Showing posts with label #t1dlookslikeme. Show all posts
Showing posts with label #t1dlookslikeme. Show all posts

Friday, November 1, 2019

#NDAM: Thank you for coming to My Diabetes Ted Talk, Day 1


My diabetes footprint.
Make your own @
JDRF.org/NDAM 

November 1, the first day of Diabetes Awareness Month. 
Somethings you need to know about diabetes - no matter the type. 
I've had t1 diabetes almost as long as I've been on the planet. 
Living with and managing diabetes is fucking hard work and all encompassing - and no matter what type of diabetes you have - so let's not fight about what type is worse. 

Some days diabetes rocks me to the core, other days diabetes plays nicely in the corner.

Every day is a day a "Diabetes Day," no matter the month - it's always by my side. 
If I hated diabetes, I'd be hating myself - and I'm done hating. 
I already have enough self esteem issues. 
Magazines and websites constantly tell us that we are not tall enough, short enough, skinny and or curvy enough. 
I don't need another reason to tear myself apart. - I already do that without blaming diabetes. 

Do I get mad at my diabetes? YES. 
Is the Pope Catholic? 

Do I work hard to have my diabetes be drama free YES. 
DO I flip my diabetes bitchswitch?
You bet your sweet ass! 

If you have diabetes - keep up the good work, get back up when you stumble and please know that you are not alone. 

If you love someone with diabetes - thanks for your support. We need and appreciate it so much. 
And we need and love you and all you do for us.

If you want to learn about diabetes - this month is a great time to learn and ask questions. 

Thank you for coming to #MyDiabetesTedTalk, Day 1

Thursday, October 31, 2019

42




ME
Photo Cred: @sweetercherise

42 years ago today and bright and early in the morning, my parents drove me to Children’s Hospital of Philadelphia - after what seemed like hours, I was diagnosed with T1 Diabetes. 
Some things I remember vividly, many things I don’t remember at all. 
Life changed that day and I can’t go back, nor can I spend much time wondering about the what-ifs. 
I embrace being the girl who lived and I’m working hard on becoming the woman I want to be. 
Every year since Diabetesaliciousness began, I’ve written a list of things that I love and am grateful for on my Diaversary
WHY? It's a good reminder that I’m still here, still alive, and there’s so much in life to love and be thankful for.

42
  1. I look fabulous in both black and jewel tones
  2. My family and friends who are family 
  3. Little kids laughing 
  4. Rereading my favorite books for inspiration or just because 
  5. Finding a new book that hits me right in the feels
  6. I can still do cartwheel on the lawn and still rock a handstand underwater
  7. Making homemade soup. Some people are bakers,  I’m a “soupier.” I love making soup form scratch - its my Zen time, allows me to be creative, AND I’M REALLY GOOD AT IT
  8. Making soup for friends and family
  9. Good Karma Hospital on Amazon Prime - I'm hooked!
  10. The ocean. It makes me feel whole and I get really antsy when I’m landlocked for too long
  11. October and November Skies at Sunset 
  12. Traveling. I LOVE IT
  13. The Diabetes Online Community - I’d be lost with you. You teach me always and bring me up when I’m feeling down. I will always fight for you and with you!
  14. Diabetes Meet-ups
  15. Manatees - my favorite sea mammals and I love them 
  16. Atlantic City Italian Sub rolls with good butter or EVOO 
  17. The Beach. See number 9 
  18. Black leather boots 
  19. Prosecco 
  20. A nice glass of Red
  21. The occasional martini
  22. Daffodils
  23. All spring and summer flowers 
  24. My veggie garden 
  25. Going to the movies 
  26. Laughing from my belly
  27. Nailing the cupcake carb count from a really top-notch bakery
  28. My mom’s engagement ring and wedding band. Every time I wear them on my right hand I think of my parents. I love them and I miss them
  29. My nieces and nephews. They own my heart 
  30. Vanilla anything
  31. Dark chocolate and Reese’s Peanut Butter Cups
  32. KerryGold Butter 
  33. Jewelry. Antique, family heirlooms, costume, handmade, Native American, the macaroni bracelet one of my students made me a few years ago. I LOVE JEWELRY
  34. Photography. I love taking pictures - especially nature photography and candids. I'm working on my photography skills - more on that in another post
  35. Photography As Art. It absolutely is and I love photographs taken by artists behind the lens
  36. Music. ALL KINDS
  37. Singing. I love to sing and at one time I was pretty good. I need to sing more
  38. Writing
  39. The sound of rain and being outside right after a storm
  40. Exploring. I love to explore. Sometimes I go out on a drive, pick an unknown road/town and explore
  41. Sea glassing
  42. Finding treasure everyday. OK, sounds corny, but it’s been my mantra as of late.
Every day as of late I tell myself to “go out and find the treasure.” 
I’m not talking about a treasure chest filled with jewels and gold (but I’m down with that,) it’s about finding and experiencing all the good in the day and in life…. Including life with diabetes. 

