Wednesday, July 29, 2009

Way Back Wednesday: Dear Mom & Dad, Inspired by all the Parents of The DOC

I've decided to follow the fabulous leads of both Scott and Amy's and do a "Way Back Wednesday," post.

I've followed their lead because:

A. Because there are some posts I LOVE, LOVE, LOVE.

And

B. Because I will be on the road all day and I really wanted to post.
The Following Post: Dear Mom and Dad, Thank -You, was originally posted on March 26th, 2008 and is inspired by all the parents in Dblogville-it's a Thank-You and a love letter to all of them. Everything they've done in the world of their Children with t1, allows them to grow up to be the fabulous adult t1's they are.

Hope it makes you smile!

Dear Mom and Dad, THANK YOU (Inspired By All the Parents In D-Blog Land)


Dear Mom and Dad -

I don't think I ever said it before, but
THANK- YOU so much for taking care of me; Debbie, and Donna.

God give you 6 kids and 3 girls with Type 1 Diabetes.

I don't know how you did it.

How did you take care of us all those years ago, before the technology and research?
Before the open forum of communication on the net and the freedom of
carb counting and insulin pumps?

Back in the days when urine testing required fizzy pills and glass tubes, a clumsy and and
inaccurate way that was used to measure our sugars way back when...Until Blood Sugar machines the size & weight of a brick came about.
These antiquated "machines" took 5 minutes to calibrate and another 5 minutes to measure your sugar. They were far from portable, required metal lancets that hurt like a bitch, and God only knows how accurate they really were. They were also VERY expensive. You bought one with money that we didn't have so that we could gain control. Instead of thanking you, I bitched about it.
I wanted to be
NORMAL & fought you tooth and nail. I'm sorry.

I don't ever remember you crying when I was diagnosed. I know you did, but you kept your tears behind closed doors and in the dark. You always entered my hospital room with a smiling face and a bunch of new "Romona" books for me to read.

I just did the Diabetes math. I was 8 at my diagnoses, Donna & Debbie we're both 12.
Donna is 20 years older than me and Debbie was 14 years older.

So, if I've got the math down correctly, 1st came Donna at the age of 12. When she was 18, Debbie was diagnosed at the age of 12.

Which means you had 6 years before 1 Diabetic daughter became 2.

You had 10 years before 2 Diabetic daughters became 3.

Donna had married and moved out four years earlier by the time of my diagnoses.
Your daily diabetes family life was just getting easier when I joined the Club of D. It must have been so hard for you to handle...And even harder for you to hear.

Mom and Dad, I'm so sorry that my diagnoses hurt you, and for what all our combined diabetes has put you both through.

You never let us feel sorry for ourselves. I never grew up with a hatred of diabetes. Though deep in my heart, I hated what it did to you. I think it really helped when dad sat me down long ago in my hospital room and said;
"Kelly it is what it is, do what you have to."And I did.
Daddy knew from experience, because he was a T1 as well.

Mom, you posted the ADA diet on our kitchen wall, right behind my seat at the kitchen table.
You measures portions fanatically, right down to the grape. You'd dole out 12 grapes for my snack. I'd give them back and say in a venomous
"Keep Em! Who can eat 12 grapes?!" But u were just doing your job and never wavered. I never experienced chicken with the skin on it until I was 21, and to this day, have never had a class of OJ that was more than 1/4 of a cup.
I don't even drink juice anymore.

.
Dad, you body surfed and swam in the ocean every summer, and you shared your love of all water sports with me. Together we became part of the waves, while maintaining good numbers.
You rode your bike every morning, and when you passed
by my bus stop Freshman year, I was embarrassed instead of proud. I'd give anything to see you peddle your bike one more time. I'm sorry.
You and mom took long walks every evening with the dog and u ou always said exercise was the key.

You were meticulous, bordering on the insane, about what you put in your body.

A militant soldier when it came to food. Only skim milk, fruit, and eating only whole grain bread before it became the rage. While I longed for "Wonder Bread," you put the kibosh white bread of any kind. I thought you were mean, but you were smart because you still let us enjoy ice cream.

Diabetes took so much from you both, most namely your daughter Debbie.
Daddy, you never recovered from her loss. Every time you spoke of her death, I heard sadness and anger all mixed together. It broke a part of you that all my jokes couldn't fix.

