'm talking to you: People with diabetes are not lazy, glutenous, self destructive saps. And regardless of our type, we don't deserve the diabetes card we were dealt.

I demand that the media stop perpetuating diabetes myths and stereotypes - and I will fight to make that happen.

I demand that the media stop running with catchy diabetes sound bites that only have a degree of “truthiness” and only represent one facet of the vast diabetes spectrum. I want the media to differentiate between the types instead of lumping everyone with diabetes together. I want the media to see the many faces of diabetes and I demand that the media do it’s job and take the time and effort to explain ALL the diabetes incarnations and facts.

And while I'm at it, I'll put some of the blame on food manufacturers for adding High Fructose Corn Syrup into everything we eat in this country. Because ironically, it wasn't until HFCS started replacing sugar in foods almost 40 years ago, that people started associating diabetes with people being over weight & lazy sons of bitches who caused their own disease.

I demand that congress not allow the Corn Refiners Association to change the name of High Corn Syrup to the friendlier and incredibly deceptive sounding “Corn Sugar.

And I will demand and fight for insurance reform so insurance companies can’t charge outrageous monthly premiums, while limiting their clients heath options in the form of denying insulin pumps, cgms, and the number bottles of insulin and test strips per month, and the likes there of. All the while, allowing their CEO's fat payoffs with options to boot!

And I'll continue to fight for a cure for type 1 diabetes every single day of my existence!I 'll fight until the day pigs fly and my feet and knees bleed because I've literally crawled to find a cure. I'll fight until I literally have no voice left. And then, I'll keep writing about it!

But as far as blaming a person with diabetes, I won't do that - because society blames us enough.

Diabetes is a disease that has many types, but we are all part of the same family and on the same side. Regardless of what type of diabetes we live with, our goals are the same.

  1. To live
  2. To live a healthy and productive life
  3. To stop the perpetuation of diabetes myths and stereotypes and educate the public on the diabetes facts
  4. To find a cure

I choose to focus not on our differences, but the qualities and goals that unite us.

Other posts regarding the Civil War include, but by no means limited too:

http://talesofswaging.blogspot.com/2010/12/not-so-civil-war.html#comment-form

http://ourdiabeticlife.blogspot.com/2010/11/us-against-them-and-my-6-things.html

http://www.diabetesdaily.com/edelman/2010/10/which-is-worse-type-1-or-type-2-diabetes.php

http://strangelydiabetic.com/2010/11/30/is-there-a-civil-war/

http://www.diabetesdaily.com/knicks/2010/11/its-not-you-its-me.php

http://lemonadelife.com/2010/11/diabetes-civil-war-my-thoughts/

http://thecornerboothcc.blogspot.com/2010/12/not-abe-lincolns-civil-war.html

http://thepoordiabetic.com/diabetes-civil-war/

http://www.tudiabetes.org/forum/topics/diabetes-civil-war-people-with?commentId=583967%3AComment%3A1357011

Dear Dblogville: I Will Be Seeing Things In a Different, But No less Beautiful Light

Dear Dblogville: I Will Be Seeing Things In a Different, But No less Beautiful Light

5th UPDATE: THIS HAD ABSOLUTELY NOTHING TO DO WITH DIABETES -and I have the test results to prove it! Nothing to do with heart or brain issues. It was a 1 in a million thing- just like me~

4th UPDATE 12/11/09: Yesterdays Brain MRI and MRA are perfectly normal. Well...as normal as a brain owned and operated by yours truly can be~

3RD UPDATE 12/7/09: HeartEKG/ Echo cardiogram/Corroded Artery tests all came back negative. Apparently, I have no blockages, incredibly little plack, a fine looking heart muscle. and a "great set of corroded arteries!"

12/3/09 2ND UPDATE: Both my Endocrinoligist & The two eye specialists (who both said I had the most beautiful looking retinas they'd ever seen on a PWD with diabetes for 32 yrs) agree that my vision loss WAS NOT caused by Diabetes.