Some days the treasure is right in front of me, other days it shows up in small ways and victories. And on the days when the treasure seems impossible to locate, I remind myself that there’s much joy to be found in the search. 

Thursday, July 19, 2018

Friends For Life Orlando, 2018

Just a few things of the many things I loved about the Children With Diabetes, Friends For Life Orlando conference, I attend last week.
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Super special coin and bracelet.
People roaming the halls of Disney’s Coronado Springs wearing green and orange bracelets, and who “get diabetes," without ever uttering the D word. I LOVE THAT. 

Littles running up to me and shouting: Mama, she has a green bracelet like me!

Realizing that the young “teen” you've mentored/been friends with for years, is now a vibrant 21 year old woman with t1d who is thriving! 
Sidebar: And who promised you (and put it in writing,) that as an adult t1 woman, she will ALWAYS keep an 8 pack of juice boxes by her bed. 
Seeing the 16 and 14 year-old t1s and the awesome 11 year old orange bracelet sibling you’ve known since they were in single digits,(and missing the 16 year old orange bracelet sibling and her mamma, who were sidelined due to an injury,) are growing and becoming and it blows your mind.

Hanging at the bar with other green/orange bracelet adults and laughing with them about everything - including all the beeps and blips from all the various diabetes electronicals.

Bumping into the little boy who told you last year that diabetes “makes him happy and sad,” and who now declares “that he loves diabetes,” and ROCKING YOUR WORLD, in the process. 
2018 and 2017.
What a difference a year makes~
Meeting a 10-year-old, green bracelet “First Timer,” and his orange bracelet wearing little sister in the lunch line, and who become super excited to make superhero capes at the Dexcom booth after you explain to them that Dex's Super Hero Cape Making Station is an actual thing. 
Then green bracelet boy discusses with you (and in great detail,) about pumping; wearing a Dex, and how he gets his love of sauerkraut from his Grandmother, as he piles his lunch plate with 3 big scoops. 
You get dTechy with him and also tell him that you can totally relate to his sauerkraut obsession because thanks to your dad, you feel the same exact way about horseradish — and you both start to giggle. 
He follows you over to the dessert table and you both go for the oatmeal cookies “because they are the best,” and the giggles continue.
A few hours later, two green and orange bracelet wearing super heroes (and one with a penchant for sauerkraut,) are rocking capes and participating in your #IwishPeopleKnewThatDiabetes booth, then head over to the Beta Bionics booth and make the crazy light thingies and then give them to you, and after you'd complimented them on their cool crazy light thingies.  :)  


My new FFL cape wearing, sauerkraut loving,
orange and green bracelet wearing, sibling Super Heroes!
Your special group of “First Timers alumni,” are now seasoned Friends for Lifers, who you have special drinks with at the pool and exchange silly texts with.
T1 Chicks & Orange Bracelet friends @ the Omnipod party for
T1 Adults at #FFLOrlando18 
D Squad goals met and exceeded because of a group of fantastical green and orange bracelet wearing chick friends who have indeed become friends for life. 
These women always encourage you throughout the year; send you wake up texts on the day you fly out to ffl; buy you unsalted almonds and water at Publix, ply you with British chocolates, understand your “L Explorer” and “GM Running Club” references, and always make you laugh!

Sitting at the bar and watching your “diabetes brothers” totally nerd out over Disney’s Avatar Ride, while you and your D-Sister can’t stop laughing at and with them.

Attending adult t1 support sessions about diabetes burnout and diabetes complications in a judgment free zone. 

Your D mama friend who once again makes sure you’re OK with juice boxes and bottled water. 

Orange bracelets who have become friends for life!

Watching your t1d friend experience FFL for the first time and through her eyes.
You forget that she’s shy because she's anything but with you. 
And you burst with pride as she reaches her goal to meet 3 new green/orange bracelet wearing friends in one hour at the bar.

Discovering that the shy little Ninja Turtle loving, 4 year old green bracelet wearing boy from last year is now a talkative, confident, and positive Spidey Super Hero with a huge smile and an amazing attitude!

Experiencing one of the worst lows of your life surrounded by people who love and help you, and continue to check in with you throughout the day, into the evening, and well into the next day - and in a way that doesn’t make you feel like a burden. 

And you are so incredibly thankful that they were there.

Realizing a few days later while talking with your diabetes brother about that low, that maybe it’s time to do something you’ve been putting off for a while. 
Sidebar: More on that later. 