Mom, you cared for her (for all of us,) with such gusto that you're heart literally started to skip beats.
The scariest moment of my life was when you and Debbie were both in separate hospitals.
I came home from school to an answering machine full of voice mail that told me nothing
and everything.
I knew one of you had gone to heaven. I was so scared it was you. I felt so guilty (yet
relieved, because I still had a mom) when I heard it was her.

What got me thinking about what you both did for me?

All the parents of Diabetics kids whose blogs I read. I hear what they go through everyday and I immediately think of you both. They tell me what you wouldn't.

Parents of diabetics are a different breed entirely.

They are strong, keeping a smile on their face when they take care of their kids, even when they feel like crying out in pain.
These parents have the
strength to say "no" to their kids, even when every fiber of their soul wants to say yes to them.
Strong enough to take their kids blood in the middle of the night, insert infusion sets that make their babies cry, give-up gluten with a smile that never seems forced, and count
carbs until it becomes second nature to everyone in the family.

These moms and dads have the fortitude to let their diabetic children grow to become independent young adults. Even when they know that independence means that their kids will make conscience mistakes in order to fit in.

Diabetic parents hate the disease, but are strong enough to not let their kids hate it, because if they did, their children would never learn to accept and love themselves.

To every parent in D-blog land,
THANK-YOU. I know when your kids are old enough, they will tell you themselves, and they will have meant from the bottom of their hearts.

To my parents,
THANK YOU. I wouldn't be here today if you hadn't worked so hard to keep me healthy.

You taught me to pick myself up by my bootstraps and move forward. I hope I'm making you proud.

Love You Both!
Kelly
#6

Monday, July 27, 2009

My Spin on the Roche / Diabetes Social Media Summit

The Diabetes Social Media Summit "Think Tank" Picture courtesy of Roche.
For a numbered legend of the photo and links to each person click here 
Thanks tudiabetes!

Many a post is already up regarding Roche’s new Media Summit- I needed a few days to rap my head around what I had just been a part of.

First off, BIG THANKS to Amy for making it happen and asking me to be a part of something that was not just historic, but incredibly life changing!

Second set of BIG THANKS go to Roche, who extended the invite and were incredibly brave to invite us all out, on their dime, and for listening to what we as Patient Bloggers  and Patients had to say - both positive and negative. As a group, we were not at a loss for words and thefact that they were willing to listen, no holds bared, was incredible!

The Day started off on an annoying note at Philadelphia International Airport when I was unable to update Diabetesaliciousness from my Blogger account via my iPhone - I even approached another iphone user at the airport and he had no luck getting the keyboard to appear in the blogger account either.

On a positive note- Leeann from The Butter Compartment was sitting at the terminal when I arrived and we were happy to find out that we were on the same plane!

The flight left about 20 minutes late but was uneventful.  The plane was a shuttle and I was happy when we landed.

When we arrived in Indiana, Leeann ran to baggage claim and I ran to the rest room. When we met up again, we were joined by  Bennet, from Your Diabetes May Vary,

who had also been on our plane.

We were met by a Driver whose name I forget, and who was not a  Roche employee, but an employee of a shuttle company whom Roche works with.  MORE ON THIS LATER.

In the lobby we were greeted by Scott S, Joe, and Gina- all whom I’d met before. Lot’s of hugs ensued and I ran up to my room to get dressed for Dinner, then I ran back to the lobby where I ran into William Lee Dubois- except I wasn’t sure if it was him or not so I just said “Hello” and smiled. We had the opportunity to talk in ernest later on.


D Ladies in the house!

At the Bar I ran into more Diabetes folks I'd met IRL; Fran, Kerri, Amy,and Bernard who I'd met on previous D-outtings, and  immediately met Chris, Scottie J, Sandra,  David from Diabetes Daily, Kitty (who I'd talked with on the phone) and Crystal for the first time in Real LIfe

I also met and  talked with both Brandy from Diabetic Sisters and Jeff Hitchcock from Children With Diabetes, , but not nearly enough, but they were awesome just the same!

 When I turned to my left there was Charlie Cherry from Diabetes Power Hour, all dressed in black and very Johnny Cash like, standing next to Chris from Diabetic Rockstar

The bar was Diabetes Blog Central and the Roche reps had a difficult time getting us out of the lobby- it was like a class reunion and people 

Scott S & his "Angels" 

were hugging, chatting, taking pics and buying drinks. We literally could have stayed there all night!

I was standing next to Amy T, Fran C, and Riva Greenberg when a Roche rep grabbed us and steered us towards the hotel entrance “ We need to start filling up the shuttle to the restaurant, so a group of us got on the shuttle and began bonding even more.

