Oct 29, 2012

Click your heels together three times...

Ahh wouldn't that just rock? Something so simple to manage diabetes?

 It is no secret that I am a fan of reality television...and all things related to E! TV...throw eggs...I love it! TONS of celebs these days are wearing blue heels!! Do we take credit for that? Did the DOC posting photos of all of us fab warriors wearing our best Blue Shoes have THAT kind of influence??

 I say yes....yes we do.

Would it matter if a celebrity fashionista had a diabetes platform to spread the good word?? Ummm...duh, yeah. But once I started noticing those shoes, I couldn't help but think, HEY?? Do they have a diabetes connection?? I literally let myself believe that yes, society having lunch on television was saying HEY...WE LOVE YOU DOC!!

Matters not. What happened was I realized that I no longer looked at Kim Kardashian as a train wreck....with great eyelashes. I started looking at her, and the lovelies on the red carpets as catalysts. What if your *platform*...heels and otherwise, isn't just diabetes??

Can you host a Pet adoption/spay neuter clinic as a Blue Heel Society advocate? You bet.

Can you host a monthly book club or dinner club wearing Blue shoes? Bingo!

Hanging out in the car show parking lot with your 1958 Porsche Speedster...wearing those blue babies.....Yes and Yes.

Because YOU aren't doing advocacy a disservice.....YOU are touching the lives of a people who like you love animals, or kids, or politics or *fill in your favorite past time* and CHANGING the way people look at diabetes. YOU are doing your passion and repping the DOC big time. 

While we don't raise money for any charity...we support you and if you want to use Blue Heel Society as your platform to raise awareness for your causes....we say try us on for size!!



Click here to join Blue Heel Society as we click our collective heels up and go change the way people see diabetes. One step at a time....

See you at the mall!

Oct 26, 2012

Scuffed White Shoes after Labor Day


I was a six year old girl, who even at that tender age....was way too fashion forward for my very traditional southern upbringing. My Aunt Judy used to say she could see me wearing a bed sheet, draped just so.... I was totally into not wearing what everyone else did....well, until "junior high"...but that's a blog for another day....

My mother bought me this little peachy chiffon number and I probably wore that dress 800 times. It became my all-occasion attire...and I loved it. Once, I got myself all dolled up to go to the *Time Saver* convenience store with mama to get the dreaded items we'd forgotten at the grocery store. Like I said, it was a special occasion dress and wearing it made me feel special. I ran into the store after my brother and caught the lace trim on a shelf and ripped that dress. Oh, the tears.




That isn't the only really impressionable memory of that dress for me.....this dress, I wore to my grandmother's funeral. There are the weird photos that my family took of all of the grandchildren around her casket. Yes, my family does that....I don't have a good reason why. Memories are memories...and that is how they preserved that one. I won't share *that* photo.

My grandmother died from of complications resulting of living with Type 2 Diabetes. At the age of 6, I knew diabetes killed people. It scared me then....and scares me now. Diabetes robbed my mother and her siblings of their mother. It robbed me and my brother, and the subsequent additions to our family of a grandmother. I knew about this disease my whole life. Never did I imagine how much I wish I could have started my efforts in advocating for the rights of people who live with or care for someone with this disease THEN. I was a somewhat bright child who was far from shy or demure. I could have been fighting the fight all along. Hindsight, no?

Fast forward a bit....I have worked most of my adult life in some form of healthcare....womb to tomb. I have embalmed bodies at a funeral home, and I have managed an endocrinology office.....irony..... in that I saw the before and after affects of what a person who lives with disease really REALLY lives with....the good, the bad, and the ugly. I saw families blame their loved ones for dying or being fat or being not proactive enough in dealing with this disease. I saw aging parents literally give up taking care of themselves because while no one could see the disease....the stigma of having *diabetes* was like wearing white shoes after labor day....white shoes with a giant black scuff. 