Standing at the ice machine on Friday afternoon after a long day of sessions, attempting to fill a ziplock bag with ice, so you can ice your broken toe (long story), and failing miserably, because the goddamn ice keeps spilling EVERY WHERE and you are about to lose your proverbial shit.
Then, and just as your about to let out a stream of expletives, you feel a slight brush against the side of your thigh and exactly where your Omnipod and purple grip are, followed by a little voice that’s barely a whisper, saying: I like your gripper and your Omnipod. 
You turn around and see a little girl with blond hair, wearing a blue and green bikini, with a pod on her belly that’s surrounded by a super cool black oval grip— and she’s looking up at you with a broad and shy smile.
And you know it must have taken all the courage she could muster to walk up and start a conversation with you.  
Your heart melts and you respond: I like yours too. 
And then you both start talking about all things diabetes — your new D friend is a year and a half in and her mom is watching and smiling. 
All of a sudden you’re not frustrated anymore. You’re happy and want to hug this amazing little girl and tell her that’s she’s exceptionally awesome, because she is, so you do. 
You’re glad you’re wearing sunglasses because you know your eyes are on the verge of leaking. 
Then her mom grabs your arm and thanks you for “doing what you do because it’s amazing,” and you feel your cheeks turning red. 
You thank the mom for all she does, tell your new friend that you’ll look for her in the pool and in the hallways and she promises to do the same. 

You say your goodbyes and walk in the direction that may (or may not,) lead your back to your room, as tears start streaming down your face and in the best of ways.

And once again you are reminded how much you need to be at the Friends for Life Conference in Orlando - for yourself and for others.  
And how much #FFlOrlando18 recharges your diabetes batteries and your spirit - and once again, you are so incredibly grateful~

Wednesday, September 6, 2017

My Omnipod Experience - Part One

Learning and discovering new things every damn day and glad that Insulet gives us 45 days to figure it out. 
There’s a learning curve when it comes to wearing the Omnipod, but so far it's been good - except for a few hiccups along the way.
I’ve taken copious amounts of notes - so many notes that I had to divide them up into two posts!
Part one is below and I hope you enjoy!
######
So this happened!
Day 1: Omnipod training with my CDE went well and I'm officially untethered!
Wearing pod on my right arm. It's weird not being tethered to my electronic pancreas ,but in a really great way!
Also, discovered that I walk freakishly close to the edge of door frames.
Seriously, why have I not realized this about myself before?  
Another also, since noticing this Kellyism, I have become better at not slamming into door frames.  
Day Day 2: Experienced absorption issues 27 hours into wearing with perfect numbers up until then. I was the wearing the pod on my arm - the one I kept banging into door frames. 
Called CS and replaced pod. More on that in part 2.
Day 5: I swam in the Atlantic ocean with my pod for the very first time - it was fantastic!
Also, it stayed securely on my person - muddy legs and all. 
Also: AWESOME. 
Actual aerial footage of my and my pod about to
go in for a dip in the Atlantic~
Day 8: I left my PDM/case on the table in a restaurant that I had just exited. 
I immediately noticed after checking my hand bag (to make sure I had my PDM,) and ran back in to retrieve it - and all the while silently praying to the Diabetes Gods that it was still there. It was and I was grateful - it has not happened since. 
Day 9: Wearing the pod on my left arm - it's working well, but I'm aware of my pump whenever I twist to exit my vehicle. 
Day 17: Getting the hang of podding and no longer waking up and reaching to check if my pump is attached to the waistband of my Pajamas. 
Same goes for reaching to disconnect every time I walk towards the bathroom to shower.
Day 35: OK, every once in a while I Still grab my waist band to disconnect before taking a shower - old habits die hard.

Maybe it’s just me
For the first few days, I kept confusing my PDM with my iPhone and whenever I was trying to take a picture of my PDM screen. 
I’d stare at the screen for a few seconds, all confused as to why I couldn’t take a screen shot. 
Unlike an iPhone you can’t take a picture of the PDM screen with said PDM and no matter how hard you try and attempt to press Home button and the nonexistent Silent switch


No matter how hard one tries, you cannot take a
screenshot with your PDM.
But you can customize your PDM~
Day 33 and since I'm being balls out honest, sometimes I still grab my iPhone when I mean to grab my PDM and then wonder "why" and out loud when I press the "Home" button and start to bitch out load because I can’t scroll down.
Then I realize why and I feel like an idiot. 

Spacial Issues
I still have them, but instead of doorknobs and edges issue with pump tubing, arm pods and door frames have become my new jam - literally.  
like I mentioned earlier in the post, for the first few days of podding, I banged my pod arm into my kitchen and bedroom door frames more often than I’d like to admit. 
Now, I'm specially more aware of my surroundings - at least when I'm wearing the pod on my arm. 