We arrived at Maggiano’s and walked into a dinning room filled with Roche Reps from every department. They walked up to us and immediately started engaging us in conversation – and we did the same. It was very strange and flattering to hear one’s blog quoted from the folks at Roche-I’m glad they did their research!

Half way into the  "getting to know you portion of the evening I would meet Ninjbetic (and ran across the dining room to hug him tight) and  CALPUMPER  in the flesh, both who experienced flight delays, for the first time- and they are wonderful!

 Dinner at Maggiano’s has been described as a 7h grade dance with Roche employees interested in life with diabetes and DBloggers willing to share. And that’s exactly what it was! I believe both sides walked away from the evening knowing the other on a personal level, and a great time was had by all!

At the Dinner/Dance with my boys!

Room 966 A.K.A - The Room of Shared Stories...and a Stalker Free Zone for those being stalked by Tim

After more chatting and giggling, we got down to the business of sharing our D story. It was amazing and I’m not sure if I can put it all into words, except to say, at that very moment there’s no place I would have rather been.

When It was my turn, I took a deep breath- (FYI, I am usually NEVER at a loss for words regarding life with D) but I have to tell you, as I looked around at the faces in room 966, I felt that I was looking into the eyes of my Diabetes, past, present, and future. And for one split second, I thought of a particular face that would have benefited the most from the DOC, but had left this world back in 1991. The emotion that had been welling inside me all night, came to the surface and I couldn’t hold back.

I talked about my “D Story” and I’m really not sure exactly what I said,

but I do remember at one point I broke my own “There’s no crying in baseball” rule and my voice began to faltered. I started to cry tears of acceptance and joy, of loss and happiness all rolled into one.

G-Ninja opened his arms and hugged me tight and made me laugh, and in that room, I felt safe.

Room 966 was also protected Chris’s virtue from his stalker Tim- so it was truly a safe haven for all!

Thursday – The Summit-

The Summit itself was 8 hours of intense Dialogue between the diabetes communities expressing our wants needs and concerns with Roche.

The first part of the morning was devoted to ways in which to reach out to the patient population, creating guidelines, and  a Manifesto for both Pharma and Patient Bloggers to follow in Social Media. Both Manny & Amy have detailed breakdowns-GO READ THEM if you haven’t already.

Roche and other Pharmaceutical companies want to enter the world of New Media and as Diabetes consumers, and we want them to- absolutely. But we,as Patient Bloggers, Patients, and Consumers require that Pharma's participation is done in a way that’s honest and upfront, and in a way where we the consumer concerns will not only be heard, but validated.

During a lunch breakout session, I told Dan Majestic, Director of Sales for Roche, “That Diabetes is a Technology based disease and we need to be able to afford the technology, because our life literally depends in it - In order to treat we need to test, and test often.”

Not only do all companies across the board need affordable testing options, (and insulin, insulin-pump, CGM and other options) we need insurance and Medicare to stop limiting the amount of strips they are willing to pay for.

For instance, Medicare will only pay for patients to test 3 times a day. How does one fix their blood sugar issue by testing 3 times a day?

All the diabetics in the room agreed that advertising MUST stop pitching the two faces of diabetes that the public knows:  

1. The Ideal Diabetic

2. The Bad Diabetic (Steel Magnolia version)

For all of us in the Dblogville and beyond, the “Ideal Diabetic” is not one whose numbers are constantly at a 97. 

The Ideal Diabetic is one who puts the guilt of the numbers aside and learns from every test taken. 

The Ideal Diabetic is one who makes mistakes and learns from them.

The Ideal Diabetic is one who voices her or his opinion and becomes not just a Diabetes Advocate for themself, but for everyone else whose lives are affected by the disease.

We in the DOC – and beyond, ARE the Ideal Diabetic-the rest of society needs to relearn what diabetes is and what it means to be a PWD.

Kelly Close, from Close Concerns mentioned that Diabetes is perceived as a character flaw- and she’s absolutely right! 

I've said it before and I'll say it again,Diabetes is the only disease (besides sexually transmitted diseases) where the patient is blamed for their disease.

A perfect example of this was what LeenAnn, Bennet, and I experienced on the car ride to our hotel. 

The 3 of us were picked up by a Black Car Service, and the following conversation transpired with our Driver, who WAS NOT a Roche Rep, but he did represent John Q Public’s ideal regarding Diabetes:

Driver: SO, what business are you all in?

Me: We are in the business of living a great life with Diabetes.