This is an updated version of last nights letter that I sent in reply to the emails in my inbox. It has some new updates, and less grammatical errors & typos. Though I did have some really good excuses for the latter, including getting my eyes dilated twice in one day, having my veins shot up with all sorts of dye- and the whole lack of vision thing.



Dearest Dtribe:

Thank you all for being such wonderful caring friends!

Without your love and positivity life would be much more difficult.

I love and appreciate every single one of you VERY much!


Tuesday was a very long day that involved multiple Doctors,tests, and a shitload of tears.

I tried keeping up on Twitter and email- but I was in a very poor calling area and couldn't access any online activity.


Plus mentally, I was dealing with some stuff.

You all know what happened on Monday, so I wont rehash.
Visually, my eye looks perfect. No pain, no redness, no goo, no outward swelling.

The good news, I have VERY LITTLE diabetic retnopothy- especially for someone whose had diabetes for 32 years.

But, a 1 in a million occurrence happened. I developed a blood clot in my eye called a retinal artery occlusion. Basically my right eye had a stroke and oxygen supply was lost to the vascular system of the eye. If it's not caught within 90 minutes of occurring,you loose your vision.
The kicker is- you don't have any symptoms. They don't know when this happened, it might have happened while I was sleeping since I woke up feeling like something was in my eye.

I've lost most of my vision in my right eye, permanently. The clot could have gone to my brain, but did not.

Yes, it was a lot to take in, and there were many moments where I couldn't speak because the fear and grief that caused a huge lump in my throat.

Thank God my friend Cathy V, and my sister Cathy M(two separate Cathy's who I love VERY much) were there to take notes and answer questions when I was to upset to.

On a positive note, I was born with an extra blood vessel in that eye- which only 15 to 20% of the population is born with.

That small, wonderful little vessel who I've decided to call "Mr Wonderful", provided my eye with some oxygen. And that wonderful blood vessel will allow me to see a bit from my right eye, once the swelling& pressure around the retinal area goes down.

The Docs are not sure if this is diabetes related or not- especially since I had very little diabetic retnopathy for someone w/D for 32 yrs.

They actually feel it could be due to heart and stroke issues that run in my family.

And they also thing it might have been some freak factor - one in a million shot.

The medical staff at both specialists office were very upset, brutally honest, and incredibly supportive.

The DON'T believe it will happen in my left eye - which is strong, and is already starting to compensate for the right.

I will be getting an ecco cardiogram & a corroded artery test to rule out any blockages.

The way I see things now will be different but no less beautiful.

I will still see the wonders that the world has to offer and experience the love of friends like all of you.

And for that, I am truly blessed.

This morning I woke up and had some sad moments.

I cried when I opened my eyes.

I guess I just need to get used to waking up too the world in a different way.

Not only did I cry, but I sobbed until I couldn't catch my breath.

Then I got up, scheduled my ecco cardiogram & corroded artery test for Friday afternoon.

To be honest, I continued to cry as I scheduled the tests.

On the bright side- my tears made the receptionists on the other end of the phone schedule me ASAP.

i've decided that I will cry when needed,but just as important, l will also continue to laugh and live.

This is a moment in my life that is a life changing one- but not necessary for the worse.

On the contrary, I will fight very hard to see (no pun intended) the gifts that this moment has given,and will continue to give me.

Like I said, the clot could have gone to my brain, the fact that it did not is indeed a gift.

The fact that my experience might get others to go to both the heart and eye Dr, is indeed a gift.

There is the gift of continuing on with life.
I will continue to live, be a Diabetes Advocate (perhaps a diabetes / Retina Artery Occlusion Advocate now) work, blog, and find the funny a regarding this most recent bump on the road of life.

And I absolutely expect all of you to do the same.

Just please don't send any braille get well cards, because I have too much on my plate and I don't have time to learn a new language just yet!

But feel free to done some new fashions inspired by yours truly by clicking HERE!

LOVE YOU ALL
k2