I will say this....until the day diabetes got personal in my life...and it did...in the worst way imaginable....I was not indifferent about this disease....I was aware. I was unsure about what it actually meant to live with but I knew that it was always popping up in my life....one little glimpse at a time. I saw physicians I worked with get very large bonuses from insurance companies if they could get a portion of their diabetes client panels to a *target* A1c. I watched nurses call those pesky non compliant diabetic patients and literally bribe them to just eat better for this month...or exercise....or fill in the blank. I was incredulous. I remember telling the nurse practitioner I worked with that those clinicians and nurses needed to go to Diabetes Rehab. Quit blaming, bribing or coercing these people and try understanding how they live and encourage them to care. Fell on deaf ears. They worked with the ones that would and the rest....well, they didn't. It was their disease....and they had to manage it. WHA??

About the dress....That dress made me feel special. People who love, live with, care for or advocate for someone with diabetes.....they are my dress now....and my perfect white shoes with the black scuff that I will wear after labor day...This family of strangers I lean on daily for compassion may lead very diverse lives... but at the end of it all, we are NOT okay with the stigmas....or the thought that someone has no fight in them because it's *just* diabetes. That's enough for me. 

Diabetes entered my family before I was born.....put it's self in my life in many manifestations....and then it preyed on my child. My D kiddo is six now, and he knows more about diabetes than ANY professional I ever worked for. And he rocks. Plain out rocks the world daily. No way in hell will I allow anyone who can be within earshot of me to not only hear about diabetes....but about how fabulous and special a community we are. Scuffed blue heels are still able to tell the story....the real one.


Oct 25, 2012

Nora's post #3...Children's Congress Application

Nora has finally finished writing all her answers for the Children's Congress application. Geez!! That was a crazy, long application process. Now it will be my turn to condense her paragraphs into no more than three pages or 1200 words. UGH!! But, I'm glad she has gone through this process...she's learned a lot, as have I. about the Special Diabetes Act and diabetes and my daughter. If you've missed the previous two posts you can find them here and here.

I'm going to combine this post with questions 3-5.

Question 3: What does the Special Diabetes Program mean to you?

The Special Diabetes Program is important to me because a cure could take longer to find. If there was no SDP then a lot of the technology wouldn't advance and help us diabetes live a better life. Without the SDP there would be no TrialNet. TrialNet is VERY important because it helped my sister get diagnosed earlier. If she hadn't been diagnosed earlier then she would've been really sick. The SDP is hope for a better future, earlier diagnosis, understanding complications, help, hope and a cure. This is what the Special Diabetes Program means to me.

Question 4: Why should the US Congress support diabetes research to help find a cure for T1D?

The US Congress should help support diabetes research because it would help diabetics have a normal life. Without the government help, these programs would not exist or they would have to spend more time fundraising instead of researching, preventing, advancing technology and finding a cure. The US Congress needs to help my sister, myself and the other 26 million diabetics have a better life!

Question 5: What have you done to promote awareness of T1D in your community?

 I have raised awareness for T1D in my community being featured as 1 of 3 diabetics in a JDRF video, Why We Joined the JDRF Advocacy Family. I have attended Promise to Remember Me Campaigns for JDRF with my local Congressmen. I celebrate, with my family, community and other T1D's, World Diabetes Day events in Downtown Cincinnati, that our local JDRF chapter hosts. I have been interviewed by local newspapers and morning news shows about T1D. I also blog about my life with diabetes at http://lovingnora.blogspot.com/. I love doing all these things because I get to meet other people just like me! I also like to mentor newly diagnosed kids. I have met a lot of new friends by spreading T1D awareness. I'm happy I know I'm not alone!

Oct 24, 2012

Guest post - "Greatness because of Diabetes"



Emma & Mini-Type1Rider 

Guest Post via http://Type1Rider.org

Type1Rider.org is pleased to present a Guest post from one of our favorite Dmom's, Author, Advocate, and Creator (with her Daughter Emma) of 'Diabetic Barbie'...Amy Ermel. We also would like to express our most profound gratitude for the masterpiece in creating BY HAND, the Mini-Type1Rider pictured above. 

First of all, I would like to say that I am honored to be writing a guest post for Type1Rider.org, thank you very much for the opportunity! My daughter, Emma is 8 years old and was diagnosed with type 1 diabetes 4 years ago. Since that day, I have learned so many things to say the least. I think I would like to dedicate this post to one in particular though...greatness.