Driver: REALLY? A great life with Diabetes? You all should take your patients to Dialysis ward- let them see what happens when Diabetics don’t take care of themselves.

I looked at Leeanne and her face was literally frozen in horror.

Bennet: WE ARE THE CLIENT.

Me: YEP, WE are People with Diabetes.

Driver: I didn’t mean to offend, really I didn’t I WAS A PATIENT in the Dialysis ward and my mom’s a diabetic.

Me: Times are different today; it’s much easier to take of your diabetes. Nothing is off limits and the technology is much more advanced than 30 years ago-it’s more advanced that 5 years ago. 

Needless to say, we were on the defense-, which is not very different than most days for those of us with the Big D.

Do I blame the Driver for his poorly chosen words that we have all heard before? NO I don't. 

I blame the way society- including Doctor’s blame the PWD. Do I want the gentleman fired? NO I DON’T. I want him and the rest of the world to be properly educated in Diabetes; it's causes,it’s issues, and it’s management to prevent conversations like this from ever having happening.

Back to the Summit:

At one point in the afternoon, Ginger Viera  mentioned the fact that we need to look at 1 number at a time and that she’d much rather "see an ad that showed a meter with a number of 310 with a real Person with Diabetes in ad that stated: This is Ginger, she woke up with a 310, now what? “ And all of us in the DOC wholeheartedly agreed.

I raised my hand and Amy handed me the mic. I stated that I wanted to see the guilt of being a diabetic be removed from the disease.

“As Diabetics, we are always saying, “I’m sorry.” Sorry to our Doctors, our friends, our parents. The guilt starts with the high numbers and the reactions we get. It becomes a Domino affect; patients start fudging logbooks, lying to our docs so we don’t have to feel guilty. Patients stop going to see their Endo’s and stop testing.”

The last 20 minutes of the day was tense when Chris from Diabetic Rockstar brought up the cost of test strips and Fran Carpenter had has back! Let me say that I was not there for Chris’s initial question- I was in the bathroom. But When I returned to the talk questions were flying across the room regarding the cost of test strips.

I wasn’t quite sure what was happening, but I do know SOMETHING MUST be done regarding the cost of being a diabetic on every level.

Scott King, of Diabetes Health had a great suggestion of offering special insurance for test strip customers without insurance- which would be wonderful  for all parties involved. More people could afford to buy the strips and test more often.

Collectively as a whole, we only had 8 hours of discussion and 8 hours isn’t enough to change the way things are done. But I believe it was a great first step in the process towards change and understanding between all parties. 

Roche was the first Pharmaceutical Company in history to openly reach-out to a group of Patient Bloggers - that move is both historical and positive on their part, and I thank them for taking that first step and asking me to take part.   

Now, if they can continue with what was started, wonderful things can happen.

END NOTE: I was the only person who stayed a second night, due an original flight that had me leaving the conference by 1pm.  I had signed up for the Roche tour and didn’t want to miss it. Roche was kind enough to change my flight in June and I was able to stay the extra night-, which was great thing because I was physically and emotionally exhausted. The Tour of the Test Strip manufacturing plant was impressive, a lot goes into to the production of those little strips, including gold, rocket science, and many peoples sweat and hard work. Both William Lee Dubois and David Mandosa have excellent recaps- READ THEM.

When I said my goodbyes to the group on the airport shuttle I was sad. I hugged everyone tight and as I got off the bus, Scottie J was getting on-“Hey what about me, where’s my hug?” As I hugged him tight and we told one another how we felt from the heart.

The car ride back was quiet, the hotel was quiet, even my dinner for one at The Cheesecake Factory was quiet- I was missing friends and trying to fully understnad what had just transpired in the past 32 hours. The waitress had to come back 4 times before I was ready to order. Note to self: Never go to the Cheese Cake Factory when you want to have a light meal and some self-reflection UNLESS you know the menu!

“I needed "more time" in every sense of the phrase,” and that's exactly what I told my waitress, and she gave it to me.  Allowing me to sitting outside on the patio, with my sunglasses on, which was good thing because I started to tear up. I missed my D friends so much, and I was so proud of what we had all accomplished that day.

 

Friday, July 24, 2009

D-Blogger Summit Teaser

I Literally just drove back from the airport (and Friday afternoon gridlock,) walked in the door, threw down my keys and “plugged in” after returning from the D-Blogger Summit at Roche Pharmaceuticals.

The event was historical and emotional, educational and explosive  AND I WAS SO HAPPY TO BE THERE FOR IT ALL.  