Black on Black pump skin 
PDM came with a black Skin. Black PDM + Black Case/ Black Skin means the potential for misplacing is an issue because diabetes or not, I am extremely nearsighted - there's a reason I avoid handbags with black lining and my wallet is not black for a reason - I can't freaking find anything in a blackened handbag - especially a black wallet.
Also, I've put aqua blue K-tape on my black remote control for the same reasons.
My Fix
I have a collection of several brightly colored and insulated, 3 and 3/4 inch X 7 inch, makeup bags. I use one of these bags daily and rotate whenever the mood strikes. 
Currently the one I'm using has owls all over it  - and people stop me every damn day because it's so cute.
 I always put the PDM (and my canister of teststrips/lancets because the PDM also acts as a meter,) back in whatever bag I’m using, ASAP and without fail.
It's now become a full fledged habit - and it didn't take 30 days!

When I go out, I put the PDM, spare pod, test strips,and insulin in said makeup bag, and place in my handbag/work bag. 

Sidebar: Lipstick, eye-drops, my driver’s license and a credit card also fit in the bag along with all of the above mentioned - VERY IMPORTANT.
Also, recently started using bright green skin for the PDM because it brings out my eyes  - but I still bag it~
Owl bag because functional and very cute!
Tune in tomorrow for Part 2, where I break down and get to the nitty gritty re: what I love about podding, as well as the learning curve when it comes to being a Podder~ 

Monday, November 14, 2016

World Diabetes Day 2016

I apologize for the radio silence this past week - there was some stuff going on in my country, the United States - I’ll leave it at that. 
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Today, Monday November 14th, 2016 is Word Diabetes Day - I’ve lived with T1 for 39 years, and I’ve known (and loved,) many people who didn’t survive the diabetes dark ages - or whose lives were severely shortened because of those diabetes dark days. 
We are so damn lucky and blessed! 
I/we survived and are surrounded and inspired daily, by a global diabetes online community. A community that has our backs and keeps fighting for every single person living with diabetes on the planet.
November 14th is also the 125th birthday of Dr. Banting and I keeping thinking of how I wouldn’t be here (and neither would you, or someone you love,)  if Dr. Banting & Company hadn’t discovered insulin. 
And not just me - most of my immediate family wouldn't be here, because my late father was diagnosed with t1 in the early 1950s. 
If insulin hadn’t been discovered and if dad hadn’t had access to it- my father would have died as a very young man - and my branch of the Kunik Family tree would have a been a small twig. 
Same goes for my dad's two younger sister's who were diagnosed in the 1940s - they wouldn't have survived, therefore my cousins never would have been born.

Last night our friend Renza from Diabetogenic in Australia ,broke the news to those of us in this hemisphere, that Google finally dedicated a Google Doodle to our hero Dr. Banting. 
As long as I’ve been a member of the Diabetes Online Community - since 2007 to be exact. My blogaversary was on November 9th - lots of things were going down in the U.S. that day and I didn’t write about this year, but I digress. 
Back to the story, since I became a member of the DOC family in “07,” the DOC has been petitioning for a #WDD Google Doodle - and now we have one!

Dr. Banting and World Diabetes Day are Google Doodlefied! 
Today I will be doing my Big Blue Test , participating in the 5th annual, 24 hour World Diabetes Day, twitter chat #WWDchat16 for those of you who only speak in hashtags. HUGE thanks to Cherise over at DCaf - for making this chat happen!
 I will be hosting the 7pm to 8pm hour tonight :) 
I will make a donation to IDF’s Life For A Child, an d I will do my best to help as many diabetes orgs as I can. 

Speaking of diabetes orgs, Kerri over at sixuntilme has a wonderful breakdown of ways you can help others living with diabetes this month and every month - and how others living with diabetes can help you - click HERE, now.  

We are on this together - now and forever! 

Tuesday, November 1, 2016

November Is National Diabetes Awareness Month - Here's My T1D Footprint - What's Yours?

November is National Diabetes Awareness Month, (#NDAM, for those who only speak in hashtags) - a month where where we "bust diabetes myths and perpetuate diabetes realities," to those sans diabetes. 

And JDRF has created a very cool tool that calculates your t1D footprint. http://www.jdrf.org/t1dlookslikeme/

We spend so much time dealing with our diabetes - now we have an easy way to get our own personal breakdown of our D numbers to help us educate others - and to remind us of how hard we work!
What's your T1D diabetes footprint look like? 

Also, if you live with LADA1.5 or t2, you work damn hard, get your D stats, too! 
I haven't had a day off from my #T1D ind 14,246 days!