When the doctor walked in the room and gave us the official diagnosis, I never would have thought that anything great or positive could have come of it. I thought that we were destined for a life of battles with food, needles, blood sugars, and insulin. I thought that it would consume us and take over every single aspect of our lives. I thought that there could never possibly be anything that would shine some light on our now darkened spirits. Boy was I wrong!

A mere 5 months after Emma was diagnosed, she approached me and asked if we could set up a lemonade stand out front of our house to raise money for "the people looking for a cure." She looked up at me with such innocent and determined eyes, that there was no way I could say no.

Seeing as how it was November, we convinced her to switch it to hot chocolate..contacted JDRF, made a few phone calls....and managed to raise $1200 in 3 hours time on November 14th (World Diabetes Day). As I sit here now thinking of that night, I can remember her face....her little 4 year old face...standing there with such hope in her eyes. She was on marshmallow duty naturally...what other job would a 4 year old want, right? She stood there for 3 hours filling cup after cup with marshmallows, chatting with hundreds of people about her diabetes, telling them that she was helping to find a cure. To say I was proud, would be the understatement of the century. That night was one of the first moments that I saw her "greatness". I saw the incredible amount of potential and drive and determination that lies within a person living with diabetes.

One day last year, Emma came home from school and told me that her friends had been talking about how there was going to be a bald version of a Barbie doll made to support kids dealing with cancer and other diseases involving hair loss. She once again looked up at me with those same innocent and determined eyes and asked me so matter of factly why there wasn't a doll out in the stores that had diabetes. I decided to make a toy insulin pump and blood sugar meter for her to play with on one of her own dolls. I thought there is no way that I could ever take on a toy manufacturer and help her make this dream a reality. I thought that it would just be left at that...a toy for only her to play with.

Well, Emma decided that she wanted other kids to be able to play with them too. She wanted other kids to have something that made them feel special. She wanted to keep going with this idea...and really, with that greatness and that drive that lies inside her....who was I to say no? So, we created a Facebook page to gain support for our campaign to make this a reality available in stores...and we have nearly 6,000 supporters.

I think back to that day of diagnosis and I want to wipe away the tears of that old me and force myself to look at my daughter through clear focused eyes. I want her to see that greatness...that drive...the flickering light that is the embers of hope that burns from her gaze. I see it now. I see it and I know that no matter what this life throws our way and no matter how many times diabetes tries to bring us to our knees.....we will make it. We will do better than just make it...we will leap over every hurdle with style and we will make things happen. We will make change happen all because of her greatness.
 You can visit Amy's Blog HERE
To purchase a "virtual cup of hot chocolate" to help Emma support JDRF, please click on the following link: http://www.canadahelps.org/GivingPages/GivingPage.aspx?gpID=21134
To support Emma in her dream of a Diabetic Barbie, or other doll[s],  please click on the following link and click "like" on her Facebook page and share with others to spread the word! : http://www.facebook.com/DiabeticBarbie 



Oct 22, 2012

A guest post from my daughter, Nora...

So apparently, I've passed on the blogging bug to my girls. I LOVE it!! Sometimes it's so much easier to write down how you feel and I respect that. We are all so busy living and putting on a brave face that sometimes we just need to get it out. And that's what my baby did...


Dear Diabetes,

It's me,Nora. Why do you have to make my life so miserable? Why can't I just be like most of the other 12 year olds in the world? You surely get in the way of a LOT but, it doesn't stop me though. I just walk right past you. I really hate you but...one thing I do like about you, is that you ONLY make me strong. So I guess no thank you but thank you? Goodness...you are complicated. Whenever I'm playing a sport you just HAVE to mess with me. I mean like excuse me but, when I play sports it's MY free time, not yours. I am not being selfish. If anyone is being selfish...it's you. You just take my life away and not in a good way. This past summer you just had to get into my sister. Is this a joke to you? It's not a joke to anyone else. Well...I'm not waisting anymore time on you right now.
Not Yours Truly,
Nora

p.s. to anyone else that is suffering with T1D ��STAY STRONG��