And yes, my mind is spinning faster than Jeff Gordon at Indy!  So much occurred in such a short amount of time that I still can’t wrap my head around it let alone decipher my notes.

However please stay tuned as I will be posting  all the Diabetesalicious™ details on Monday!  

Tuesday, July 21, 2009

An Addendum To "What Diabetes Has Given Me."

And addendum to my previous post: Flashback Friday-What Diabetes Has Given Me

After posting on Friday,I received an email from one of the women I had lunch with on Thursday, who was also a Type 1 and had been diagnosed her last year of college. What she wrote has been on my mind for days, and I hesitated writing about it-but I am, for several reasons. It's how I feel, and I think it's how many others might feel regarding their own life with diabetes.

" Kelly - Thanks also for sharing your personal story. When you live with diabetes, it's hard to imagine someone else's life being "more" impacted than your own... But I have to say, you're life hasn't just been impacted, it seems to be created around diabetes... And your approach to it all now is really remarkable!"

A life created around diabetes ? A remarkable approach? I don’t know about that.

I ran away from any and all things having to do with diabetes my whole life. Diagnosed at 8, by the time I was 19, I’d had my fill of it. Living with a family of type 1’s, the last thing I wanted to do was go to college and learn about Diabetes.

When I was in my early 20’s my sister died from Diabetes complications. Part of my heart broke when she died and another portion was filled with guilt (that followed me for years, still does actually) and I continued to run away from the diabetes world.

I’d continually run into people (parents of CWD’s, coworkers, my mailman, etc) who would ask about life with diabetes. I’d be positive and answer their questions, and leave it at that.

When I was 26 my 16-year-old nephew was diagnosed with "the diabetes", and while I was there for him on every level, telling him "that life is what you make of it, regardless of diabetes -You can do anything Brendan, diabetes or not!”

I still stayed far away from the diabetes community as a whole. But damn if Diabetes "didn’t keep pulling me back in!"

In my early 30’s I went on the pump and became consumed with telling any and all who would listen that the pump and glucose testing equaled freedom.

Three years ago I started working with Diabetes Orgs and Diabetes patient groups.

18 months ago I found out about the DOC and I started my blog.

Diabetes has given me something else - MY PASSION.

Friday, July 17, 2009

Flashback Friday: What Diabetes Has Given Me

Yesterday I had a marathon lunch with some new dfriends and we talked about many things. Life in general; growing up with diabetes and other health issues, and how those health issues help to shape you as a whole. 

I mentioned that there are many gifts associated with diabetes and other conditions, you just need to be aware of what they are. Sometimes you don't realize the gifts or the reasons until many years later. But when you finally realize the gifts that were given also helped shaped your sense of purpose, you become EXTREMELY grateful ~

Then I went home and found the following entry titled "What Diabetes Has Given Me," which I wrote back on 12/6/2007-back when Diabetesaliciousness was just a few months old and I didn't know many in Dblogville. 

It's Friday - I was having a blog flashback- and I hope you enjoy it~



So instead of complaining about Diabetes, I felt that I needed to make a statement about the positive, (yes positive) things Diabetes has given me in my life. Let me know if you agree.

1. Diabetes has given me Humor. When I was diagnosed at the age of 8 - on Halloween and my parents anniversary no less, I don't remember crying, really I don't. I do remember trying to make my mom and dad laugh so they wouldn't cry. I remember spending 3 weeks at Children's Hospital in Philadelphia injecting saline solution into an orange and doing my best to make the other patients on the 3rd floor smile and giggle so they wouldn't be scared of needles; x-rays, and upcoming surgeries.

Was I scared? Yes, more than anything. Did I show it? No. I laughed at it because I didn't want anyone to see me cry. In my 8 year old head, I knew that my family was upset and that my diagnoses had changed the whole family dynamic. If they saw me cry, then they would cry and I didn't want to be the cause of that.

Sometimes at night, when the hospital was at it's most quiet, the tears would start to fall as I thought about needles for life and saying so long to my beloved Pixie Sticks and Peanut Butter Cups. But then I'd watch late night television and get lost in the magic. Johnny Carson and reruns of Hogans Heroes and Bewitched would make me forget just long enough to halt the waterworks and drift off to sleep. 

When I finally came home from the hospital, I spent the next few weeks making my classmates laugh when it came to my new diagnoses. I did this in many ways. I would raise my eyebrows "A La Groucho Marxs" as I reached for my apple to eat in the middle of class, knowing full well that the substitute teacher has no clue that I was diabetic. Hilarity would ensue when she would start reprimand me and I would say sweetly, "But I'm a diabetic, I'll go into shock if I don't eat."
I would educate a whole school yard full of children on diabetes, by doing my Rosanna Rosanna Dana impersonation. It went a little something like this: "Dr. Richard Fader from Fort Lee NJ writes, Dear Rosanna Rosanna Danna, whats all this talk about Diabetes; what the heck is it, and can I catch it?" Then I would explain in my own way what it was and that it wasn't contagious. Thanks Gilda Radner - U taught me so much and always made me laugh!

Would I have a great sense of humor and irony without the "big D?" Magic 8 ball says "Most Likely,"
but would they be as developed? Not bloody likely.

2. Diabetes had given me Empathy. I think all of us are born with a sense of empathy, but being a child or adult with diabetes most certainly hones that skill and allows most of us to be a good friend to all who need one.

Most kids who have diabetes, or have a family member with it, know what it's like to have a bad day. We understand the fear of not fitting in and sticking out like a sore thumb.
Diabetics become good friends and good listeners and these gifts last us for life. 


3. Diabetes allows me to know my body's idiosyncrasies. I know when I'm going to be sick two-weeks before I'm symptomatic. My blood sugars run high for no apparent reason and I can start pre-treat. When I say pre-treat I mean bolus and basal accordingly, get enough sleep, pop some zinc lozenges, drink some Airborne, and O.D on the chicken soup & Vitamin C.

4. Diabetes allows me to pull myself up by my bootstraps on a daily basis, because Diabetes has taught me that everyone has issues, it can always be worse, and I have no choice but to forge ahead.

Tuesday, July 14, 2009

It’s All About The Numbers…. As in 14,000 ! And No Diabetes Police Allowed!

Actual Aerial footage of Kelly K's (k2's) lunchtime Blood Sugar

Based on a suggestion made to TuDiabetes/EstuDiabetes Founder Manny Hernandez from TuDiabetes member & Diabetic Living Magazine's Kelly Rawlings-14,000 people with diabetes (10,000 from Tu Diabetes & and 4000 from EstuDiabetes) will take 5 seconds this afternoon at 4pm EST, and simultaneously take & post their individual blood sugars to raise awareness of the important role monitoring blood sugars plays in managing diabetes!

Hope your reading this insurance companies! Talk about strength in numbers! And not one single member of the dreaded Diabetes Police will be in attendance!

NO DIABETES POLICE ALLOWED!

Here’s the link: 14k Strong TuDiabetes


Time Zone Breakdown:

* 1:00 pm PT
* 2:00 pm MT
* 3:00 pm CT
* 4:00 pm ET
* 8:00:00 pm GMT

READY? AIM, TEST!


Monday, July 13, 2009

How Many Diabetics Does it Take To....

How many diabetics does it take (on a 24 X 7 basis btw,) to test blood sugars; count carbs, bolus/inject accordingly, exercise daily, continually educate her or himself and others (with out blowing a gasket or throwing a punch when they say something offensive,) check the occasional keytone, get themselves to their Endocrinologists appointment every 3 months, deal with insurance companies continually wanting to deny them care and or coverage, and not loose it entirely when his or her numbers get wacky for no reason at all?

Image: Pablo Picasso (Spanish,1882-1973), Girl Before a Mirror (1932).

The answer is ONE- take a look in the mirror and give that person with diabetes a big round of applause, because YOU ROCK!


Saturday, July 4, 2009

Stars And Strips Forever.......And Muppets?

Wishing you and yours a wonderful July 4th-with lots of love, luck, and laughter.
Be safe,laugh loud,test often,& "Bolus baby, BOLUS!"

The Attached video made me smile and reminded me of growing up!
Anything with The Swedish Chef & Animal catches my eye. Hope it makes you chuckle!




Wednesday, July 1, 2009

Murphy's Law Gets All Tricked Out Diabetes Style~

Actual Aerial footage of Infusion set incident # 517

Diabetes & ripped infusion set: 1, Kelly & her white dress shirt: 0

Diabetes, I laugh in your face-HA,HA,TRIPLE DOG HA!!

Diabetes can drive you nuts on so many levels, fashion being the least important of course, but no less annoying.

I find in times like these,when Murphy's Law gets all "tricked out diabetes style," (because this never seems to happen when I'm wearing black,navy, or purple) it's best to laugh, and quickly reach for some cold water and soap.

Which is exactly what I did~